Incidental Mutation 'R1730:Igfn1'
ID |
199145 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Igfn1
|
Ensembl Gene |
ENSMUSG00000051985 |
Gene Name |
immunoglobulin-like and fibronectin type III domain containing 1 |
Synonyms |
9830123M21Rik |
MMRRC Submission |
039762-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.076)
|
Stock # |
R1730 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
135881316-135934080 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 135910213 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Tryptophan
at position 124
(R124W)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000129680
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000166193]
|
AlphaFold |
no structure available at present |
Predicted Effect |
unknown
Transcript: ENSMUST00000124134
AA Change: R3W
|
SMART Domains |
Protein: ENSMUSP00000119230 Gene: ENSMUSG00000051985 AA Change: R3W
Domain | Start | End | E-Value | Type |
IG
|
73 |
159 |
1.29e-6 |
SMART |
IG_like
|
258 |
344 |
5.45e1 |
SMART |
IG
|
354 |
435 |
1.79e0 |
SMART |
IG
|
445 |
524 |
3.54e-4 |
SMART |
IG
|
538 |
624 |
4.86e-2 |
SMART |
FN3
|
627 |
711 |
3.99e-10 |
SMART |
FN3
|
727 |
810 |
9.1e-14 |
SMART |
FN3
|
828 |
911 |
1.5e-14 |
SMART |
IG
|
938 |
1021 |
6.41e-2 |
SMART |
FN3
|
1024 |
1106 |
3.2e-9 |
SMART |
IGc2
|
1152 |
1219 |
4.89e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000166193
AA Change: R124W
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000129680 Gene: ENSMUSG00000051985 AA Change: R124W
Domain | Start | End | E-Value | Type |
low complexity region
|
90 |
101 |
N/A |
INTRINSIC |
IG
|
193 |
279 |
1.29e-6 |
SMART |
PDB:2LHU|A
|
302 |
365 |
8e-7 |
PDB |
IG_like
|
378 |
464 |
5.45e1 |
SMART |
IG
|
474 |
555 |
1.79e0 |
SMART |
low complexity region
|
724 |
739 |
N/A |
INTRINSIC |
internal_repeat_2
|
838 |
1006 |
9.98e-5 |
PROSPERO |
low complexity region
|
1067 |
1084 |
N/A |
INTRINSIC |
internal_repeat_2
|
1812 |
1967 |
9.98e-5 |
PROSPERO |
Pfam:I-set
|
2054 |
2139 |
6.2e-8 |
PFAM |
IG
|
2153 |
2239 |
4.86e-2 |
SMART |
FN3
|
2242 |
2326 |
3.99e-10 |
SMART |
FN3
|
2342 |
2425 |
9.1e-14 |
SMART |
FN3
|
2443 |
2526 |
1.5e-14 |
SMART |
IG
|
2553 |
2636 |
6.41e-2 |
SMART |
FN3
|
2639 |
2721 |
3.2e-9 |
SMART |
IGc2
|
2767 |
2834 |
4.89e-7 |
SMART |
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.5%
- 20x: 92.9%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 198 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
T |
C |
6: 91,896,259 (GRCm39) |
I369T |
possibly damaging |
Het |
Aass |
T |
C |
6: 23,121,018 (GRCm39) |
D82G |
probably damaging |
Het |
Abi3bp |
G |
A |
16: 56,488,642 (GRCm39) |
V1258I |
possibly damaging |
Het |
Acad11 |
T |
A |
9: 103,941,081 (GRCm39) |
V41E |
probably benign |
Het |
Aff1 |
T |
G |
5: 103,981,378 (GRCm39) |
L514V |
probably damaging |
Het |
Ankdd1b |
G |
T |
13: 96,597,411 (GRCm39) |
T7K |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,401,312 (GRCm39) |
I1111V |
probably benign |
Het |
Bag3 |
A |
T |
7: 128,125,583 (GRCm39) |
M1L |
possibly 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 |
Carmil1 |
T |
C |
13: 24,225,672 (GRCm39) |
