Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre1 |
T |
C |
17: 57,709,620 (GRCm39) |
W121R |
unknown |
Het |
Adprh |
C |
T |
16: 38,270,578 (GRCm39) |
G76S |
possibly damaging |
Het |
Arhgap31 |
T |
C |
16: 38,423,976 (GRCm39) |
T697A |
probably benign |
Het |
Ces2f |
T |
C |
8: 105,680,705 (GRCm39) |
M489T |
probably benign |
Het |
Clec5a |
A |
G |
6: 40,561,314 (GRCm39) |
Y44H |
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,833,426 (GRCm39) |
H950R |
probably damaging |
Het |
Dennd10 |
A |
G |
19: 60,805,972 (GRCm39) |
T86A |
possibly damaging |
Het |
Dgkz |
G |
T |
2: 91,766,210 (GRCm39) |
P784T |
probably benign |
Het |
Dok1 |
T |
C |
6: 83,008,293 (GRCm39) |
D463G |
possibly damaging |
Het |
Eif4a2 |
C |
A |
16: 22,927,941 (GRCm39) |
Q94K |
probably benign |
Het |
Epg5 |
T |
C |
18: 78,055,956 (GRCm39) |
L1710P |
probably damaging |
Het |
Fign |
A |
G |
2: 63,808,988 (GRCm39) |
|
probably benign |
Het |
Gbp10 |
T |
C |
5: 105,372,137 (GRCm39) |
|
probably null |
Het |
Gga2 |
G |
T |
7: 121,597,299 (GRCm39) |
D363E |
probably benign |
Het |
Glis2 |
T |
A |
16: 4,429,195 (GRCm39) |
F133I |
possibly damaging |
Het |
Isg20 |
A |
G |
7: 78,566,333 (GRCm39) |
D94G |
probably damaging |
Het |
Kif23 |
T |
C |
9: 61,839,096 (GRCm39) |
D319G |
probably benign |
Het |
Lbr |
C |
A |
1: 181,663,759 (GRCm39) |
R87L |
probably damaging |
Het |
Map3k9 |
T |
C |
12: 81,771,513 (GRCm39) |
T715A |
probably benign |
Het |
Mapk14 |
T |
C |
17: 28,944,820 (GRCm39) |
|
probably null |
Het |
Mpp4 |
A |
C |
1: 59,169,226 (GRCm39) |
C341W |
probably benign |
Het |
Mroh9 |
C |
T |
1: 162,875,551 (GRCm39) |
|
probably null |
Het |
Myo16 |
T |
C |
8: 10,322,630 (GRCm39) |
V20A |
probably damaging |
Het |
Or12e8 |
T |
C |
2: 87,188,249 (GRCm39) |
S154P |
probably damaging |
Het |
Or52p2 |
A |
T |
7: 102,237,436 (GRCm39) |
C171* |
probably null |
Het |
Or7c19 |
A |
T |
8: 85,957,308 (GRCm39) |
L61F |
probably benign |
Het |
Pofut2 |
C |
T |
10: 77,099,127 (GRCm39) |
R186W |
probably damaging |
Het |
Ppp1r1b |
T |
A |
11: 98,241,392 (GRCm39) |
|
probably null |
Het |
Slc34a2 |
A |
G |
5: 53,218,218 (GRCm39) |
I166V |
probably damaging |
Het |
Slc4a2 |
A |
G |
5: 24,637,928 (GRCm39) |
T375A |
probably benign |
Het |
Slitrk5 |
C |
A |
14: 111,916,432 (GRCm39) |
H19N |
probably benign |
Het |
Stoml1 |
T |
C |
9: 58,163,996 (GRCm39) |
V105A |
probably damaging |
Het |
Stt3b |
C |
A |
9: 115,075,329 (GRCm39) |
|
probably benign |
Het |
Thbs4 |
T |
C |
13: 92,913,488 (GRCm39) |
E144G |
probably benign |
Het |
Tns3 |
A |
G |
11: 8,498,937 (GRCm39) |
Y49H |
probably damaging |
Het |
Vmn2r87 |
C |
T |
10: 130,315,586 (GRCm39) |
W160* |
probably null |
Het |
Zfp647 |
T |
A |
15: 76,801,968 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Sptb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Sptb
|
APN |
12 |
76,668,105 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00160:Sptb
|
APN |
12 |
76,669,943 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00229:Sptb
|
APN |
12 |
76,667,527 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00820:Sptb
|
APN |
12 |
76,679,251 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01309:Sptb
|
APN |
12 |
76,634,237 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01408:Sptb
|
APN |
12 |
76,659,921 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01450:Sptb
|
APN |
12 |
76,671,014 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01455:Sptb
|
APN |
12 |
76,659,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Sptb
|
APN |
12 |
76,659,329 (GRCm39) |
splice site |
probably benign |
|
IGL02070:Sptb
|
APN |
12 |
76,652,313 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02346:Sptb
|
APN |
12 |
76,667,788 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02452:Sptb
|
APN |
12 |
76,655,810 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02515:Sptb
|
APN |
12 |
76,653,261 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02545:Sptb
|
APN |
12 |
