Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
C |
1: 71,353,183 (GRCm39) |
D753G |
probably benign |
Het |
Adat2 |
T |
C |
10: 13,432,590 (GRCm39) |
|
probably benign |
Het |
Ahsa2 |
A |
G |
11: 23,440,426 (GRCm39) |
L275S |
probably benign |
Het |
Arhgef38 |
C |
T |
3: 132,837,828 (GRCm39) |
D118N |
possibly damaging |
Het |
Bicra |
A |
T |
7: 15,709,726 (GRCm39) |
H1097Q |
probably benign |
Het |
C4b |
T |
C |
17: 34,950,104 (GRCm39) |
T1389A |
possibly damaging |
Het |
Cd180 |
A |
G |
13: 102,841,535 (GRCm39) |
S194G |
probably benign |
Het |
Chgb |
C |
A |
2: 132,635,434 (GRCm39) |
Q459K |
probably benign |
Het |
Clvs1 |
G |
T |
4: 9,449,385 (GRCm39) |
|
probably benign |
Het |
Cpox |
G |
A |
16: 58,492,923 (GRCm39) |
G186R |
probably damaging |
Het |
Cul5 |
A |
G |
9: 53,553,975 (GRCm39) |
|
probably benign |
Het |
Epsti1 |
G |
A |
14: 78,212,021 (GRCm39) |
R249K |
probably benign |
Het |
Gabrg1 |
A |
T |
5: 70,952,025 (GRCm39) |
Y90* |
probably null |
Het |
Gabrp |
T |
C |
11: 33,504,980 (GRCm39) |
R274G |
probably damaging |
Het |
Gm6401 |
C |
T |
14: 41,788,851 (GRCm39) |
E73K |
possibly damaging |
Het |
Hectd4 |
C |
T |
5: 121,486,857 (GRCm39) |
T3284M |
possibly damaging |
Het |
Lpar6 |
T |
C |
14: 73,476,882 (GRCm39) |
V281A |
possibly damaging |
Het |
Med18 |
G |
T |
4: 132,186,924 (GRCm39) |
Q192K |
possibly damaging |
Het |
Mis18bp1 |
A |
G |
12: 65,208,704 (GRCm39) |
V3A |
probably benign |
Het |
Mpped2 |
G |
T |
2: 106,613,968 (GRCm39) |
|
probably benign |
Het |
Ms4a10 |
A |
G |
19: 10,946,035 (GRCm39) |
V32A |
probably benign |
Het |
Mthfd1l |
T |
A |
10: 3,968,601 (GRCm39) |
|
probably null |
Het |
Myh1 |
A |
T |
11: 67,097,213 (GRCm39) |
Q422L |
possibly damaging |
Het |
Myo3b |
A |
T |
2: 70,085,721 (GRCm39) |
Q819L |
possibly damaging |
Het |
Ncoa1 |
G |
A |
12: 4,324,818 (GRCm39) |
T921I |
possibly damaging |
Het |
Or10d4b |
A |
G |
9: 39,534,694 (GRCm39) |
I92V |
probably damaging |
Het |
Or6c214 |
A |
G |
10: 129,591,238 (GRCm39) |
L27P |
possibly damaging |
Het |
Or8c16 |
A |
C |
9: 38,130,361 (GRCm39) |
T81P |
probably damaging |
Het |
Phf3 |
A |
G |
1: 30,843,734 (GRCm39) |
S1742P |
probably benign |
Het |
Plxdc2 |
G |
A |
2: 16,655,043 (GRCm39) |
|
probably null |
Het |
Poc5 |
A |
G |
13: 96,538,123 (GRCm39) |
T263A |
probably benign |
Het |
Prss41 |
T |
A |
17: 24,061,396 (GRCm39) |
I132F |
probably damaging |
Het |
Pxylp1 |
A |
G |
9: 96,707,195 (GRCm39) |
I329T |
probably benign |
Het |
Rbm27 |
T |
C |
18: 42,466,464 (GRCm39) |
|
probably null |
Het |
Rnps1-ps |
T |
C |
6: 7,982,857 (GRCm39) |
|
noncoding transcript |
Het |
Rpgrip1l |
A |
T |
8: 91,987,411 (GRCm39) |
V882E |
probably damaging |
Het |
Sec16b |
T |
C |
1: 157,388,369 (GRCm39) |
S579P |
probably benign |
Het |
Senp7 |
A |
G |
16: 55,996,249 (GRCm39) |
E776G |
probably damaging |
Het |
Smc2 |
A |
G |
4: 52,449,638 (GRCm39) |
I207V |
probably benign |
Het |
Spata31e5 |
A |
G |