T635A |
probably damaging |
Het |
Ccdc93 |
C |
T |
1: 121,383,855 (GRCm39) |
P192L |
probably benign |
Het |
Ccdc93 |
T |
C |
1: 121,389,668 (GRCm39) |
V237A |
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 |
Cep63 |
T |
A |
9: 102,496,066 (GRCm39) |
I114F |
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 |
Cnr1 |
A |
G |
4: 33,943,851 (GRCm39) |
T80A |
possibly damaging |
Het |
Cntnap5a |
C |
A |
1: 116,382,734 (GRCm39) |
L1001I |
probably benign |
Het |
Cntnap5a |
C |
T |
1: 116,382,873 (GRCm39) |
T1047I |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,382,831 (GRCm39) |
L1033S |
probably benign |
Het |
Col12a1 |
A |
C |
9: 79,535,660 (GRCm39) |
V2612G |
possibly damaging |
Het |
Crb1 |
T |
C |
1: 139,162,517 (GRCm39) |
M1214V |
probably benign |
Het |
Crb1 |
C |
T |
1: 139,171,155 (GRCm39) |
R684H |
probably benign |
Het |
Crb1 |
C |
T |
1: 139,170,733 (GRCm39) |
G825R |
probably damaging |
Het |
Crb1 |
G |
A |
1: 139,168,876 (GRCm39) |
P881S |
probably damaging |
Het |
Crb1 |
A |
T |
1: 139,165,360 (GRCm39) |
H921Q |
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 |
Cyp2c29 |
A |
T |
19: 39,313,389 (GRCm39) |
H295L |
possibly damaging |
Het |
Cyp2c68 |
A |
T |
19: 39,687,719 (GRCm39) |
M426K |
possibly damaging |
Het |
Ddx59 |
T |
C |
1: 136,344,791 (GRCm39) |
V154A |
probably benign |
Het |
Dsel |
G |
C |
1: 111,787,724 (GRCm39) |
T937S |
probably benign |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dsg2 |
G |
A |
18: 20,724,937 (GRCm39) |
V448I |
probably benign |
Het |
Dstyk |
C |
T |
1: 132,384,722 (GRCm39) |
L739F |
probably damaging |
Het |
En1 |
A |
G |
1: 120,531,350 (GRCm39) |
S197G |
unknown |
Het |
Eogt |
T |
C |
6: 97,090,825 (GRCm39) |
D438G |
probably damaging |
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 |
Etnk2 |
A |
G |
1: 133,291,661 (GRCm39) |
S54G |
probably benign |
Het |
Etnppl |
A |
G |
3: 130,414,398 (GRCm39) |
T98A |
probably damaging |
Het |
Eya2 |
G |
T |
2: 165,529,583 (GRCm39) |
G109W |
probably damaging |
Het |
Fam131b |
T |
G |
6: 42,295,514 (GRCm39) |
Q221P |
possibly damaging |
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 |
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: 130,739,317 (GRCm39) |
I206V |
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 |
Gabarap |
C |
T |
11: 69,882,515 (GRCm39) |
|
probably benign |
Het |
Gatad2a |
G |
T |
8: 70,362,586 (GRCm39) |
H600N |
probably damaging |
Het |
Gba2 |
A |
G |
4: 43,578,242 (GRCm39) |
C36R |
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 |
Gm10961 |
T |
C |
3: 107,540,310 (GRCm39) |
|
probably benign |
Het |
Gm4847 |
T |
C |
1: 166,465,908 (GRCm39) |
D227G |
possibly damaging |
Het |
Gpr37l1 |
C |
A |
1: 135,089,268 (GRCm39) |
E266* |
probably null |
Het |
Gucy1a2 |
A |
T |
9: 3,634,957 (GRCm39) |
N334Y |
probably benign |
Het |
H2-D1 |
A |
G |
17: 35,482,381 (GRCm39) |
T34A |
probably damaging |
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 |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Kcna5 |
A |
T |
6: 126,510,823 (GRCm39) |
I435N |
probably damaging |
Het |
Kcnj5 |
T |
C |
9: 32,233,488 (GRCm39) |
