Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010109A12Rik |
A |
G |
5: 93,354,434 (GRCm39) |
|
probably benign |
Het |
4930563M21Rik |
C |
T |
9: 55,896,760 (GRCm39) |
V283I |
possibly damaging |
Het |
Acot11 |
C |
T |
4: 106,617,327 (GRCm39) |
G240R |
probably damaging |
Het |
Allc |
T |
A |
12: 28,607,388 (GRCm39) |
H288L |
probably damaging |
Het |
Atg16l1 |
T |
C |
1: 87,702,576 (GRCm39) |
I279T |
possibly damaging |
Het |
Atp6v1b1 |
A |
G |
6: 83,728,857 (GRCm39) |
|
probably benign |
Het |
Barhl1 |
G |
A |
2: 28,805,495 (GRCm39) |
P66L |
probably benign |
Het |
Brd8dc |
T |
A |
18: 34,713,894 (GRCm39) |
M244L |
probably benign |
Het |
Cfap58 |
A |
T |
19: 47,943,856 (GRCm39) |
D352V |
probably benign |
Het |
Cyp3a44 |
T |
A |
5: 145,731,781 (GRCm39) |
K122* |
probably null |
Het |
Dnai1 |
G |
T |
4: 41,625,308 (GRCm39) |
R424L |
probably benign |
Het |
Dync1li2 |
G |
T |
8: 105,167,167 (GRCm39) |
H79Q |
probably damaging |
Het |
Fem1b |
A |
G |
9: 62,704,015 (GRCm39) |
V415A |
possibly damaging |
Het |
Fgb |
C |
T |
3: 82,954,094 (GRCm39) |
S48N |
possibly damaging |
Het |
Gm5624 |
T |
C |
14: 44,799,332 (GRCm39) |
D31G |
possibly damaging |
Het |
Gzmn |
T |
A |
14: 56,403,432 (GRCm39) |
I226F |
probably damaging |
Het |
H2-T5 |
A |
T |
17: 36,476,622 (GRCm39) |
V284E |
probably damaging |
Het |
Il31ra |
T |
C |
13: 112,683,902 (GRCm39) |
S184G |
probably damaging |
Het |
Insrr |
C |
T |
3: 87,720,873 (GRCm39) |
R1044C |
probably damaging |
Het |
Kcnj15 |
A |
G |
16: 95,097,193 (GRCm39) |
S272G |
probably damaging |
Het |
Kcnk16 |
C |
T |
14: 20,312,997 (GRCm39) |
A106T |
probably benign |
Het |
Kmt2b |
A |
G |
7: 30,283,984 (GRCm39) |
V876A |
probably damaging |
Het |
Large2 |
G |
T |
2: 92,201,215 (GRCm39) |
|
probably benign |
Het |
Maml2 |
A |
T |
9: 13,532,847 (GRCm39) |
|
probably benign |
Het |
Me1 |
A |
G |
9: 86,464,851 (GRCm39) |
L533P |
possibly damaging |
Het |
Muc16 |
A |
G |
9: 18,477,986 (GRCm39) |
|
probably null |
Het |
Nova2 |
C |
A |
7: 18,692,419 (GRCm39) |
T516K |
probably damaging |
Het |
Or1l4 |
T |
A |
2: 37,092,118 (GRCm39) |
N288K |
probably damaging |
Het |
Or56b1 |
T |
C |
7: 104,285,094 (GRCm39) |
I71T |
probably damaging |
Het |
Otogl |
G |
A |
10: 107,612,978 (GRCm39) |
|
silent |
Het |
Ppp2r1a |
T |
A |
17: 21,176,087 (GRCm39) |
V103E |
probably benign |
Het |
Prl3d3 |
G |
A |
13: 27,341,147 (GRCm39) |
|
probably null |
Het |
Rhbdf1 |
G |
T |
11: 32,164,042 (GRCm39) |
A288E |
possibly damaging |
Het |
Rnf213 |
T |
C |
11: 119,321,147 (GRCm39) |
S1202P |
possibly damaging |
Het |
Slc25a17 |
A |
G |
15: 81,222,154 (GRCm39) |
V106A |
probably benign |
Het |
Slc4a4 |
T |
G |
5: 89,318,624 (GRCm39) |
S640A |
probably benign |
Het |
Smc4 |
T |
A |
3: 68,924,105 (GRCm39) |
Y298N |
probably damaging |
Het |
Tek |
G |
T |
4: 94,741,732 (GRCm39) |
