Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,141,973 (GRCm39) |
H3R |
probably benign |
Het |
Actg2 |
A |
T |
6: 83,499,866 (GRCm39) |
F128Y |
possibly damaging |
Het |
Ankrd6 |
G |
A |
4: 32,822,241 (GRCm39) |
T176M |
probably damaging |
Het |
Atp6ap1l |
T |
C |
13: 91,046,826 (GRCm39) |
D117G |
probably damaging |
Het |
Cd209b |
A |
G |
8: 3,968,714 (GRCm39) |
I284T |
probably damaging |
Het |
Cfl2 |
C |
T |
12: 54,908,143 (GRCm39) |
A123T |
probably benign |
Het |
Cgnl1 |
T |
C |
9: 71,631,822 (GRCm39) |
T510A |
probably benign |
Het |
Chn2 |
G |
T |
6: 54,249,963 (GRCm39) |
R24M |
probably damaging |
Het |
Cyfip2 |
T |
C |
11: 46,161,474 (GRCm39) |
I339V |
probably benign |
Het |
Etl4 |
C |
T |
2: 20,748,886 (GRCm39) |
P539L |
possibly damaging |
Het |
Fras1 |
A |
G |
5: 96,918,512 (GRCm39) |
D3516G |
probably benign |
Het |
Frem2 |
T |
C |
3: 53,433,317 (GRCm39) |
Y2669C |
probably damaging |
Het |
Gga2 |
G |
T |
7: 121,601,943 (GRCm39) |
H205N |
probably damaging |
Het |
Gm5592 |
G |
A |
7: 40,938,491 (GRCm39) |
G591D |
probably benign |
Het |
Gtf3c1 |
A |
T |
7: 125,246,622 (GRCm39) |
C1562* |
probably null |
Het |
Heatr3 |
T |
A |
8: 88,864,939 (GRCm39) |
C59S |
probably damaging |
Het |
Heatr5b |
A |
G |
17: 79,060,603 (GRCm39) |
M2024T |
possibly damaging |
Het |
Jarid2 |
T |
C |
13: 45,055,732 (GRCm39) |
S313P |
probably damaging |
Het |
Lzts3 |
A |
G |
2: 130,477,285 (GRCm39) |
S502P |
probably damaging |
Het |
Or5d36 |
A |
G |
2: 87,901,579 (GRCm39) |
V49A |
probably benign |
Het |
Pcdhb2 |
A |
T |
18: 37,428,594 (GRCm39) |
D189V |
probably damaging |
Het |
Pias3 |
G |
T |
3: 96,606,982 (GRCm39) |
G82C |
probably damaging |
Het |
Polg |
T |
C |
7: 79,105,285 (GRCm39) |
E753G |
probably damaging |
Het |
Pus10 |
T |
C |
11: 23,668,654 (GRCm39) |
|
probably null |
Het |
Pxn |
A |
G |
5: 115,684,966 (GRCm39) |
R264G |
probably damaging |
Het |
Rag1 |
A |
G |
2: 101,472,416 (GRCm39) |
Y909H |
probably damaging |
Het |
Rell2 |
A |
G |
18: 38,091,267 (GRCm39) |
H144R |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Ryr2 |
C |
T |
13: 11,602,323 (GRCm39) |
V4520I |
possibly damaging |
Het |
Scp2 |
A |
G |
4: 107,921,181 (GRCm39) |
F10L |
probably benign |
Het |
Slc9b2 |
T |
C |
3: 135,035,598 (GRCm39) |
Y356H |
probably benign |
Het |
Stra6 |
T |
A |
9: 58,058,501 (GRCm39) |
V454E |
probably damaging |
Het |
Tbc1d8 |
T |
C |
1: 39,411,512 (GRCm39) |
N1108S |
probably benign |
Het |
Tep1 |
C |
T |
14: 51,081,191 (GRCm39) |
R1349Q |
possibly damaging |
Het |
Tmem132d |
T |
C |
5: 128,345,884 (GRCm39) |
R213G |
probably benign |
Het |
Ubash3a |
T |
C |
17: 31,456,249 (GRCm39) |
Y506H |
probably damaging |
Het |
Xcr1 |
A |
C |
9: 123,685,561 (GRCm39) |
V67G |
probably damaging |
Het |
Zranb2 |
C |
A |
3: 157,243,227 (GRCm39) |
C74* |
probably null |
Het |
|
Other mutations in Sorcs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Sorcs1
|
APN |
19 |
50,178,492 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00983:Sorcs1
|
APN |
19 |
50,164,566 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01125:Sorcs1
|
APN |
19 |
50,216,639 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01320:Sorcs1
|
APN |
19 |
50,276,517 (GRCm39) |
splice site |
probably benign |
|
IGL01445:Sorcs1
|
APN |
19 |
50,141,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01682:Sorcs1
|
APN |
19 |
50,169,944 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01799:Sorcs1
|
APN |
19 |
50,218,647 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02044:Sorcs1
|
APN |
19 |
50,276,597 (GRCm39) |
splice site |
probably benign |
|
IGL02111:Sorcs1
|
APN |
19 |
50,218,683 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02364:Sorcs1
|