1: 28,817,664 (GRCm39) |
F123L |
probably benign |
Het |
Spats2 |
A |
G |
15: 99,078,569 (GRCm39) |
T211A |
probably benign |
Het |
Sphkap |
A |
T |
1: 83,254,552 (GRCm39) |
S779T |
probably damaging |
Het |
Syt11 |
A |
T |
3: 88,656,148 (GRCm39) |
M1K |
probably null |
Het |
Tacc2 |
A |
G |
7: 130,225,585 (GRCm39) |
T757A |
possibly damaging |
Het |
Tecta |
A |
C |
9: 42,256,789 (GRCm39) |
M1629R |
probably benign |
Het |
Ufsp2 |
T |
A |
8: 46,437,137 (GRCm39) |
I101N |
probably damaging |
Het |
Unc13b |
T |
A |
4: 43,235,368 (GRCm39) |
C892S |
probably damaging |
Het |
Ush1c |
A |
G |
7: 45,874,361 (GRCm39) |
|
probably benign |
Het |
Vwde |
A |
T |
6: 13,208,381 (GRCm39) |
V167E |
probably benign |
Het |
Wdfy4 |
A |
G |
14: 32,862,608 (GRCm39) |
L588P |
probably damaging |
Het |
Zfyve1 |
T |
C |
12: 83,621,595 (GRCm39) |
T267A |
probably damaging |
Het |
|
Other mutations in Hoxc9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01413:Hoxc9
|
APN |
15 |
102,892,432 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01418:Hoxc9
|
APN |
15 |
102,892,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R0498:Hoxc9
|
UTSW |
15 |
102,892,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R1436:Hoxc9
|
UTSW |
15 |
102,890,304 (GRCm39) |
missense |
probably benign |
0.03 |
R2059:Hoxc9
|
UTSW |
15 |
102,892,555 (GRCm39) |
missense |
probably benign |
0.01 |
R2414:Hoxc9
|
UTSW |
15 |
102,892,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R2900:Hoxc9
|
UTSW |
15 |
102,890,185 (GRCm39) |
missense |
probably benign |
0.00 |
R3807:Hoxc9
|
UTSW |
15 |
102,890,116 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3821:Hoxc9
|
UTSW |
15 |
102,890,596 (GRCm39) |
missense |
probably benign |
0.32 |
R4824:Hoxc9
|
UTSW |
15 |
102,890,225 (GRCm39) |
nonsense |
probably null |
|
R5165:Hoxc9
|
UTSW |
15 |
102,892,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R5700:Hoxc9
|
UTSW |
15 |
102,890,313 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5701:Hoxc9
|
UTSW |
15 |
102,890,313 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6003:Hoxc9
|
UTSW |
15 |
102,890,311 (GRCm39) |
missense |
probably benign |
0.15 |
R6145:Hoxc9
|
UTSW |
15 |
102,892,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R6570:Hoxc9
|
UTSW |
15 |
102,890,185 (GRCm39) |
missense |
probably benign |
0.00 |
R7312:Hoxc9
|
UTSW |
15 |
102,890,593 (GRCm39) |
missense |
probably benign |
0.02 |
R7434:Hoxc9
|
UTSW |
15 |
102,892,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R8080:Hoxc9
|
UTSW |
15 |
102,890,551 (GRCm39) |
missense |
probably benign |
0.22 |
R8519:Hoxc9
|
UTSW |
15 |
102,892,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R8792:Hoxc9
|
UTSW |
15 |
102,890,226 (GRCm39) |
missense |
probably benign |
0.00 |
R9705:Hoxc9
|
UTSW |
15 |
102,890,362 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9717:Hoxc9
|
UTSW |
15 |
102,890,551 (GRCm39) |
missense |
probably benign |
0.22 |
|