I276V |
probably damaging |
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 |
A |
G |
1: 136,396,017 (GRCm39) |
N108D |
probably benign |
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 |
Klhl20 |
A |
G |
1: 160,930,560 (GRCm39) |
V314A |
possibly 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 |
A |
T |
1: 134,915,747 (GRCm39) |
S334T |
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 |
Lin7b |
A |
T |
7: 45,019,351 (GRCm39) |
H72Q |
probably benign |
Het |
Lmod1 |
C |
T |
1: 135,291,811 (GRCm39) |
T222I |
probably benign |
Het |
Map3k9 |
A |
T |
12: 81,769,000 (GRCm39) |
V1016E |
probably damaging |
Het |
Mcam |
T |
C |
9: 44,046,003 (GRCm39) |
L6P |
probably damaging |
Het |
Mgam |
A |
G |
6: 40,641,794 (GRCm39) |
H549R |
possibly damaging |
Het |
Mrc1 |
T |
C |
2: 14,332,655 (GRCm39) |
V1285A |
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 |
Myh7b |
A |
G |
2: 155,467,592 (GRCm39) |
D739G |
possibly damaging |
Het |
Nav1 |
A |
T |
1: 135,512,465 (GRCm39) |
D198E |
possibly damaging |
Het |
Nfkbib |
A |
T |
7: 28,461,480 (GRCm39) |
Y86N |
probably damaging |
Het |
Nfrkb |
C |
T |
9: 31,325,932 (GRCm39) |
T1125M |
probably benign |
Het |
Nr5a2 |
C |
A |
1: 136,879,863 (GRCm39) |
R35L |
probably benign |
Het |
Nrip1 |
G |
T |
16: 76,089,778 (GRCm39) |
T593K |
probably benign |
Het |
Obscn |
A |
G |
11: 58,964,459 (GRCm39) |
Y726H |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Olfml2b |
G |
A |
1: 170,509,358 (GRCm39) |
G569S |
probably damaging |
Het |
Optc |
C |
G |
1: 133,832,908 (GRCm39) |
S64T |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or10v5 |
T |
A |
19: 11,805,445 (GRCm39) |
Q315L |
probably benign |
Het |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or4f14b |
T |
C |
2: 111,775,633 (GRCm39) |
H56R |
probably benign |
Het |
Or7c19 |
A |
C |
8: 85,957,477 (GRCm39) |
M118L |
probably benign |
Het |
Or8d2 |
T |
A |
9: 38,760,268 (GRCm39) |
I286K |
probably damaging |
Het |
Or8g32 |
T |
C |
9: 39,305,518 (GRCm39) |
Y144H |
probably benign |
Het |
Or9g3 |
T |
A |
2: 85,590,586 (GRCm39) |
I45F |
possibly damaging |
Het |
Pard6g |
T |
A |
18: 80,123,040 (GRCm39) |
F25I |
probably damaging |
Het |
Parp6 |
C |
A |
9: 59,540,821 (GRCm39) |
C291* |
probably null |
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 |
Plekha6 |
C |
G |
1: 133,215,584 (GRCm39) |
T792S |
probably benign |
Het |
Polr2i |
T |
C |
7: 29,932,493 (GRCm39) |
C67R |
probably damaging |
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 |
Ptgfrn |
T |
C |
3: 100,963,758 (GRCm39) |
N618S |
possibly damaging |
Het |
Ptpn7 |
A |
G |
1: 135,062,213 (GRCm39) |
Q53R |
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 |
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 |
Rab29 |
A |
G |
1: 131,799,848 (GRCm39) |
Q141R |
probably benign |
Het |
Rad17 |
C |
T |
13: 100,759,314 (GRCm39) |
R571Q |
probably 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 |
A |
C |
1: 133,284,195 (GRCm39) |
K187Q |
probably benign |
Het |
Rims1 |
C |
T |
1: 22,416,753 (GRCm39) |
|
probably null |
Het |
Rnpep |
C |
T |
1: 135,190,834 (GRCm39) |
A571T |
possibly damaging |
