Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcyap1r1 |
A |
G |
6: 55,457,078 (GRCm39) |
T270A |
probably null |
Het |
Adgrv1 |
A |
T |
13: 81,681,241 (GRCm39) |
|
probably benign |
Het |
Aldh1b1 |
A |
T |
4: 45,803,383 (GRCm39) |
D307V |
probably benign |
Het |
Aldh3a2 |
A |
T |
11: 61,153,065 (GRCm39) |
C220* |
probably null |
Het |
Ank2 |
T |
C |
3: 126,753,444 (GRCm39) |
Y279C |
probably damaging |
Het |
Anks1 |
T |
C |
17: 28,210,351 (GRCm39) |
Y444H |
probably benign |
Het |
Asph |
G |
T |
4: 9,531,968 (GRCm39) |
T383K |
probably benign |
Het |
Asphd1 |
G |
T |
7: 126,547,747 (GRCm39) |
S185R |
possibly damaging |
Het |
Bcl2a1d |
T |
A |
9: 88,613,748 (GRCm39) |
I9F |
probably damaging |
Het |
Bcl2l11 |
T |
C |
2: 127,970,961 (GRCm39) |
|
probably benign |
Het |
C2cd3 |
T |
G |
7: 100,062,581 (GRCm39) |
S656A |
possibly damaging |
Het |
Cd5l |
T |
C |
3: 87,274,929 (GRCm39) |
V156A |
probably damaging |
Het |
Cdh8 |
G |
C |
8: 99,757,536 (GRCm39) |
N687K |
probably damaging |
Het |
Cdk19 |
A |
G |
10: 40,352,232 (GRCm39) |
D338G |
probably benign |
Het |
Cenpf |
A |
G |
1: 189,390,728 (GRCm39) |
C1035R |
probably damaging |
Het |
Cep290 |
A |
G |
10: 100,384,776 (GRCm39) |
R1845G |
probably benign |
Het |
Cep295nl |
G |
T |
11: 118,224,650 (GRCm39) |
Q65K |
probably damaging |
Het |
Ciz1 |
T |
C |
2: 32,262,300 (GRCm39) |
|
probably benign |
Het |
Clasrp |
T |
C |
7: 19,324,173 (GRCm39) |
D234G |
possibly damaging |
Het |
Dctd |
C |
T |
8: 48,590,449 (GRCm39) |
|
probably benign |
Het |
Ddr2 |
A |
G |
1: 169,832,340 (GRCm39) |
V150A |
probably benign |
Het |
Dennd10 |
A |
G |
19: 60,819,252 (GRCm39) |
E120G |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,120,604 (GRCm39) |
S74P |
probably benign |
Het |
Dnttip2 |
C |
A |
3: 122,078,750 (GRCm39) |
A743E |
probably damaging |
Het |
Dysf |
A |
T |
6: 84,044,005 (GRCm39) |
Q281L |
possibly damaging |
Het |
Ece2 |
A |
G |
16: 20,462,905 (GRCm39) |
E610G |
probably damaging |
Het |
Edem3 |
T |
G |
1: 151,679,982 (GRCm39) |
|
probably null |
Het |
Ext1 |
G |
T |
15: 52,955,773 (GRCm39) |
N441K |
probably benign |
Het |
Fam118a |
A |
G |
15: 84,942,969 (GRCm39) |
R333G |
probably damaging |
Het |
Fat4 |
C |
T |
3: 38,945,754 (GRCm39) |
T1549I |
probably damaging |
Het |
Fbxo4 |
A |
G |
15: 4,005,394 (GRCm39) |
V162A |
probably damaging |
Het |
Fgd2 |
A |
G |
17: 29,592,223 (GRCm39) |
H385R |
possibly damaging |
Het |
Garnl3 |
A |
T |
2: 32,977,100 (GRCm39) |
M1K |
probably null |
Het |
Gm37267 |
T |
G |
1: 180,338,083 (GRCm39) |
|
noncoding transcript |
Het |
Gpbar1 |
C |
T |
1: 74,318,702 (GRCm39) |
A315V |
probably damaging |
Het |
Grm2 |
T |
C |
9: 106,524,844 (GRCm39) |
I624V |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,468,836 (GRCm39) |
I5042V |
probably benign |
Het |
Hnf4g |
T |
C |
3: 3,716,448 (GRCm39) |
Y291H |
possibly damaging |
Het |
Ighm |
A |
G |
12: 113,385,241 (GRCm39) |
S240P |
unknown |
Het |
Igkv4-91 |
A |
G |
6: 68,745,604 (GRCm39) |
I98T |
probably damaging |
Het |
Krt72 |
T |
C |
15: 101,694,469 (GRCm39) |
N142S |
probably damaging |
Het |
