Incidental Mutation 'R1728:Hectd4'
ID |
198554 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Hectd4
|
Ensembl Gene |
ENSMUSG00000042744 |
Gene Name |
HECT domain E3 ubiquitin protein ligase 4 |
Synonyms |
Gm15800 |
MMRRC Submission |
039760-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.927)
|
Stock # |
R1728 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
121358282-121506640 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 121439902 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Phenylalanine
at position 1134
(Y1134F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000048345
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042614]
[ENSMUST00000100769]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000042614
AA Change: Y1134F
PolyPhen 2
Score 0.514 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000048345 Gene: ENSMUSG00000042744 AA Change: Y1134F
Domain | Start | End | E-Value | Type |
low complexity region
|
224 |
234 |
N/A |
INTRINSIC |
low complexity region
|
266 |
282 |
N/A |
INTRINSIC |
low complexity region
|
553 |
564 |
N/A |
INTRINSIC |
low complexity region
|
725 |
735 |
N/A |
INTRINSIC |
low complexity region
|
1252 |
1265 |
N/A |
INTRINSIC |
coiled coil region
|
1372 |
1398 |
N/A |
INTRINSIC |
low complexity region
|
1551 |
1562 |
N/A |
INTRINSIC |
low complexity region
|
1725 |
1741 |
N/A |
INTRINSIC |
low complexity region
|
1892 |
1904 |
N/A |
INTRINSIC |
low complexity region
|
2656 |
2666 |
N/A |
INTRINSIC |
low complexity region
|
2857 |
2872 |
N/A |
INTRINSIC |
low complexity region
|
2901 |
2917 |
N/A |
INTRINSIC |
low complexity region
|
2921 |
2933 |
N/A |
INTRINSIC |
low complexity region
|
3232 |
3246 |
N/A |
INTRINSIC |
low complexity region
|
3275 |
3335 |
N/A |
INTRINSIC |
low complexity region
|
3441 |
3448 |
N/A |
INTRINSIC |
low complexity region
|
3473 |
3506 |
N/A |
INTRINSIC |
low complexity region
|
3512 |
3533 |
N/A |
INTRINSIC |
low complexity region
|
3540 |
3554 |
N/A |
INTRINSIC |
low complexity region
|
3794 |
3822 |
N/A |
INTRINSIC |
HECTc
|
4048 |
4412 |
4.78e-11 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000100769
|
SMART Domains |
Protein: ENSMUSP00000098332 Gene: ENSMUSG00000042744
Domain | Start | End | E-Value | Type |
coiled coil region
|
35 |
61 |
N/A |
INTRINSIC |
low complexity region
|
214 |
225 |
N/A |
INTRINSIC |
low complexity region
|
388 |
404 |
N/A |
INTRINSIC |
low complexity region
|
555 |
567 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128514
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000148368
|
Predicted Effect |
unknown
Transcript: ENSMUST00000201669
AA Change: Y494F
|
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.0%
- 20x: 91.4%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 223 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447A16Rik |
G |
A |
15: 37,439,844 (GRCm39) |
|
probably benign |
Het |
Aadat |
A |
G |
8: 60,979,746 (GRCm39) |
T203A |
probably damaging |
Het |
Abca13 |
T |
A |
11: 9,199,680 (GRCm39) |
F104L |
probably benign |
Het |
Acox1 |
T |
A |
11: 116,089,109 (GRCm39) |
|
probably null |
Het |
Adam34l |
T |
C |
8: 44,078,620 (GRCm39) |
N535D |
probably damaging |
Het |
Adamts17 |
C |
T |
7: 66,799,704 (GRCm39) |
R1060* |
probably null |
Het |
Adgrg6 |
T |
C |
10: 14,315,526 (GRCm39) |
T593A |
probably damaging |
Het |
Ankrd12 |
G |
T |
17: 66,291,071 (GRCm39) |
P1454Q |
probably benign |
Het |
Ap2m1 |
T |
A |
16: 20,358,088 (GRCm39) |
N35K |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,401,312 (GRCm39) |
I1111V |
probably benign |
Het |
Atr |
G |
A |
9: 95,779,634 (GRCm39) |
V1331I |
probably benign |
Het |
Bola1 |
C |
T |
3: 96,104,426 (GRCm39) |
G56D |
probably benign |
Het |
Brsk1 |
A |
G |
7: 4,707,218 (GRCm39) |
D257G |
probably damaging |
Het |
C4bp |
C |
G |
1: 130,570,725 (GRCm39) |
V284L |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,046,454 (GRCm39) |
F1761S |
probably benign |
Het |
Camsap2 |
C |
T |
1: 136,209,053 (GRCm39) |
R802Q |
probably benign |
Het |
Cbs |
G |
T |
17: 31,839,923 (GRCm39) |
A337E |
probably benign |
Het |
Ccdc186 |
A |
C |
19: 56,797,652 (GRCm39) |
H306Q |
probably benign |
Het |
Ccdc93 |
T |
C |
1: 121,389,668 (GRCm39) |
V237A |
probably benign |
Het |
Ccdc93 |
C |
T |
1: 121,383,855 (GRCm39) |
P192L |
probably benign |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cd55 |
C |
A |
1: 130,387,370 (GRCm39) |
A143S |
probably benign |
Het |
Cdh19 |
C |
A |
1: 110,821,114 (GRCm39) |
E541D |
probably damaging |
Het |
Cdh20 |
C |
G |
1: 109,993,465 (GRCm39) |
L307V |
possibly damaging |
Het |
Cfh |
C |
T |
1: 140,075,435 (GRCm39) |
V268I |
possibly damaging |
Het |
Cfhr2 |
A |
G |
1: 139,741,180 (GRCm39) |
M265T |
probably benign |
Het |
Cfhr2 |
A |
C |
1: 139,741,197 (GRCm39) |
N259K |
probably benign |
Het |
Chi3l1 |
C |
T |
1: 134,116,267 (GRCm39) |
A250V |
probably damaging |
Het |
Chrnb1 |
C |
A |
11: 69,676,588 (GRCm39) |
D388Y |
probably damaging |
Het |
Clcn1 |
T |
A |
6: 42,276,448 (GRCm39) |
F360Y |
possibly damaging |
Het |
Clgn |
A |
G |
8: 84,149,659 (GRCm39) |
S387G |
probably damaging |
Het |
Cntnap5a |
C |
T |
1: 116,382,873 (GRCm39) |