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 |
Sctr |
T |
C |
1: 119,959,386 (GRCm39) |
F110L |
probably benign |
Het |
Sctr |
G |
A |
1: 119,990,987 (GRCm39) |
S440N |
possibly damaging |
Het |
Sele |
T |
G |
1: 163,882,192 (GRCm39) |
V559G |
probably benign |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Serpinb10 |
C |
T |
1: 107,466,203 (GRCm39) |
S63F |
probably damaging |
Het |
Serpinb2 |
C |
A |
1: 107,451,564 (GRCm39) |
A239E |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,620 (GRCm39) |
H258Y |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,624 (GRCm39) |
T259I |
probably benign |
Het |
Serpinb2 |
A |
C |
1: 107,452,273 (GRCm39) |
S284R |
probably benign |
Het |
Serpinb2 |
G |
A |
1: 107,443,365 (GRCm39) |
A55T |
probably damaging |
Het |
Serpinb8 |
A |
C |
1: 107,534,734 (GRCm39) |
L268F |
probably benign |
Het |
Serpinb8 |
A |
G |
1: 107,525,257 (GRCm39) |
S20G |
probably benign |
Het |
Serpinb8 |
G |
A |
1: 107,526,684 (GRCm39) |
A75T |
probably benign |
Het |
Setd1a |
T |
A |
7: 127,384,296 (GRCm39) |
Y382* |
probably null |
Het |
Sipa1l2 |
A |
T |
8: 126,206,880 (GRCm39) |
|
probably null |
Het |
Slc25a41 |
T |
C |
17: 57,346,921 (GRCm39) |
E10G |
probably benign |
Het |
Slc26a9 |
C |
T |
1: 131,691,608 (GRCm39) |
A617V |
probably benign |
Het |
Slc36a1 |
A |
G |
11: 55,114,498 (GRCm39) |
D192G |
probably damaging |
Het |
Steap3 |
G |
A |
1: 120,162,108 (GRCm39) |
A350V |
probably benign |
Het |
Steap3 |
T |
C |
1: 120,155,480 (GRCm39) |
N493S |
probably benign |
Het |
Susd4 |
A |
G |
1: 182,681,543 (GRCm39) |
E128G |
probably damaging |
Het |
Synpo2l |
G |
A |
14: 20,715,887 (GRCm39) |
P233S |
probably damaging |
Het |
Tbc1d17 |
A |
C |
7: 44,494,555 (GRCm39) |
S227A |
probably damaging |
Het |
Tfg |
G |
T |
16: 56,533,152 (GRCm39) |
N2K |
probably damaging |
Het |
Thsd7b |
A |
C |
1: 130,044,368 (GRCm39) |
Q1116P |
probably benign |
Het |
Thsd7b |
G |
C |
1: 129,605,920 (GRCm39) |
A554P |
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 |
Tmem143 |
G |
A |
7: 45,556,426 (GRCm39) |
D144N |
possibly damaging |
Het |
Tnnt2 |
C |
T |
1: 135,773,244 (GRCm39) |
|
probably benign |
Het |
Trim47 |
A |
G |
11: 115,996,864 (GRCm39) |
L630P |
probably damaging |
Het |
Ttk |
A |
G |
9: 83,750,645 (GRCm39) |
N691S |
possibly damaging |
Het |
Ttn |
T |
G |
2: 76,547,336 (GRCm39) |
T32237P |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Ube2t |
C |
T |
1: 134,899,905 (GRCm39) |
A149V |
probably benign |
Het |
Uggt1 |
T |
C |
1: 36,260,342 (GRCm39) |
T158A |
probably benign |
Het |
Usp9y |
A |
T |
Y: 1,367,093 (GRCm39) |
V998D |
probably benign |
Het |
Vwa5b2 |
C |
T |
16: 20,419,675 (GRCm39) |
P644S |
probably damaging |
Het |
Wars1 |
A |
C |
12: 108,841,667 (GRCm39) |
F160C |
probably damaging |
Het |
Zc3h11a |
G |
A |
1: 133,549,892 (GRCm39) |
P695S |
probably benign |
Het |
Zc3h11a |
C |
T |
1: 133,552,359 (GRCm39) |
V583I |
probably benign |
Het |
Zfp541 |
A |
G |
7: 15,811,898 (GRCm39) |
T184A |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 6,821,938 (GRCm39) |
D375G |