Kynu |
T |
A |
2: 43,569,830 (GRCm39) |
Y371N |
possibly damaging |
Het |
Ly9 |
G |
T |
1: 171,434,898 (GRCm39) |
|
probably benign |
Het |
Man1a2 |
C |
A |
3: 100,524,372 (GRCm39) |
V359F |
probably damaging |
Het |
Mast1 |
T |
C |
8: 85,647,287 (GRCm39) |
I623M |
probably damaging |
Het |
Mb |
A |
G |
15: 76,906,687 (GRCm39) |
|
probably null |
Het |
Mcm4 |
A |
C |
16: 15,452,374 (GRCm39) |
L113* |
probably null |
Het |
Mcub |
C |
T |
3: 129,710,685 (GRCm39) |
W249* |
probably null |
Het |
Mme |
T |
A |
3: 63,247,453 (GRCm39) |
V246E |
probably benign |
Het |
Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
Mrpl38 |
A |
G |
11: 116,025,098 (GRCm39) |
Y232H |
probably damaging |
Het |
Myh7b |
T |
A |
2: 155,455,420 (GRCm39) |
M89K |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,796,536 (GRCm39) |
S892G |
possibly damaging |
Het |
Nt5dc3 |
A |
G |
10: 86,652,941 (GRCm39) |
Y245C |
probably damaging |
Het |
Ntn1 |
CCTTCTTCT |
CCTTCT |
11: 68,103,852 (GRCm39) |
|
probably benign |
Het |
Or12d12 |
T |
A |
17: 37,611,095 (GRCm39) |
T73S |
probably benign |
Het |
Or12d14-ps1 |
A |
T |
17: 37,673,337 (GRCm39) |
I107L |
probably benign |
Het |
Or14a259 |
A |
T |
7: 86,012,692 (GRCm39) |
N284K |
probably damaging |
Het |
Or5m12 |
T |
A |
2: 85,734,715 (GRCm39) |
I228F |
probably benign |
Het |
Or8b36 |
G |
T |
9: 37,937,822 (GRCm39) |
C240F |
probably damaging |
Het |
Or8k28 |
A |
T |
2: 86,286,153 (GRCm39) |
I154N |
possibly damaging |
Het |
Palld |
A |
T |
8: 62,002,815 (GRCm39) |
|
probably benign |
Het |
Pcdhga10 |
T |
C |
18: 37,881,253 (GRCm39) |
V338A |
probably damaging |
Het |
Pcdhga11 |
A |
G |
18: 37,890,459 (GRCm39) |
Y489C |
probably damaging |
Het |
Pgm2 |
T |
C |
5: 64,261,237 (GRCm39) |
Y244H |
probably benign |
Het |
Phactr4 |
A |
T |
4: 132,105,759 (GRCm39) |
S102R |
probably damaging |
Het |
Plekha5 |
A |
G |
6: 140,471,636 (GRCm39) |
Y20C |
probably damaging |
Het |
Rdh19 |
A |
G |
10: 127,696,013 (GRCm39) |
D255G |
probably benign |
Het |
Rgs3 |
T |
C |
4: 62,549,532 (GRCm39) |
V438A |
probably benign |
Het |
Rnf186 |
A |
G |
4: 138,695,254 (GRCm39) |
T265A |
probably benign |
Het |
Ror1 |
T |
C |
4: 100,283,195 (GRCm39) |
F420S |
probably benign |
Het |
Rtkn2 |
A |
G |
10: 67,841,463 (GRCm39) |
K204E |
probably damaging |
Het |
Rundc1 |
A |
G |
11: 101,324,874 (GRCm39) |
T527A |
probably benign |
Het |
Samd4 |
T |
C |
14: 47,303,920 (GRCm39) |
S301P |
probably damaging |
Het |
Scaf1 |
G |
A |
7: 44,655,303 (GRCm39) |
|
probably benign |
Het |
Stab2 |
T |
C |
10: 86,778,099 (GRCm39) |
D743G |
probably damaging |
Het |
Stim1 |
A |
T |
7: 102,003,779 (GRCm39) |
I71F |
probably damaging |
Het |
Stk17b |
T |
C |
1: 53,796,693 (GRCm39) |
D358G |
probably benign |
Het |
Sun2 |
A |
G |
15: 79,611,765 (GRCm39) |
Y551H |
probably damaging |
Het |
Tas2r110 |
A |
T |
6: 132,845,091 (GRCm39) |
T41S |
probably benign |
Het |
Tead3 |
T |
A |
17: 28,552,589 (GRCm39) |
E268V |
probably damaging |
Het |
Tead3 |
A |
G |
17: 28,553,962 (GRCm39) |
S131P |
probably benign |
Het |
Tepsin |
A |
T |
11: 119,982,351 (GRCm39) |
