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 |
Hectd4 |
A |
T |
5: 121,439,902 (GRCm39) |
Y1134F |
possibly damaging |
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 |
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 Tecta |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00466:Tecta
|
APN |
9 |
42,243,844 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00925:Tecta
|
APN |
9 |
42,286,331 (GRCm39) |
missense |
probably benign |
|
IGL00960:Tecta
|
APN |
9 |
42,270,376 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL00974:Tecta
|
APN |
9 |
42,242,670 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01070:Tecta
|
APN |
9 |
42,306,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01284:Tecta
|
APN |
9 |
42,256,916 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01324:Tecta
|
APN |
9 |
42,256,727 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01694:Tecta
|
APN |
9 |
42,278,475 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01861:Tecta
|
APN |
9 |
42,284,658 (GRCm39) |
missense |
probably benign |
|
IGL02010:Tecta
|
APN |
9 |
42,248,489 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02397:Tecta
|
APN |
9 |
42,306,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03031:Tecta
|
APN |
9 |
42,256,789 (GRCm39) |
missense |
probably benign |
|
IGL03208:Tecta
|
APN |
9 |
42,248,396 (GRCm39) |
splice site |
probably benign |
|
IGL03249:Tecta
|
APN |
9 |
42,303,182 (GRCm39) |
missense |
probably benign |
0.20 |
cover
|
UTSW |
9 |
42,255,183 (GRCm39) |
missense |
probably benign |
0.05 |
lid
|
UTSW |
9 |
42,284,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R0004:Tecta
|
UTSW |
9 |
42,256,774 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0045:Tecta
|
UTSW |
9 |
42,286,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R0045:Tecta
|
UTSW |
9 |
42,286,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Tecta
|
UTSW |
9 |
42,263,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Tecta
|
UTSW |
9 |
42,278,524 (GRCm39) |
missense |
probably benign |
0.00 |
R0157:Tecta
|
UTSW |
9 |
42,286,307 (GRCm39) |
missense |
probably benign |
|
R0180:Tecta
|
UTSW |
9 |
42,278,109 (GRCm39) |
missense |
probably benign |
|
R0299:Tecta
|
UTSW |
9 |
42,263,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R0345:Tecta
|
UTSW |
9 |
42,295,514 (GRCm39) |
missense |
probably damaging |
0.98 |
R0370:Tecta
|
UTSW |
9 |
42,278,100 (GRCm39) |
missense |
probably benign |
|
R0465:Tecta
|
UTSW |
9 |
42,270,714 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0466:Tecta
|
UTSW |
9 |
42,284,369 (GRCm39) |
missense |
probably benign |
|
R0479:Tecta
|
UTSW |
9 |
42,249,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R0498:Tecta
|
UTSW |
9 |
42,288,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R0499:Tecta
|
UTSW |
9 |
42,263,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R0519:Tecta
|
UTSW |
9 |
42,259,188 (GRCm39) |
splice site |
probably benign |
|
R0584:Tecta
|
UTSW |
9 |
42,259,204 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0589:Tecta
|
UTSW |
9 |
42,256,930 (GRCm39) |
missense |
probably benign |
0.01 |
R0607:Tecta
|
UTSW |
9 |
42,299,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Tecta
|
UTSW |
9 |
42,295,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R0905:Tecta
|
UTSW |
9 |
42,250,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R1216:Tecta
|
UTSW |
9 |
42,289,203 (GRCm39) |
missense |
probably benign |
0.44 |
R1239:Tecta
|
UTSW |
9 |
42,243,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Tecta
|
UTSW |
9 |
42,243,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R1553:Tecta
|
UTSW |
9 |
42,259,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Tecta
|
UTSW |
9 |
42,270,597 (GRCm39) |
missense |
probably damaging |
0.96 |
R1729:Tecta
|
UTSW |
9 |
42,303,218 (GRCm39) |
missense |
probably benign |
0.12 |
R1762:Tecta
|
UTSW |
9 |
42,286,605 (GRCm39) |
