Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933402J07Rik |
C |
T |
8: 88,312,691 (GRCm39) |
Q159* |
probably null |
Het |
Abca12 |
C |
A |
1: 71,302,647 (GRCm39) |
V2191L |
probably benign |
Het |
Adam34 |
A |
G |
8: 44,105,538 (GRCm39) |
Y36H |
probably benign |
Het |
Adprm |
A |
G |
11: 66,929,055 (GRCm39) |
V312A |
probably benign |
Het |
Anapc2 |
T |
C |
2: 25,162,682 (GRCm39) |
L52P |
probably benign |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
Apoc4 |
T |
A |
7: 19,412,560 (GRCm39) |
T62S |
probably damaging |
Het |
Arfgef1 |
C |
T |
1: 10,270,103 (GRCm39) |
A349T |
probably benign |
Het |
Arhgap32 |
A |
G |
9: 32,027,436 (GRCm39) |
E2G |
possibly damaging |
Het |
Atg4c |
C |
A |
4: 99,109,463 (GRCm39) |
N143K |
possibly damaging |
Het |
C1qtnf12 |
A |
G |
4: 156,050,922 (GRCm39) |
N297S |
probably benign |
Het |
Cadps2 |
G |
T |
6: 23,838,998 (GRCm39) |
|
probably benign |
Het |
Ccdc63 |
C |
G |
5: 122,265,628 (GRCm39) |
A71P |
possibly damaging |
Het |
Cdca2 |
T |
C |
14: 67,952,258 (GRCm39) |
K38E |
probably damaging |
Het |
Cyp2j11 |
G |
A |
4: 96,204,595 (GRCm39) |
T317I |
probably damaging |
Het |
Dab2 |
T |
C |
15: 6,446,398 (GRCm39) |
V5A |
probably benign |
Het |
Dennd3 |
A |
T |
15: 73,426,909 (GRCm39) |
H762L |
probably benign |
Het |
Disp1 |
A |
G |
1: 182,869,936 (GRCm39) |
F828S |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,406,587 (GRCm39) |
M552V |
probably benign |
Het |
Dock2 |
A |
G |
11: 34,179,472 (GRCm39) |
|
probably null |
Het |
Dsel |
A |
T |
1: 111,787,987 (GRCm39) |
N849K |
probably benign |
Het |
Fah |
A |
T |
7: 84,244,042 (GRCm39) |
I239N |
probably damaging |
Het |
Flt4 |
T |
C |
11: 49,536,824 (GRCm39) |
Y1265H |
probably benign |
Het |
Ghdc |
T |
C |
11: 100,660,018 (GRCm39) |
E243G |
probably benign |
Het |
Glb1 |
T |
C |
9: 114,279,716 (GRCm39) |
Y375H |
probably damaging |
Het |
Gm6619 |
A |
G |
6: 131,466,021 (GRCm39) |
I40V |
probably benign |
Het |
Gpld1 |
T |
C |
13: 25,146,630 (GRCm39) |
V225A |
probably benign |
Het |
Hectd4 |
T |
C |
5: 121,391,921 (GRCm39) |
|
probably benign |
Het |
Igdcc4 |
A |
G |
9: 65,032,617 (GRCm39) |
I542V |
possibly damaging |
Het |
Igsf9b |
T |
C |
9: 27,245,633 (GRCm39) |
L1200P |
probably damaging |
Het |
Itgb7 |
C |
T |
15: 102,130,553 (GRCm39) |
V378M |
probably damaging |
Het |
Krt84 |
T |
C |
15: 101,438,019 (GRCm39) |
E312G |
possibly damaging |
Het |
Man2a2 |
A |
G |
7: 80,017,532 (GRCm39) |
W250R |
probably damaging |
Het |
Mcam |
T |
C |
9: 44,047,932 (GRCm39) |
V59A |
probably damaging |
Het |
Mfrp |
T |
C |
9: 44,015,015 (GRCm39) |
L314P |
probably benign |
Het |
Mgat5 |
T |
C |
1: 127,396,987 (GRCm39) |
V578A |
probably damaging |
Het |
Mycbp2 |
G |
A |
14: 103,393,358 (GRCm39) |
H3068Y |
probably damaging |
Het |
Myh1 |
A |
C |
11: 67,113,234 (GRCm39) |
D1873A |
probably benign |
Het |
Nek9 |
A |
G |
12: 85,376,677 (GRCm39) |
W235R |
probably damaging |
Het |
Or9g19 |
T |
C |
2: 85,600,342 (GRCm39) |
S66P |
probably damaging |
Het |
Parvb |
A |
G |
15: 84,116,369 (GRCm39) |
K33E |
possibly damaging |
Het |
Pecr |
T |
C |
1: 72,316,517 (GRCm39) |
R63G |
possibly damaging |
Het |
Pkhd1l1 |
T |
G |
15: 44,363,378 (GRCm39) |
