Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
C |
T |
7: 45,629,449 (GRCm39) |
V1293M |
probably damaging |
Het |
Agt |
A |
G |
8: 125,290,537 (GRCm39) |
W257R |
possibly damaging |
Het |
Arhgef11 |
T |
A |
3: 87,620,406 (GRCm39) |
N457K |
probably benign |
Het |
Bcl3 |
G |
T |
7: 19,554,082 (GRCm39) |
H95Q |
probably benign |
Het |
C1d |
T |
A |
11: 17,213,662 (GRCm39) |
N64K |
probably damaging |
Het |
Casc3 |
C |
T |
11: 98,713,607 (GRCm39) |
R280C |
probably damaging |
Het |
Cd300c2 |
C |
T |
11: 114,891,466 (GRCm39) |
S136N |
probably benign |
Het |
Cdh8 |
A |
G |
8: 99,757,672 (GRCm39) |
V642A |
possibly damaging |
Het |
Cep290 |
A |
T |
10: 100,331,706 (GRCm39) |
I180F |
possibly damaging |
Het |
Copz2 |
A |
G |
11: 96,744,887 (GRCm39) |
E86G |
probably damaging |
Het |
Cplane1 |
A |
G |
15: 8,230,635 (GRCm39) |
I971V |
probably benign |
Het |
Cracdl |
A |
G |
1: 37,652,537 (GRCm39) |
V1090A |
probably benign |
Het |
Csf3r |
A |
T |
4: 125,923,712 (GRCm39) |
D74V |
possibly damaging |
Het |
Cyp11b1 |
T |
G |
15: 74,710,789 (GRCm39) |
E257A |
possibly damaging |
Het |
Dlg2 |
A |
G |
7: 92,024,875 (GRCm39) |
Q580R |
probably damaging |
Het |
Dnai2 |
A |
T |
11: 114,645,275 (GRCm39) |
K570M |
unknown |
Het |
Dock8 |
A |
G |
19: 25,133,281 (GRCm39) |
K1143E |
probably benign |
Het |
Dxo |
T |
C |
17: 35,058,099 (GRCm39) |
S394P |
probably benign |
Het |
Etl4 |
A |
G |
2: 20,810,977 (GRCm39) |
D1388G |
probably benign |
Het |
F13a1 |
C |
A |
13: 37,209,692 (GRCm39) |
R91L |
probably damaging |
Het |
Fam50b |
C |
T |
13: 34,930,856 (GRCm39) |
R111* |
probably null |
Het |
Fat2 |
T |
G |
11: 55,202,535 (GRCm39) |
N180H |
probably damaging |
Het |
Fitm2 |
A |
T |
2: 163,311,768 (GRCm39) |
H148Q |
probably benign |
Het |
Fjx1 |
A |
T |
2: 102,281,156 (GRCm39) |
S260T |
possibly damaging |
Het |
Fos |
T |
C |
12: 85,522,466 (GRCm39) |
L165P |
probably damaging |
Het |
Gm39115 |
C |
A |
7: 141,689,710 (GRCm39) |
C21F |
unknown |
Het |
Gucy1a1 |
C |
T |
3: 82,005,000 (GRCm39) |
C595Y |
probably damaging |
Het |
Hectd4 |
G |
T |
5: 121,467,172 (GRCm39) |
W2478L |
possibly damaging |
Het |
I830077J02Rik |
T |
A |
3: 105,836,060 (GRCm39) |
K9N |
probably damaging |
Het |
Ift70a1 |
T |
C |
2: 75,811,519 (GRCm39) |
D188G |
probably benign |
Het |
Ireb2 |
T |
C |
9: 54,811,265 (GRCm39) |
F723L |
possibly damaging |
Het |
Itpr1 |
G |
A |
6: 108,496,309 (GRCm39) |
V2580I |
probably damaging |
Het |
Kcnu1 |
G |
A |
8: 26,382,092 (GRCm39) |
G481R |
probably damaging |
Het |
Kdm3b |
G |
T |
18: 34,926,129 (GRCm39) |
A90S |
probably benign |
Het |
Klra8 |
A |
G |
6: 130,105,056 (GRCm39) |
V23A |
probably damaging |
Het |
Lig4 |
A |
G |
8: 10,023,777 (GRCm39) |
M1T |
probably null |
Het |
Lpin3 |
C |
T |
2: 160,737,273 (GRCm39) |
P107S |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 41,265,867 (GRCm39) |
K1100* |
probably null |
Het |
Obscn |
G |
A |
11: 58,929,700 (GRCm39) |
H5172Y |
probably damaging |
Het |
Or10a3m |
T |
A |
7: 108,313,418 (GRCm39) |
M286K |
possibly damaging |
Het |
Or4p20 |
A |
G |
2: 88,253,745 (GRCm39) |
I208T |
probably benign |
Het |
Or5ae1 |
C |
T |
7: 84,565,787 (GRCm39) |
H267Y |
probably benign |
Het |
Or6z1 |
T |
A |
7: 6,504,734 (GRCm39) |
T170S |
probably damaging |
Het |
Or8c14-ps1 |
A |
T |
9: 38,101,498 (GRCm39) |
H159L |
possibly damaging |
Het |
Orc3 |
A |
G |
4: 34,593,173 (GRCm39) |
L298P |
probably damaging |
Het |
Otub1 |
A |
G |
19: 7,177,360 (GRCm39) |
F96L |
probably damaging |
Het |
Pcnx3 |
A |
G |
19: 5,736,670 (GRCm39) |
S156P |
probably benign |
Het |
Pde3b |
A |
G |
7: 114,126,129 (GRCm39) |
M788V |