missense |
probably benign |
0.30 |
R1778:Tecta
|
UTSW |
9 |
42,254,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Tecta
|
UTSW |
9 |
42,289,345 (GRCm39) |
missense |
probably benign |
|
R1796:Tecta
|
UTSW |
9 |
42,295,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Tecta
|
UTSW |
9 |
42,303,320 (GRCm39) |
missense |
probably damaging |
0.97 |
R1871:Tecta
|
UTSW |
9 |
42,248,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R1871:Tecta
|
UTSW |
9 |
42,248,472 (GRCm39) |
missense |
probably damaging |
0.98 |
R1911:Tecta
|
UTSW |
9 |
42,249,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Tecta
|
UTSW |
9 |
42,248,575 (GRCm39) |
nonsense |
probably null |
|
R2135:Tecta
|
UTSW |
9 |
42,251,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R2171:Tecta
|
UTSW |
9 |
42,270,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R2220:Tecta
|
UTSW |
9 |
42,303,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R2372:Tecta
|
UTSW |
9 |
42,299,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R2570:Tecta
|
UTSW |
9 |
42,243,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R2939:Tecta
|
UTSW |
9 |
42,289,290 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2940:Tecta
|
UTSW |
9 |
42,289,290 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3081:Tecta
|
UTSW |
9 |
42,289,290 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3407:Tecta
|
UTSW |
9 |
42,249,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Tecta
|
UTSW |
9 |
42,303,402 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3771:Tecta
|
UTSW |
9 |
42,242,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R3772:Tecta
|
UTSW |
9 |
42,242,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Tecta
|
UTSW |
9 |
42,242,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R3832:Tecta
|
UTSW |
9 |
42,250,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4378:Tecta
|
UTSW |
9 |
42,278,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R4480:Tecta
|
UTSW |
9 |
42,284,529 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4485:Tecta
|
UTSW |
9 |
42,248,570 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4804:Tecta
|
UTSW |
9 |
42,309,533 (GRCm39) |
missense |
probably benign |
|
R4869:Tecta
|
UTSW |
9 |
42,286,830 (GRCm39) |
missense |
probably benign |
0.02 |
R4944:Tecta
|
UTSW |
9 |
42,241,573 (GRCm39) |
missense |
probably benign |
0.05 |
R5008:Tecta
|
UTSW |
9 |
42,284,358 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5014:Tecta
|
UTSW |
9 |
42,284,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5125:Tecta
|
UTSW |
9 |
42,286,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R5178:Tecta
|
UTSW |
9 |
42,286,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R5180:Tecta
|
UTSW |
9 |
42,248,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Tecta
|
UTSW |
9 |
42,256,964 (GRCm39) |
missense |
probably benign |
0.04 |
R5230:Tecta
|
UTSW |
9 |
42,306,239 (GRCm39) |
missense |
probably damaging |
0.96 |
R5330:Tecta
|
UTSW |
9 |
42,249,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5387:Tecta
|
UTSW |
9 |
42,286,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R5614:Tecta
|
UTSW |
9 |
42,250,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R5708:Tecta
|
UTSW |
9 |
42,250,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R5738:Tecta
|
UTSW |
9 |
42,284,474 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5770:Tecta
|
UTSW |
9 |
42,256,885 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5839:Tecta
|
UTSW |
9 |
42,284,272 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5839:Tecta
|
UTSW |
9 |
42,242,319 (GRCm39) |
missense |
probably benign |
0.03 |
R6119:Tecta
|
UTSW |
9 |
42,284,371 (GRCm39) |
missense |
probably benign |
0.00 |
R6246:Tecta
|
UTSW |
9 |
42,289,204 (GRCm39) |
missense |
probably benign |
0.07 |
R6377:Tecta
|
UTSW |
9 |
42,255,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R6416:Tecta
|
UTSW |
