Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adtrp |
C |
T |
13: 41,981,735 (GRCm39) |
V13I |
probably damaging |
Het |
Ak2 |
A |
G |
4: 128,902,013 (GRCm39) |
K229E |
probably benign |
Het |
Atp13a4 |
A |
T |
16: 29,241,502 (GRCm39) |
V741D |
probably damaging |
Het |
Bdp1 |
A |
T |
13: 100,197,697 (GRCm39) |
M896K |
probably benign |
Het |
Ccser1 |
C |
T |
6: 61,288,547 (GRCm39) |
R237C |
probably benign |
Het |
Cdk7 |
A |
G |
13: 100,859,182 (GRCm39) |
|
probably benign |
Het |
CK137956 |
A |
G |
4: 127,845,180 (GRCm39) |
S188P |
probably benign |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dbndd2 |
A |
G |
2: 164,330,563 (GRCm39) |
D72G |
probably damaging |
Het |
Disp3 |
A |
T |
4: 148,344,423 (GRCm39) |
I493N |
probably damaging |
Het |
Dnaaf10 |
A |
T |
11: 17,179,832 (GRCm39) |
T278S |
probably benign |
Het |
Epx |
T |
C |
11: 87,755,650 (GRCm39) |
D678G |
probably damaging |
Het |
Fbxw5 |
G |
T |
2: 25,394,810 (GRCm39) |
V235L |
probably damaging |
Het |
Fmo4 |
T |
A |
1: 162,621,741 (GRCm39) |
D490V |
probably damaging |
Het |
Fuca2 |
A |
G |
10: 13,382,518 (GRCm39) |
Y268C |
probably damaging |
Het |
Gm4787 |
C |
T |
12: 81,425,544 (GRCm39) |
V205I |
probably damaging |
Het |
Gpat3 |
G |
A |
5: 101,045,687 (GRCm39) |
R437K |
probably benign |
Het |
Herc2 |
A |
G |
7: 55,834,121 (GRCm39) |
S3109G |
probably damaging |
Het |
Hr |
G |
A |
14: 70,808,888 (GRCm39) |
R1117H |
probably damaging |
Het |
Htra4 |
T |
A |
8: 25,523,593 (GRCm39) |
D324V |
probably damaging |
Het |
Kcnd3 |
A |
G |
3: 105,366,853 (GRCm39) |
Y241C |
probably damaging |
Het |
Kcp |
G |
A |
6: 29,489,071 (GRCm39) |
L1072F |
probably damaging |
Het |
Lrrc52 |
T |
C |
1: 167,294,028 (GRCm39) |
N86D |
probably benign |
Het |
Mindy4 |
A |
G |
6: 55,188,247 (GRCm39) |
T26A |
probably damaging |
Het |
Mre11a |
A |
T |
9: 14,707,101 (GRCm39) |
N117Y |
probably damaging |
Het |
Mrgprb1 |
A |
T |
7: 48,097,076 (GRCm39) |
S279T |
possibly damaging |
Het |
Myh13 |
T |
G |
11: 67,241,064 (GRCm39) |
S814A |
probably benign |
Het |
Ncapd2 |
A |
G |
6: 125,153,678 (GRCm39) |
V679A |
possibly damaging |
Het |
Nipbl |
A |
T |
15: 8,379,771 (GRCm39) |
V1007D |
probably damaging |
Het |
Nlrp12 |
T |
A |
7: 3,277,049 (GRCm39) |
H960L |
probably damaging |
Het |
Or3a1c |
T |
A |
11: 74,046,769 (GRCm39) |
M263K |
possibly damaging |
Het |
Or4a72 |
C |
T |
2: 89,405,558 (GRCm39) |
V171I |
probably benign |
Het |
Or7e169 |
A |
G |
9: 19,757,709 (GRCm39) |
S69P |
probably benign |
Het |
Pklr |
A |
G |
3: 89,050,545 (GRCm39) |
Y402C |
probably damaging |
Het |
Prdm2 |
T |
C |
4: 142,859,334 (GRCm39) |
T1319A |
possibly damaging |
Het |
Rif1 |
T |
A |
2: 51,982,358 (GRCm39) |
V541E |
probably damaging |
Het |
Ryk |
T |
A |
9: 102,758,855 (GRCm39) |
I248N |
possibly damaging |
Het |
Shisa2 |
A |
T |
14: 59,867,134 (GRCm39) |
I129F |
probably damaging |
Het |
Snap25 |
T |
G |
2: 136,611,973 (GRCm39) |
|
probably benign |
Het |
Spata31g1 |
C |
T |
4: 42,974,131 (GRCm39) |
Q1155* |
probably null |
Het |
Tas2r140 |
A |
G |
6: 40,469,154 (GRCm39) |
K328R |
possibly damaging |
Het |
Tas2r140 |
T |
C |
6: 133,032,213 (GRCm39) |
T182A |
probably benign |
Het |
Thumpd2 |
G |
A |
17: 81,372,387 (GRCm39) |
R35C |
probably damaging |
Het |
