Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr2a |
A |
G |
2: 48,782,166 (GRCm39) |
Y233C |
probably damaging |
Het |
Agl |
A |
G |
3: 116,584,814 (GRCm39) |
S169P |
probably damaging |
Het |
Arid1b |
C |
T |
17: 5,341,332 (GRCm39) |
Q879* |
probably null |
Het |
Bbs2 |
A |
G |
8: 94,819,178 (GRCm39) |
S64P |
probably damaging |
Het |
Bend7 |
G |
A |
2: 4,768,052 (GRCm39) |
R336Q |
probably damaging |
Het |
Cacna2d2 |
A |
G |
9: 107,391,313 (GRCm39) |
T447A |
probably benign |
Het |
Ccdc168 |
T |
A |
1: 44,096,955 (GRCm39) |
Y1381F |
probably benign |
Het |
Ccdc169 |
A |
T |
3: 55,049,740 (GRCm39) |
|
probably benign |
Het |
Cdan1 |
A |
G |
2: 120,560,546 (GRCm39) |
S275P |
possibly damaging |
Het |
Cdh15 |
A |
G |
8: 123,588,802 (GRCm39) |
N292S |
probably null |
Het |
Cmtm1 |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
8: 105,036,102 (GRCm39) |
|
probably benign |
Het |
Cnnm1 |
A |
G |
19: 43,430,301 (GRCm39) |
H473R |
probably benign |
Het |
Cplx4 |
G |
A |
18: 66,103,157 (GRCm39) |
|
probably benign |
Het |
Crb1 |
C |
T |
1: 139,265,109 (GRCm39) |
G103E |
probably damaging |
Het |
Dnaja3 |
T |
A |
16: 4,512,346 (GRCm39) |
V250E |
possibly damaging |
Het |
Dync2h1 |
T |
G |
9: 7,129,727 (GRCm39) |
Q1757P |
probably damaging |
Het |
Edem3 |
A |
G |
1: 151,683,202 (GRCm39) |
Q626R |
probably damaging |
Het |
Eif2b1 |
T |
C |
5: 124,716,862 (GRCm39) |
|
probably benign |
Het |
Esf1 |
T |
A |
2: 139,996,801 (GRCm39) |
K521* |
probably null |
Het |
Fbxl3 |
A |
C |
14: 103,320,730 (GRCm39) |
V239G |
probably damaging |
Het |
Fhip2a |
A |
G |
19: 57,367,051 (GRCm39) |
D198G |
probably benign |
Het |
Fto |
A |
G |
8: 92,118,107 (GRCm39) |
|
probably benign |
Het |
Gm5773 |
T |
C |
3: 93,681,090 (GRCm39) |
L254P |
probably damaging |
Het |
Gm5916 |
A |
T |
9: 36,032,012 (GRCm39) |
W91R |
probably benign |
Het |
Gpam |
A |
T |
19: 55,077,269 (GRCm39) |
L174H |
probably damaging |
Het |
Grk1 |
G |
A |
8: 13,464,478 (GRCm39) |
R450Q |
probably damaging |
Het |
Hc |
G |
A |
2: 34,927,636 (GRCm39) |
A326V |
probably benign |
Het |
Hectd4 |
T |
C |
5: 121,442,511 (GRCm39) |
I1317T |
probably benign |
Het |
Hlcs |
A |
G |
16: 94,068,383 (GRCm39) |
V426A |
possibly damaging |
Het |
Ighv1-23 |
T |
C |
12: 114,728,376 (GRCm39) |
|
probably benign |
Het |
Itgax |
G |
A |
7: 127,740,474 (GRCm39) |
V754I |
probably benign |
Het |
Krt24 |
T |
A |
11: 99,173,556 (GRCm39) |
D255V |
probably damaging |
Het |
Lnpk |
T |
C |
2: 74,403,935 (GRCm39) |
|
probably benign |
Het |
Loxhd1 |
G |
T |
18: 77,454,237 (GRCm39) |
R478L |
probably damaging |
Het |
Lrrc56 |
A |
G |
7: 140,789,537 (GRCm39) |
Q518R |
probably benign |
Het |
Mbl1 |
A |
T |
14: 40,880,786 (GRCm39) |
I225F |
probably damaging |
Het |
Mmp21 |
T |
C |
7: 133,277,651 (GRCm39) |
S392G |
probably benign |
Het |
Mug2 |
T |
G |
6: 122,058,551 (GRCm39) |
F1318V |
probably damaging |
Het |
Myo5c |