T1047I |
probably benign |
Het |
Cntnap5a |
C |
A |
1: 116,382,734 (GRCm39) |
L1001I |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,382,831 (GRCm39) |
L1033S |
probably benign |
Het |
Coil |
G |
A |
11: 88,864,802 (GRCm39) |
V10I |
probably damaging |
Het |
Col4a1 |
G |
A |
8: 11,262,712 (GRCm39) |
P1256S |
possibly damaging |
Het |
Copa |
T |
A |
1: 171,939,554 (GRCm39) |
F597Y |
probably benign |
Het |
Crb1 |
G |
A |
1: 139,168,876 (GRCm39) |
P881S |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,170,733 (GRCm39) |
G825R |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,171,155 (GRCm39) |
R684H |
probably benign |
Het |
Crb1 |
T |
C |
1: 139,162,517 (GRCm39) |
M1214V |
probably benign |
Het |
Crb1 |
A |
T |
1: 139,165,360 (GRCm39) |
H921Q |
probably benign |
Het |
Crybg1 |
T |
A |
10: 43,880,015 (GRCm39) |
Q391L |
probably damaging |
Het |
Cspg4 |
G |
T |
9: 56,805,821 (GRCm39) |
V2211L |
probably benign |
Het |
Cxcr4 |
C |
T |
1: 128,517,014 (GRCm39) |
V216I |
probably benign |
Het |
Cyb5r1 |
C |
T |
1: 134,335,405 (GRCm39) |
R147W |
probably damaging |
Het |
Ddx59 |
T |
C |
1: 136,344,791 (GRCm39) |
V154A |
probably benign |
Het |
Dhx30 |
T |
C |
9: 109,927,819 (GRCm39) |
H101R |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 117,880,666 (GRCm39) |
D3818V |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,960,345 (GRCm39) |
C2572Y |
possibly damaging |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dsel |
G |
C |
1: 111,787,724 (GRCm39) |
T937S |
probably benign |
Het |
Dstyk |
C |
T |
1: 132,384,722 (GRCm39) |
L739F |
probably damaging |
Het |
Ehf |
T |
G |
2: 103,104,251 (GRCm39) |
T186P |
possibly damaging |
Het |
En1 |
A |
G |
1: 120,531,350 (GRCm39) |
S197G |
unknown |
Het |
Etnk2 |
C |
A |
1: 133,293,325 (GRCm39) |
D89E |
probably benign |
Het |
Etnk2 |
G |
T |
1: 133,293,503 (GRCm39) |
G149W |
probably damaging |
Het |
Etnk2 |
C |
T |
1: 133,293,554 (GRCm39) |
R166* |
probably null |
Het |
Etnk2 |
G |
A |
1: 133,293,555 (GRCm39) |
R166Q |
probably benign |
Het |
Etnk2 |
T |
A |
1: 133,304,653 (GRCm39) |
V292E |
probably benign |
Het |
Fam187b |
C |
T |
7: 30,688,445 (GRCm39) |
Q268* |
probably null |
Het |
Fam72a |
C |
T |
1: 131,466,633 (GRCm39) |
T139M |
probably benign |
Het |
Fam72a |
T |
C |
1: 131,458,406 (GRCm39) |
I56T |
probably benign |
Het |
Fat3 |
A |
C |
9: 15,907,611 (GRCm39) |
V2797G |
possibly damaging |
Het |
Fcamr |
A |
C |
1: 130,732,364 (GRCm39) |
N117T |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,739,317 (GRCm39) |
I206V |
probably benign |
Het |
Fcamr |
G |
A |
1: 130,740,366 (GRCm39) |
G262S |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,429 (GRCm39) |
I283V |
probably benign |
Het |
Fcamr |
T |
C |
1: 130,740,475 (GRCm39) |
V298A |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,546 (GRCm39) |
M322V |
probably benign |
Het |
Fcamr |
C |
T |
1: 130,740,553 (GRCm39) |
P324L |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,742,334 (GRCm39) |
N574D |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,732,306 (GRCm39) |
R98G |
probably benign |
Het |
Fcmr |
T |
C |
1: 130,806,006 (GRCm39) |
S321P |
probably benign |
Het |
Fcmr |
A |
G |
1: 130,803,711 (GRCm39) |
T172A |
probably benign |
Het |
Fut10 |
T |
A |
8: 31,691,418 (GRCm39) |
S88T |
probably benign |
Het |
Gabarap |
C |
T |
11: 69,882,515 (GRCm39) |
|
probably benign |
Het |
Gli2 |
G |
T |
1: 118,929,774 (GRCm39) |
H44Q |
probably benign |
Het |
Gli2 |
C |
T |
1: 118,795,817 (GRCm39) |
A113T |
possibly damaging |
Het |
Glrx2 |
C |
T |
1: 143,615,478 (GRCm39) |
A27V |
possibly damaging |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gpr25 |
G |
A |
1: 136,188,448 (GRCm39) |
P55L |
probably benign |
Het |
Gse1 |
G |
A |
8: 121,294,992 (GRCm39) |
|
probably benign |
Het |
Heatr4 |
T |
C |
12: 84,014,346 (GRCm39) |
I630M |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,887,666 (GRCm39) |
P2466L |
probably damaging |
Het |
Igfn1 |
C |
T |
1: 135,899,865 (GRCm39) |
R482Q |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,898,149 (GRCm39) |
S806G |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,895,937 (GRCm39) |
A1543V |
probably benign |
Het |
Igfn1 |
C |
T |
1: 135,907,653 (GRCm39) |
A231T |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,910,213 (GRCm39) |
R124W |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,926,363 (GRCm39) |
E29G |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,926,421 (GRCm39) |
I10V |
unknown |
Het |
Ikbke |
T |
C |
1: 131,197,560 (GRCm39) |
S447G |
probably benign |
Het |
Ikbke |
C |
A |
1: 131,193,674 (GRCm39) |
A459S |
probably benign |
Het |
Ildr1 |
A |
T |
16: 36,528,698 (GRCm39) |
T48S |
possibly damaging |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Ipo9 |
CTC |
CTCTTC |
1: 135,314,009 (GRCm39) |
|
probably benign |
Het |
Itprid1 |
T |
C |
6: 55,945,526 (GRCm39) |
F749S |
probably benign |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Kcnh5 |
T |
C |
12: 75,184,465 (GRCm39) |
D86G |
probably benign |
Het |
Kcnt2 |
G |
A |
1: 140,282,285 (GRCm39) |
S90N |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,713 (GRCm39) |
K340E |
probably damaging |
