Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930018M24Rik |
T |
C |
14: 51,134,414 (GRCm39) |
D76G |
possibly damaging |
Het |
Adamtsl3 |
A |
T |
7: 82,260,958 (GRCm39) |
R1631W |
probably damaging |
Het |
Alg5 |
C |
T |
3: 54,646,254 (GRCm39) |
H40Y |
probably benign |
Het |
B3galt1 |
T |
C |
2: 67,949,095 (GRCm39) |
L270P |
probably damaging |
Het |
Ceacam3 |
A |
G |
7: 16,893,860 (GRCm39) |
Y457C |
probably damaging |
Het |
Cenpa |
A |
T |
5: 30,830,736 (GRCm39) |
R124W |
probably damaging |
Het |
Cfap44 |
A |
G |
16: 44,275,894 (GRCm39) |
T1385A |
possibly damaging |
Het |
Chd9 |
A |
T |
8: 91,738,078 (GRCm39) |
H1570L |
possibly damaging |
Het |
Cmtm4 |
T |
C |
8: 105,084,356 (GRCm39) |
I113V |
probably benign |
Het |
Dmxl1 |
T |
C |
18: 50,024,693 (GRCm39) |
I1789T |
possibly damaging |
Het |
Dpf3 |
G |
A |
12: 83,371,714 (GRCm39) |
R174W |
probably damaging |
Het |
Dusp26 |
T |
C |
8: 31,584,169 (GRCm39) |
L92P |
probably damaging |
Het |
Fndc7 |
T |
A |
3: 108,770,208 (GRCm39) |
T659S |
possibly damaging |
Het |
Fry |
A |
G |
5: 150,282,546 (GRCm39) |
H357R |
possibly damaging |
Het |
G0s2 |
A |
T |
1: 192,954,859 (GRCm39) |
L75H |
probably damaging |
Het |
Gm5493 |
A |
G |
17: 22,969,065 (GRCm39) |
T82A |
probably benign |
Het |
Herc2 |
T |
C |
7: 55,854,164 (GRCm39) |
V3690A |
probably benign |
Het |
Igf2bp3 |
C |
A |
6: 49,064,734 (GRCm39) |
V537F |
probably damaging |
Het |
Kntc1 |
C |
T |
5: 123,956,538 (GRCm39) |
R2101W |
possibly damaging |
Het |
Kpna2rt |
T |
C |
17: 90,217,635 (GRCm39) |
E37G |
probably damaging |
Het |
Mrgpra6 |
G |
T |
7: 46,835,657 (GRCm39) |
P255T |
probably damaging |
Het |
Ncor2 |
A |
G |
5: 125,125,364 (GRCm39) |
V229A |
probably benign |
Het |
Nos1ap |
T |
A |
1: 170,176,968 (GRCm39) |
K145M |
probably damaging |
Het |
Or6c210 |
T |
A |
10: 129,495,969 (GRCm39) |
I98K |
possibly damaging |
Het |
Or7g21 |
T |
A |
9: 19,032,676 (GRCm39) |
C142S |
probably benign |
Het |
Ppt2 |
C |
A |
17: 34,844,823 (GRCm39) |
M140I |
probably benign |
Het |
Ppwd1 |
A |
G |
13: 104,356,906 (GRCm39) |
I203T |
probably damaging |
Het |
Prpf6 |
A |
G |
2: 181,287,381 (GRCm39) |
T589A |
probably benign |
Het |
Psd4 |
T |
C |
2: 24,287,427 (GRCm39) |
L453P |
probably benign |
Het |
Ptpn14 |
A |
G |
1: 189,519,038 (GRCm39) |
T23A |
probably damaging |
Het |
Rxrb |
T |
C |
17: 34,256,381 (GRCm39) |
L374P |
probably damaging |
Het |
Scaf4 |
T |
C |
16: 90,041,198 (GRCm39) |
E710G |
unknown |
Het |
Sik1 |
C |
T |
17: 32,069,802 (GRCm39) |
V216I |
probably damaging |
Het |
Skint8 |
C |
A |
4: 111,807,390 (GRCm39) |
L359M |
probably damaging |
Het |
Slc30a5 |
T |
A |
13: 100,950,380 (GRCm39) |
K236* |
probably null |
Het |
Slc38a4 |
A |
C |
15: 96,910,871 (GRCm39) |
S135A |
probably damaging |
Het |
Slc9a1 |
T |
A |