Tnxb |
A |
T |
17: 34,937,443 (GRCm39) |
N3811Y |
probably damaging |
Het |
Tpte |
A |
C |
8: 22,835,901 (GRCm39) |
N428T |
probably damaging |
Het |
Trpm6 |
A |
G |
19: 18,831,629 (GRCm39) |
D1498G |
probably benign |
Het |
Tsc2 |
C |
T |
17: 24,842,444 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,703,277 (GRCm39) |
|
probably benign |
Het |
Wdr24 |
A |
G |
17: 26,045,017 (GRCm39) |
I251V |
probably benign |
Het |
Zc3h6 |
T |
C |
2: 128,848,006 (GRCm39) |
Y278H |
probably damaging |
Het |
Zfat |
A |
G |
15: 67,990,783 (GRCm39) |
|
probably null |
Het |
Zfp442 |
A |
T |
2: 150,250,042 (GRCm39) |
V620E |
possibly damaging |
Het |
Zfp788 |
A |
G |
7: 41,298,984 (GRCm39) |
H540R |
probably damaging |
Het |
|
Other mutations in Snx31 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Snx31
|
APN |
15 |
36,545,761 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01627:Snx31
|
APN |
15 |
36,517,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02514:Snx31
|
APN |
15 |
36,525,728 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03069:Snx31
|
APN |
15 |
36,525,749 (GRCm39) |
nonsense |
probably null |
|
IGL03182:Snx31
|
APN |
15 |
36,525,833 (GRCm39) |
missense |
probably benign |
0.00 |
R0755:Snx31
|
UTSW |
15 |
36,534,576 (GRCm39) |
missense |
probably damaging |
0.99 |
R1005:Snx31
|
UTSW |
15 |
36,517,837 (GRCm39) |
splice site |
probably benign |
|
R1463:Snx31
|
UTSW |
15 |
36,539,444 (GRCm39) |
missense |
probably null |
1.00 |
R1513:Snx31
|
UTSW |
15 |
36,545,745 (GRCm39) |
missense |
probably damaging |
0.99 |
R3404:Snx31
|
UTSW |
15 |
36,525,799 (GRCm39) |
missense |
probably benign |
0.00 |
R3720:Snx31
|
UTSW |
15 |
36,523,704 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4152:Snx31
|
UTSW |
15 |
36,525,785 (GRCm39) |
missense |
probably benign |
|
R4474:Snx31
|
UTSW |
15 |
36,546,256 (GRCm39) |
intron |
probably benign |
|
R4729:Snx31
|
UTSW |
15 |
36,523,698 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4998:Snx31
|
UTSW |
15 |
36,539,513 (GRCm39) |
missense |
probably damaging |
0.96 |
R5010:Snx31
|
UTSW |
15 |
36,555,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R5375:Snx31
|
UTSW |
15 |
36,525,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R5893:Snx31
|
UTSW |
15 |
36,523,601 (GRCm39) |
missense |
probably damaging |
0.98 |
R5970:Snx31
|
UTSW |
15 |
36,523,634 (GRCm39) |
nonsense |
probably null |
|
R6211:Snx31
|
UTSW |
15 |
36,547,030 (GRCm39) |
missense |
probably damaging |
0.98 |
R7198:Snx31
|
UTSW |
15 |
36,555,455 (GRCm39) |
missense |
probably benign |
0.04 |
R7293:Snx31
|
UTSW |
15 |
36,523,596 (GRCm39) |
missense |
probably damaging |
0.97 |
R7329:Snx31
|
UTSW |
15 |
36,555,621 (GRCm39) |
missense |
probably benign |
0.00 |
R7741:Snx31
|
UTSW |
15 |
36,523,587 (GRCm39) |
critical splice donor site |
probably null |
|
R8057:Snx31
|
UTSW |
15 |
36,523,606 (GRCm39) |
missense |
probably damaging |
0.98 |
R8791:Snx31
|
UTSW |
15 |
36,537,678 (GRCm39) |
missense |
probably benign |
0.01 |
R8806:Snx31
|
UTSW |
15 |
36,537,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R9349:Snx31
|
UTSW |
15 |
36,555,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Snx31
|
UTSW |
15 |
36,534,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|