9 |
42,286,563 (GRCm39) |
missense |
probably damaging |
0.97 |
R6595:Tecta
|
UTSW |
9 |
42,295,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R6850:Tecta
|
UTSW |
9 |
42,255,134 (GRCm39) |
missense |
probably benign |
0.20 |
R6859:Tecta
|
UTSW |
9 |
42,303,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R6861:Tecta
|
UTSW |
9 |
42,248,633 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6939:Tecta
|
UTSW |
9 |
42,259,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R6996:Tecta
|
UTSW |
9 |
42,278,082 (GRCm39) |
missense |
probably benign |
|
R7069:Tecta
|
UTSW |
9 |
42,306,237 (GRCm39) |
missense |
probably benign |
0.03 |
R7104:Tecta
|
UTSW |
9 |
42,278,239 (GRCm39) |
missense |
probably benign |
0.00 |
R7129:Tecta
|
UTSW |
9 |
42,259,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R7220:Tecta
|
UTSW |
9 |
42,255,183 (GRCm39) |
missense |
probably benign |
0.05 |
R7251:Tecta
|
UTSW |
9 |
42,299,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R7307:Tecta
|
UTSW |
9 |
42,289,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Tecta
|
UTSW |
9 |
42,248,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R7355:Tecta
|
UTSW |
9 |
42,278,438 (GRCm39) |
nonsense |
probably null |
|
R7635:Tecta
|
UTSW |
9 |
42,242,283 (GRCm39) |
missense |
probably benign |
0.11 |
R7653:Tecta
|
UTSW |
9 |
42,248,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7723:Tecta
|
UTSW |
9 |
42,278,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R7939:Tecta
|
UTSW |
9 |
42,299,519 (GRCm39) |
missense |
probably damaging |
0.99 |
R7966:Tecta
|
UTSW |
9 |
42,306,258 (GRCm39) |
missense |
probably damaging |
0.98 |
R7967:Tecta
|
UTSW |
9 |
42,289,251 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8000:Tecta
|
UTSW |
9 |
42,278,480 (GRCm39) |
nonsense |
probably null |
|
R8064:Tecta
|
UTSW |
9 |
42,306,251 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8117:Tecta
|
UTSW |
9 |
42,288,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Tecta
|
UTSW |
9 |
42,270,465 (GRCm39) |
missense |
probably damaging |
0.97 |
R8284:Tecta
|
UTSW |
9 |
42,289,325 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8315:Tecta
|
UTSW |
9 |
42,299,121 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8321:Tecta
|
UTSW |
9 |
42,284,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R8332:Tecta
|
UTSW |
9 |
42,286,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R8437:Tecta
|
UTSW |
9 |
42,243,856 (GRCm39) |
missense |
probably damaging |
0.98 |
R8496:Tecta
|
UTSW |
9 |
42,241,547 (GRCm39) |
missense |
probably benign |
0.01 |
R8514:Tecta
|
UTSW |
9 |
42,284,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R8683:Tecta
|
UTSW |
9 |
42,278,268 (GRCm39) |
missense |
probably damaging |
0.96 |
R8856:Tecta
|
UTSW |
9 |
42,284,597 (GRCm39) |
missense |
probably benign |
0.13 |
R8886:Tecta
|
UTSW |
9 |
42,278,359 (GRCm39) |
missense |
probably benign |
0.37 |
R9047:Tecta
|
UTSW |
9 |
42,286,375 (GRCm39) |
missense |
probably benign |
0.00 |
R9106:Tecta
|
UTSW |
9 |
42,278,479 (GRCm39) |
missense |
probably benign |
0.05 |
R9332:Tecta
|
UTSW |
9 |
42,284,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Tecta
|
UTSW |
9 |
42,249,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R9462:Tecta
|
UTSW |
9 |
42,248,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R9535:Tecta
|
UTSW |
9 |
42,270,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R9564:Tecta
|
UTSW |
9 |
42,249,123 (GRCm39) |
missense |
probably damaging |
0.97 |
R9592:Tecta
|
UTSW |
9 |
42,250,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R9715:Tecta
|
UTSW |
9 |
42,286,596 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tecta
|
UTSW |
9 |
42,303,390 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Tecta
|
UTSW |
9 |
42,286,872 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Tecta
|
UTSW |
9 |
42,303,366 (GRCm39) |
missense |
probably damaging |
1.00 |
|