Het |
Kif14 |
G |
A |
1: 136,406,103 (GRCm39) |
A556T |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,418,070 (GRCm39) |
S868G |
probably benign |
Het |
Kif14 |
C |
T |
1: 136,431,169 (GRCm39) |
L1189F |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,443,699 (GRCm39) |
F1291L |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,453,521 (GRCm39) |
V1433A |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,017 (GRCm39) |
N108D |
probably benign |
Het |
Kif1b |
T |
C |
4: 149,272,179 (GRCm39) |
T1541A |
probably damaging |
Het |
Kif21b |
A |
G |
1: 136,087,859 (GRCm39) |
I983V |
possibly damaging |
Het |
Kif26a |
T |
C |
12: 112,143,219 (GRCm39) |
S1158P |
possibly damaging |
Het |
Kmt2d |
A |
G |
15: 98,763,013 (GRCm39) |
C279R |
probably damaging |
Het |
Kpna3 |
T |
A |
14: 61,605,150 (GRCm39) |
E499V |
probably benign |
Het |
Krt16 |
T |
C |
11: 100,138,533 (GRCm39) |
E205G |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,761 (GRCm39) |
R346C |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,119 (GRCm39) |
P132S |
possibly damaging |
Het |
Lax1 |
T |
C |
1: 133,608,307 (GRCm39) |
N145D |
probably benign |
Het |
Lax1 |
G |
A |
1: 133,611,372 (GRCm39) |
P67S |
probably damaging |
Het |
Lax1 |
T |
C |
1: 133,607,716 (GRCm39) |
R342G |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,914,826 (GRCm39) |
V641I |
probably benign |
Het |
Lgr6 |
G |
T |
1: 134,918,373 (GRCm39) |
H263N |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,931,214 (GRCm39) |
S3N |
probably benign |
Het |
Lmod1 |
C |
T |
1: 135,291,811 (GRCm39) |
T222I |
probably benign |
Het |
Mb21d2 |
A |
G |
16: 28,647,173 (GRCm39) |
V267A |
probably benign |
Het |
Mfrp |
A |
G |
9: 44,015,884 (GRCm39) |
T334A |
possibly damaging |
Het |
Morc1 |
T |
A |
16: 48,432,660 (GRCm39) |
D709E |
probably benign |
Het |
Mrgpra2b |
A |
G |
7: 47,114,627 (GRCm39) |
I35T |
probably benign |
Het |
Mroh3 |
G |
C |
1: 136,119,882 (GRCm39) |
Q440E |
possibly damaging |
Het |
Mybph |
C |
T |
1: 134,125,218 (GRCm39) |
R249C |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,392,614 (GRCm39) |
C3206S |
probably damaging |
Het |
Nav1 |
A |
T |
1: 135,512,465 (GRCm39) |
D198E |
possibly damaging |
Het |
Ndufaf7 |
A |
T |
17: 79,245,058 (GRCm39) |
K59M |
probably damaging |
Het |
Necab3 |
T |
C |
2: 154,388,795 (GRCm39) |
S208G |
probably benign |
Het |
Nr5a2 |
C |
A |
1: 136,879,863 (GRCm39) |
R35L |
probably benign |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Optc |
C |
G |
1: 133,832,908 (GRCm39) |
S64T |
probably benign |
Het |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or3a1c |
A |
G |
11: 74,046,802 (GRCm39) |
D274G |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or5m13b |
T |
A |
2: 85,754,466 (GRCm39) |
L285I |
possibly damaging |
Het |
Or8b12i |
A |
T |
9: 20,082,209 (GRCm39) |
Y219* |
probably null |
Het |
Otoa |
T |
C |
7: 120,724,662 (GRCm39) |
V447A |
probably benign |
Het |
Papss1 |
A |
G |
3: 131,311,728 (GRCm39) |
N319D |
probably benign |
Het |
Patj |
G |
A |
4: 98,320,017 (GRCm39) |
G428D |
possibly damaging |
Het |
Pcdhb3 |
G |
A |
18: 37,434,931 (GRCm39) |
G299D |
probably damaging |
Het |
Pcsk4 |
T |
C |
10: 80,159,404 (GRCm39) |
D432G |
probably damaging |
Het |
Pde5a |
G |
T |
3: 122,541,889 (GRCm39) |
L126F |
probably damaging |
Het |
Pigr |
C |
T |
1: 130,772,259 (GRCm39) |
A159V |
possibly damaging |
Het |
Pik3c2b |
C |
T |
1: 132,994,365 (GRCm39) |
P110S |
probably benign |
Het |
Pinx1 |
A |
G |
14: 64,115,559 (GRCm39) |
|
probably null |
Het |
Plec |
C |
A |
15: 76,061,892 (GRCm39) |
E2547* |
probably null |
Het |
Plekha6 |
C |
G |
1: 133,215,584 (GRCm39) |
T792S |
probably benign |
Het |
Ppfia4 |
G |
A |
1: 134,227,059 (GRCm39) |
P1159S |
probably benign |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Prrx1 |
T |
A |
1: 163,089,536 (GRCm39) |
N97I |
probably damaging |
Het |
Ptpn7 |
A |
G |
1: 135,062,213 (GRCm39) |
Q53R |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,035,575 (GRCm39) |
V400A |
probably benign |
Het |
Ptprc |
C |
A |
1: 138,035,562 (GRCm39) |
E402D |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,035,561 (GRCm39) |
S405P |
probably benign |
Het |
Ptprc |
T |
G |
1: 138,027,414 (GRCm39) |
N478T |
probably benign |
Het |
Ptprc |
T |
C |
1: 138,039,992 (GRCm39) |
K212E |
possibly damaging |
Het |
Rab29 |
A |
G |
1: 131,799,848 (GRCm39) |
Q141R |
probably benign |
Het |
Rbsn |
A |
T |
6: 92,167,000 (GRCm39) |
L548Q |
possibly damaging |
Het |
Ren1 |
C |
T |
1: 133,281,975 (GRCm39) |
T32I |
probably benign |
Het |
Ren1 |
T |
A |
1: 133,281,944 (GRCm39) |
W22R |
probably damaging |
Het |
Ren1 |
C |
G |
1: 133,287,745 (GRCm39) |
L360V |
probably benign |
Het |
Ren1 |
A |
T |
1: 133,287,721 (GRCm39) |
N352Y |
probably benign |
Het |
Ren1 |
A |
T |
1: 133,286,817 (GRCm39) |
E315D |
probably benign |
Het |
Ren1 |
C |
A |
1: 133,286,720 (GRCm39) |
|
probably null |
Het |
Ren1 |
A |
C |
1: 133,284,195 (GRCm39) |
K187Q |
probably benign |
Het |
Rnpep |
C |
T |
1: 135,190,834 (GRCm39) |
A571T |
possibly damaging |
Het |
Rnpep |
G |
C |
1: 135,211,715 (GRCm39) |
A11G |
probably benign |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Ro60 |