76,654,754 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02644:Sptb
|
APN |
12 |
76,652,391 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02878:Sptb
|
APN |
12 |
76,667,527 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03007:Sptb
|
APN |
12 |
76,668,115 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03220:Sptb
|
APN |
12 |
76,659,684 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03343:Sptb
|
APN |
12 |
76,630,330 (GRCm39) |
unclassified |
probably benign |
|
IGL03098:Sptb
|
UTSW |
12 |
76,668,273 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4472001:Sptb
|
UTSW |
12 |
76,667,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Sptb
|
UTSW |
12 |
76,669,724 (GRCm39) |
missense |
probably damaging |
0.99 |
R0365:Sptb
|
UTSW |
12 |
76,647,157 (GRCm39) |
missense |
probably benign |
0.12 |
R0373:Sptb
|
UTSW |
12 |
76,668,145 (GRCm39) |
missense |
probably benign |
0.03 |
R0704:Sptb
|
UTSW |
12 |
76,630,368 (GRCm39) |
missense |
probably damaging |
0.99 |
R1005:Sptb
|
UTSW |
12 |
76,648,633 (GRCm39) |
critical splice donor site |
probably null |
|
R1109:Sptb
|
UTSW |
12 |
76,650,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Sptb
|
UTSW |
12 |
76,659,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R1358:Sptb
|
UTSW |
12 |
76,668,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R1358:Sptb
|
UTSW |
12 |
76,668,095 (GRCm39) |
frame shift |
probably null |
|
R1459:Sptb
|
UTSW |
12 |
76,658,657 (GRCm39) |
missense |
probably benign |
0.01 |
R1518:Sptb
|
UTSW |
12 |
76,650,798 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1628:Sptb
|
UTSW |
12 |
76,630,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1668:Sptb
|
UTSW |
12 |
76,667,943 (GRCm39) |
missense |
probably benign |
|
R1677:Sptb
|
UTSW |
12 |
76,676,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R1687:Sptb
|
UTSW |
12 |
76,650,473 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1695:Sptb
|
UTSW |
12 |
76,667,641 (GRCm39) |
missense |
probably benign |
0.10 |
R1708:Sptb
|
UTSW |
12 |
76,659,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R1761:Sptb
|
UTSW |
12 |
76,659,382 (GRCm39) |
missense |
probably damaging |
0.96 |
R1925:Sptb
|
UTSW |
12 |
76,669,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Sptb
|
UTSW |
12 |
76,679,246 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2373:Sptb
|
UTSW |
12 |
76,667,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R2517:Sptb
|
UTSW |
12 |
76,696,643 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2918:Sptb
|
UTSW |
12 |
76,645,532 (GRCm39) |
missense |
probably damaging |
0.97 |
R2961:Sptb
|
UTSW |
12 |
76,650,356 (GRCm39) |
missense |
probably benign |
0.19 |
R3409:Sptb
|
UTSW |
12 |
76,657,589 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3410:Sptb
|
UTSW |
12 |
76,657,589 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3411:Sptb
|
UTSW |
12 |
76,657,589 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3744:Sptb
|
UTSW |
12 |
76,647,174 (GRCm39) |
missense |
probably benign |
|
R4112:Sptb
|
UTSW |
12 |
76,644,553 (GRCm39) |
missense |
probably damaging |
0.99 |
R4177:Sptb
|
UTSW |
12 |
76,659,953 (GRCm39) |
missense |
probably benign |
0.25 |
R4194:Sptb
|
UTSW |
12 |
76,659,784 (GRCm39) |
missense |
probably benign |
0.44 |
R4301:Sptb
|
UTSW |
12 |
76,659,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R4555:Sptb
|
UTSW |
12 |
76,659,625 (GRCm39) |
missense |
probably benign |
0.03 |
R4619:Sptb
|
UTSW |
12 |
76,630,581 (GRCm39) |
nonsense |
probably null |
|
R4620:Sptb
|
UTSW |
12 |
76,630,581 (GRCm39) |
nonsense |
probably null |
|
R4625:Sptb
|
UTSW |
12 |
76,634,100 (GRCm39) |
splice site |
probably null |
|
R4728:Sptb
|
UTSW |
12 |
76,630,153 (GRCm39) |
missense |
probably benign |
0.00 |
R4751:Sptb
|
UTSW |
12 |
76,673,884 (GRCm39) |
missense |
probably benign |
0.07 |
R4810:Sptb
|
UTSW |
12 |
76,669,971 (GRCm39) |
nonsense |
probably null |
|
R4888:Sptb
|
UTSW |
12 |
76,655,811 (GRCm39) |