4: 133,139,571 (GRCm39) |
V263D |
probably damaging |
Het |
Socs2 |
T |
C |
10: 95,228,745 (GRCm39) |
I168M |
unknown |
Het |
Spag9 |
C |
A |
11: 93,959,838 (GRCm39) |
D342E |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,469,825 (GRCm39) |
S4508P |
possibly damaging |
Het |
Stat5b |
C |
A |
11: 100,675,080 (GRCm39) |
E710* |
probably null |
Het |
Stip1 |
G |
A |
19: 7,009,883 (GRCm39) |
P213L |
probably damaging |
Het |
Tarbp1 |
A |
T |
8: 127,177,425 (GRCm39) |
L749Q |
probably damaging |
Het |
Thsd7b |
T |
G |
1: 129,523,270 (GRCm39) |
S24R |
probably benign |
Het |
Upp2 |
T |
C |
2: 58,680,107 (GRCm39) |
V293A |
probably damaging |
Het |
Vmn2r65 |
C |
T |
7: 84,590,047 (GRCm39) |
C623Y |
probably damaging |
Het |
Vps54 |
T |
C |
11: 21,258,799 (GRCm39) |
V742A |
probably damaging |
Het |
|
Other mutations in 2610028H24Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02400:2610028H24Rik
|
APN |
10 |
76,290,644 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02951:2610028H24Rik
|
APN |
10 |
76,290,536 (GRCm39) |
splice site |
probably benign |
|
PIT4283001:2610028H24Rik
|
UTSW |
10 |
76,285,093 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R0013:2610028H24Rik
|
UTSW |
10 |
76,293,346 (GRCm39) |
missense |
probably benign |
0.32 |
R0295:2610028H24Rik
|
UTSW |
10 |
76,290,642 (GRCm39) |
missense |
probably damaging |
0.99 |
R2018:2610028H24Rik
|
UTSW |
10 |
76,293,899 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2019:2610028H24Rik
|
UTSW |
10 |
76,293,899 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2128:2610028H24Rik
|
UTSW |
10 |
76,293,349 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2129:2610028H24Rik
|
UTSW |
10 |
76,293,349 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4776:2610028H24Rik
|
UTSW |
10 |
76,293,346 (GRCm39) |
missense |
probably benign |
0.16 |
R5808:2610028H24Rik
|
UTSW |
10 |
76,286,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R5896:2610028H24Rik
|
UTSW |
10 |
76,288,664 (GRCm39) |
missense |
probably benign |
0.01 |
R5990:2610028H24Rik
|
UTSW |
10 |
76,285,123 (GRCm39) |
missense |
probably benign |
0.08 |
R6238:2610028H24Rik
|
UTSW |
10 |
76,285,096 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6505:2610028H24Rik
|
UTSW |
10 |
76,285,115 (GRCm39) |
missense |
probably benign |
0.02 |
R7741:2610028H24Rik
|
UTSW |
10 |
76,290,551 (GRCm39) |
missense |
probably damaging |
0.99 |
R9210:2610028H24Rik
|
UTSW |
10 |
76,287,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R9558:2610028H24Rik
|
UTSW |
10 |
76,290,576 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:2610028H24Rik
|
UTSW |
10 |
76,293,925 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1176:2610028H24Rik
|
UTSW |
10 |
76,288,697 (GRCm39) |
missense |
probably damaging |
1.00 |
|