C |
T |
1: 143,635,752 (GRCm39) |
V465I |
probably benign |
Het |
Ryr2 |
C |
T |
13: 11,602,308 (GRCm39) |
V4525M |
possibly damaging |
Het |
Sctr |
G |
A |
1: 119,990,987 (GRCm39) |
S440N |
possibly damaging |
Het |
Sctr |
T |
C |
1: 119,959,386 (GRCm39) |
F110L |
probably benign |
Het |
Serpinb10 |
C |
T |
1: 107,466,203 (GRCm39) |
S63F |
probably damaging |
Het |
Serpinb2 |
G |
A |
1: 107,443,365 (GRCm39) |
A55T |
probably damaging |
Het |
Serpinb2 |
A |
C |
1: 107,452,273 (GRCm39) |
S284R |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,624 (GRCm39) |
T259I |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,620 (GRCm39) |
H258Y |
probably benign |
Het |
Serpinb2 |
C |
A |
1: 107,451,564 (GRCm39) |
A239E |
probably benign |
Het |
Serpinb8 |
A |
G |
1: 107,525,257 (GRCm39) |
S20G |
probably benign |
Het |
Serpinb8 |
A |
C |
1: 107,534,734 (GRCm39) |
L268F |
probably benign |
Het |
Serpinb8 |
G |
A |
1: 107,526,684 (GRCm39) |
A75T |
probably benign |
Het |
Sis |
A |
T |
3: 72,872,978 (GRCm39) |
C53* |
probably null |
Het |
Slc13a5 |
C |
T |
11: 72,157,285 (GRCm39) |
|
probably null |
Het |
Slc26a9 |
C |
T |
1: 131,691,608 (GRCm39) |
A617V |
probably benign |
Het |
Slc26a9 |
C |
A |
1: 131,693,750 (GRCm39) |
R747S |
probably benign |
Het |
Slc9a8 |
T |
C |
2: 167,266,065 (GRCm39) |
F14S |
probably benign |
Het |
Spock3 |
T |
C |
8: 63,802,011 (GRCm39) |
L330P |
probably damaging |
Het |
Stab2 |
T |
G |
10: 86,773,903 (GRCm39) |
R809S |
probably benign |
Het |
Steap3 |
T |
C |
1: 120,155,480 (GRCm39) |
N493S |
probably benign |
Het |
Steap3 |
G |
A |
1: 120,162,108 (GRCm39) |
A350V |
probably benign |
Het |
Tecta |
G |
A |
9: 42,303,218 (GRCm39) |
T138I |
probably benign |
Het |
Thsd7b |
G |
C |
1: 129,605,920 (GRCm39) |
A554P |
probably benign |
Het |
Thsd7b |
A |
C |
1: 130,044,368 (GRCm39) |
Q1116P |
probably benign |
Het |
Thsd7b |
C |
T |
1: 129,556,628 (GRCm39) |
T328I |
probably damaging |
Het |
Thsd7b |
T |
A |
1: 129,595,674 (GRCm39) |
F498Y |
probably benign |
Het |
Tnnt2 |
C |
T |
1: 135,773,244 (GRCm39) |
|
probably benign |
Het |
Traf7 |
A |
G |
17: 24,731,353 (GRCm39) |
F228L |
probably damaging |
Het |
Trhr |
A |
G |
15: 44,060,549 (GRCm39) |
E23G |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,577,968 (GRCm39) |
T779A |
probably benign |
Het |
Tusc2 |
A |
T |
9: 107,441,830 (GRCm39) |
I68F |
probably damaging |
Het |
Ube2t |
C |
T |
1: 134,899,905 (GRCm39) |
A149V |
probably benign |
Het |
Upf2 |
A |
T |
2: 6,032,261 (GRCm39) |
S191C |
probably damaging |
Het |
Usp24 |
A |
G |
4: 106,217,618 (GRCm39) |
N447S |
possibly damaging |
Het |
Usp42 |
T |
C |
5: 143,700,381 (GRCm39) |
D1214G |
probably damaging |
Het |
Vcam1 |
T |
A |
3: 115,908,164 (GRCm39) |
I633L |
probably benign |
Het |
Vmn2r73 |
T |
C |
7: 85,507,086 (GRCm39) |
Y742C |
probably damaging |
Het |
Vmn2r81 |
C |
A |
10: 79,106,489 (GRCm39) |
T489K |
probably benign |
Het |
Ypel1 |
C |
G |
16: 16,907,283 (GRCm39) |
|
probably benign |
Het |
Zan |
C |
A |
5: 137,413,280 (GRCm39) |
|
probably benign |
Het |
Zc3h11a |
C |
T |
1: 133,552,359 (GRCm39) |
V583I |
probably benign |
Het |
Zc3h11a |
G |
A |
1: 133,549,892 (GRCm39) |
P695S |
probably benign |
Het |
Zfp616 |
A |
C |
11: 73,976,597 (GRCm39) |
K955N |
probably damaging |
Het |
Zfyve9 |
A |
C |
4: 108,575,698 (GRCm39) |
V461G |
possibly damaging |
Het |
Zp3r |
A |
G |
1: 130,524,551 (GRCm39) |
L164P |
probably benign |
Het |
Zp3r |
C |
A |
1: 130,547,151 (GRCm39) |
E8D |
possibly damaging |
Het |
|
Other mutations in Hectd4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00156:Hectd4
|
APN |
5 |
121,501,933 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL00976:Hectd4
|
APN |
5 |
121,487,169 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01085:Hectd4
|
APN |
5 |
121,469,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01112:Hectd4
|
APN |
5 |
121,445,013 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01402:Hectd4
|
APN |
5 |
121,477,480 (GRCm39) |
splice site |
probably benign |
|
IGL01474:Hectd4
|
APN |
5 |
121,474,712 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01503:Hectd4
|
APN |
5 |
121,456,714 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01548:Hectd4
|
APN |
5 |
121,502,723 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01656:Hectd4
|
APN |
5 |
121,460,763 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01756:Hectd4
|
APN |
5 |
121,482,887 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01819:Hectd4
|
APN |
5 |
121,466,481 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02080:Hectd4
|
APN |
5 |
121,504,669 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02488:Hectd4
|
APN |
5 |
121,430,150 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02490:Hectd4
|
APN |
5 |
121,456,676 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02558:Hectd4
|
APN |
5 |
121,482,848 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02626:Hectd4
|
APN |
5 |
121,491,944 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02649:Hectd4
|
APN |
5 |
121,487,465 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02736:Hectd4
|
APN |
5 |
