Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn2 |
T |
A |
13: 12,290,065 (GRCm39) |
T734S |
probably damaging |
Het |
Acvr2a |
A |
T |
2: 48,760,324 (GRCm39) |
T27S |
possibly damaging |
Het |
Ankhd1 |
T |
A |
18: 36,781,432 (GRCm39) |
N2161K |
probably damaging |
Het |
Apba3 |
A |
G |
10: 81,107,542 (GRCm39) |
Y350C |
probably damaging |
Het |
Bnipl |
T |
A |
3: 95,157,181 (GRCm39) |
R47S |
possibly damaging |
Het |
Cacna1b |
C |
T |
2: 24,651,800 (GRCm39) |
M126I |
probably damaging |
Het |
Cep112 |
G |
A |
11: 108,461,187 (GRCm39) |
E329K |
probably damaging |
Het |
Cep55 |
T |
A |
19: 38,057,558 (GRCm39) |
Y187N |
probably damaging |
Het |
Cngb3 |
T |
C |
4: 19,415,690 (GRCm39) |
I400T |
possibly damaging |
Het |
Csad |
T |
C |
15: 102,096,028 (GRCm39) |
N142D |
probably benign |
Het |
Dars1 |
A |
T |
1: 128,306,595 (GRCm39) |
I195N |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 50,050,698 (GRCm39) |
L2454Q |
probably benign |
Het |
Emc1 |
A |
T |
4: 139,093,841 (GRCm39) |
E650D |
probably benign |
Het |
Enam |
A |
G |
5: 88,650,603 (GRCm39) |
D704G |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,477,683 (GRCm39) |
I2220N |
probably damaging |
Het |
Fat4 |
T |
C |
3: 39,035,566 (GRCm39) |
S3073P |
probably benign |
Het |
Fbxl4 |
T |
C |
4: 22,403,624 (GRCm39) |
M399T |
probably benign |
Het |
Gcsh |
G |
A |
8: 117,715,909 (GRCm39) |
T58M |
possibly damaging |
Het |
Ghrhr |
T |
C |
6: 55,356,726 (GRCm39) |
Y108H |
probably damaging |
Het |
Gm5431 |
A |
T |
11: 48,780,058 (GRCm39) |
I566N |
probably damaging |
Het |
Gnb5 |
A |
T |
9: 75,234,511 (GRCm39) |
D70V |
probably damaging |
Het |
Grin2c |
G |
T |
11: 115,141,492 (GRCm39) |
S875R |
probably benign |
Het |
Itch |
A |
C |
2: 155,044,141 (GRCm39) |
Q482P |
probably benign |
Het |
Krt87 |
T |
C |
15: 101,336,314 (GRCm39) |
E113G |
probably damaging |
Het |
Map4 |
A |
G |
9: 109,900,116 (GRCm39) |
E934G |
probably damaging |
Het |
Mkx |
A |
G |
18: 7,000,675 (GRCm39) |
L89P |
probably damaging |
Het |
Myo15a |
T |
A |
11: 60,400,847 (GRCm39) |
Y2982* |
probably null |
Het |
Nedd4 |
C |
T |
9: 72,632,356 (GRCm39) |
L397F |
possibly damaging |
Het |
Nom1 |
A |
G |
5: 29,641,019 (GRCm39) |
D353G |
probably benign |
Het |
Notch1 |
A |
T |
2: 26,353,816 (GRCm39) |
L1937* |
probably null |
Het |
Nrxn2 |
A |
T |
19: 6,540,139 (GRCm39) |
D820V |
probably damaging |
Het |
Nup210 |
A |
T |
6: 91,032,226 (GRCm39) |
N47K |
probably benign |
Het |
Or1j12 |
T |
A |
2: 36,342,600 (GRCm39) |
M1K |
probably null |
Het |
Or4p21 |
G |
A |
2: 88,277,054 (GRCm39) |
T76I |
probably benign |
Het |
Or6d14 |
A |
T |
6: 116,533,578 (GRCm39) |
Q64L |
probably damaging |
Het |
Pcolce2 |
A |
T |
9: 95,576,742 (GRCm39) |
I338F |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,799,046 (GRCm39) |
M2755T |
possibly damaging |
Het |
Plekhg4 |
TAGTCGATGCCCGAGTC |
TAGTC |
8: 106,103,084 (GRCm39) |
|
probably benign |
Het |
Rab3a |
T |
C |
8: 71,209,872 (GRCm39) |
S51P |
probably benign |
Het |
Scn10a |
G |
A |
9: 119,438,070 (GRCm39) |
A1933V |
probably benign |
Het |
Serpina1c |
T |
A |
12: 103,862,370 (GRCm39) |
Y315F |
probably damaging |
Het |
Slc29a4 |
A |
C |
5: 142,698,650 (GRCm39) |
I104L |
possibly damaging |
Het |
Spag16 |
G |
A |
1: 69,897,681 (GRCm39) |