A |
G |
9: 75,202,487 (GRCm39) |
N1447S |
probably null |
Het |
Nbea |
A |
C |
3: 55,948,297 (GRCm39) |
V543G |
probably damaging |
Het |
Necap1 |
A |
G |
6: 122,857,706 (GRCm39) |
I96V |
probably benign |
Het |
Nr3c2 |
T |
A |
8: 77,937,377 (GRCm39) |
M872K |
possibly damaging |
Het |
Nrf1 |
C |
T |
6: 30,118,967 (GRCm39) |
T362M |
probably benign |
Het |
Or14j2 |
T |
C |
17: 37,885,618 (GRCm39) |
E232G |
probably damaging |
Het |
Pcare |
A |
G |
17: 72,056,930 (GRCm39) |
S916P |
probably benign |
Het |
Plekhm3 |
T |
C |
1: 64,859,149 (GRCm39) |
E685G |
probably damaging |
Het |
Robo4 |
CGG |
CG |
9: 37,322,786 (GRCm39) |
|
probably null |
Het |
Sbk3 |
A |
T |
7: 4,970,422 (GRCm39) |
S316T |
probably benign |
Het |
Serpinb9e |
T |
C |
13: 33,441,767 (GRCm39) |
L233P |
probably damaging |
Het |
Set |
T |
A |
2: 29,959,422 (GRCm39) |
S132T |
possibly damaging |
Het |
Slc17a4 |
C |
T |
13: 24,092,800 (GRCm39) |
E11K |
possibly damaging |
Het |
Slc22a6 |
T |
A |
19: 8,595,917 (GRCm39) |
N86K |
possibly damaging |
Het |
Slco1a6 |
A |
G |
6: 142,032,325 (GRCm39) |
L600P |
probably damaging |
Het |
Sp8 |
A |
G |
12: 118,812,246 (GRCm39) |
K34E |
possibly damaging |
Het |
Tcf12 |
G |
A |
9: 71,792,525 (GRCm39) |
P53S |
probably damaging |
Het |
Tcf3 |
A |
G |
10: 80,246,045 (GRCm39) |
V626A |
probably damaging |
Het |
Trpc4ap |
A |
G |
2: 155,514,908 (GRCm39) |
|
probably null |
Het |
Ttc3 |
T |
A |
16: 94,230,479 (GRCm39) |
V892D |
probably damaging |
Het |
Tub |
G |
T |
7: 108,625,978 (GRCm39) |
R243L |
possibly damaging |
Het |
Tubgcp5 |
A |
G |
7: 55,473,433 (GRCm39) |
Y837C |
probably damaging |
Het |
Utp25 |
A |
T |
1: 192,810,687 (GRCm39) |
D105E |
probably benign |
Het |
Wdhd1 |
A |
T |
14: 47,506,181 (GRCm39) |
Y244* |
probably null |
Het |
Xdh |
T |
A |
17: 74,232,027 (GRCm39) |
T228S |
probably benign |
Het |
Zfp418 |
A |
C |
7: 7,185,534 (GRCm39) |
Q499P |
probably benign |
Het |
Zfpm1 |
G |
A |
8: 123,062,269 (GRCm39) |
E443K |
possibly damaging |
Het |
Zfy1 |
T |
C |
Y: 725,950 (GRCm39) |
H605R |
possibly damaging |
Het |
|
Other mutations in Spen |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01133:Spen
|
APN |
4 |
141,217,212 (GRCm39) |
missense |
unknown |
|
IGL01357:Spen
|
APN |
4 |
141,244,424 (GRCm39) |
missense |
unknown |
|
IGL02184:Spen
|
APN |
4 |
141,214,917 (GRCm39) |
missense |
unknown |
|
IGL02226:Spen
|
APN |
4 |
141,205,457 (GRCm39) |
missense |
unknown |
|
IGL02321:Spen
|
APN |
4 |
141,244,441 (GRCm39) |
missense |
unknown |
|
IGL02350:Spen
|
APN |
4 |
141,204,890 (GRCm39) |
missense |
unknown |
|
IGL02357:Spen
|
APN |
4 |
141,204,890 (GRCm39) |
missense |
unknown |
|
IGL02627:Spen
|
APN |
4 |
141,200,326 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02683:Spen
|
APN |
4 |
141,198,956 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02945:Spen
|
APN |
4 |
141,221,624 (GRCm39) |
missense |
unknown |