probably 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 Igfn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00753:Igfn1
|
APN |
1 |
135,894,464 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02299:Igfn1
|
APN |
1 |
135,881,755 (GRCm39) |
utr 3 prime |
probably benign |
|
Bounty
|
UTSW |
1 |
135,904,655 (GRCm39) |
critical splice donor site |
probably null |
|
R2276_Igfn1_773
|
UTSW |
1 |
135,892,479 (GRCm39) |
missense |
probably damaging |
0.98 |
R4058_Igfn1_315
|
UTSW |
1 |
135,897,494 (GRCm39) |
missense |
probably benign |
0.07 |
R0144:Igfn1
|
UTSW |
1 |
135,889,751 (GRCm39) |
missense |
probably damaging |
0.99 |
R0190:Igfn1
|
UTSW |
1 |
135,889,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R0350:Igfn1
|
UTSW |
1 |
135,884,505 (GRCm39) |
nonsense |
probably null |
|
R0413:Igfn1
|
UTSW |
1 |
135,895,334 (GRCm39) |
missense |
probably benign |
0.23 |
R0504:Igfn1
|
UTSW |
1 |
135,896,267 (GRCm39) |
missense |
probably benign |
0.00 |
R0606:Igfn1
|
UTSW |
1 |
135,887,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R0681:Igfn1
|
UTSW |
1 |
135,891,591 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0825:Igfn1
|
UTSW |
1 |
135,890,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0839:Igfn1
|
UTSW |
1 |
135,882,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R1066:Igfn1
|
UTSW |
1 |
135,898,463 (GRCm39) |
missense |
probably benign |
|
R1078:Igfn1
|
UTSW |
1 |
135,902,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R1224:Igfn1
|
UTSW |
1 |
135,897,494 (GRCm39) |
missense |
probably benign |
0.07 |
R1569:Igfn1
|
UTSW |
1 |
135,896,771 (GRCm39) |
missense |
probably benign |
|
R1626:Igfn1
|
UTSW |
1 |
135,896,705 (GRCm39) |
missense |
probably benign |
0.29 |
R1663:Igfn1
|
UTSW |
1 |
135,896,046 (GRCm39) |
missense |
probably benign |
0.15 |
R1677:Igfn1
|
UTSW |
1 |
135,898,839 (GRCm39) |
missense |
probably damaging |
0.99 |
R1709:Igfn1
|
UTSW |
1 |
135,883,311 (GRCm39) |
missense |
probably benign |
0.24 |
R1728:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1728:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1729:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1729:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1729:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1729:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1729:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1730:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1746:Igfn1
|
UTSW |
1 |
135,897,561 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1762:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1783:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1783:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1783:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1783:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1783:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1783:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1784:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1785:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Igfn1
|
UTSW |
1 |
135,897,126 (GRCm39) |
missense |
probably benign |
|
R1866:Igfn1
|
UTSW |
1 |
135,902,606 (GRCm39) |
splice site |
