Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700129C05Rik |
T |
A |
14: 59,380,128 (GRCm39) |
T57S |
possibly damaging |
Het |
Adamts1 |
A |
G |
16: 85,594,629 (GRCm39) |
Y670H |
possibly damaging |
Het |
Akr1b7 |
A |
T |
6: 34,396,343 (GRCm39) |
I185F |
probably damaging |
Het |
Ankfn1 |
T |
C |
11: 89,312,097 (GRCm39) |
N683D |
probably benign |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Chrna5 |
T |
A |
9: 54,913,749 (GRCm39) |
W432R |
probably damaging |
Het |
Chrng |
T |
A |
1: 87,136,836 (GRCm39) |
L235Q |
probably damaging |
Het |
Ciao1 |
A |
T |
2: 127,088,631 (GRCm39) |
C97* |
probably null |
Het |
Cpt2 |
G |
T |
4: 107,764,745 (GRCm39) |
H340N |
probably damaging |
Het |
Dmtn |
A |
T |
14: 70,842,777 (GRCm39) |
M328K |
possibly damaging |
Het |
Dusp10 |
T |
A |
1: 183,806,506 (GRCm39) |
V413E |
probably damaging |
Het |
Epha3 |
A |
T |
16: 63,431,443 (GRCm39) |
L487* |
probably null |
Het |
Esco2 |
A |
G |
14: 66,068,641 (GRCm39) |
V223A |
probably damaging |
Het |
Fryl |
A |
T |
5: 73,245,739 (GRCm39) |
D1139E |
possibly damaging |
Het |
Gemin4 |
A |
G |
11: 76,104,408 (GRCm39) |
S118P |
probably damaging |
Het |
Gm3604 |
A |
G |
13: 62,518,060 (GRCm39) |
I79T |
probably damaging |
Het |
Gpatch3 |
T |
C |
4: 133,302,117 (GRCm39) |
V16A |
probably benign |
Het |
Hcn4 |
A |
G |
9: 58,731,063 (GRCm39) |
N90S |
unknown |
Het |
Hr |
C |
T |
14: 70,799,293 (GRCm39) |
H593Y |
possibly damaging |
Het |
Igkv4-50 |
A |
G |
6: 69,677,951 (GRCm39) |
V51A |
probably damaging |
Het |
Insr |
C |
A |
8: 3,223,602 (GRCm39) |
V844F |
probably benign |
Het |
Kcns2 |
T |
C |
15: 34,839,318 (GRCm39) |
F227S |
possibly damaging |
Het |
Map4k1 |
A |
G |
7: 28,686,563 (GRCm39) |
I162V |
probably benign |
Het |
Naip2 |
T |
C |
13: 100,291,468 (GRCm39) |
S1157G |
probably benign |
Het |
Neurog2 |
A |
G |
3: 127,427,550 (GRCm39) |
E58G |
probably damaging |
Het |
Or4x6 |
T |
C |
2: 89,949,087 (GRCm39) |
Y285C |
probably damaging |
Het |
Or5h25 |
T |
A |
16: 58,930,793 (GRCm39) |
Y60F |
probably damaging |
Het |
Or7e174 |
T |
G |
9: 20,012,154 (GRCm39) |
L33W |
probably damaging |
Het |
Orc4 |
A |
T |
2: 48,800,248 (GRCm39) |
M300K |
probably benign |
Het |
Plch1 |
T |
C |
3: 63,648,105 (GRCm39) |
D422G |
possibly damaging |
Het |
Prox1 |
T |
C |
1: 189,855,583 (GRCm39) |
E683G |
probably benign |
Het |
Pxdn |
A |
G |
12: 30,056,704 (GRCm39) |
D1305G |
probably damaging |
Het |
Rcor3 |
C |
A |
1: 191,822,173 (GRCm39) |
G8V |
probably damaging |
Het |
Rex2 |
T |
G |
4: 147,142,329 (GRCm39) |
I272M |
probably damaging |
Het |
Rpa2 |
T |
C |
4: 132,496,014 (GRCm39) |
S12P |
possibly damaging |
Het |
Samd15 |
C |
A |
12: 87,248,350 (GRCm39) |
P345Q |
probably damaging |
Het |
Sema5a |
T |
A |
15: 32,673,574 (GRCm39) |
I804N |
probably damaging |
Het |
Sgsm3 |
G |
A |
15: 80,891,667 (GRCm39) |
R165H |
possibly damaging |
Het |
Slc22a30 |
T |
G |
19: 8,313,072 (GRCm39) |
M467L |
unknown |
Het |
Slc2a5 |
T |
C |
4: 150,226,642 (GRCm39) |
I368T |
probably benign |
Het |
Slc8a1 |
A |
T |
17: 81,749,200 (GRCm39) |
|
probably null |
Het |
Snap91 |
T |
C |
9: 86,688,547 (GRCm39) |
T331A |
possibly damaging |
Het |
Soat2 |
G |
T |
15: 102,062,456 (GRCm39) |
|
probably null |
Het |
Sptbn4 |
