Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alkbh3 |
T |
A |
2: 93,838,458 (GRCm39) |
T38S |
probably benign |
Het |
Btbd8 |
T |
C |
5: 107,656,422 (GRCm39) |
V895A |
possibly damaging |
Het |
Cdkn2c |
A |
G |
4: 109,522,209 (GRCm39) |
|
probably benign |
Het |
Clca4b |
A |
C |
3: 144,631,939 (GRCm39) |
C189G |
probably damaging |
Het |
Clec4f |
T |
A |
6: 83,629,682 (GRCm39) |
N292I |
possibly damaging |
Het |
Dkk3 |
A |
C |
7: 111,748,234 (GRCm39) |
S123R |
probably benign |
Het |
Dock1 |
C |
T |
7: 134,748,209 (GRCm39) |
A1557V |
probably benign |
Het |
E130308A19Rik |
C |
T |
4: 59,719,676 (GRCm39) |
Q403* |
probably null |
Het |
F5 |
G |
A |
1: 164,012,177 (GRCm39) |
|
probably null |
Het |
Fam98c |
T |
A |
7: 28,852,187 (GRCm39) |
D326V |
probably damaging |
Het |
Firrm |
G |
A |
1: 163,786,868 (GRCm39) |
Q734* |
probably null |
Het |
Frem2 |
A |
C |
3: 53,458,767 (GRCm39) |
V2034G |
possibly damaging |
Het |
Galnt2 |
G |
A |
8: 124,958,318 (GRCm39) |
G18D |
probably damaging |
Het |
Grhl3 |
T |
C |
4: 135,284,176 (GRCm39) |
E222G |
probably benign |
Het |
Hif3a |
A |
C |
7: 16,778,293 (GRCm39) |
|
probably benign |
Het |
Ibtk |
C |
T |
9: 85,601,946 (GRCm39) |
G755D |
probably damaging |
Het |
Laptm4b |
A |
G |
15: 34,277,630 (GRCm39) |
N187S |
probably benign |
Het |
Lrba |
A |
G |
3: 86,232,380 (GRCm39) |
T776A |
probably damaging |
Het |
Matcap2 |
A |
T |
9: 22,341,775 (GRCm39) |
K149* |
probably null |
Het |
Mfhas1 |
T |
A |
8: 36,058,104 (GRCm39) |
W860R |
possibly damaging |
Het |
Mon2 |
A |
C |
10: 122,859,844 (GRCm39) |
W811G |
probably damaging |
Het |
Nup42 |
A |
G |
5: 24,380,505 (GRCm39) |
T167A |
probably benign |
Het |
Or10j2 |
A |
G |
1: 173,097,898 (GRCm39) |
D52G |
probably benign |
Het |
Or2z2 |
C |
A |
11: 58,345,873 (GRCm39) |
A301S |
probably damaging |
Het |
Or4k45 |
T |
C |
2: 111,395,249 (GRCm39) |
D180G |
probably damaging |
Het |
Or5w10 |
T |
C |
2: 87,375,093 (GRCm39) |
Y265C |
probably damaging |
Het |
Or8j3c |
T |
C |
2: 86,254,021 (GRCm39) |
|
probably null |
Het |
Pgap2 |
T |
C |
7: 101,886,629 (GRCm39) |
L217P |
probably damaging |
Het |
Pik3c2b |
T |
G |
1: 133,005,056 (GRCm39) |
|
probably benign |
Het |
Ppfia3 |
T |
A |
7: 45,006,092 (GRCm39) |
D149V |
probably damaging |
Het |
Prkcb |
C |
T |
7: 122,200,063 (GRCm39) |
|
probably benign |
Het |
Prl |
A |
G |
13: 27,245,562 (GRCm39) |
D97G |
probably benign |
Het |
Psma5-ps |
T |
C |
10: 85,149,698 (GRCm39) |
|
noncoding transcript |
Het |
Rnf112 |
T |
C |
11: 61,340,231 (GRCm39) |
|
probably benign |
Het |
Slc17a8 |
C |
A |
10: 89,412,465 (GRCm39) |
G323* |
probably null |
Het |
Snx19 |
T |
C |
9: 30,343,660 (GRCm39) |
F607L |
possibly damaging |
Het |
Suco |
A |
G |
1: 161,655,256 (GRCm39) |
S1079P |
probably damaging |
Het |
Taf5 |
T |
C |
19: 47,056,649 (GRCm39) |
L149P |
probably benign |
Het |
Taf6l |
T |
C |
19: 8,752,630 (GRCm39) |
M379V |
probably benign |
Het |
Tcf25 |
T |
C |
8: 124,126,031 (GRCm39) |
F558L |
probably damaging |
Het |
Tlcd1 |
T |
C |
