Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Ak2 |
T |
A |
4: 128,902,040 (GRCm39) |
F238I |
probably damaging |
Het |
Akap8l |
T |
C |
17: 32,557,266 (GRCm39) |
Y115C |
probably damaging |
Het |
Alms1 |
T |
A |
6: 85,606,190 (GRCm39) |
N2613K |
possibly damaging |
Het |
Antxr1 |
C |
T |
6: 87,194,255 (GRCm39) |
|
probably null |
Het |
Ap3b1 |
A |
T |
13: 94,664,765 (GRCm39) |
R901S |
unknown |
Het |
Arhgap45 |
A |
G |
10: 79,861,310 (GRCm39) |
E491G |
probably damaging |
Het |
Capn11 |
C |
T |
17: 45,950,600 (GRCm39) |
R293Q |
possibly damaging |
Het |
Cdx1 |
C |
T |
18: 61,152,971 (GRCm39) |
V212I |
probably benign |
Het |
Clca4b |
G |
A |
3: 144,627,624 (GRCm39) |
T449I |
probably benign |
Het |
Clec14a |
T |
C |
12: 58,314,612 (GRCm39) |
I337V |
probably benign |
Het |
Clip4 |
A |
C |
17: 72,096,878 (GRCm39) |
M1L |
probably damaging |
Het |
Exoc3l4 |
T |
C |
12: 111,389,851 (GRCm39) |
I142T |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,890,843 (GRCm38) |
I575N |
probably benign |
Het |
Gad1-ps |
A |
T |
10: 99,280,395 (GRCm39) |
|
noncoding transcript |
Het |
Golga7 |
C |
T |
8: 23,740,360 (GRCm39) |
A57T |
probably damaging |
Het |
Gpa33 |
A |
G |
1: 165,974,360 (GRCm39) |
T66A |
possibly damaging |
Het |
Gpr141b |
A |
G |
13: 19,913,465 (GRCm39) |
|
noncoding transcript |
Het |
Gpr45 |
A |
G |
1: 43,072,218 (GRCm39) |
Y287C |
probably damaging |
Het |
H2-Eb1 |
C |
A |
17: 34,533,229 (GRCm39) |
Y150* |
probably null |
Het |
Hsd17b8 |
T |
C |
17: 34,245,435 (GRCm39) |
D233G |
probably null |
Het |
Ifna6 |
A |
T |
4: 88,745,906 (GRCm39) |
Q85L |
probably damaging |
Het |
Igkv9-120 |
G |
A |
6: 68,027,257 (GRCm39) |
W57* |
probably null |
Het |
Ivns1abp |
G |
T |
1: 151,229,760 (GRCm39) |
L149F |
probably benign |
Het |
Kank4 |
A |
G |
4: 98,653,698 (GRCm39) |
|
probably null |
Het |
Lama2 |
A |
T |
10: 27,066,540 (GRCm39) |
C1114S |
probably damaging |
Het |
Lmbr1l |
A |
C |
15: 98,805,489 (GRCm39) |
D337E |
possibly damaging |
Het |
Ly75 |
T |
C |
2: 60,138,655 (GRCm39) |
D1404G |
probably damaging |
Het |
Muc4 |
A |
G |
16: 32,575,011 (GRCm39) |
T1199A |
probably benign |
Het |
Nalcn |
A |
G |
14: 123,532,818 (GRCm39) |
I1314T |
probably damaging |
Het |
Nhlrc1 |
A |
G |
13: 47,167,193 (GRCm39) |
F355L |
probably benign |
Het |
Or2y16 |
T |
C |
11: 49,335,140 (GRCm39) |
V154A |
probably benign |
Het |
Or4k39 |
C |
T |
2: 111,238,818 (GRCm39) |
|
noncoding transcript |
Het |
Or5b21 |
A |
T |
19: 12,839,171 (GRCm39) |
T11S |
probably benign |
Het |
Pcsk1 |
A |
G |
13: 75,246,026 (GRCm39) |
T135A |
possibly damaging |
Het |
Ptpru |
T |
A |
4: 131,547,501 (GRCm39) |
Y112F |
possibly damaging |
Het |
Rbbp8 |
A |
G |
18: 11,875,699 (GRCm39) |