missense |
probably benign |
0.00 |
R4894:Sptb
|
UTSW |
12 |
76,671,768 (GRCm39) |
critical splice donor site |
probably null |
|
R5114:Sptb
|
UTSW |
12 |
76,656,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R5191:Sptb
|
UTSW |
12 |
76,659,608 (GRCm39) |
missense |
probably benign |
0.12 |
R5479:Sptb
|
UTSW |
12 |
76,646,625 (GRCm39) |
missense |
probably benign |
0.04 |
R5646:Sptb
|
UTSW |
12 |
76,634,215 (GRCm39) |
missense |
probably benign |
|
R5725:Sptb
|
UTSW |
12 |
76,669,888 (GRCm39) |
missense |
probably benign |
0.25 |
R5727:Sptb
|
UTSW |
12 |
76,669,888 (GRCm39) |
missense |
probably benign |
0.25 |
R5797:Sptb
|
UTSW |
12 |
76,650,473 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5874:Sptb
|
UTSW |
12 |
76,645,501 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5952:Sptb
|
UTSW |
12 |
76,679,158 (GRCm39) |
missense |
probably benign |
0.02 |
R5956:Sptb
|
UTSW |
12 |
76,650,942 (GRCm39) |
missense |
probably benign |
|
R6298:Sptb
|
UTSW |
12 |
76,667,428 (GRCm39) |
critical splice donor site |
probably null |
|
R6470:Sptb
|
UTSW |
12 |
76,659,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R6477:Sptb
|
UTSW |
12 |
76,653,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Sptb
|
UTSW |
12 |
76,659,954 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6854:Sptb
|
UTSW |
12 |
76,650,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R6969:Sptb
|
UTSW |
12 |
76,654,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R6987:Sptb
|
UTSW |
12 |
76,660,021 (GRCm39) |
missense |
probably benign |
0.00 |
R7023:Sptb
|
UTSW |
12 |
76,671,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R7366:Sptb
|
UTSW |
12 |
76,650,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R7379:Sptb
|
UTSW |
12 |
76,657,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Sptb
|
UTSW |
12 |
76,671,003 (GRCm39) |
missense |
probably damaging |
0.98 |
R7392:Sptb
|
UTSW |
12 |
76,671,003 (GRCm39) |
missense |
probably damaging |
0.98 |
R7477:Sptb
|
UTSW |
12 |
76,675,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R7653:Sptb
|
UTSW |
12 |
76,675,271 (GRCm39) |
missense |
probably benign |
0.06 |
R7684:Sptb
|
UTSW |
12 |
76,658,969 (GRCm39) |
missense |
probably benign |
0.06 |
R7733:Sptb
|
UTSW |
12 |
76,644,695 (GRCm39) |
splice site |
probably null |
|
R7846:Sptb
|
UTSW |
12 |
76,655,300 (GRCm39) |
nonsense |
probably null |
|
R8048:Sptb
|
UTSW |
12 |
76,675,333 (GRCm39) |
missense |
probably benign |
0.02 |
R8261:Sptb
|
UTSW |
12 |
76,668,036 (GRCm39) |
missense |
probably benign |
0.06 |
R8324:Sptb
|
UTSW |
12 |
76,665,936 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8512:Sptb
|
UTSW |
12 |
76,648,826 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8515:Sptb
|
UTSW |
12 |
76,658,815 (GRCm39) |
missense |
probably benign |
0.10 |
R8558:Sptb
|
UTSW |
12 |
76,659,561 (GRCm39) |
missense |
probably benign |
0.09 |
R8872:Sptb
|
UTSW |
12 |
76,658,813 (GRCm39) |
missense |
probably benign |
0.37 |
R8907:Sptb
|
UTSW |
12 |
76,634,186 (GRCm39) |
missense |
probably benign |
0.16 |
R9047:Sptb
|
UTSW |
12 |
76,679,308 (GRCm39) |
splice site |
probably benign |
|
R9079:Sptb
|
UTSW |
12 |
76,677,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R9166:Sptb
|
UTSW |
12 |
76,673,776 (GRCm39) |
missense |
probably damaging |
0.96 |
R9381:Sptb
|
UTSW |
12 |
76,634,292 (GRCm39) |
missense |
probably benign |
|
R9601:Sptb
|
UTSW |
12 |
76,667,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R9680:Sptb
|
UTSW |
12 |
76,677,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R9771:Sptb
|
UTSW |
12 |
76,650,353 (GRCm39) |
missense |
probably damaging |
1.00 |
X0057:Sptb
|
UTSW |
12 |
76,677,513 (GRCm39) |
missense |
probably benign |
|
Z1176:Sptb
|
UTSW |
12 |
76,667,507 (GRCm39) |
nonsense |
probably null |
|
Z1177:Sptb
|
UTSW |
12 |
76,653,219 (GRCm39) |
missense |
probably benign |
0.22 |
Z1177:Sptb
|
UTSW |
12 |
76,630,358 (GRCm39) |
missense |
probably damaging |
1.00 |
|