11: 78,070,444 (GRCm39) |
V102A |
probably benign |
Het |
Tmc5 |
G |
T |
7: 118,226,456 (GRCm39) |
A274S |
probably benign |
Het |
Toporsl |
C |
T |
4: 52,611,624 (GRCm39) |
H506Y |
probably benign |
Het |
Ubtd1 |
T |
C |
19: 42,022,109 (GRCm39) |
L127P |
possibly damaging |
Het |
Usp24 |
A |
C |
4: 106,295,967 (GRCm39) |
|
probably benign |
Het |
Usp24 |
C |
A |
4: 106,295,969 (GRCm39) |
|
probably benign |
Het |
Usp43 |
T |
G |
11: 67,746,581 (GRCm39) |
D1042A |
probably benign |
Het |
Whrn |
T |
C |
4: 63,337,709 (GRCm39) |
T48A |
possibly damaging |
Het |
Wnt2b |
A |
G |
3: 104,862,032 (GRCm39) |
I102T |
probably benign |
Het |
Zmat4 |
A |
G |
8: 24,287,389 (GRCm39) |
Y45C |
probably damaging |
Het |
|
Other mutations in Zfp763 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03291:Zfp763
|
APN |
17 |
33,238,860 (GRCm39) |
missense |
probably damaging |
0.96 |
R0346:Zfp763
|
UTSW |
17 |
33,238,721 (GRCm39) |
missense |
probably benign |
0.26 |
R0675:Zfp763
|
UTSW |
17 |
33,238,774 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0683:Zfp763
|
UTSW |
17 |
33,237,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R1494:Zfp763
|
UTSW |
17 |
33,240,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R1521:Zfp763
|
UTSW |
17 |
33,252,276 (GRCm39) |
start codon destroyed |
probably benign |
0.03 |
R1607:Zfp763
|
UTSW |
17 |
33,238,881 (GRCm39) |
missense |
probably benign |
0.08 |
R1627:Zfp763
|
UTSW |
17 |
33,240,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R1714:Zfp763
|
UTSW |
17 |
33,238,591 (GRCm39) |
missense |
probably damaging |
0.99 |
R1993:Zfp763
|
UTSW |
17 |
33,237,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Zfp763
|
UTSW |
17 |
33,238,752 (GRCm39) |
missense |
probably benign |
|
R4420:Zfp763
|
UTSW |
17 |
33,237,455 (GRCm39) |
missense |
probably benign |
0.43 |
R4612:Zfp763
|
UTSW |
17 |
33,237,922 (GRCm39) |
missense |
probably benign |
0.05 |
R5114:Zfp763
|
UTSW |
17 |
33,237,949 (GRCm39) |
missense |
probably damaging |
0.99 |
R5426:Zfp763
|
UTSW |
17 |
33,238,569 (GRCm39) |
missense |
probably benign |
|
R5503:Zfp763
|
UTSW |
17 |
33,238,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5534:Zfp763
|
UTSW |
17 |
33,240,768 (GRCm39) |
missense |
probably damaging |
0.97 |
R6133:Zfp763
|
UTSW |
17 |
33,237,675 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7141:Zfp763
|
UTSW |
17 |
33,237,769 (GRCm39) |
missense |
probably damaging |
0.97 |
R7365:Zfp763
|
UTSW |
17 |
33,252,352 (GRCm39) |
start gained |
probably benign |
|
R7430:Zfp763
|
UTSW |
17 |
33,238,506 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7552:Zfp763
|
UTSW |
17 |
33,237,625 (GRCm39) |
missense |
probably benign |
|
R8277:Zfp763
|
UTSW |
17 |
33,252,294 (GRCm39) |
start gained |
probably benign |
|
R8446:Zfp763
|
UTSW |
17 |
33,238,473 (GRCm39) |
missense |
probably benign |
0.28 |
R8964:Zfp763
|
UTSW |
17 |
33,240,710 (GRCm39) |
missense |
probably benign |
0.25 |
R9662:Zfp763
|
UTSW |
17 |
33,240,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|