V144I |
possibly damaging |
Het |
Sult2a8 |
T |
A |
7: 14,161,778 (GRCm39) |
I23L |
probably benign |
Het |
Thoc1 |
T |
A |
18: 9,986,300 (GRCm39) |
V344D |
probably damaging |
Het |
Tnn |
G |
C |
1: 159,924,798 (GRCm39) |
Y1185* |
probably null |
Het |
Trpc4 |
A |
G |
3: 54,209,614 (GRCm39) |
I660V |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,571,144 (GRCm39) |
Y1222H |
probably benign |
Het |
Usp4 |
A |
G |
9: 108,250,885 (GRCm39) |
E531G |
probably benign |
Het |
Vmn2r93 |
C |
T |
17: 18,525,428 (GRCm39) |
S362L |
probably damaging |
Het |
Zfhx3 |
G |
T |
8: 109,526,885 (GRCm39) |
E927D |
probably damaging |
Het |
Zfp644 |
A |
T |
5: 106,786,469 (GRCm39) |
M1K |
probably null |
Het |
Zp2 |
T |
C |
7: 119,737,529 (GRCm39) |
H252R |
probably benign |
Het |
|
Other mutations in Spata22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02016:Spata22
|
APN |
11 |
73,226,857 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02833:Spata22
|
APN |
11 |
73,234,569 (GRCm39) |
missense |
probably benign |
0.00 |
R0147:Spata22
|
UTSW |
11 |
73,221,979 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R0304:Spata22
|
UTSW |
11 |
73,231,275 (GRCm39) |
nonsense |
probably null |
|
R1855:Spata22
|
UTSW |
11 |
73,231,385 (GRCm39) |
missense |
probably benign |
0.00 |
R1967:Spata22
|
UTSW |
11 |
73,221,953 (GRCm39) |
unclassified |
probably benign |
|
R2073:Spata22
|
UTSW |
11 |
73,227,052 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2087:Spata22
|
UTSW |
11 |
73,231,079 (GRCm39) |
missense |
probably benign |
0.11 |
R2256:Spata22
|
UTSW |
11 |
73,231,301 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2509:Spata22
|
UTSW |
11 |
73,236,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R2849:Spata22
|
UTSW |
11 |
73,244,571 (GRCm39) |
nonsense |
probably null |
|
R2883:Spata22
|
UTSW |
11 |
73,235,504 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3236:Spata22
|
UTSW |
11 |
73,236,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R3237:Spata22
|
UTSW |
11 |
73,236,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R4560:Spata22
|
UTSW |
11 |
73,236,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Spata22
|
UTSW |
11 |
73,236,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R5171:Spata22
|
UTSW |
11 |
73,227,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R5893:Spata22
|
UTSW |
11 |
73,227,073 (GRCm39) |
nonsense |
probably null |
|
R6401:Spata22
|
UTSW |
11 |
73,224,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R6493:Spata22
|
UTSW |
11 |
73,244,572 (GRCm39) |
makesense |
probably null |
|
R6496:Spata22
|
UTSW |
11 |
73,231,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R6647:Spata22
|
UTSW |
11 |
73,245,526 (GRCm39) |
splice site |
probably null |
|
R6838:Spata22
|
UTSW |
11 |
73,236,759 (GRCm39) |
missense |
probably benign |
|
R7099:Spata22
|
UTSW |
11 |
73,231,225 (GRCm39) |
missense |
probably benign |
|
R7396:Spata22
|
UTSW |
11 |
73,236,702 (GRCm39) |
missense |
probably damaging |
0.98 |
R7453:Spata22
|
UTSW |
11 |
73,226,816 (GRCm39) |
splice site |
probably null |
|
R7748:Spata22
|
UTSW |
11 |
73,227,080 (GRCm39) |
missense |
probably null |
0.99 |
R8870:Spata22
|
UTSW |
11 |
73,231,091 (GRCm39) |
missense |
probably damaging |
1.00 |
|