|
probably null |
Het |
Plekha5 |
T |
C |
6: 140,516,129 (GRCm39) |
V270A |
probably damaging |
Het |
Prr14l |
T |
C |
5: 32,988,046 (GRCm39) |
D483G |
probably benign |
Het |
Rimkla |
T |
A |
4: 119,331,779 (GRCm39) |
M140L |
possibly damaging |
Het |
Senp1 |
C |
T |
15: 97,956,196 (GRCm39) |
V408I |
possibly damaging |
Het |
Tada2a |
T |
C |
11: 83,970,455 (GRCm39) |
D432G |
probably damaging |
Het |
Themis |
T |
A |
10: 28,544,723 (GRCm39) |
I23N |
probably damaging |
Het |
Thnsl1 |
T |
C |
2: 21,217,344 (GRCm39) |
I366T |
probably benign |
Het |
Tmem131 |
C |
A |
1: 36,851,690 (GRCm39) |
V938L |
probably benign |
Het |
Tmem178b |
A |
T |
6: 40,184,435 (GRCm39) |
Q111L |
probably damaging |
Het |
Vmn1r195 |
C |
G |
13: 22,462,934 (GRCm39) |
L135V |
possibly damaging |
Het |
Vmn2r-ps36 |
C |
T |
7: 7,431,539 (GRCm39) |
|
noncoding transcript |
Het |
Zfp956 |
G |
A |
6: 47,940,805 (GRCm39) |
R388H |
probably damaging |
Het |
Zfr2 |
T |
G |
10: 81,077,950 (GRCm39) |
V259G |
probably benign |
Het |
|
Other mutations in Stambpl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00496:Stambpl1
|
APN |
19 |
34,217,430 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01779:Stambpl1
|
APN |
19 |
34,217,427 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01817:Stambpl1
|
APN |
19 |
34,211,393 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02582:Stambpl1
|
APN |
19 |
34,212,612 (GRCm39) |
missense |
probably benign |
0.01 |
R1639:Stambpl1
|
UTSW |
19 |
34,213,707 (GRCm39) |
missense |
probably benign |
0.11 |
R1707:Stambpl1
|
UTSW |
19 |
34,216,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Stambpl1
|
UTSW |
19 |
34,204,121 (GRCm39) |
missense |
probably damaging |
0.99 |
R1768:Stambpl1
|
UTSW |
19 |
34,204,121 (GRCm39) |
missense |
probably damaging |
0.99 |
R1887:Stambpl1
|
UTSW |
19 |
34,213,808 (GRCm39) |
missense |
probably benign |
0.38 |
R2362:Stambpl1
|
UTSW |
19 |
34,213,754 (GRCm39) |
missense |
probably benign |
0.31 |
R4342:Stambpl1
|
UTSW |
19 |
34,211,446 (GRCm39) |
missense |
probably benign |
0.00 |
R4689:Stambpl1
|
UTSW |
19 |
34,213,691 (GRCm39) |
missense |
probably benign |
0.11 |
R5533:Stambpl1
|
UTSW |
19 |
34,211,316 (GRCm39) |
splice site |
probably null |
|
R5647:Stambpl1
|
UTSW |
19 |
34,211,686 (GRCm39) |
missense |
probably benign |
0.03 |
R6353:Stambpl1
|
UTSW |
19 |
34,211,520 (GRCm39) |
splice site |
probably null |
|
R6402:Stambpl1
|
UTSW |
19 |
34,211,539 (GRCm39) |
missense |
probably benign |
0.00 |
R7334:Stambpl1
|
UTSW |
19 |
34,204,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R7413:Stambpl1
|
UTSW |
19 |
34,204,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R7728:Stambpl1
|
UTSW |
19 |
34,213,721 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8257:Stambpl1
|
UTSW |
19 |
34,208,901 (GRCm39) |
missense |
probably damaging |
0.99 |
R8341:Stambpl1
|
UTSW |
19 |
34,211,401 (GRCm39) |
missense |
probably benign |
0.44 |
R9163:Stambpl1
|
UTSW |
19 |
34,212,634 (GRCm39) |
missense |
probably benign |
0.01 |
R9694:Stambpl1
|
UTSW |
19 |
34,211,535 (GRCm39) |
missense |
probably benign |
|
Z1088:Stambpl1
|
UTSW |
19 |
34,204,027 (GRCm39) |
missense |
probably damaging |
0.96 |
|