|
IGL02950:Spen
|
APN |
4 |
141,196,819 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Spen
|
APN |
4 |
141,203,448 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03019:Spen
|
APN |
4 |
141,206,227 (GRCm39) |
missense |
unknown |
|
IGL03038:Spen
|
APN |
4 |
141,265,550 (GRCm39) |
missense |
unknown |
|
IGL03334:Spen
|
APN |
4 |
141,197,280 (GRCm39) |
missense |
probably damaging |
1.00 |
filtered
|
UTSW |
4 |
141,204,683 (GRCm39) |
missense |
unknown |
|
mentholated
|
UTSW |
4 |
141,196,711 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0105:Spen
|
UTSW |
4 |
141,197,121 (GRCm39) |
splice site |
probably benign |
|
R0268:Spen
|
UTSW |
4 |
141,204,868 (GRCm39) |
missense |
unknown |
|
R0359:Spen
|
UTSW |
4 |
141,244,181 (GRCm39) |
missense |
unknown |
|
R0394:Spen
|
UTSW |
4 |
141,201,514 (GRCm39) |
missense |
probably benign |
0.03 |
R0423:Spen
|
UTSW |
4 |
141,206,647 (GRCm39) |
missense |
unknown |
|
R0433:Spen
|
UTSW |
4 |
141,211,069 (GRCm39) |
missense |
unknown |
|
R0462:Spen
|
UTSW |
4 |
141,200,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0687:Spen
|
UTSW |
4 |
141,215,339 (GRCm39) |
missense |
unknown |
|
R0699:Spen
|
UTSW |
4 |
141,201,702 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0865:Spen
|
UTSW |
4 |
141,199,181 (GRCm39) |
missense |
probably benign |
0.11 |
R0918:Spen
|
UTSW |
4 |
141,212,875 (GRCm39) |
missense |
unknown |
|
R1034:Spen
|
UTSW |
4 |
141,203,063 (GRCm39) |
missense |
probably benign |
0.33 |
R1341:Spen
|
UTSW |
4 |
141,196,711 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1401:Spen
|
UTSW |
4 |
141,199,132 (GRCm39) |
missense |
probably damaging |
0.98 |
R1509:Spen
|
UTSW |
4 |
141,202,946 (GRCm39) |
missense |
probably benign |
0.00 |
R1509:Spen
|
UTSW |
4 |
141,203,011 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1561:Spen
|
UTSW |
4 |
141,199,694 (GRCm39) |
nonsense |
probably null |
|
R1589:Spen
|
UTSW |
4 |
141,215,335 (GRCm39) |
missense |
unknown |
|
R1640:Spen
|
UTSW |
4 |
141,196,254 (GRCm39) |
missense |
probably damaging |
0.98 |
R1758:Spen
|
UTSW |
4 |
141,203,686 (GRCm39) |
missense |
unknown |
|
R1764:Spen
|
UTSW |
4 |
141,200,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Spen
|
UTSW |
4 |
141,200,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Spen
|
UTSW |
4 |
141,197,654 (GRCm39) |
missense |
probably benign |
0.17 |
R1916:Spen
|
UTSW |
4 |
141,199,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Spen
|
UTSW |
4 |
141,200,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R2295:Spen
|
UTSW |
4 |
141,204,584 (GRCm39) |
missense |
unknown |
|
R2379:Spen
|
UTSW |
4 |
141,244,238 (GRCm39) |
missense |
unknown |
|
R2404:Spen
|
UTSW |
4 |
141,205,216 (GRCm39) |
missense |
unknown |
|
R3719:Spen
|
UTSW |
4 |
141,244,494 (GRCm39) |
missense |
unknown |
|
R3889:Spen
|
UTSW |
4 |
141,205,192 (GRCm39) |
missense |
unknown |
|
R3945:Spen
|
