Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12b |
G |
A |
12: 70,215,822 (GRCm39) |
G88S |
probably damaging |
Het |
Acot10 |
A |
G |
15: 20,666,051 (GRCm39) |
F230S |
probably benign |
Het |
Akap12 |
G |
T |
10: 4,303,273 (GRCm39) |
A28S |
probably benign |
Het |
Anks1 |
C |
A |
17: 28,205,227 (GRCm39) |
T262K |
probably damaging |
Het |
Arfgap3 |
A |
G |
15: 83,197,710 (GRCm39) |
Y349H |
possibly damaging |
Het |
Cacna1g |
G |
A |
11: 94,357,054 (GRCm39) |
|
probably benign |
Het |
Camsap2 |
T |
A |
1: 136,225,528 (GRCm39) |
E199D |
probably benign |
Het |
Ccdc13 |
A |
T |
9: 121,656,429 (GRCm39) |
M128K |
probably benign |
Het |
Ccdc38 |
T |
C |
10: 93,405,797 (GRCm39) |
|
probably null |
Het |
Cep95 |
G |
A |
11: 106,704,641 (GRCm39) |
V499I |
probably benign |
Het |
Cpne6 |
G |
C |
14: 55,749,459 (GRCm39) |
M6I |
probably benign |
Het |
Cpne6 |
A |
T |
14: 55,752,706 (GRCm39) |
I299F |
probably damaging |
Het |
Cse1l |
T |
A |
2: 166,769,428 (GRCm39) |
Y278* |
probably null |
Het |
Dip2c |
A |
G |
13: 9,625,179 (GRCm39) |
N558D |
possibly damaging |
Het |
Edar |
A |
T |
10: 58,464,460 (GRCm39) |
C60S |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,201,698 (GRCm39) |
N459D |
probably benign |
Het |
Fbxw8 |
C |
T |
5: 118,251,785 (GRCm39) |
V243M |
possibly damaging |
Het |
Fem1b |
G |
A |
9: 62,704,810 (GRCm39) |
A150V |
possibly damaging |
Het |
Gpatch3 |
CAGGAGGAGGAGGAGGAG |
CAGGAGGAGGAGGAG |
4: 133,305,613 (GRCm39) |
|
probably benign |
Het |
Grin2c |
T |
C |
11: 115,147,020 (GRCm39) |
T392A |
probably benign |
Het |
Idh3a |
T |
A |
9: 54,493,829 (GRCm39) |
|
probably null |
Het |
Itpk1 |
T |
C |
12: 102,572,362 (GRCm39) |
E117G |
probably damaging |
Het |
Kif12 |
G |
T |
4: 63,084,121 (GRCm39) |
P627Q |
probably damaging |
Het |
Krtap15-1 |
T |
A |
16: 88,626,255 (GRCm39) |
F88L |
probably benign |
Het |
Mcm7 |
C |
T |
5: 138,168,653 (GRCm39) |
V13I |
probably benign |
Het |
Mlh1 |
T |
C |
9: 111,081,980 (GRCm39) |
N248D |
possibly damaging |
Het |
Or2i1 |
T |
C |
17: 37,507,833 (GRCm39) |
N342S |
probably benign |
Het |
Or4k15 |
A |
G |
14: 50,364,039 (GRCm39) |
N2D |
probably benign |
Het |
Or52z12 |
T |
C |
7: 103,233,900 (GRCm39) |
Y224H |
probably damaging |
Het |
Per2 |
T |
C |
1: 91,376,555 (GRCm39) |
H106R |
probably damaging |
Het |
Pfkl |
T |
A |
10: 77,827,229 (GRCm39) |
T486S |
probably benign |
Het |
Prkdc |
T |
C |
16: 15,485,595 (GRCm39) |
V474A |
possibly damaging |
Het |
Scamp4 |
C |
A |
10: 80,445,256 (GRCm39) |
Q34K |
probably damaging |
Het |
Serpinb3b |
A |
G |
1: 107,082,395 (GRCm39) |
Y290H |
probably damaging |
Het |
Sft2d2 |
G |
T |
1: 165,011,564 (GRCm39) |
A110E |
probably benign |
Het |
Siglecf |
T |
A |
7: 43,001,377 (GRCm39) |
L115* |
probably null |
Het |
Slc6a11 |
C |
T |
6: 114,111,626 (GRCm39) |
T103M |
probably damaging |
Het |
Slco1a1 |
T |
A |
6: 141,892,313 (GRCm39) |
K18* |
probably null |
Het |
Spata1 |
A |
T |
3: 146,193,154 (GRCm39) |
Y112* |
probably null |
Het |
Tbc1d32 |