probably null |
|
R1921:Igfn1
|
UTSW |
1 |
135,893,801 (GRCm39) |
critical splice donor site |
probably null |
|
R1984:Igfn1
|
UTSW |
1 |
135,889,782 (GRCm39) |
missense |
probably benign |
0.39 |
R2049:Igfn1
|
UTSW |
1 |
135,902,590 (GRCm39) |
splice site |
probably benign |
|
R2049:Igfn1
|
UTSW |
1 |
135,898,376 (GRCm39) |
missense |
probably benign |
|
R2098:Igfn1
|
UTSW |
1 |
135,906,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:Igfn1
|
UTSW |
1 |
135,902,590 (GRCm39) |
splice site |
probably benign |
|
R2141:Igfn1
|
UTSW |
1 |
135,902,590 (GRCm39) |
splice site |
probably benign |
|
R2276:Igfn1
|
UTSW |
1 |
135,892,479 (GRCm39) |
missense |
probably damaging |
0.98 |
R2425:Igfn1
|
UTSW |
1 |
135,890,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Igfn1
|
UTSW |
1 |
135,897,275 (GRCm39) |
missense |
probably benign |
|
R2504:Igfn1
|
UTSW |
1 |
135,897,054 (GRCm39) |
missense |
probably benign |
0.07 |
R3109:Igfn1
|
UTSW |
1 |
135,925,586 (GRCm39) |
missense |
probably benign |
0.12 |
R3421:Igfn1
|
UTSW |
1 |
135,904,655 (GRCm39) |
critical splice donor site |
probably null |
|
R3423:Igfn1
|
UTSW |
1 |
135,926,379 (GRCm39) |
missense |
probably benign |
0.01 |
R3705:Igfn1
|
UTSW |
1 |
135,896,147 (GRCm39) |
missense |
probably benign |
|
R3871:Igfn1
|
UTSW |
1 |
135,896,574 (GRCm39) |
missense |
probably benign |
0.03 |
R3875:Igfn1
|
UTSW |
1 |
135,882,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R3953:Igfn1
|
UTSW |
1 |
135,894,918 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3955:Igfn1
|
UTSW |
1 |
135,894,918 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3957:Igfn1
|
UTSW |
1 |
135,894,918 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3965:Igfn1
|
UTSW |
1 |
135,895,557 (GRCm39) |
missense |
probably benign |
|
R4006:Igfn1
|
UTSW |
1 |
135,910,100 (GRCm39) |
splice site |
probably null |
|
R4058:Igfn1
|
UTSW |
1 |
135,897,494 (GRCm39) |
missense |
probably benign |
0.07 |
R4059:Igfn1
|
UTSW |
1 |
135,897,494 (GRCm39) |
missense |
probably benign |
0.07 |
R4370:Igfn1
|
UTSW |
1 |
135,895,844 (GRCm39) |
missense |
probably benign |
0.00 |
R4380:Igfn1
|
UTSW |
1 |
135,895,509 (GRCm39) |
missense |
probably benign |
0.00 |
R4495:Igfn1
|
UTSW |
1 |
135,897,416 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4628:Igfn1
|
UTSW |
1 |
135,887,468 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4672:Igfn1
|
UTSW |
1 |
135,893,107 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4682:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R4702:Igfn1
|
UTSW |
1 |
135,894,947 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4744:Igfn1
|
UTSW |
1 |
135,910,196 (GRCm39) |
missense |
probably benign |
0.07 |
R4777:Igfn1
|
UTSW |
1 |
135,882,600 (GRCm39) |
missense |
probably benign |
|
R4806:Igfn1
|
UTSW |
1 |
135,895,095 (GRCm39) |
missense |
probably benign |
0.01 |
R4840:Igfn1
|
UTSW |
1 |
135,895,778 (GRCm39) |
missense |
probably benign |
0.00 |
R4894:Igfn1
|
UTSW |
1 |
135,882,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4998:Igfn1
|
UTSW |
1 |
135,882,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Igfn1
|
UTSW |
1 |