G830* |
probably null |
Het |
Tgfb1 |
A |
T |
7: 25,388,587 (GRCm39) |
|
probably benign |
Het |
Themis |
T |
C |
10: 28,657,903 (GRCm39) |
I157T |
probably damaging |
Het |
Trmt12 |
A |
G |
15: 58,744,514 (GRCm39) |
|
probably benign |
Het |
Trrap |
T |
C |
5: 144,793,760 (GRCm39) |
W3654R |
probably damaging |
Het |
Tspan3 |
C |
T |
9: 56,054,724 (GRCm39) |
G108S |
probably damaging |
Het |
Ugt1a10 |
T |
A |
1: 87,983,979 (GRCm39) |
|
probably null |
Het |
Vps13b |
A |
G |
15: 35,770,829 (GRCm39) |
K2091E |
probably benign |
Het |
Wdr62 |
A |
T |
7: 29,971,045 (GRCm39) |
V184D |
probably damaging |
Het |
|
Other mutations in Zfp958 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01950:Zfp958
|
APN |
8 |
4,678,917 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02185:Zfp958
|
APN |
8 |
4,678,990 (GRCm39) |
nonsense |
probably null |
|
IGL02716:Zfp958
|
APN |
8 |
4,675,967 (GRCm39) |
critical splice donor site |
probably null |
|
R1118:Zfp958
|
UTSW |
8 |
4,676,169 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1119:Zfp958
|
UTSW |
8 |
4,676,169 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1478:Zfp958
|
UTSW |
8 |
4,679,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Zfp958
|
UTSW |
8 |
4,679,147 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1837:Zfp958
|
UTSW |
8 |
4,678,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Zfp958
|
UTSW |
8 |
4,678,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R3763:Zfp958
|
UTSW |
8 |
4,676,226 (GRCm39) |
critical splice donor site |
probably null |
|
R5257:Zfp958
|
UTSW |
8 |
4,678,456 (GRCm39) |
missense |
probably benign |
0.28 |
R5258:Zfp958
|
UTSW |
8 |
4,678,456 (GRCm39) |
missense |
probably benign |
0.28 |
R5304:Zfp958
|
UTSW |
8 |
4,676,196 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5512:Zfp958
|
UTSW |
8 |
4,675,838 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5907:Zfp958
|
UTSW |
8 |
4,679,072 (GRCm39) |
missense |
probably benign |
0.01 |
R6604:Zfp958
|
UTSW |
8 |
4,678,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R6688:Zfp958
|
UTSW |
8 |
4,678,940 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6981:Zfp958
|
UTSW |
8 |
4,676,170 (GRCm39) |
missense |
probably benign |
0.00 |
R7010:Zfp958
|
UTSW |
8 |
4,678,377 (GRCm39) |
missense |
probably benign |
0.13 |
R7140:Zfp958
|
UTSW |
8 |
4,678,481 (GRCm39) |
missense |
probably benign |
0.05 |
R8096:Zfp958
|
UTSW |
8 |
4,663,273 (GRCm39) |
start gained |
probably benign |
|
R8491:Zfp958
|
UTSW |
8 |
4,676,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R8673:Zfp958
|
UTSW |
8 |
4,678,268 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8847:Zfp958
|
UTSW |
8 |
4,678,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Zfp958
|
UTSW |
8 |
4,678,298 (GRCm39) |
missense |
probably damaging |
1.00 |
|