121,480,782 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02861:Hectd4
|
APN |
5 |
121,445,067 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02880:Hectd4
|
APN |
5 |
121,503,116 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02889:Hectd4
|
APN |
5 |
121,503,116 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02953:Hectd4
|
APN |
5 |
121,503,116 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02969:Hectd4
|
APN |
5 |
121,503,116 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03031:Hectd4
|
APN |
5 |
121,486,857 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL03066:Hectd4
|
APN |
5 |
121,503,116 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03160:Hectd4
|
APN |
5 |
121,397,942 (GRCm39) |
missense |
probably benign |
|
IGL03181:Hectd4
|
APN |
5 |
121,492,021 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03265:Hectd4
|
APN |
5 |
121,398,002 (GRCm39) |
splice site |
probably benign |
|
IGL03375:Hectd4
|
APN |
5 |
121,466,445 (GRCm39) |
missense |
possibly damaging |
0.72 |
Achilles
|
UTSW |
5 |
121,445,444 (GRCm39) |
nonsense |
probably null |
|
agamemnon
|
UTSW |
5 |
121,391,921 (GRCm39) |
splice site |
probably benign |
|
clymnestra
|
UTSW |
5 |
121,472,438 (GRCm39) |
missense |
possibly damaging |
0.86 |
hector
|
UTSW |
5 |
121,453,500 (GRCm39) |
missense |
probably damaging |
1.00 |
helen
|
UTSW |
5 |
121,448,726 (GRCm39) |
missense |
probably damaging |
0.97 |
Merriwether
|
UTSW |
5 |
121,491,614 (GRCm39) |
missense |
possibly damaging |
0.53 |
PIT4466001:Hectd4
|
UTSW |
5 |
121,471,123 (GRCm39) |
critical splice donor site |
probably null |
|
R0018:Hectd4
|
UTSW |
5 |
121,392,242 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0024:Hectd4
|
UTSW |
5 |
121,446,639 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0030:Hectd4
|
UTSW |
5 |
121,400,651 (GRCm39) |
nonsense |
probably null |
|
R0080:Hectd4
|
UTSW |
5 |
121,487,435 (GRCm39) |
missense |
probably benign |
0.18 |
R0110:Hectd4
|
UTSW |
5 |
121,443,736 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0110:Hectd4
|
UTSW |
5 |
121,419,959 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0115:Hectd4
|
UTSW |
5 |
121,433,569 (GRCm39) |
splice site |
probably benign |
|
R0128:Hectd4
|
UTSW |
5 |
121,487,306 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0131:Hectd4
|
UTSW |
5 |
121,471,087 (GRCm39) |
missense |
probably benign |
0.44 |
R0131:Hectd4
|
UTSW |
5 |
121,471,087 (GRCm39) |
missense |
probably benign |
0.44 |
R0132:Hectd4
|
UTSW |
5 |
121,471,087 (GRCm39) |
missense |
probably benign |
0.44 |
R0244:Hectd4
|
UTSW |
5 |
121,467,668 (GRCm39) |
missense |
probably benign |
0.33 |
R0281:Hectd4
|
UTSW |
5 |
121,392,314 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0329:Hectd4
|
UTSW |
5 |
121,397,927 (GRCm39) |
missense |
probably benign |
|
R0410:Hectd4
|
UTSW |
5 |
121,424,329 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0422:Hectd4
|
UTSW |
5 |
121,481,145 (GRCm39) |
splice site |
probably null |
|
R0442:Hectd4
|
UTSW |
5 |
121,462,045 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0449:Hectd4
|
UTSW |
5 |
121,502,653 (GRCm39) |
splice site |
probably null |
|
R0469:Hectd4
|
UTSW |
5 |
121,443,736 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0469:Hectd4
|
UTSW |
5 |
121,419,959 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0481:Hectd4
|
UTSW |
5 |
121,433,569 (GRCm39) |
splice site |
probably benign |
|
R0510:Hectd4
|
UTSW |
5 |
121,443,736 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0510:Hectd4
|
UTSW |
5 |
121,419,959 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0520:Hectd4
|
UTSW |
5 |
121,469,770 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0534:Hectd4
|
UTSW |
5 |
121,486,539 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0603:Hectd4
|
UTSW |
5 |
121,442,400 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0617:Hectd4
|
UTSW |
5 |
121,481,295 (GRCm39) |
splice site |
probably benign |
|
R0622:Hectd4
|
UTSW |
5 |
121,486,688 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0626:Hectd4
|
UTSW |
5 |
121,415,887 (GRCm39) |
missense |
probably benign |
0.18 |
R0708:Hectd4
|
UTSW |
5 |
121,424,526 (GRCm39) |
critical splice donor site |
probably null |
|
R0710:Hectd4
|
UTSW |
5 |
121,474,691 (GRCm39) |
missense |
probably benign |
0.08 |
R0763:Hectd4
|
UTSW |
5 |
121,445,096 (GRCm39) |
unclassified |
probably benign |
|
R0764:Hectd4
|
UTSW |
5 |
121,424,832 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1123:Hectd4
|
UTSW |
5 |
121,424,799 (GRCm39) |
missense |
probably damaging |
0.96 |
R1129:Hectd4
|
UTSW |
5 |
121,448,662 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1204:Hectd4
|
UTSW |
5 |
121,488,548 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1237:Hectd4
|
UTSW |
5 |
121,459,570 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1257:Hectd4
|
UTSW |
5 |
121,456,687 (GRCm39) |
nonsense |
probably null |
|
R1391:Hectd4
|
UTSW |
5 |
121,491,758 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1395:Hectd4
|
UTSW |
5 |
121,466,576 (GRCm39) |
critical splice donor site |
probably null |
|
R1468:Hectd4
|
UTSW |
5 |
121,487,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1468:Hectd4