135,892,564 (GRCm39) |
missense |
probably benign |
|
R5108:Igfn1
|
UTSW |
1 |
135,910,179 (GRCm39) |
missense |
probably benign |
|
R5120:Igfn1
|
UTSW |
1 |
135,901,240 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5127:Igfn1
|
UTSW |
1 |
135,887,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R5231:Igfn1
|
UTSW |
1 |
135,894,474 (GRCm39) |
missense |
probably benign |
0.26 |
R5286:Igfn1
|
UTSW |
1 |
135,895,599 (GRCm39) |
missense |
probably benign |
0.10 |
R5307:Igfn1
|
UTSW |
1 |
135,892,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R5380:Igfn1
|
UTSW |
1 |
135,893,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R5553:Igfn1
|
UTSW |
1 |
135,895,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R5660:Igfn1
|
UTSW |
1 |
135,898,152 (GRCm39) |
missense |
probably benign |
0.01 |
R5779:Igfn1
|
UTSW |
1 |
135,894,578 (GRCm39) |
missense |
probably benign |
0.16 |
R5818:Igfn1
|
UTSW |
1 |
135,893,864 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5832:Igfn1
|
UTSW |
1 |
135,902,533 (GRCm39) |
missense |
probably damaging |
0.96 |
R5933:Igfn1
|
UTSW |
1 |
135,898,341 (GRCm39) |
nonsense |
probably null |
|
R5966:Igfn1
|
UTSW |
1 |
135,893,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R6116:Igfn1
|
UTSW |
1 |
135,898,205 (GRCm39) |
missense |
probably benign |
0.00 |
R6297:Igfn1
|
UTSW |
1 |
135,892,399 (GRCm39) |
critical splice donor site |
probably null |
|
R6652:Igfn1
|
UTSW |
1 |
135,891,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Igfn1
|
UTSW |
1 |
135,897,605 (GRCm39) |
missense |
probably benign |
|
R6816:Igfn1
|
UTSW |
1 |
135,887,466 (GRCm39) |
missense |
probably benign |
0.02 |
R6886:Igfn1
|
UTSW |
1 |
135,901,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R6888:Igfn1
|
UTSW |
1 |
135,910,218 (GRCm39) |
missense |
probably benign |
0.33 |
R6975:Igfn1
|
UTSW |
1 |
135,896,183 (GRCm39) |
missense |
probably damaging |
0.96 |
R7105:Igfn1
|
UTSW |
1 |
135,911,956 (GRCm39) |
missense |
probably benign |
0.11 |
R7114:Igfn1
|
UTSW |
1 |
135,894,519 (GRCm39) |
missense |
probably benign |
0.01 |
R7233:Igfn1
|
UTSW |
1 |
135,897,873 (GRCm39) |
missense |
probably benign |
0.41 |
R7276:Igfn1
|
UTSW |
1 |
135,926,376 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7354:Igfn1
|
UTSW |
1 |
135,903,770 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7358:Igfn1
|
UTSW |
1 |
135,891,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7380:Igfn1
|
UTSW |
1 |
135,889,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Igfn1
|
UTSW |
1 |
135,894,785 (GRCm39) |
missense |
probably benign |
0.00 |
R7513:Igfn1
|
UTSW |
1 |
135,887,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R7718:Igfn1
|
UTSW |
1 |
135,896,774 (GRCm39) |
missense |
probably benign |
|
R7769:Igfn1
|
UTSW |
1 |
135,910,143 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7810:Igfn1
|
UTSW |
1 |
135,902,527 (GRCm39) |
missense |
probably damaging |
0.98 |
R7917:Igfn1
|
UTSW |
1 |
135,899,706 (GRCm39) |
missense |
probably damaging |
0.99 |
R7952:Igfn1
|
UTSW |
1 |
135,891,693 (GRCm39) |
missense |
probably damaging |
0.99 |
R8041:Igfn1
|
UTSW |
1 |
