Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
T |
5: 88,118,524 (GRCm39) |
I3F |
probably benign |
Het |
4930590J08Rik |
A |
G |
6: 91,894,016 (GRCm39) |
N211S |
probably benign |
Het |
A2ml1 |
A |
T |
6: 128,524,196 (GRCm39) |
Y1145* |
probably null |
Het |
Abca7 |
A |
G |
10: 79,850,064 (GRCm39) |
D1972G |
probably benign |
Het |
Adamts19 |
A |
T |
18: 59,185,687 (GRCm39) |
D1187V |
probably damaging |
Het |
Adcy6 |
G |
C |
15: 98,497,888 (GRCm39) |
I421M |
probably damaging |
Het |
Afap1 |
C |
A |
5: 36,131,835 (GRCm39) |
H387Q |
probably damaging |
Het |
Atp8b1 |
C |
T |
18: 64,678,335 (GRCm39) |
V854M |
probably damaging |
Het |
Auts2 |
C |
T |
5: 131,516,302 (GRCm39) |
|
probably benign |
Het |
Cbll1 |
T |
C |
12: 31,537,855 (GRCm39) |
D300G |
probably damaging |
Het |
Cd200r4 |
A |
T |
16: 44,653,412 (GRCm39) |
T61S |
possibly damaging |
Het |
Chmp4c |
G |
T |
3: 10,454,744 (GRCm39) |
V207L |
probably benign |
Het |
Cntn5 |
T |
C |
9: 9,976,321 (GRCm39) |
T413A |
possibly damaging |
Het |
Cox7a2 |
T |
A |
9: 79,665,863 (GRCm39) |
|
probably null |
Het |
Cwc27 |
A |
G |
13: 104,933,814 (GRCm39) |
L236P |
probably damaging |
Het |
Diaph1 |
A |
G |
18: 38,029,146 (GRCm39) |
|
probably null |
Het |
Dst |
T |
A |
1: 34,299,453 (GRCm39) |
|
probably benign |
Het |
Ear1 |
T |
A |
14: 44,056,583 (GRCm39) |
H95L |
probably damaging |
Het |
Enpp1 |
T |
A |
10: 24,517,732 (GRCm39) |
H898L |
probably benign |
Het |
Entpd5 |
G |
A |
12: 84,429,069 (GRCm39) |
R321* |
probably null |
Het |
Ercc6l2 |
C |
A |
13: 63,972,685 (GRCm39) |
N177K |
possibly damaging |
Het |
Ergic1 |
T |
C |
17: 26,860,680 (GRCm39) |
|
probably null |
Het |
Erich6 |
A |
T |
3: 58,534,019 (GRCm39) |
I336N |
probably benign |
Het |
Fmnl2 |
A |
G |
2: 52,995,549 (GRCm39) |
E424G |
probably damaging |
Het |
Galnt3 |
A |
T |
2: 65,914,550 (GRCm39) |
D622E |
probably damaging |
Het |
Gjd4 |
T |
A |
18: 9,280,569 (GRCm39) |
T170S |
probably damaging |
Het |
Gm5611 |
G |
A |
9: 16,941,903 (GRCm39) |
|
noncoding transcript |
Het |
Gpc5 |
T |
A |
14: 115,636,662 (GRCm39) |
N448K |
probably benign |
Het |
Klra3 |
G |
C |
6: 130,310,107 (GRCm39) |
R138G |
probably benign |
Het |
Maco1 |
A |
G |
4: 134,531,818 (GRCm39) |
V617A |
probably damaging |
Het |
Man2b2 |
T |
C |
5: 36,978,271 (GRCm39) |
T338A |
probably benign |
Het |
Mbtps1 |
A |
T |
8: 120,272,864 (GRCm39) |
S94T |
probably benign |
Het |
Muc3a |
A |
T |
5: 137,244,538 (GRCm39) |
S205T |
unknown |
Het |
Nav2 |
C |
A |
7: 49,195,682 (GRCm39) |
D1019E |
probably damaging |
Het |
Neurl4 |
T |
A |
11: 69,794,252 (GRCm39) |
L236* |
probably null |
Het |
Or13c25 |
A |
G |
4: 52,911,260 (GRCm39) |
V178A |
probably benign |
Het |
Plcxd3 |
T |
C |
15: 4,546,093 (GRCm39) |
|
probably benign |
Het |
Pprc1 |
T |
C |
19: 46,059,965 (GRCm39) |
|
probably benign |
Het |
Prkaa2 |
T |
A |
4: 104,932,647 (GRCm39) |
N67I |
probably damaging |
Het |
Prom1 |
T |
A |
5: 44,175,695 (GRCm39) |
Y508F |
probably benign |
Het |
Prx |
A |
G |
7: 27,216,683 (GRCm39) |
M534V |
probably damaging |
Het |
Rps6kc1 |
C |
T |
1: 190,603,965 (GRCm39) |
R219Q |
possibly damaging |
Het |
Sbf2 |
T |
C |
7: 109,977,250 (GRCm39) |
