Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
G |
A |
3: 137,775,520 (GRCm39) |
V1570I |
probably damaging |
Het |
Alx4 |
A |
G |
2: 93,473,106 (GRCm39) |
R35G |
probably damaging |
Het |
Apod |
T |
C |
16: 31,116,211 (GRCm39) |
D173G |
probably benign |
Het |
Atp8b3 |
G |
A |
10: 80,361,858 (GRCm39) |
T731I |
possibly damaging |
Het |
Birc6 |
A |
C |
17: 74,947,145 (GRCm39) |
T2955P |
probably benign |
Het |
Cdh15 |
G |
A |
8: 123,587,612 (GRCm39) |
D179N |
probably damaging |
Het |
Cntnap5c |
G |
T |
17: 58,717,263 (GRCm39) |
V1282L |
probably benign |
Het |
Crocc2 |
G |
A |
1: 93,141,372 (GRCm39) |
R1175H |
probably benign |
Het |
Dbh |
A |
G |
2: 27,064,836 (GRCm39) |
D349G |
probably damaging |
Het |
Dync1h1 |
A |
G |
12: 110,605,278 (GRCm39) |
I2372V |
probably benign |
Het |
Fer1l4 |
A |
T |
2: 155,889,007 (GRCm39) |
W389R |
probably damaging |
Het |
Fndc1 |
T |
C |
17: 7,984,036 (GRCm39) |
T1297A |
unknown |
Het |
Gart |
T |
C |
16: 91,422,321 (GRCm39) |
N732S |
probably damaging |
Het |
Gas2l2 |
T |
C |
11: 83,313,924 (GRCm39) |
I463V |
probably benign |
Het |
Gm5591 |
G |
A |
7: 38,220,072 (GRCm39) |
S267L |
probably benign |
Het |
Gzmk |
A |
G |
13: 113,309,657 (GRCm39) |
V92A |
probably damaging |
Het |
Hspg2 |
C |
T |
4: 137,273,884 (GRCm39) |
R2680W |
probably damaging |
Het |
Insyn2a |
A |
G |
7: 134,520,270 (GRCm39) |
Y87H |
probably damaging |
Het |
Kcnh3 |
G |
A |
15: 99,131,982 (GRCm39) |
V646M |
probably damaging |
Het |
Kcnk7 |
A |
C |
19: 5,756,463 (GRCm39) |
I230L |
probably benign |
Het |
Kif3b |
C |
T |
2: 153,158,594 (GRCm39) |
R132* |
probably null |
Het |
Klra5 |
T |
C |
6: 129,885,776 (GRCm39) |
S128G |
probably benign |
Het |
Krba1 |
C |
T |
6: 48,383,282 (GRCm39) |
R4* |
probably null |
Het |
Krt1c |
T |
A |
15: 101,726,026 (GRCm39) |
I171F |
probably damaging |
Het |
Lss |
A |
G |
10: 76,372,089 (GRCm39) |
D148G |
probably benign |
Het |
Mavs |
G |
T |
2: 131,082,370 (GRCm39) |
A85S |
probably damaging |
Het |
Mipep |
T |
C |
14: 61,140,865 (GRCm39) |
C566R |
probably damaging |
Het |
Myocd |
T |
A |
11: 65,069,254 (GRCm39) |
|
probably benign |
Het |
Ndufa9 |
C |
T |
6: 126,804,498 (GRCm39) |
|
probably null |
Het |
Nolc1 |
G |
A |
19: 46,071,959 (GRCm39) |
G583D |
probably damaging |
Het |
Nucb2 |
T |
C |
7: 116,127,059 (GRCm39) |
|
probably null |
Het |
Or1i2 |
T |
C |
10: 78,448,409 (GRCm39) |
D22G |
probably benign |
Het |
Or52e19 |
C |
T |
7: 102,959,165 (GRCm39) |
T79I |
probably benign |
Het |
Or5p63 |
A |
T |
7: 107,811,301 (GRCm39) |
I145N |
possibly damaging |
Het |
Pank4 |
C |
A |
4: 155,061,076 (GRCm39) |
D508E |
probably benign |
Het |
Phb1 |
T |
A |
11: 95,562,416 (GRCm39) |
|
probably benign |
Het |
Pign |
T |
A |
1: 105,449,715 (GRCm39) |
|
probably benign |
Het |
Plec |
T |
C |
15: 76,076,382 (GRCm39) |
K349E |
probably benign |
Het |
Ppp1r3c |
A |
T |
19: 36,711,743 (GRCm39) |
V9E |
possibly damaging |
Het |
Rap1gap |
T |
A |
4: 137,443,422 (GRCm39) |
V130D |
probably damaging |
Het |
Senp3 |
T |
A |
11: 69,567,944 (GRCm39) |
Y432F |
probably benign |
Het |
Serpina3f |
T |
C |
12: 104,183,549 (GRCm39) |
I137T |
possibly damaging |
Het |
Slc46a3 |
T |
A |
5: 147,823,540 (GRCm39) |
K101* |
probably null |
Het |
Snph |
G |
A |
2: 151,436,434 (GRCm39) |
Q96* |
probably null |
Het |
Srbd1 |
A |
T |
17: 86,416,693 (GRCm39) |
F488L |
probably benign |
Het |
Ssc5d |
A |
T |
7: 4,932,524 (GRCm39) |
H396L |
probably damaging |
Het |
Sulf1 |
A |
C |
1: 12,856,876 (GRCm39) |
R42S |
probably damaging |
Het |
Taf1a |
T |
A |
1: 183,181,752 (GRCm39) |
|
probably benign |
Het |
Thoc5 |
T |
A |
11: 4,876,218 (GRCm39) |
M609K |
probably damaging |
Het |
Tiam2 |
A |
T |
17: 3,568,617 (GRCm39) |
I1588F |
probably damaging |
Het |
Tmcc1 |
C |
T |
6: 116,020,247 (GRCm39) |
V402I |
probably damaging |
Het |
Tmprss15 |
T |
C |
16: 78,818,358 (GRCm39) |
D524G |
probably damaging |
Het |
Trbv31 |
T |
C |
6: 41,534,901 (GRCm39) |
I21V |
probably benign |
Het |
Vmn1r74 |
A |
T |
7: 11,581,398 (GRCm39) |
T233S |
possibly damaging |
Het |
Vmn1r74 |
G |
C |
7: 11,581,403 (GRCm39) |
Q234H |
probably damaging |
Het |
Vsx1 |
A |
T |
2: 150,530,529 (GRCm39) |
S118T |
probably benign |
Het |
Wnt9b |
G |
A |
11: 103,621,949 (GRCm39) |
T236I |
probably benign |
Het |
Zbtb21 |
T |
C |
16: 97,751,092 (GRCm39) |
T1092A |
possibly damaging |
Het |
Zc3hc1 |
G |
A |
6: 30,387,523 (GRCm39) |
T52I |
probably benign |
Het |
Zfp558 |
T |
A |
9: 18,367,577 (GRCm39) |
N404Y |
possibly damaging |
Het |
Zfp735 |
A |
T |
11: 73,602,031 (GRCm39) |
D325V |
probably damaging |
Het |
Zhx3 |
A |
T |
2: 160,623,879 (GRCm39) |
M96K |
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 |
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 |
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 |
|