UTSW |
4 |
141,204,664 (GRCm39) |
missense |
unknown |
|
R4227:Spen
|
UTSW |
4 |
141,249,458 (GRCm39) |
missense |
unknown |
|
R4326:Spen
|
UTSW |
4 |
141,204,683 (GRCm39) |
missense |
unknown |
|
R4382:Spen
|
UTSW |
4 |
141,200,450 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4542:Spen
|
UTSW |
4 |
141,204,097 (GRCm39) |
missense |
unknown |
|
R4757:Spen
|
UTSW |
4 |
141,200,390 (GRCm39) |
nonsense |
probably null |
|
R4771:Spen
|
UTSW |
4 |
141,199,907 (GRCm39) |
missense |
probably benign |
0.14 |
R5072:Spen
|
UTSW |
4 |
141,249,613 (GRCm39) |
missense |
unknown |
|
R5121:Spen
|
UTSW |
4 |
141,203,410 (GRCm39) |
missense |
probably benign |
0.00 |
R5176:Spen
|
UTSW |
4 |
141,203,587 (GRCm39) |
missense |
unknown |
|
R5290:Spen
|
UTSW |
4 |
141,201,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R5291:Spen
|
UTSW |
4 |
141,215,390 (GRCm39) |
missense |
unknown |
|
R5293:Spen
|
UTSW |
4 |
141,199,717 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5511:Spen
|
UTSW |
4 |
141,244,149 (GRCm39) |
missense |
unknown |
|
R5511:Spen
|
UTSW |
4 |
141,202,375 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5772:Spen
|
UTSW |
4 |
141,205,495 (GRCm39) |
missense |
unknown |
|
R5834:Spen
|
UTSW |
4 |
141,199,154 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5858:Spen
|
UTSW |
4 |
141,201,182 (GRCm39) |
missense |
probably benign |
0.05 |
R6214:Spen
|
UTSW |
4 |
141,206,423 (GRCm39) |
missense |
unknown |
|
R6232:Spen
|
UTSW |
4 |
141,244,333 (GRCm39) |
missense |
unknown |
|
R6345:Spen
|
UTSW |
4 |
141,198,944 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6419:Spen
|
UTSW |
4 |
141,203,621 (GRCm39) |
missense |
unknown |
|
R6455:Spen
|
UTSW |
4 |
141,202,820 (GRCm39) |
missense |
probably damaging |
0.97 |
R6979:Spen
|
UTSW |
4 |
141,205,374 (GRCm39) |
missense |
unknown |
|
R6994:Spen
|
UTSW |
4 |
141,220,770 (GRCm39) |
missense |
unknown |
|
R7018:Spen
|
UTSW |
4 |
141,220,755 (GRCm39) |
missense |
unknown |
|
R7040:Spen
|
UTSW |
4 |
141,221,693 (GRCm39) |
missense |
unknown |
|
R7127:Spen
|
UTSW |
4 |
141,203,419 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7218:Spen
|
UTSW |
4 |
141,199,961 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7234:Spen
|
UTSW |
4 |
141,206,446 (GRCm39) |
missense |
unknown |
|
R7316:Spen
|
UTSW |
4 |
141,204,365 (GRCm39) |
missense |
unknown |
|
R7350:Spen
|
UTSW |
4 |
141,206,696 (GRCm39) |
missense |
unknown |
|
R7356:Spen
|
UTSW |
4 |
141,199,235 (GRCm39) |
nonsense |
probably null |
|
R7400:Spen
|
UTSW |
4 |
141,201,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R7470:Spen
|
UTSW |
4 |
141,206,605 (GRCm39) |
missense |
unknown |
|
R7698:Spen
|
UTSW |
4 |
141,200,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R7858:Spen
|
UTSW |
4 |
141,215,442 (GRCm39) |
splice site |
probably null |
|
R8033:Spen
|
UTSW |
4 |
141,199,057 (GRCm39) |
missense |
probably benign |