135,895,797 (GRCm39) |
nonsense |
probably null |
|
R8233:Igfn1
|
UTSW |
1 |
135,895,782 (GRCm39) |
missense |
probably benign |
0.00 |
R8354:Igfn1
|
UTSW |
1 |
135,887,619 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8363:Igfn1
|
UTSW |
1 |
135,891,625 (GRCm39) |
missense |
probably benign |
0.01 |
R8428:Igfn1
|
UTSW |
1 |
135,895,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R8731:Igfn1
|
UTSW |
1 |
135,925,574 (GRCm39) |
missense |
probably benign |
0.02 |
R8756:Igfn1
|
UTSW |
1 |
135,895,698 (GRCm39) |
missense |
probably benign |
0.10 |
R8797:Igfn1
|
UTSW |
1 |
135,902,573 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8913:Igfn1
|
UTSW |
1 |
135,891,579 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8927:Igfn1
|
UTSW |
1 |
135,905,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Igfn1
|
UTSW |
1 |
135,905,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9087:Igfn1
|
UTSW |
1 |
135,902,606 (GRCm39) |
splice site |
probably null |
|
R9109:Igfn1
|
UTSW |
1 |
135,926,327 (GRCm39) |
missense |
probably benign |
0.26 |
R9113:Igfn1
|
UTSW |
1 |
135,883,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R9117:Igfn1
|
UTSW |
1 |
135,902,528 (GRCm39) |
missense |
probably benign |
0.03 |
R9205:Igfn1
|
UTSW |
1 |
135,903,695 (GRCm39) |
missense |
probably damaging |
0.96 |
R9251:Igfn1
|
UTSW |
1 |
135,894,409 (GRCm39) |
splice site |
probably benign |
|
R9260:Igfn1
|
UTSW |
1 |
135,907,694 (GRCm39) |
missense |
probably benign |
0.45 |
R9275:Igfn1
|
UTSW |
1 |
135,901,185 (GRCm39) |
missense |
probably damaging |
0.96 |
R9277:Igfn1
|
UTSW |
1 |
135,887,520 (GRCm39) |
missense |
probably damaging |
0.98 |
R9278:Igfn1
|
UTSW |
1 |
135,901,185 (GRCm39) |
missense |
probably damaging |
0.96 |
R9287:Igfn1
|
UTSW |
1 |
135,925,544 (GRCm39) |
missense |
probably benign |
0.33 |
R9298:Igfn1
|
UTSW |
1 |
135,926,327 (GRCm39) |
missense |
probably benign |
0.26 |
R9356:Igfn1
|
UTSW |
1 |
135,899,825 (GRCm39) |
nonsense |
probably null |
|
R9371:Igfn1
|
UTSW |
1 |
135,906,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9532:Igfn1
|
UTSW |
1 |
135,897,229 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9653:Igfn1
|
UTSW |
1 |
135,883,323 (GRCm39) |
nonsense |
probably null |
|
R9666:Igfn1
|
UTSW |
1 |
135,897,692 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9741:Igfn1
|
UTSW |
1 |
135,895,383 (GRCm39) |
missense |
probably benign |
0.00 |
R9748:Igfn1
|
UTSW |
1 |
135,926,336 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9796:Igfn1
|
UTSW |
1 |
135,897,611 (GRCm39) |
missense |
probably benign |
0.26 |
Z1176:Igfn1
|
UTSW |
1 |
135,899,738 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Igfn1
|
UTSW |
1 |
135,897,305 (GRCm39) |
missense |
probably benign |
0.26 |
Z1177:Igfn1
|
UTSW |
1 |
135,883,547 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Igfn1
|
UTSW |
1 |
135,910,164 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Predicted Primers |
PCR Primer
(F):5'- GCTTGGTAAAGCAGAGCAGACTCC -3'
(R):5'- AGAGCCTACTCCTTCCCTGAGAAAC -3'
Sequencing Primer
(F):5'- AAGCAGAGATGGTGTGTTCCC -3'
(R):5'- CCTGAGAAACTGGCCTAGTG -3'
|
Posted On |
2014-05-23 |