probably damaging |
Het |
Pias4 |
A |
G |
10: 80,992,844 (GRCm39) |
|
probably null |
Het |
Polg |
A |
G |
7: 79,114,743 (GRCm39) |
C73R |
probably benign |
Het |
Ptbp2 |
T |
C |
3: 119,541,467 (GRCm39) |
Y190C |
probably damaging |
Het |
Rab33b |
T |
A |
3: 51,401,050 (GRCm39) |
F175I |
probably damaging |
Het |
Rfx1 |
A |
G |
8: 84,806,515 (GRCm39) |
T108A |
probably benign |
Het |
Ribc2 |
A |
G |
15: 85,019,461 (GRCm39) |
D81G |
probably benign |
Het |
Rnf213 |
T |
G |
11: 119,340,149 (GRCm39) |
M3460R |
|
Het |
Rsf1 |
T |
A |
7: 97,266,103 (GRCm39) |
S86T |
|
Het |
Rxfp2 |
C |
A |
5: 149,973,068 (GRCm39) |
T181N |
possibly damaging |
Het |
Samm50 |
G |
A |
15: 84,094,702 (GRCm39) |
E365K |
possibly damaging |
Het |
Shld2 |
A |
C |
14: 33,989,942 (GRCm39) |
N321K |
probably benign |
Het |
Slc22a18 |
T |
C |
7: 143,051,123 (GRCm39) |
V334A |
probably damaging |
Het |
Slc23a3 |
A |
T |
1: 75,110,085 (GRCm39) |
C97S |
probably benign |
Het |
Smchd1 |
T |
A |
17: 71,714,244 (GRCm39) |
H873L |
probably benign |
Het |
Snrpa1 |
G |
A |
7: 65,720,381 (GRCm39) |
G195R |
probably benign |
Het |
Stox1 |
A |
G |
10: 62,501,543 (GRCm39) |
V339A |
probably damaging |
Het |
Tlx1 |
A |
G |
19: 45,142,036 (GRCm39) |
E220G |
probably damaging |
Het |
Tmem71 |
C |
A |
15: 66,413,421 (GRCm39) |
|
probably null |
Het |
Tmprss3 |
T |
C |
17: 31,413,976 (GRCm39) |
D56G |
possibly damaging |
Het |
Trabd |
A |
G |
15: 88,970,107 (GRCm39) |
R368G |
probably benign |
Het |
Trf |
A |
G |
9: 103,094,675 (GRCm39) |
I461T |
probably damaging |
Het |
Trpm3 |
A |
G |
19: 22,676,226 (GRCm39) |
T133A |
possibly damaging |
Het |
Trpv3 |
G |
A |
11: 73,186,209 (GRCm39) |
V667I |
possibly damaging |
Het |
Vps13b |
T |
A |
15: 35,455,246 (GRCm39) |
N718K |
probably benign |
Het |
Zdbf2 |
T |
C |
1: 63,345,166 (GRCm39) |
S1182P |
possibly damaging |
Het |
Zfp13 |
T |
C |
17: 23,795,866 (GRCm39) |
D235G |
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,227,987 (GRCm39) |
E1874G |
probably damaging |
Het |
Zfp503 |
T |
C |
14: 22,036,277 (GRCm39) |
K213R |
probably benign |
Het |
Zkscan2 |
A |
G |
7: 123,084,651 (GRCm39) |
V491A |
probably damaging |
Het |
|
Other mutations in Sphkap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Sphkap
|
APN |
1 |
83,258,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00337:Sphkap
|
APN |
1 |
83,317,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00470:Sphkap
|
APN |
1 |
83,255,631 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL00577:Sphkap
|
APN |
1 |
83,256,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00657:Sphkap
|
APN |
1 |
83,254,096 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01868:Sphkap
|
APN |
1 |
83,258,120 (GRCm39) |
splice site |
probably null |
|
IGL02101:Sphkap
|
APN |
1 |
83,268,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02471:Sphkap
|
APN |
1 |
83,253,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02945:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03031:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03059:Sphkap
|
APN |
1 |
83,234,963 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03085:Sphkap
|
APN |
1 |
83,258,075 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03355:Sphkap
|
APN |
1 |
83,258,224 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03356:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03368:Sphkap
|
APN |
1 |
83,253,397 (GRCm39) |
missense |
probably benign |
0.14 |
R0294:Sphkap
|
UTSW |
1 |
83,255,966 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0308:Sphkap
|
UTSW |
1 |
83,254,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R0478:Sphkap