C |
A |
7: 27,071,697 (GRCm39) |
R1589L |
probably damaging |
Het |
Stk38l |
A |
G |
6: 146,677,152 (GRCm39) |
Y443C |
probably damaging |
Het |
Sult5a1 |
T |
C |
8: 123,872,117 (GRCm39) |
I242V |
probably benign |
Het |
Susd3 |
T |
C |
13: 49,384,638 (GRCm39) |
R262G |
probably benign |
Het |
Syt9 |
A |
G |
7: 107,035,784 (GRCm39) |
D267G |
probably damaging |
Het |
Tbce |
A |
G |
13: 14,185,172 (GRCm39) |
V172A |
probably benign |
Het |
Tcstv3 |
A |
T |
13: 120,779,107 (GRCm39) |
D2V |
possibly damaging |
Het |
Tmod1 |
T |
A |
4: 46,083,593 (GRCm39) |
S7R |
possibly damaging |
Het |
Ubqln4 |
C |
T |
3: 88,462,731 (GRCm39) |
|
probably benign |
Het |
Ucp2 |
T |
C |
7: 100,146,514 (GRCm39) |
|
probably null |
Het |
Usp30 |
G |
A |
5: 114,258,308 (GRCm39) |
S306N |
probably benign |
Het |
Usp5 |
A |
T |
6: 124,794,970 (GRCm39) |
I660N |
probably damaging |
Het |
Vmn1r43 |
A |
G |
6: 89,846,547 (GRCm39) |
V313A |
possibly damaging |
Het |
Wdr49 |
T |
C |
3: 75,265,744 (GRCm39) |
H234R |
possibly damaging |
Het |
Wdr70 |
T |
C |
15: 8,065,327 (GRCm39) |
D245G |
possibly damaging |
Het |
Zc3h6 |
A |
G |
2: 128,859,172 (GRCm39) |
K1068E |
probably benign |
Het |
Zfp141 |
T |
C |
7: 42,124,856 (GRCm39) |
K539E |
probably benign |
Het |
Zfp758 |
T |
A |
17: 22,593,872 (GRCm39) |
H119Q |
possibly damaging |
Het |
|
Other mutations in Iqcn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6811:Iqcn
|
UTSW |
8 |
71,169,422 (GRCm39) |
missense |
probably benign |
0.05 |
R6850:Iqcn
|
UTSW |
8 |
71,163,425 (GRCm39) |
missense |
probably damaging |
0.97 |
R7029:Iqcn
|
UTSW |
8 |
71,161,511 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7203:Iqcn
|
UTSW |
8 |
71,169,597 (GRCm39) |
missense |
probably benign |
0.26 |
R7260:Iqcn
|
UTSW |
8 |
71,161,397 (GRCm39) |
missense |
probably benign |
0.00 |
R7263:Iqcn
|
UTSW |
8 |
71,163,425 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7327:Iqcn
|
UTSW |
8 |
71,169,453 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7401:Iqcn
|
UTSW |
8 |
71,169,921 (GRCm39) |
missense |
probably benign |
0.03 |
R7542:Iqcn
|
UTSW |
8 |
71,161,415 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7733:Iqcn
|
UTSW |
8 |
71,170,100 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7873:Iqcn
|
UTSW |
8 |
71,163,989 (GRCm39) |
missense |
probably benign |
0.29 |
R8015:Iqcn
|
UTSW |
8 |
71,169,441 (GRCm39) |
missense |
probably benign |
0.02 |
R8039:Iqcn
|
UTSW |
8 |
71,163,555 (GRCm39) |
missense |
probably benign |
0.09 |
R8061:Iqcn
|
UTSW |
8 |
71,161,224 (GRCm39) |
missense |
probably benign |
|
R8094:Iqcn
|
UTSW |
8 |
71,162,067 (GRCm39) |
missense |
probably benign |
|
R8498:Iqcn
|
UTSW |
8 |
71,162,625 (GRCm39) |
missense |
probably benign |
0.19 |
R8542:Iqcn
|
UTSW |
8 |
71,166,520 (GRCm39) |
splice site |
probably null |
|
R8709:Iqcn
|
UTSW |
8 |
71,162,372 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9141:Iqcn
|
UTSW |
8 |
71,162,421 (GRCm39) |
missense |
probably benign |
0.15 |
R9313:Iqcn
|
UTSW |
8 |
71,161,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R9324:Iqcn
|
UTSW |
8 |
71,161,794 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1177:Iqcn
|
UTSW |
8 |
71,169,752 (GRCm39) |
missense |
possibly damaging |
0.92 |
|