Y628C |
probably damaging |
Het |
Slc1a2 |
A |
T |
2: 102,607,855 (GRCm39) |
D501V |
probably benign |
Het |
Spata31 |
A |
T |
13: 65,069,196 (GRCm39) |
Q448L |
probably damaging |
Het |
Stxbp5 |
T |
A |
10: 9,713,836 (GRCm39) |
R234S |
probably damaging |
Het |
Tifab |
A |
G |
13: 56,324,101 (GRCm39) |
V114A |
probably benign |
Het |
Tiprl |
A |
G |
1: 165,055,975 (GRCm39) |
M49T |
probably benign |
Het |
Tlr12 |
A |
G |
4: 128,511,545 (GRCm39) |
L235P |
possibly damaging |
Het |
Trim43b |
A |
T |
9: 88,967,411 (GRCm39) |
C407* |
probably null |
Het |
Txndc17 |
C |
A |
11: 72,098,533 (GRCm39) |
F28L |
probably damaging |
Het |
Vmn2r27 |
T |
C |
6: 124,177,649 (GRCm39) |
R452G |
probably damaging |
Het |
Vmn2r3 |
T |
A |
3: 64,182,538 (GRCm39) |
D387V |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,875,712 (GRCm39) |
I2699T |
probably damaging |
Het |
Zfp944 |
G |
T |
17: 22,558,697 (GRCm39) |
Y183* |
probably null |
Het |
|
Other mutations in Stk35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00850:Stk35
|
APN |
2 |
129,643,912 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02609:Stk35
|
APN |
2 |
129,643,721 (GRCm39) |
missense |
probably damaging |
1.00 |
fingernails
|
UTSW |
2 |
129,652,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256_Stk35_331
|
UTSW |
2 |
129,652,427 (GRCm39) |
nonsense |
probably null |
|
skinned
|
UTSW |
2 |
129,653,155 (GRCm39) |
intron |
probably benign |
|
R0045:Stk35
|
UTSW |
2 |
129,642,488 (GRCm39) |
nonsense |
probably null |
|
R0306:Stk35
|
UTSW |
2 |
129,643,683 (GRCm39) |
nonsense |
probably null |
|
R0784:Stk35
|
UTSW |
2 |
129,652,722 (GRCm39) |
nonsense |
probably null |
|
R2256:Stk35
|
UTSW |
2 |
129,652,427 (GRCm39) |
nonsense |
probably null |
|
R2507:Stk35
|
UTSW |
2 |
129,643,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R2508:Stk35
|
UTSW |
2 |
129,643,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R3848:Stk35
|
UTSW |
2 |
129,642,656 (GRCm39) |
missense |
probably benign |
0.13 |
R3872:Stk35
|
UTSW |
2 |
129,652,495 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4466:Stk35
|
UTSW |
2 |
129,643,436 (GRCm39) |
missense |
probably damaging |
0.99 |
R5144:Stk35
|
UTSW |
2 |
129,652,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R6267:Stk35
|
UTSW |
2 |
129,652,808 (GRCm39) |
nonsense |
probably null |
|
R6296:Stk35
|
UTSW |
2 |
129,652,808 (GRCm39) |
nonsense |
probably null |
|
R6480:Stk35
|
UTSW |
2 |
129,652,607 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6807:Stk35
|
UTSW |
2 |
129,643,573 (GRCm39) |
missense |
probably damaging |
0.97 |
R7203:Stk35
|
UTSW |
2 |
129,643,513 (GRCm39) |
missense |
probably benign |
|
R7476:Stk35
|
UTSW |
2 |
129,652,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R8505:Stk35
|
UTSW |
2 |
129,643,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R8998:Stk35
|
UTSW |
2 |
129,652,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R8999:Stk35
|
UTSW |
2 |
129,652,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Stk35
|
UTSW |
2 |
129,652,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R9760:Stk35
|
UTSW |
2 |
129,642,605 (GRCm39) |
missense |
probably benign |
|
|