Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300003K06Rik |
T |
A |
11: 99,728,163 (GRCm39) |
S227C |
unknown |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Adamts15 |
C |
T |
9: 30,813,786 (GRCm39) |
R793H |
probably damaging |
Het |
Ankra2 |
A |
G |
13: 98,407,644 (GRCm39) |
E38G |
probably damaging |
Het |
Aqp8 |
G |
A |
7: 123,061,807 (GRCm39) |
C8Y |
probably damaging |
Het |
Atg9b |
A |
G |
5: 24,597,017 (GRCm39) |
|
probably benign |
Het |
Atp6v1b1 |
A |
G |
6: 83,735,339 (GRCm39) |
E469G |
possibly damaging |
Het |
B4gat1 |
T |
A |
19: 5,089,241 (GRCm39) |
Y79* |
probably null |
Het |
BB019430 |
T |
A |
10: 58,540,014 (GRCm39) |
|
noncoding transcript |
Het |
Ccr2 |
C |
T |
9: 123,906,239 (GRCm39) |
T173I |
possibly damaging |
Het |
Cfap43 |
T |
C |
19: 47,885,538 (GRCm39) |
D359G |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,566,639 (GRCm39) |
E1022G |
possibly damaging |
Het |
Drd2 |
T |
A |
9: 49,318,259 (GRCm39) |
C400* |
probably null |
Het |
Efcab7 |
T |
A |
4: 99,766,941 (GRCm39) |
H495Q |
probably damaging |
Het |
Faim |
T |
C |
9: 98,874,195 (GRCm39) |
V29A |
probably benign |
Het |
Fancd2 |
T |
C |
6: 113,526,326 (GRCm39) |
S350P |
probably damaging |
Het |
Fbxw16 |
T |
C |
9: 109,270,285 (GRCm39) |
E152G |
probably benign |
Het |
Kif17 |
T |
C |
4: 138,025,643 (GRCm39) |
|
probably null |
Het |
Kif24 |
A |
T |
4: 41,428,604 (GRCm39) |
S119T |
probably damaging |
Het |
Ly6k |
A |
T |
15: 74,670,429 (GRCm39) |
S38T |
probably benign |
Het |
Mapk10 |
A |
G |
5: 103,061,158 (GRCm39) |
S430P |
probably damaging |
Het |
Megf10 |
G |
A |
18: 57,410,180 (GRCm39) |
A654T |
probably benign |
Het |
Mlph |
T |
C |
1: 90,867,536 (GRCm39) |
L450P |
probably damaging |
Het |
Otof |
T |
C |
5: 30,532,323 (GRCm39) |
D1603G |
probably damaging |
Het |
Pdcd11 |
T |
C |
19: 47,116,771 (GRCm39) |
S1580P |
possibly damaging |
Het |
Rad54b |
G |
A |
4: 11,595,919 (GRCm39) |
R232H |
possibly damaging |
Het |
Sar1b |
C |
T |
11: 51,670,576 (GRCm39) |
T40I |
possibly damaging |
Het |
Scyl2 |
C |
T |
10: 89,496,124 (GRCm39) |
S242N |
probably benign |
Het |
Sema4b |
A |
G |
7: 79,874,715 (GRCm39) |
N702D |
possibly damaging |
Het |
Slc16a11 |
A |
G |
11: 70,107,172 (GRCm39) |
I394V |
probably benign |
Het |
Stard9 |
A |
C |
2: 120,531,851 (GRCm39) |
T2703P |
probably damaging |
Het |
Stat5b |
A |
T |
11: 100,695,733 (GRCm39) |
L83Q |
possibly damaging |
Het |
Tas2r119 |
T |
A |
15: 32,177,932 (GRCm39) |
V166D |
possibly damaging |
Het |
Tmem117 |
T |
A |
15: 94,612,839 (GRCm39) |
I125N |
probably benign |
Het |
Tmem39a |
T |
C |
16: 38,393,568 (GRCm39) |
I89T |
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,178,565 (GRCm39) |
H3272Q |
probably damaging |
Het |
Vmn1r7 |
T |
C |
6: 57,001,591 (GRCm39) |
E223G |
probably damaging |
Het |
Vmn2r78 |
T |
C |
7: 86,603,796 (GRCm39) |
V658A |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,343,410 (GRCm39) |
T1884S |
possibly damaging |
Het |
Xkr4 |
A |
T |
1: 3,286,901 (GRCm39) |
F430I |
probably damaging |
Het |
Yae1d1 |
A |
G |
13: 18,164,200 (GRCm39) |
M1T |
probably null |
Het |
Zfand4 |
T |
C |
6: 116,265,084 (GRCm39) |
V183A |
probably damaging |
Het |
|
Other mutations in Calhm3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
FR4304:Calhm3
|
UTSW |
19 |
47,140,335 (GRCm39) |
frame shift |
probably null |
|
R1203:Calhm3
|
UTSW |
19 |
47,143,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R1863:Calhm3
|
UTSW |
19 |
47,140,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Calhm3
|
UTSW |
19 |
47,143,908 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1951:Calhm3
|
UTSW |
19 |
47,140,256 (GRCm39) |
missense |
probably benign |
0.00 |
R2089:Calhm3
|
UTSW |
19 |
47,140,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Calhm3
|
UTSW |
19 |
47,140,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Calhm3
|
UTSW |
19 |
47,140,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R2273:Calhm3
|
UTSW |
19 |
47,145,986 (GRCm39) |
missense |
probably damaging |
0.96 |
R2274:Calhm3
|
UTSW |
19 |
47,145,986 (GRCm39) |
missense |
probably damaging |
0.96 |
R2436:Calhm3
|
UTSW |
19 |
47,140,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R3702:Calhm3
|
UTSW |
19 |
47,140,187 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5758:Calhm3
|
UTSW |
19 |
47,140,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R5938:Calhm3
|
UTSW |
19 |
47,140,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6948:Calhm3
|
UTSW |
19 |
47,140,344 (GRCm39) |
missense |
probably damaging |
0.99 |
R9190:Calhm3
|
UTSW |
19 |
47,146,121 (GRCm39) |
missense |
probably benign |
0.00 |
|