M505K |
possibly damaging |
Het |
Trbv28 |
A |
G |
6: 41,248,668 (GRCm39) |
Y66C |
possibly damaging |
Het |
Ttc6 |
A |
G |
12: 57,749,142 (GRCm39) |
Q1358R |
probably damaging |
Het |
Ttll2 |
C |
T |
17: 7,618,998 (GRCm39) |
V310I |
probably benign |
Het |
Uaca |
T |
C |
9: 60,753,283 (GRCm39) |
V76A |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,663,425 (GRCm39) |
T2789S |
probably benign |
Het |
Yipf4 |
T |
C |
17: 74,801,089 (GRCm39) |
F136L |
probably benign |
Het |
Zdhhc1 |
CGGGGG |
CGGGGGG |
8: 106,210,376 (GRCm39) |
|
probably null |
Het |
Zfp804b |
A |
T |
5: 6,926,479 (GRCm39) |
D51E |
probably damaging |
Het |
Zfyve9 |
C |
T |
4: 108,538,183 (GRCm39) |
G969R |
probably damaging |
Het |
|
Other mutations in Srgap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00677:Srgap2
|
APN |
1 |
131,284,438 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01738:Srgap2
|
APN |
1 |
131,224,164 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01933:Srgap2
|
APN |
1 |
131,339,593 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01964:Srgap2
|
APN |
1 |
131,217,316 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02028:Srgap2
|
APN |
1 |
131,224,173 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02159:Srgap2
|
APN |
1 |
131,247,404 (GRCm39) |
splice site |
probably benign |
|
IGL02326:Srgap2
|
APN |
1 |
131,284,645 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02396:Srgap2
|
APN |
1 |
131,220,413 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02407:Srgap2
|
APN |
1 |
131,247,340 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02444:Srgap2
|
APN |
1 |
131,252,891 (GRCm39) |
splice site |
probably null |
|
IGL02559:Srgap2
|
APN |
1 |
131,452,674 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02900:Srgap2
|
APN |
1 |
131,339,534 (GRCm39) |
splice site |
probably benign |
|
IGL03150:Srgap2
|
APN |
1 |
131,238,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0008:Srgap2
|
UTSW |
1 |
131,283,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R0008:Srgap2
|
UTSW |
1 |
131,283,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R0016:Srgap2
|
UTSW |
1 |
131,277,200 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0016:Srgap2
|
UTSW |
1 |
131,277,200 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0044:Srgap2
|
UTSW |
1 |
131,247,289 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0441:Srgap2
|
UTSW |
1 |
131,264,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R0580:Srgap2
|
UTSW |
1 |
131,277,239 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0882:Srgap2
|
UTSW |
1 |
131,217,253 (GRCm39) |
missense |
probably benign |
0.00 |
R1412:Srgap2
|
UTSW |
1 |
131,228,151 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1501:Srgap2
|
UTSW |
1 |
131,220,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R1740:Srgap2
|
UTSW |
1 |
131,217,126 (GRCm39) |
missense |
probably benign |
0.00 |
R1764:Srgap2
|
UTSW |
1 |
131,247,275 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1772:Srgap2
|
UTSW |
1 |
131,247,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R1776:Srgap2