|
UTSW |
5 |
121,487,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1545:Hectd4
|
UTSW |
5 |
121,462,019 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1553:Hectd4
|
UTSW |
5 |
121,487,322 (GRCm39) |
missense |
probably benign |
0.00 |
R1572:Hectd4
|
UTSW |
5 |
121,439,941 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1662:Hectd4
|
UTSW |
5 |
121,455,308 (GRCm39) |
missense |
probably benign |
0.01 |
R1705:Hectd4
|
UTSW |
5 |
121,436,167 (GRCm39) |
missense |
probably benign |
|
R1715:Hectd4
|
UTSW |
5 |
121,482,881 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1736:Hectd4
|
UTSW |
5 |
121,487,593 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1768:Hectd4
|
UTSW |
5 |
121,496,366 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1775:Hectd4
|
UTSW |
5 |
121,429,254 (GRCm39) |
splice site |
probably benign |
|
R1784:Hectd4
|
UTSW |
5 |
121,439,902 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1843:Hectd4
|
UTSW |
5 |
121,435,243 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1914:Hectd4
|
UTSW |
5 |
121,460,357 (GRCm39) |
missense |
probably benign |
0.08 |
R1915:Hectd4
|
UTSW |
5 |
121,460,357 (GRCm39) |
missense |
probably benign |
0.08 |
R2024:Hectd4
|
UTSW |
5 |
121,419,981 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2103:Hectd4
|
UTSW |
5 |
121,493,692 (GRCm39) |
missense |
probably benign |
0.04 |
R2108:Hectd4
|
UTSW |
5 |
121,471,487 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2124:Hectd4
|
UTSW |
5 |
121,456,702 (GRCm39) |
missense |
probably damaging |
0.97 |
R2150:Hectd4
|
UTSW |
5 |
121,391,921 (GRCm39) |
splice site |
probably benign |
|
R2192:Hectd4
|
UTSW |
5 |
121,453,206 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2301:Hectd4
|
UTSW |
5 |
121,491,600 (GRCm39) |
missense |
probably benign |
0.18 |
R2324:Hectd4
|
UTSW |
5 |
121,453,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R2331:Hectd4
|
UTSW |
5 |
121,458,089 (GRCm39) |
missense |
probably benign |
0.05 |
R2504:Hectd4
|
UTSW |
5 |
121,402,030 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2504:Hectd4
|
UTSW |
5 |
121,358,683 (GRCm39) |
missense |
unknown |
|
R2904:Hectd4
|
UTSW |
5 |
121,430,787 (GRCm39) |
splice site |
probably benign |
|
R3843:Hectd4
|
UTSW |
5 |
121,397,936 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3934:Hectd4
|
UTSW |
5 |
121,458,164 (GRCm39) |
critical splice donor site |
probably null |
|
R3944:Hectd4
|
UTSW |
5 |
121,441,588 (GRCm39) |
splice site |
probably benign |
|
R4133:Hectd4
|
UTSW |
5 |
121,415,897 (GRCm39) |
critical splice donor site |
probably null |
|
R4271:Hectd4
|
UTSW |
5 |
121,358,567 (GRCm39) |
small deletion |
probably benign |
|
R4413:Hectd4
|
UTSW |
5 |
121,488,544 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4456:Hectd4
|
UTSW |
5 |
121,446,334 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4489:Hectd4
|
UTSW |
5 |
121,424,320 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4539:Hectd4
|
UTSW |
5 |
121,452,970 (GRCm39) |
nonsense |
probably null |
|
R4564:Hectd4
|
UTSW |
5 |
121,488,494 (GRCm39) |
missense |
probably benign |
0.33 |
R4582:Hectd4
|
UTSW |
5 |
121,424,482 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4629:Hectd4
|
UTSW |
5 |
121,435,266 (GRCm39) |
missense |
probably benign |
0.01 |
R4633:Hectd4
|
UTSW |
5 |
121,487,279 (GRCm39) |
missense |
probably benign |
0.33 |
R4643:Hectd4
|
UTSW |
5 |
121,487,118 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4679:Hectd4
|
UTSW |
5 |
121,463,314 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4681:Hectd4
|
UTSW |
5 |
121,441,678 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4734:Hectd4
|
UTSW |
5 |
121,480,040 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4739:Hectd4
|
UTSW |
5 |
121,486,505 (GRCm39) |
missense |
probably benign |
|
R4781:Hectd4
|
UTSW |
5 |
121,444,170 (GRCm39) |
critical splice donor site |
probably null |
|
R4860:Hectd4
|
UTSW |
5 |
121,443,881 (GRCm39) |
missense |
probably benign |
0.04 |
R4860:Hectd4
|
UTSW |
5 |
121,443,881 (GRCm39) |
missense |
probably benign |
0.04 |
R4869:Hectd4
|
UTSW |
5 |
121,460,735 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4909:Hectd4
|
UTSW |
5 |
121,401,954 (GRCm39) |
missense |
probably benign |
0.18 |
R4922:Hectd4
|
UTSW |
5 |
121,497,378 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4925:Hectd4
|
UTSW |
5 |
121,460,753 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5004:Hectd4
|
UTSW |
5 |
121,467,628 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5004:Hectd4
|
UTSW |
5 |
121,466,262 (GRCm39) |
splice site |
probably null |
|
R5129:Hectd4
|
UTSW |
5 |
121,481,573 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5217:Hectd4
|
UTSW |
5 |
121,491,614 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5267:Hectd4
|
UTSW |
5 |
121,482,887 (GRCm39) |
missense |
probably benign |
0.28 |
R5344:Hectd4
|
UTSW |
5 |
121,481,739 (GRCm39) |
missense |
probably benign |
0.28 |
R5345:Hectd4
|
UTSW |
5 |
121,402,037 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5347:Hectd4
|
UTSW |
5 |
121,442,511 (GRCm39) |
missense |
probably benign |
0.33 |
R5360:Hectd4
|