|
UTSW |
1 |
83,256,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Sphkap
|
UTSW |
1 |
83,258,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R0678:Sphkap
|
UTSW |
1 |
83,256,349 (GRCm39) |
missense |
probably benign |
0.03 |
R1216:Sphkap
|
UTSW |
1 |
83,268,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R1253:Sphkap
|
UTSW |
1 |
83,256,619 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1532:Sphkap
|
UTSW |
1 |
83,234,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Sphkap
|
UTSW |
1 |
83,256,121 (GRCm39) |
missense |
probably benign |
0.03 |
R1655:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1657:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1700:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1701:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1734:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1736:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1743:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1744:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1760:Sphkap
|
UTSW |
1 |
83,255,265 (GRCm39) |
missense |
probably benign |
0.29 |
R1893:Sphkap
|
UTSW |
1 |
83,256,687 (GRCm39) |
missense |
probably benign |
0.02 |
R1937:Sphkap
|
UTSW |
1 |
83,245,162 (GRCm39) |
nonsense |
probably null |
|
R1986:Sphkap
|
UTSW |
1 |
83,255,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1995:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R2001:Sphkap
|
UTSW |
1 |
83,254,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R2004:Sphkap
|
UTSW |
1 |
83,255,632 (GRCm39) |
missense |
probably benign |
0.04 |
R2111:Sphkap
|
UTSW |
1 |
83,253,602 (GRCm39) |
missense |
probably benign |
0.00 |
R2112:Sphkap
|
UTSW |
1 |
83,253,602 (GRCm39) |
missense |
probably benign |
0.00 |
R2156:Sphkap
|
UTSW |
1 |
83,255,710 (GRCm39) |
missense |
probably benign |
0.03 |
R2182:Sphkap
|
UTSW |
1 |
83,254,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R2271:Sphkap
|
UTSW |
1 |
83,234,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R3712:Sphkap
|
UTSW |
1 |
83,254,833 (GRCm39) |
missense |
probably benign |
0.27 |
R3919:Sphkap
|
UTSW |
1 |
83,254,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R3980:Sphkap
|
UTSW |
1 |
83,245,215 (GRCm39) |
splice site |
probably null |
|
R4130:Sphkap
|
UTSW |
1 |
83,255,619 (GRCm39) |
missense |
probably damaging |
0.96 |
R4539:Sphkap
|
UTSW |
1 |
83,255,514 (GRCm39) |
missense |
probably benign |
0.00 |
R4602:Sphkap
|
UTSW |
1 |
83,256,782 (GRCm39) |
nonsense |
probably null |
|
R4735:Sphkap
|
UTSW |
1 |
83,256,838 (GRCm39) |
missense |
probably benign |
0.01 |
R4793:Sphkap
|
UTSW |
1 |
83,255,805 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4849:Sphkap
|
UTSW |
1 |
83,255,105 (GRCm39) |
missense |
probably benign |
0.03 |
R4880:Sphkap
|
UTSW |
1 |
83,266,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Sphkap
|
UTSW |
1 |
83,258,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Sphkap
|
UTSW |
1 |
83,253,885 (GRCm39) |
missense |
probably benign |
0.04 |
R5331:Sphkap
|
UTSW |
1 |
83,254,503 (GRCm39) |
missense |
probably benign |
0.08 |
R5632:Sphkap
|
UTSW |
1 |
83,256,006 (GRCm39) |
missense |
probably benign |
0.01 |
R5647:Sphkap
|
UTSW |
1 |
83,385,720 (GRCm39) |
missense |
probably damaging |
0.98 |
R5751:Sphkap
|
UTSW |
1 |
83,253,618 (GRCm39) |
missense |
probably benign |
0.27 |
R5935:Sphkap
|
UTSW |
1 |
83,317,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R5999:Sphkap
|
UTSW |
1 |
83,245,126 (GRCm39) |
missense |
probably benign |
0.02 |
R6232:Sphkap
|
UTSW |
1 |