G |
A |
10: 56,056,620 (GRCm39) |
T440I |
probably benign |
Het |
Vmn1r159 |
A |
G |
7: 22,542,588 (GRCm39) |
V148A |
probably damaging |
Het |
Wnt16 |
C |
T |
6: 22,297,934 (GRCm39) |
R267C |
probably damaging |
Het |
Xylt1 |
A |
C |
7: 117,148,125 (GRCm39) |
S230R |
probably benign |
Het |
Zfp334 |
T |
C |
2: 165,223,017 (GRCm39) |
H342R |
probably damaging |
Het |
|
Other mutations in Gm5422 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01306:Gm5422
|
APN |
10 |
31,125,432 (GRCm39) |
exon |
noncoding transcript |
|
IGL01569:Gm5422
|
APN |
10 |
31,125,897 (GRCm39) |
exon |
noncoding transcript |
|
IGL01645:Gm5422
|
APN |
10 |
31,126,069 (GRCm39) |
exon |
noncoding transcript |
|
IGL02273:Gm5422
|
APN |
10 |
31,126,003 (GRCm39) |
exon |
noncoding transcript |
|
IGL02603:Gm5422
|
APN |
10 |
31,125,436 (GRCm39) |
exon |
noncoding transcript |
|
IGL02928:Gm5422
|
APN |
10 |
31,126,250 (GRCm39) |
exon |
noncoding transcript |
|
IGL03003:Gm5422
|
APN |
10 |
31,126,840 (GRCm39) |
exon |
noncoding transcript |
|
IGL03274:Gm5422
|
APN |
10 |
31,126,348 (GRCm39) |
exon |
noncoding transcript |
|
IGL03297:Gm5422
|
APN |
10 |
31,125,727 (GRCm39) |
exon |
noncoding transcript |
|
R0010:Gm5422
|
UTSW |
10 |
31,125,750 (GRCm39) |
exon |
noncoding transcript |
|
R0506:Gm5422
|
UTSW |
10 |
31,126,318 (GRCm39) |
exon |
noncoding transcript |
|
R0560:Gm5422
|
UTSW |
10 |
31,125,240 (GRCm39) |
exon |
noncoding transcript |
|
R0573:Gm5422
|
UTSW |
10 |
31,126,156 (GRCm39) |
exon |
noncoding transcript |
|
R0652:Gm5422
|
UTSW |
10 |
31,125,277 (GRCm39) |
exon |
noncoding transcript |
|
R1210:Gm5422
|
UTSW |
10 |
31,126,719 (GRCm39) |
intron |
noncoding transcript |
|
R1259:Gm5422
|
UTSW |
10 |
31,125,111 (GRCm39) |
exon |
noncoding transcript |
|
R1352:Gm5422
|
UTSW |
10 |
31,126,731 (GRCm39) |
intron |
noncoding transcript |
|
R1631:Gm5422
|
UTSW |
10 |
31,125,802 (GRCm39) |
exon |
noncoding transcript |
|
R1707:Gm5422
|
UTSW |
10 |
31,124,458 (GRCm39) |
exon |
noncoding transcript |
|
R1893:Gm5422
|
UTSW |
10 |
31,125,609 (GRCm39) |
exon |
noncoding transcript |
|
R2011:Gm5422
|
UTSW |
10 |
31,124,764 (GRCm39) |
exon |
noncoding transcript |
|
R2132:Gm5422
|
UTSW |
10 |
31,124,929 (GRCm39) |
exon |
noncoding transcript |
|
R3427:Gm5422
|
UTSW |
10 |
31,124,842 (GRCm39) |
exon |
noncoding transcript |
|
R3772:Gm5422
|
UTSW |
10 |
31,124,510 (GRCm39) |
exon |
noncoding transcript |
|
R4703:Gm5422
|
UTSW |
10 |
31,125,608 (GRCm39) |
exon |
noncoding transcript |
|
R5539:Gm5422
|
UTSW |
10 |
31,124,646 (GRCm39) |
exon |
noncoding transcript |
|
R5603:Gm5422
|
UTSW |
10 |
31,126,840 (GRCm39) |
exon |
noncoding transcript |
|
R5660:Gm5422
|
UTSW |
10 |
31,126,048 (GRCm39) |
exon |
noncoding transcript |
|
R6124:Gm5422
|
UTSW |
10 |
31,125,396 (GRCm39) |
exon |
noncoding transcript |
|
R6178:Gm5422
|
UTSW |
10 |
31,125,688 (GRCm39) |
exon |
noncoding transcript |
|
R8263:Gm5422
|
UTSW |
10 |
31,125,099 (GRCm39) |
missense |
noncoding transcript |
|
|