UTSW |
5 |
121,453,464 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5363:Hectd4
|
UTSW |
5 |
121,448,666 (GRCm39) |
missense |
probably benign |
0.04 |
R5445:Hectd4
|
UTSW |
5 |
121,404,337 (GRCm39) |
missense |
probably benign |
0.00 |
R5479:Hectd4
|
UTSW |
5 |
121,445,011 (GRCm39) |
missense |
probably benign |
|
R5507:Hectd4
|
UTSW |
5 |
121,419,164 (GRCm39) |
missense |
unknown |
|
R5552:Hectd4
|
UTSW |
5 |
121,480,914 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5691:Hectd4
|
UTSW |
5 |
121,486,878 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5745:Hectd4
|
UTSW |
5 |
121,491,565 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5757:Hectd4
|
UTSW |
5 |
121,486,682 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5845:Hectd4
|
UTSW |
5 |
121,445,587 (GRCm39) |
critical splice donor site |
probably null |
|
R5869:Hectd4
|
UTSW |
5 |
121,481,288 (GRCm39) |
critical splice donor site |
probably null |
|
R5913:Hectd4
|
UTSW |
5 |
121,462,037 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5920:Hectd4
|
UTSW |
5 |
121,446,334 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5943:Hectd4
|
UTSW |
5 |
121,460,357 (GRCm39) |
missense |
probably benign |
0.01 |
R6219:Hectd4
|
UTSW |
5 |
121,446,941 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6250:Hectd4
|
UTSW |
5 |
121,477,561 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6301:Hectd4
|
UTSW |
5 |
121,392,283 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6428:Hectd4
|
UTSW |
5 |
121,488,508 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6446:Hectd4
|
UTSW |
5 |
121,472,438 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6453:Hectd4
|
UTSW |
5 |
121,488,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R6513:Hectd4
|
UTSW |
5 |
121,494,259 (GRCm39) |
splice site |
probably null |
|
R6540:Hectd4
|
UTSW |
5 |
121,441,634 (GRCm39) |
missense |
probably benign |
0.33 |
R6706:Hectd4
|
UTSW |
5 |
121,458,147 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6720:Hectd4
|
UTSW |
5 |
121,445,444 (GRCm39) |
nonsense |
probably null |
|
R6736:Hectd4
|
UTSW |
5 |
121,415,788 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6776:Hectd4
|
UTSW |
5 |
121,491,574 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7033:Hectd4
|
UTSW |
5 |
121,502,631 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7038:Hectd4
|
UTSW |
5 |
121,437,660 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7175:Hectd4
|
UTSW |
5 |
121,411,692 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7180:Hectd4
|
UTSW |
5 |
121,446,405 (GRCm39) |
missense |
probably benign |
0.01 |
R7234:Hectd4
|
UTSW |
5 |
121,467,136 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7253:Hectd4
|
UTSW |
5 |
121,452,944 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7349:Hectd4
|
UTSW |
5 |
121,448,726 (GRCm39) |
missense |
probably damaging |
0.97 |
R7450:Hectd4
|
UTSW |
5 |
121,419,995 (GRCm39) |
missense |
probably benign |
0.00 |
R7467:Hectd4
|
UTSW |
5 |
121,462,024 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7475:Hectd4
|
UTSW |
5 |
121,496,196 (GRCm39) |
splice site |
probably null |
|
R7482:Hectd4
|
UTSW |
5 |
121,501,941 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7512:Hectd4
|
UTSW |
5 |
121,435,172 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7525:Hectd4
|
UTSW |
5 |
121,481,728 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7559:Hectd4
|
UTSW |
5 |
121,453,573 (GRCm39) |
splice site |
probably null |
|
R7560:Hectd4
|
UTSW |
5 |
121,392,405 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7561:Hectd4
|
UTSW |
5 |
121,429,288 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7576:Hectd4
|
UTSW |
5 |
121,487,522 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7584:Hectd4
|
UTSW |
5 |
121,456,798 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7648:Hectd4
|
UTSW |
5 |
121,392,434 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7663:Hectd4
|
UTSW |
5 |
121,462,094 (GRCm39) |
missense |
probably benign |
0.06 |
R7692:Hectd4
|
UTSW |
5 |
121,459,627 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7725:Hectd4
|
UTSW |
5 |
121,358,680 (GRCm39) |
missense |
unknown |
|
R7731:Hectd4
|
UTSW |
5 |
121,445,077 (GRCm39) |
missense |
probably benign |
0.00 |
R7732:Hectd4
|
UTSW |
5 |
121,474,692 (GRCm39) |
missense |
probably benign |
0.14 |
R7782:Hectd4
|
UTSW |
5 |
121,443,784 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7854:Hectd4
|
UTSW |
5 |
121,467,631 (GRCm39) |
missense |
probably benign |
0.27 |
R7898:Hectd4
|
UTSW |
5 |
121,469,880 (GRCm39) |
missense |
probably benign |
0.18 |
R7910:Hectd4
|
UTSW |
5 |
121,392,291 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7962:Hectd4
|
UTSW |
5 |
121,448,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R8003:Hectd4
|
UTSW |
5 |
121,477,581 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8098:Hectd4
|
UTSW |
5 |
121,459,461 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8110:Hectd4
|
UTSW |
5 |
121,471,012 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8118:Hectd4
|
UTSW |
5 |
121,424,439 (GRCm39) |
missense |
probably benign |
0.33 |
R8171:Hectd4
|
UTSW |