APN |
19 |
50,322,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02378:Sorcs1
|
APN |
19 |
50,171,109 (GRCm39) |
nonsense |
probably null |
|
IGL02498:Sorcs1
|
APN |
19 |
50,666,606 (GRCm39) |
missense |
probably benign |
|
IGL02658:Sorcs1
|
APN |
19 |
50,178,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Sorcs1
|
APN |
19 |
50,666,368 (GRCm39) |
nonsense |
probably null |
|
IGL02942:Sorcs1
|
APN |
19 |
50,463,875 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03057:Sorcs1
|
APN |
19 |
50,248,194 (GRCm39) |
nonsense |
probably null |
|
IGL03230:Sorcs1
|
APN |
19 |
50,230,531 (GRCm39) |
missense |
probably damaging |
1.00 |
P0033:Sorcs1
|
UTSW |
19 |
50,141,345 (GRCm39) |
missense |
probably damaging |
0.98 |
R0109:Sorcs1
|
UTSW |
19 |
50,367,329 (GRCm39) |
splice site |
probably benign |
|
R0115:Sorcs1
|
UTSW |
19 |
50,624,891 (GRCm39) |
intron |
probably benign |
|
R0242:Sorcs1
|
UTSW |
19 |
50,216,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Sorcs1
|
UTSW |
19 |
50,216,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Sorcs1
|
UTSW |
19 |
50,301,480 (GRCm39) |
splice site |
probably null |
|
R0481:Sorcs1
|
UTSW |
19 |
50,624,891 (GRCm39) |
intron |
probably benign |
|
R0581:Sorcs1
|
UTSW |
19 |
50,241,139 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0669:Sorcs1
|
UTSW |
19 |
50,230,380 (GRCm39) |
splice site |
probably benign |
|
R0980:Sorcs1
|
UTSW |
19 |
50,220,761 (GRCm39) |
missense |
probably benign |
0.04 |
R1158:Sorcs1
|
UTSW |
19 |
50,132,598 (GRCm39) |
unclassified |
probably benign |
|
R1519:Sorcs1
|
UTSW |
19 |
50,241,025 (GRCm39) |
missense |
probably benign |
0.05 |
R1669:Sorcs1
|
UTSW |
19 |
50,463,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R1779:Sorcs1
|
UTSW |
19 |
50,163,481 (GRCm39) |
splice site |
probably benign |
|
R1783:Sorcs1
|
UTSW |
19 |
50,216,747 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1927:Sorcs1
|
UTSW |
19 |
50,210,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Sorcs1
|
UTSW |
19 |
50,221,082 (GRCm39) |
missense |
probably damaging |
0.96 |
R1936:Sorcs1
|
UTSW |
19 |
50,221,082 (GRCm39) |
missense |
probably damaging |
0.96 |
R2109:Sorcs1
|
UTSW |
19 |
50,666,630 (GRCm39) |
missense |
probably benign |
|
R2206:Sorcs1
|
UTSW |
19 |
50,218,655 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2207:Sorcs1
|
UTSW |
19 |
50,218,655 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3031:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R3032:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R3107:Sorcs1
|
UTSW |
19 |
50,199,088 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3508:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R3738:Sorcs1
|
UTSW |
19 |
50,139,659 (GRCm39) |
missense |
probably benign |
0.03 |
R4212:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R4213:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R4385:Sorcs1
|
UTSW |
19 |
50,178,599 (GRCm39) |
missense |
probably benign |
0.01 |
R4424:Sorcs1
|
UTSW |
19 |
50,367,379 (GRCm39) |
missense |
probably damaging |
0.97 |
R4603:Sorcs1
|
UTSW |
19 |
50,301,402 (GRCm39) |
critical splice donor site |
probably null |
|
R4679:Sorcs1
|
UTSW |
19 |
50,171,107 (GRCm39) |
missense |
probably benign |
|
R4780:Sorcs1
|
UTSW |
19 |
50,132,419 (GRCm39) |
unclassified |
probably benign |
|
R4781:Sorcs1
|
UTSW |
19 |
50,171,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Sorcs1
|
UTSW |
19 |
50,218,740 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4823:Sorcs1
|
UTSW |
19 |
50,666,578 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4883:Sorcs1
|
UTSW |
19 |
50,220,741 (GRCm39) |
missense |
probably benign |
0.00 |
R5091:Sorcs1
|
UTSW |
19 |
50,248,190 (GRCm39) |
