Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm5 |
A |
T |
7: 119,137,511 (GRCm39) |
I402F |
probably damaging |
Het |
Acvr2b |
T |
C |
9: 119,261,570 (GRCm39) |
Y388H |
probably damaging |
Het |
Adh1 |
G |
A |
3: 137,988,512 (GRCm39) |
D162N |
possibly damaging |
Het |
C6 |
G |
T |
15: 4,822,236 (GRCm39) |
R585I |
probably damaging |
Het |
Ccdc169 |
T |
A |
3: 55,070,732 (GRCm39) |
|
probably null |
Het |
Cdh13 |
T |
A |
8: 119,401,916 (GRCm39) |
M106K |
probably damaging |
Het |
Cep78 |
C |
T |
19: 15,938,359 (GRCm39) |
E530K |
probably damaging |
Het |
Cyfip1 |
T |
A |
7: 55,546,487 (GRCm39) |
L533Q |
probably damaging |
Het |
Etl4 |
T |
C |
2: 20,811,460 (GRCm39) |
V1181A |
probably benign |
Het |
Galnt7 |
T |
G |
8: 57,984,769 (GRCm39) |
|
probably benign |
Het |
Gm11595 |
G |
A |
11: 99,663,498 (GRCm39) |
R61C |
unknown |
Het |
Gucy1a1 |
T |
A |
3: 82,016,560 (GRCm39) |
I143F |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,613,050 (GRCm39) |
N1410D |
possibly damaging |
Het |
Ltbp2 |
G |
A |
12: 84,856,020 (GRCm39) |
T741I |
probably benign |
Het |
Mdc1 |
T |
C |
17: 36,163,397 (GRCm39) |
S982P |
probably benign |
Het |
Mfsd4b2 |
A |
G |
10: 39,798,193 (GRCm39) |
|
probably benign |
Het |
Mrgprb5 |
T |
G |
7: 47,818,172 (GRCm39) |
I188L |
probably benign |
Het |
Naip6 |
T |
A |
13: 100,436,862 (GRCm39) |
S554C |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,220,957 (GRCm39) |
N1715D |
probably damaging |
Het |
Nav3 |
A |
T |
10: 109,605,119 (GRCm39) |
S985T |
possibly damaging |
Het |
Nme7 |
A |
G |
1: 164,155,866 (GRCm39) |
Q22R |
probably benign |
Het |
Or52i2 |
T |
C |
7: 102,319,927 (GRCm39) |
W267R |
probably damaging |
Het |
Otulinl |
C |
T |
15: 27,658,151 (GRCm39) |
D290N |
probably damaging |
Het |
Pabir1 |
A |
G |
19: 24,453,948 (GRCm39) |
V258A |
probably benign |
Het |
Ppp1r9a |
A |
G |
6: 5,115,322 (GRCm39) |
E815G |
probably damaging |
Het |
Ppp2r2c |
T |
A |
5: 37,083,744 (GRCm39) |
I95N |
probably damaging |
Het |
Ppp4r4 |
G |
A |
12: 103,569,225 (GRCm39) |
E717K |
possibly damaging |
Het |
Prdm2 |
A |
G |
4: 142,860,138 (GRCm39) |
S1051P |
possibly damaging |
Het |
Rnf214 |
T |
C |
9: 45,811,084 (GRCm39) |
D193G |
probably damaging |
Het |
Sirpb1b |
G |
T |
3: 15,608,244 (GRCm39) |
T167K |
probably damaging |
Het |
Slc16a3 |
C |
A |
11: 120,847,532 (GRCm39) |
S240* |
probably null |
Het |
Snx14 |
T |
A |
9: 88,267,891 (GRCm39) |
|
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,256,866 (GRCm39) |
|
probably benign |
Het |
Taar7b |
A |
T |
10: 23,875,874 (GRCm39) |
D13V |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,066,506 (GRCm39) |
E740G |
probably damaging |
Het |
Unc79 |
C |
T |
12: 103,115,279 (GRCm39) |
A2054V |
possibly damaging |
Het |
Zfp106 |
A |
G |
2: 120,354,034 (GRCm39) |
V211A |
probably benign |
Het |
Zfp112 |
A |
G |
7: 23,825,379 (GRCm39) |
H449R |
probably benign |
Het |
|
Other mutations in Stk-ps2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01088:Stk-ps2
|
APN |
1 |
46,069,010 (GRCm39) |
exon |
noncoding transcript |
|
IGL01859:Stk-ps2
|
APN |
1 |
46,069,202 (GRCm39) |
exon |
noncoding transcript |
|
IGL01949:Stk-ps2
|
APN |
1 |
46,069,148 (GRCm39) |
exon |
noncoding transcript |
|
IGL02338:Stk-ps2
|
APN |
1 |
46,069,337 (GRCm39) |
exon |
noncoding transcript |
|
R0087:Stk-ps2
|
UTSW |
1 |
46,069,049 (GRCm39) |
exon |
noncoding transcript |
|
R0139:Stk-ps2
|
UTSW |
1 |
46,068,955 (GRCm39) |
exon |
noncoding transcript |
|
R0627:Stk-ps2
|
UTSW |
1 |
46,068,851 (GRCm39) |
exon |
noncoding transcript |
|
R3086:Stk-ps2
|
UTSW |
1 |
46,068,236 (GRCm39) |
unclassified |
noncoding transcript |
|
R3763:Stk-ps2
|
UTSW |
1 |
46,069,081 (GRCm39) |
exon |
noncoding transcript |
|
R4817:Stk-ps2
|
UTSW |
1 |
46,068,125 (GRCm39) |
unclassified |
noncoding transcript |
|
R4951:Stk-ps2
|
UTSW |
1 |
46,068,602 (GRCm39) |
unclassified |
noncoding transcript |
|
|