5 |
121,456,819 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8234:Hectd4
|
UTSW |
5 |
121,477,607 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8289:Hectd4
|
UTSW |
5 |
121,404,424 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8292:Hectd4
|
UTSW |
5 |
121,455,288 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8348:Hectd4
|
UTSW |
5 |
121,358,319 (GRCm39) |
start gained |
probably benign |
|
R8397:Hectd4
|
UTSW |
5 |
121,397,957 (GRCm39) |
missense |
probably damaging |
0.98 |
R8436:Hectd4
|
UTSW |
5 |
121,446,421 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8436:Hectd4
|
UTSW |
5 |
121,481,210 (GRCm39) |
missense |
probably benign |
0.00 |
R8443:Hectd4
|
UTSW |
5 |
121,467,172 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8448:Hectd4
|
UTSW |
5 |
121,358,319 (GRCm39) |
start gained |
probably benign |
|
R8516:Hectd4
|
UTSW |
5 |
121,487,073 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8519:Hectd4
|
UTSW |
5 |
121,442,489 (GRCm39) |
nonsense |
probably null |
|
R8553:Hectd4
|
UTSW |
5 |
121,491,661 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8557:Hectd4
|
UTSW |
5 |
121,448,714 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8725:Hectd4
|
UTSW |
5 |
121,488,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R8751:Hectd4
|
UTSW |
5 |
121,501,838 (GRCm39) |
nonsense |
probably null |
|
R8769:Hectd4
|
UTSW |
5 |
121,419,936 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8803:Hectd4
|
UTSW |
5 |
121,461,994 (GRCm39) |
missense |
probably benign |
0.01 |
R8887:Hectd4
|
UTSW |
5 |
121,433,541 (GRCm39) |
missense |
probably benign |
0.44 |
R8982:Hectd4
|
UTSW |
5 |
121,466,305 (GRCm39) |
missense |
probably benign |
0.02 |
R8988:Hectd4
|
UTSW |
5 |
121,415,819 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8991:Hectd4
|
UTSW |
5 |
121,496,347 (GRCm39) |
missense |
probably benign |
0.33 |
R8994:Hectd4
|
UTSW |
5 |
121,441,629 (GRCm39) |
missense |
probably benign |
0.33 |
R8995:Hectd4
|
UTSW |
5 |
121,392,422 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9049:Hectd4
|
UTSW |
5 |
121,451,955 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9093:Hectd4
|
UTSW |
5 |
121,411,677 (GRCm39) |
missense |
probably benign |
0.14 |
R9106:Hectd4
|
UTSW |
5 |
121,467,619 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9137:Hectd4
|
UTSW |
5 |
121,496,238 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9146:Hectd4
|
UTSW |
5 |
121,487,097 (GRCm39) |
missense |
probably benign |
0.33 |
R9154:Hectd4
|
UTSW |
5 |
121,391,967 (GRCm39) |
missense |
|
|
R9162:Hectd4
|
UTSW |
5 |
121,445,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9166:Hectd4
|
UTSW |
5 |
121,446,690 (GRCm39) |
missense |
probably damaging |
0.96 |
R9183:Hectd4
|
UTSW |
5 |
121,437,551 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9207:Hectd4
|
UTSW |
5 |
121,433,496 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9291:Hectd4
|
UTSW |
5 |
121,487,028 (GRCm39) |
missense |
probably benign |
0.14 |
R9300:Hectd4
|
UTSW |
5 |
121,486,952 (GRCm39) |
missense |
probably benign |
0.33 |
R9314:Hectd4
|
UTSW |
5 |
121,437,708 (GRCm39) |
critical splice donor site |
probably null |
|
R9381:Hectd4
|
UTSW |
5 |
121,472,492 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9432:Hectd4
|
UTSW |
5 |
121,460,864 (GRCm39) |
missense |
probably benign |
0.01 |
R9491:Hectd4
|
UTSW |
5 |
121,452,981 (GRCm39) |
missense |
probably damaging |
0.97 |
R9532:Hectd4
|
UTSW |
5 |
121,502,616 (GRCm39) |
missense |
probably benign |
0.00 |
R9557:Hectd4
|
UTSW |
5 |
121,459,617 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9561:Hectd4
|
UTSW |
5 |
121,472,532 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9593:Hectd4
|
UTSW |
5 |
121,424,844 (GRCm39) |
nonsense |
probably null |
|
R9704:Hectd4
|
UTSW |
5 |
121,448,744 (GRCm39) |
missense |
probably benign |
0.00 |
R9705:Hectd4
|
UTSW |
5 |
121,448,744 (GRCm39) |
missense |
probably benign |
0.00 |
R9712:Hectd4
|
UTSW |
5 |
121,448,744 (GRCm39) |
missense |
probably benign |
0.00 |
R9713:Hectd4
|
UTSW |
5 |
121,448,744 (GRCm39) |
missense |
probably benign |
0.00 |
R9726:Hectd4
|
UTSW |
5 |
121,448,744 (GRCm39) |
missense |
probably benign |
0.00 |
R9732:Hectd4
|
UTSW |
5 |
121,392,254 (GRCm39) |
nonsense |
probably null |
|
R9750:Hectd4
|
UTSW |
5 |
121,448,744 (GRCm39) |
missense |
probably benign |
0.00 |
R9752:Hectd4
|
UTSW |
5 |
121,472,415 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9752:Hectd4
|
UTSW |
5 |
121,448,744 (GRCm39) |
missense |
probably benign |
0.00 |
R9772:Hectd4
|
UTSW |
5 |
121,448,744 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Hectd4
|
UTSW |
5 |
121,487,700 (GRCm39) |
missense |
probably benign |
0.04 |
X0027:Hectd4
|
UTSW |
5 |
121,459,467 (GRCm39) |
missense |
probably benign |
0.27 |
Z1088:Hectd4
|
UTSW |
5 |
121,433,566 (GRCm39) |
splice site |
probably null |
|
Z1177:Hectd4
|
UTSW |
5 |
121,496,383 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- GATCTTAGTGTCCCTGTGCCAACC -3'
(R):5'- CCATACCAATGTGGCCCTAACTAGC -3'
Sequencing Primer
(F):5'- TACCAGGGTCTGGCTATAAATG -3'
(R):5'- GTGGCCCTAACTAGCTAACTATGTG -3'
|
Posted On |
2014-05-23 |