Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
T |
A |
7: 40,643,381 (GRCm39) |
L441Q |
probably damaging |
Het |
Abca15 |
A |
T |
7: 119,953,746 (GRCm39) |
E550V |
probably damaging |
Het |
Adcy4 |
A |
G |
14: 56,010,213 (GRCm39) |
F690L |
probably benign |
Het |
Aspg |
T |
A |
12: 112,080,906 (GRCm39) |
N132K |
probably damaging |
Het |
B430305J03Rik |
A |
T |
3: 61,271,414 (GRCm39) |
Y110* |
probably null |
Het |
Cep135 |
A |
G |
5: 76,778,796 (GRCm39) |
E741G |
possibly damaging |
Het |
Cplane1 |
T |
C |
15: 8,239,567 (GRCm39) |
V1256A |
possibly damaging |
Het |
Dkkl1 |
T |
C |
7: 44,859,539 (GRCm39) |
K128E |
probably damaging |
Het |
Duox2 |
A |
T |
2: 122,115,249 (GRCm39) |
M1101K |
probably benign |
Het |
Gpr89 |
T |
C |
3: 96,787,484 (GRCm39) |
|
probably null |
Het |
Hormad1 |
T |
C |
3: 95,473,997 (GRCm39) |
|
probably null |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Itga2 |
A |
G |
13: 114,998,911 (GRCm39) |
F658S |
possibly damaging |
Het |
Kcnc4 |
T |
C |
3: 107,355,279 (GRCm39) |
I390V |
possibly damaging |
Het |
Krt84 |
G |
T |
15: 101,441,112 (GRCm39) |
H27N |
probably benign |
Het |
Lama5 |
A |
G |
2: 179,821,277 (GRCm39) |
I3095T |
possibly damaging |
Het |
Mef2a |
G |
T |
7: 66,884,896 (GRCm39) |
S406* |
probably null |
Het |
Ms4a1 |
T |
C |
19: 11,230,596 (GRCm39) |
T202A |
probably benign |
Het |
Nrbp2 |
A |
G |
15: 75,960,801 (GRCm39) |
S294P |
probably damaging |
Het |
Or6b13 |
A |
G |
7: 139,782,548 (GRCm39) |
V45A |
probably benign |
Het |
Or6c215 |
A |
G |
10: 129,638,172 (GRCm39) |
V74A |
probably benign |
Het |
Pde4b |
C |
T |
4: 102,344,589 (GRCm39) |
L155F |
probably damaging |
Het |
Pds5a |
A |
G |
5: 65,777,928 (GRCm39) |
S6P |
probably damaging |
Het |
Ralgapa2 |
A |
T |
2: 146,293,704 (GRCm39) |
L150Q |
probably damaging |
Het |
Reln |
C |
T |
5: 22,101,809 (GRCm39) |
V3374I |
probably damaging |
Het |
Rgs12 |
T |
G |
5: 35,180,466 (GRCm39) |
S253A |
possibly damaging |
Het |
Sap130 |
C |
A |
18: 31,786,607 (GRCm39) |
T266K |
probably damaging |
Het |
Sis |
T |
C |
3: 72,857,155 (GRCm39) |
I379V |
possibly damaging |
Het |
Slc39a10 |
T |
A |
1: 46,875,021 (GRCm39) |
I94F |
possibly damaging |
Het |
Srsf12 |
A |
G |
4: 33,231,069 (GRCm39) |
R188G |
probably damaging |
Het |
Ssxb9 |
T |
G |
X: 8,238,022 (GRCm39) |
S130R |
probably damaging |
Het |
Tg |
A |
G |
15: 66,629,729 (GRCm39) |
D470G |
probably benign |
Het |
Urb1 |
T |
C |
16: 90,573,095 (GRCm39) |
Q979R |
probably benign |
Het |
Vmn1r28 |
G |
A |
6: 58,242,702 (GRCm39) |
A182T |
probably benign |
Het |
Zfp78 |
T |
A |
7: 6,382,251 (GRCm39) |
C402S |
probably damaging |
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 |
|
IGL01680:Sptb
|
APN |
12 |
76,677,456 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|