83,258,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Sphkap
|
UTSW |
1 |
83,256,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6474:Sphkap
|
UTSW |
1 |
83,256,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R6602:Sphkap
|
UTSW |
1 |
83,253,479 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6674:Sphkap
|
UTSW |
1 |
83,255,555 (GRCm39) |
missense |
probably benign |
0.37 |
R6716:Sphkap
|
UTSW |
1 |
83,339,949 (GRCm39) |
critical splice donor site |
probably null |
|
R6803:Sphkap
|
UTSW |
1 |
83,258,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R6880:Sphkap
|
UTSW |
1 |
83,234,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R6941:Sphkap
|
UTSW |
1 |
83,385,811 (GRCm39) |
start gained |
probably benign |
|
R7170:Sphkap
|
UTSW |
1 |
83,243,706 (GRCm39) |
missense |
probably damaging |
0.99 |
R7263:Sphkap
|
UTSW |
1 |
83,254,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Sphkap
|
UTSW |
1 |
83,241,547 (GRCm39) |
missense |
probably benign |
0.02 |
R7640:Sphkap
|
UTSW |
1 |
83,256,649 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7722:Sphkap
|
UTSW |
1 |
83,256,642 (GRCm39) |
missense |
probably benign |
0.00 |
R7810:Sphkap
|
UTSW |
1 |
83,254,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R7887:Sphkap
|
UTSW |
1 |
83,255,133 (GRCm39) |
missense |
probably benign |
0.00 |
R7974:Sphkap
|
UTSW |
1 |
83,256,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7990:Sphkap
|
UTSW |
1 |
83,245,066 (GRCm39) |
missense |
probably damaging |
0.99 |
R8096:Sphkap
|
UTSW |
1 |
83,255,279 (GRCm39) |
missense |
probably damaging |
0.98 |
R8110:Sphkap
|
UTSW |
1 |
83,256,492 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8125:Sphkap
|
UTSW |
1 |
83,241,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R8153:Sphkap
|
UTSW |
1 |
83,255,730 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8245:Sphkap
|
UTSW |
1 |
83,256,492 (GRCm39) |
missense |
probably benign |
0.14 |
R8394:Sphkap
|
UTSW |
1 |
83,253,797 (GRCm39) |
missense |
probably benign |
0.08 |
R8508:Sphkap
|
UTSW |
1 |
83,254,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Sphkap
|
UTSW |
1 |
83,254,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R8673:Sphkap
|
UTSW |
1 |
83,253,561 (GRCm39) |
missense |
probably benign |
0.01 |
R8674:Sphkap
|
UTSW |
1 |
83,255,565 (GRCm39) |
missense |
probably benign |
0.04 |
R8682:Sphkap
|
UTSW |
1 |
83,256,997 (GRCm39) |
missense |
probably benign |
0.21 |
R8837:Sphkap
|
UTSW |
1 |
83,253,384 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8857:Sphkap
|
UTSW |
1 |
83,258,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Sphkap
|
UTSW |
1 |
83,256,685 (GRCm39) |
missense |
probably benign |
0.21 |
R8916:Sphkap
|
UTSW |
1 |
83,255,108 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8944:Sphkap
|
UTSW |
1 |
83,256,927 (GRCm39) |
missense |
probably benign |
0.39 |
R9154:Sphkap
|
UTSW |
1 |
83,234,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R9579:Sphkap
|
UTSW |
1 |
83,255,295 (GRCm39) |
missense |
probably damaging |
0.99 |
R9616:Sphkap
|
UTSW |
1 |
83,254,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R9781:Sphkap
|
UTSW |
1 |
83,255,772 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1088:Sphkap
|
UTSW |
1 |
83,256,325 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Sphkap
|
UTSW |
1 |
83,254,329 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sphkap
|
UTSW |
1 |
83,258,163 (GRCm39) |
missense |
possibly damaging |
0.61 |
Z1176:Sphkap
|
UTSW |
1 |
83,253,754 (GRCm39) |
nonsense |
probably null |
|
Z1177:Sphkap
|
UTSW |
1 |
83,254,152 (GRCm39) |
missense |
probably damaging |
0.96 |
|