critical splice donor site |
probably null |
|
R5105:Sorcs1
|
UTSW |
19 |
50,213,579 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5437:Sorcs1
|
UTSW |
19 |
50,241,040 (GRCm39) |
missense |
probably benign |
0.19 |
R5574:Sorcs1
|
UTSW |
19 |
50,210,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R5734:Sorcs1
|
UTSW |
19 |
50,171,213 (GRCm39) |
missense |
probably benign |
0.04 |
R6045:Sorcs1
|
UTSW |
19 |
50,178,555 (GRCm39) |
nonsense |
probably null |
|
R6091:Sorcs1
|
UTSW |
19 |
50,276,539 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6119:Sorcs1
|
UTSW |
19 |
50,276,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R6226:Sorcs1
|
UTSW |
19 |
50,169,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R6337:Sorcs1
|
UTSW |
19 |
50,132,562 (GRCm39) |
missense |
probably benign |
0.00 |
R6378:Sorcs1
|
UTSW |
19 |
50,213,615 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6782:Sorcs1
|
UTSW |
19 |
50,164,560 (GRCm39) |
nonsense |
probably null |
|
R6792:Sorcs1
|
UTSW |
19 |
50,666,606 (GRCm39) |
missense |
probably benign |
|
R6891:Sorcs1
|
UTSW |
19 |
50,213,557 (GRCm39) |
nonsense |
probably null |
|
R7151:Sorcs1
|
UTSW |
19 |
50,301,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R7223:Sorcs1
|
UTSW |
19 |
50,178,480 (GRCm39) |
missense |
probably benign |
0.06 |
R7356:Sorcs1
|
UTSW |
19 |
50,163,595 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7471:Sorcs1
|
UTSW |
19 |
50,250,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R7474:Sorcs1
|
UTSW |
19 |
50,141,550 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7503:Sorcs1
|
UTSW |
19 |
50,141,490 (GRCm39) |
missense |
probably benign |
|
R7506:Sorcs1
|
UTSW |
19 |
50,171,112 (GRCm39) |
nonsense |
probably null |
|
R7573:Sorcs1
|
UTSW |
19 |
50,141,234 (GRCm39) |
nonsense |
probably null |
|
R7867:Sorcs1
|
UTSW |
19 |
50,218,698 (GRCm39) |
nonsense |
probably null |
|
R7911:Sorcs1
|
UTSW |
19 |
50,132,470 (GRCm39) |
missense |
unknown |
|
R8032:Sorcs1
|
UTSW |
19 |
50,463,846 (GRCm39) |
missense |
probably benign |
0.28 |
R8063:Sorcs1
|
UTSW |
19 |
50,132,415 (GRCm39) |
missense |
unknown |
|
R8463:Sorcs1
|
UTSW |
19 |
50,248,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8682:Sorcs1
|
UTSW |
19 |
50,367,398 (GRCm39) |
missense |
probably damaging |
0.99 |
R8724:Sorcs1
|
UTSW |
19 |
50,139,658 (GRCm39) |
missense |
probably benign |
0.33 |
R8926:Sorcs1
|
UTSW |
19 |
50,241,096 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9160:Sorcs1
|
UTSW |
19 |
50,213,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R9173:Sorcs1
|
UTSW |
19 |
50,220,753 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9203:Sorcs1
|
UTSW |
19 |
50,250,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R9229:Sorcs1
|
UTSW |
19 |
50,141,300 (GRCm39) |
missense |
probably benign |
0.17 |
R9398:Sorcs1
|
UTSW |
19 |
50,213,651 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9430:Sorcs1
|
UTSW |
19 |
50,199,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9510:Sorcs1
|
UTSW |
19 |
50,666,521 (GRCm39) |
missense |
probably benign |
0.04 |
R9511:Sorcs1
|
UTSW |
19 |
50,666,521 (GRCm39) |
missense |
probably benign |
0.04 |
R9744:Sorcs1
|
UTSW |
19 |
50,215,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9777:Sorcs1
|
UTSW |
19 |
50,248,190 (GRCm39) |
critical splice donor site |
probably null |
|
X0024:Sorcs1
|
UTSW |
19 |
50,171,201 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1088:Sorcs1
|
UTSW |
19 |
50,210,581 (GRCm39) |
missense |
probably benign |
0.16 |
Z1177:Sorcs1
|
UTSW |
19 |
50,322,037 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sorcs1
|
UTSW |
19 |
50,215,180 (GRCm39) |
missense |
probably null |
1.00 |
|