|
UTSW |
1 |
131,339,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R2393:Srgap2
|
UTSW |
1 |
131,259,872 (GRCm39) |
missense |
probably benign |
0.00 |
R3011:Srgap2
|
UTSW |
1 |
131,238,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R3149:Srgap2
|
UTSW |
1 |
131,220,327 (GRCm39) |
missense |
probably benign |
0.00 |
R3150:Srgap2
|
UTSW |
1 |
131,220,327 (GRCm39) |
missense |
probably benign |
0.00 |
R3800:Srgap2
|
UTSW |
1 |
131,238,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Srgap2
|
UTSW |
1 |
131,220,314 (GRCm39) |
splice site |
probably null |
|
R5454:Srgap2
|
UTSW |
1 |
131,217,475 (GRCm39) |
missense |
probably benign |
0.08 |
R5536:Srgap2
|
UTSW |
1 |
131,228,128 (GRCm39) |
splice site |
probably null |
|
R6113:Srgap2
|
UTSW |
1 |
131,283,243 (GRCm39) |
splice site |
probably null |
|
R6174:Srgap2
|
UTSW |
1 |
131,217,354 (GRCm39) |
missense |
probably benign |
0.00 |
R6180:Srgap2
|
UTSW |
1 |
131,277,279 (GRCm39) |
missense |
probably benign |
0.00 |
R6341:Srgap2
|
UTSW |
1 |
131,219,367 (GRCm39) |
missense |
probably benign |
0.02 |
R6357:Srgap2
|
UTSW |
1 |
131,283,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R6363:Srgap2
|
UTSW |
1 |
131,226,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R6770:Srgap2
|
UTSW |
1 |
131,226,248 (GRCm39) |
missense |
probably benign |
0.00 |
R6934:Srgap2
|
UTSW |
1 |
131,244,969 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7007:Srgap2
|
UTSW |
1 |
131,247,275 (GRCm39) |
missense |
probably benign |
0.15 |
R7077:Srgap2
|
UTSW |
1 |
131,272,187 (GRCm39) |
missense |
|
|
R7147:Srgap2
|
UTSW |
1 |
131,238,332 (GRCm39) |
missense |
|
|
R7326:Srgap2
|
UTSW |
1 |
131,219,351 (GRCm39) |
nonsense |
probably null |
|
R7467:Srgap2
|
UTSW |
1 |
131,220,405 (GRCm39) |
missense |
probably damaging |
0.97 |
R7500:Srgap2
|
UTSW |
1 |
131,364,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7579:Srgap2
|
UTSW |
1 |
131,220,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R7923:Srgap2
|
UTSW |
1 |
131,228,151 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7989:Srgap2
|
UTSW |
1 |
131,226,170 (GRCm39) |
missense |
|
|
R8283:Srgap2
|
UTSW |
1 |
131,291,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R8708:Srgap2
|
UTSW |
1 |
131,273,544 (GRCm39) |
nonsense |
probably null |
|
R8784:Srgap2
|
UTSW |
1 |
131,223,212 (GRCm39) |
missense |
unknown |
|
R8970:Srgap2
|
UTSW |
1 |
131,226,104 (GRCm39) |
missense |
|
|
R9001:Srgap2
|
UTSW |
1 |
131,291,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R9006:Srgap2
|
UTSW |
1 |
131,283,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Srgap2
|
UTSW |
1 |
131,217,346 (GRCm39) |
missense |
probably benign |
|
R9389:Srgap2
|
UTSW |
1 |
131,283,365 (GRCm39) |
missense |
probably damaging |
0.96 |
R9599:Srgap2
|
UTSW |
1 |
131,272,164 (GRCm39) |
missense |
|
|
R9616:Srgap2
|
UTSW |
1 |
131,252,828 (GRCm39) |
missense |
|
|
X0022:Srgap2
|
UTSW |
1 |
131,339,687 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Srgap2
|
UTSW |
1 |
131,283,248 (GRCm39) |
critical splice donor site |
probably null |
|
|