0.03 |
R8064:Spen
|
UTSW |
4 |
141,203,011 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8159:Spen
|
UTSW |
4 |
141,202,314 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8187:Spen
|
UTSW |
4 |
141,200,216 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8463:Spen
|
UTSW |
4 |
141,249,590 (GRCm39) |
missense |
unknown |
|
R8557:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8558:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8672:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8673:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8674:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8714:Spen
|
UTSW |
4 |
141,215,314 (GRCm39) |
missense |
unknown |
|
R8735:Spen
|
UTSW |
4 |
141,197,129 (GRCm39) |
missense |
probably benign |
0.32 |
R8762:Spen
|
UTSW |
4 |
141,200,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8877:Spen
|
UTSW |
4 |
141,199,137 (GRCm39) |
nonsense |
probably null |
|
R8878:Spen
|
UTSW |
4 |
141,204,520 (GRCm39) |
missense |
unknown |
|
R8937:Spen
|
UTSW |
4 |
141,201,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R8939:Spen
|
UTSW |
4 |
141,202,969 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8968:Spen
|
UTSW |
4 |
141,197,701 (GRCm39) |
missense |
probably benign |
0.02 |
R8971:Spen
|
UTSW |
4 |
141,201,889 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9016:Spen
|
UTSW |
4 |
141,200,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R9072:Spen
|
UTSW |
4 |
141,203,702 (GRCm39) |
missense |
unknown |
|
R9073:Spen
|
UTSW |
4 |
141,203,702 (GRCm39) |
missense |
unknown |
|
R9120:Spen
|
UTSW |
4 |
141,200,233 (GRCm39) |
missense |
|
|
R9136:Spen
|
UTSW |
4 |
141,249,623 (GRCm39) |
missense |
unknown |
|
R9138:Spen
|
UTSW |
4 |
141,196,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R9150:Spen
|
UTSW |
4 |
141,244,468 (GRCm39) |
missense |
unknown |
|
R9225:Spen
|
UTSW |
4 |
141,202,943 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9492:Spen
|
UTSW |
4 |
141,199,098 (GRCm39) |
missense |
probably benign |
0.26 |
R9537:Spen
|
UTSW |
4 |
141,244,156 (GRCm39) |
small deletion |
probably benign |
|
R9537:Spen
|
UTSW |
4 |
141,199,015 (GRCm39) |
missense |
probably benign |
0.15 |
R9602:Spen
|
UTSW |
4 |
141,205,183 (GRCm39) |
missense |
unknown |
|
R9609:Spen
|
UTSW |
4 |
141,215,419 (GRCm39) |
missense |
unknown |
|
R9686:Spen
|
UTSW |
4 |
141,199,946 (GRCm39) |
missense |
probably benign |
0.27 |
R9697:Spen
|
UTSW |
4 |
141,196,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9713:Spen
|
UTSW |
4 |
141,244,331 (GRCm39) |
missense |
unknown |
|
T0722:Spen
|
UTSW |
4 |
141,201,664 (GRCm39) |
missense |
probably benign |
0.33 |
T0975:Spen
|
UTSW |
4 |
141,201,664 (GRCm39) |
missense |
probably benign |
0.33 |
Z1088:Spen
|
UTSW |
4 |
141,205,287 (GRCm39) |
missense |
unknown |
|
Z1088:Spen
|
UTSW |
4 |
141,205,288 (GRCm39) |
missense |
unknown |
|
|