S871G |
probably benign |
Het |
Rhoj |
A |
T |
12: 75,440,743 (GRCm39) |
I135F |
probably damaging |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Semp2l2b |
T |
A |
10: 21,942,742 (GRCm39) |
T413S |
possibly damaging |
Het |
Slc11a2 |
A |
G |
15: 100,301,169 (GRCm39) |
Y295H |
probably damaging |
Het |
Slc22a28 |
A |
T |
19: 8,108,795 (GRCm39) |
C116S |
probably damaging |
Het |
Synpo |
T |
C |
18: 60,729,022 (GRCm39) |
D1060G |
probably damaging |
Het |
Tectb |
T |
C |
19: 55,181,059 (GRCm39) |
S310P |
probably benign |
Het |
Tmc6 |
A |
G |
11: 117,666,441 (GRCm39) |
S288P |
possibly damaging |
Het |
Tpo |
A |
G |
12: 30,169,490 (GRCm39) |
S82P |
probably benign |
Het |
Ttyh3 |
T |
A |
5: 140,617,307 (GRCm39) |
M321L |
probably benign |
Het |
Usp8 |
A |
G |
2: 126,584,345 (GRCm39) |
D518G |
probably benign |
Het |
Vmn2r11 |
A |
G |
5: 109,202,772 (GRCm39) |
W102R |
probably benign |
Het |
Vps13a |
G |
A |
19: 16,692,464 (GRCm39) |
H817Y |
probably benign |
Het |
Vps51 |
A |
G |
19: 6,118,224 (GRCm39) |
V757A |
probably benign |
Het |
Washc4 |
T |
C |
10: 83,405,892 (GRCm39) |
S463P |
probably damaging |
Het |
Zfp423 |
T |
C |
8: 88,508,955 (GRCm39) |
N442S |
probably damaging |
Het |
|
Other mutations in Ska1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02146:Ska1
|
APN |
18 |
74,329,981 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02685:Ska1
|
APN |
18 |
74,330,119 (GRCm39) |
missense |
probably benign |
0.00 |
R0831:Ska1
|
UTSW |
18 |
74,330,570 (GRCm39) |
splice site |
probably benign |
|
R2087:Ska1
|
UTSW |
18 |
74,339,920 (GRCm39) |
missense |
probably benign |
0.06 |
R2232:Ska1
|
UTSW |
18 |
74,330,137 (GRCm39) |
splice site |
probably null |
|
R4658:Ska1
|
UTSW |
18 |
74,330,111 (GRCm39) |
missense |
probably benign |
0.01 |
R5876:Ska1
|
UTSW |
18 |
74,330,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R6019:Ska1
|
UTSW |
18 |
74,332,992 (GRCm39) |
missense |
probably benign |
0.13 |
R6049:Ska1
|
UTSW |
18 |
74,335,671 (GRCm39) |
missense |
probably benign |
0.00 |
R6885:Ska1
|
UTSW |
18 |
74,339,910 (GRCm39) |
missense |
probably benign |
0.41 |
R7549:Ska1
|
UTSW |
18 |
74,333,088 (GRCm39) |
missense |
probably benign |
0.01 |
R7701:Ska1
|
UTSW |
18 |
74,335,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R7757:Ska1
|
UTSW |
18 |
74,330,044 (GRCm39) |
missense |
probably benign |
0.00 |
R8141:Ska1
|
UTSW |
18 |
74,339,907 (GRCm39) |
missense |
probably benign |
0.20 |
R8266:Ska1
|
UTSW |
18 |
74,337,412 (GRCm39) |
missense |
probably benign |
0.15 |
R8963:Ska1
|
UTSW |
18 |
74,330,639 (GRCm39) |
missense |
probably damaging |
0.96 |
R9671:Ska1
|
UTSW |
18 |
74,333,010 (GRCm39) |
missense |
probably damaging |
0.99 |
|