Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf1 |
C |
A |
17: 43,609,975 (GRCm39) |
Y176* |
probably null |
Het |
Akap13 |
T |
A |
7: 75,375,068 (GRCm39) |
M1900K |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,585,332 (GRCm39) |
E381G |
probably damaging |
Het |
Ap3s1 |
T |
C |
18: 46,891,183 (GRCm39) |
|
probably null |
Het |
Cacna1e |
G |
T |
1: 154,364,551 (GRCm39) |
S341* |
probably null |
Het |
Camk1d |
G |
A |
2: 5,359,539 (GRCm39) |
S161L |
probably damaging |
Het |
Cdh23 |
G |
T |
10: 60,173,630 (GRCm39) |
H1619Q |
probably benign |
Het |
Chd7 |
T |
A |
4: 8,838,629 (GRCm39) |
I1276N |
probably damaging |
Het |
Clca3a1 |
A |
G |
3: 144,719,662 (GRCm39) |
V436A |
probably damaging |
Het |
Ctcfl |
G |
A |
2: 172,959,196 (GRCm39) |
P177S |
probably benign |
Het |
Dab2ip |
A |
G |
2: 35,620,539 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Epc1 |
A |
T |
18: 6,449,011 (GRCm39) |
S495R |
probably benign |
Het |
Espl1 |
A |
G |
15: 102,230,758 (GRCm39) |
|
probably null |
Het |
Eya4 |
T |
C |
10: 22,985,753 (GRCm39) |
E583G |
possibly damaging |
Het |
Fam111a |
C |
G |
19: 12,565,913 (GRCm39) |
T554R |
probably benign |
Het |
Fbh1 |
A |
T |
2: 11,767,771 (GRCm39) |
I359N |
probably damaging |
Het |
Fer1l6 |
T |
C |
15: 58,490,751 (GRCm39) |
C1023R |
probably damaging |
Het |
Helz2 |
G |
C |
2: 180,877,940 (GRCm39) |
P953A |
probably benign |
Het |
Ifi204 |
G |
T |
1: 173,587,808 (GRCm39) |
S117Y |
probably damaging |
Het |
Ift70a1 |
T |
C |
2: 75,810,088 (GRCm39) |
*665W |
probably null |
Het |
Igfn1 |
G |
A |
1: 135,882,520 (GRCm39) |
T2775M |
probably damaging |
Het |
Igsf9 |
A |
G |
1: 172,325,634 (GRCm39) |
T1101A |
probably benign |
Het |
Ipo13 |
A |
C |
4: 117,760,638 (GRCm39) |
I614S |
probably damaging |
Het |
Ipo13 |
A |
G |
4: 117,761,687 (GRCm39) |
I476T |
possibly damaging |
Het |
Kdm2b |
C |
A |
5: 123,079,030 (GRCm39) |
E308* |
probably null |
Het |
Klhl20 |
A |
T |
1: 160,937,102 (GRCm39) |
M91K |
possibly damaging |
Het |
Klrb1f |
T |
C |
6: 129,030,151 (GRCm39) |
F64L |
probably benign |
Het |
Ldlrad3 |
C |
T |
2: 101,888,293 (GRCm39) |
C106Y |
probably damaging |
Het |
Lilra6 |
T |
C |
7: 3,915,530 (GRCm39) |
T161A |
probably benign |
Het |
Lrriq1 |
A |
T |
10: 102,997,613 (GRCm39) |
M1334K |
possibly damaging |
Het |
Mepe |
C |
G |
5: 104,473,268 (GRCm39) |
P3R |
probably damaging |
Het |
Mgat4e |
A |
G |
1: 134,468,856 (GRCm39) |
V396A |
probably benign |
Het |
Nfx1 |
T |
G |
4: 40,996,877 (GRCm39) |
S651A |
probably damaging |
Het |
Or10ak13 |
A |
T |
4: 118,639,483 (GRCm39) |
C100S |
probably damaging |
Het |
Or2w6 |
T |
C |
13: 21,843,352 (GRCm39) |
N47S |
probably damaging |
Het |
Or4c109 |
T |
C |
2: 88,817,783 (GRCm39) |
I254M |
possibly damaging |
Het |
Rag2 |
T |
C |
2: 101,460,022 (GRCm39) |
S111P |
probably damaging |
Het |
Rai1 |
T |
A |
11: 60,077,572 (GRCm39) |
D545E |
probably damaging |
Het |
Ralgps1 |
A |
G |
2: 33,033,115 (GRCm39) |
V498A |
possibly damaging |
Het |
Rasal2 |
G |
A |
1: 157,020,374 (GRCm39) |
S205L |
probably damaging |
Het |
Rec8 |
T |
C |
14: 55,862,787 (GRCm39) |
L582P |
probably damaging |
Het |
Retn |
G |
A |
8: 3,707,358 (GRCm39) |
R106H |
probably damaging |
Het |
Rnf112 |
A |
G |
11: 61,343,488 (GRCm39) |
L116P |
probably damaging |
Het |
Rnf213 |
T |
C |
11: 119,372,066 (GRCm39) |
Y4885H |
probably damaging |
Het |
Sacm1l |
A |
G |
9: 123,411,409 (GRCm39) |
I399M |
probably benign |
Het |
Sez6 |
G |
T |
11: 77,866,086 (GRCm39) |
G738V |
probably damaging |
Het |
Spata17 |
A |
G |
1: 186,872,643 (GRCm39) |
V56A |
probably benign |
Het |
Spata31d1a |
A |
T |
13: 59,849,542 (GRCm39) |
V862D |
probably damaging |
Het |
Srpk2 |
C |
A |
5: 23,750,527 (GRCm39) |
G59W |
probably damaging |
Het |
Tyro3 |
T |
C |
2: 119,632,779 (GRCm39) |
S96P |
probably damaging |
Het |
Ube2v1 |
A |
G |
2: 167,452,280 (GRCm39) |
S108P |
probably damaging |
Het |
Usp2 |
C |
T |
9: 43,987,125 (GRCm39) |
S141L |
probably benign |
Het |
Vamp5 |
T |
C |
6: 72,347,181 (GRCm39) |
D46G |
possibly damaging |
Het |
Vmn1r23 |
T |
A |
6: 57,903,310 (GRCm39) |
Q156L |
probably benign |
Het |
Vmn2r6 |
C |
T |
3: 64,454,829 (GRCm39) |
S490N |
probably benign |
Het |
Vps39 |
A |
T |
2: 120,183,440 (GRCm39) |
I10N |
probably damaging |
Het |
Vwf |
C |
T |
6: 125,622,897 (GRCm39) |
Q1755* |
probably null |
Het |
Wdfy4 |
A |
T |
14: 32,877,717 (GRCm39) |
H82Q |
probably benign |
Het |
Wdr24 |
T |
C |
17: 26,045,101 (GRCm39) |
Y279H |
probably damaging |
Het |
Wdr72 |
A |
G |
9: 74,117,843 (GRCm39) |
T852A |
probably benign |
Het |
Zfp1 |
T |
A |
8: 112,396,355 (GRCm39) |
C92* |
probably null |
Het |
Zfp1004 |
T |
A |
2: 150,033,899 (GRCm39) |
C104* |
probably null |
Het |
Zfp426 |
A |
T |
9: 20,386,369 (GRCm39) |
|
probably benign |
Het |
Zfp442 |
C |
T |
2: 150,253,130 (GRCm39) |
|
probably null |
Het |
Zfp74 |
T |
C |
7: 29,635,470 (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 |
|
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 |
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 |
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 |
|