Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alk |
T |
C |
17: 72,207,781 (GRCm39) |
I985V |
probably damaging |
Het |
Anapc2 |
A |
C |
2: 25,164,794 (GRCm39) |
R59S |
possibly damaging |
Het |
Ankhd1 |
T |
A |
18: 36,711,696 (GRCm39) |
D165E |
probably benign |
Het |
Asb8 |
A |
T |
15: 98,034,054 (GRCm39) |
V167D |
probably damaging |
Het |
Atp5pf |
A |
G |
16: 84,625,360 (GRCm39) |
M81T |
probably benign |
Het |
Bcl7b |
A |
G |
5: 135,208,950 (GRCm39) |
T138A |
probably damaging |
Het |
Cdh23 |
A |
G |
10: 60,146,566 (GRCm39) |
L2869P |
probably damaging |
Het |
Chl1 |
T |
C |
6: 103,706,186 (GRCm39) |
S1174P |
probably benign |
Het |
Clec2g |
T |
C |
6: 128,925,699 (GRCm39) |
I36T |
unknown |
Het |
Denr |
A |
G |
5: 124,046,182 (GRCm39) |
D4G |
probably benign |
Het |
Dnajc10 |
T |
C |
2: 80,155,096 (GRCm39) |
|
probably benign |
Het |
Egf |
C |
T |
3: 129,496,104 (GRCm39) |
|
probably null |
Het |
Galnt10 |
A |
C |
11: 57,616,409 (GRCm39) |
Y108S |
probably damaging |
Het |
Gls |
C |
T |
1: 52,207,558 (GRCm39) |
G602D |
probably damaging |
Het |
Grb10 |
G |
T |
11: 11,895,599 (GRCm39) |
Q242K |
probably damaging |
Het |
Hspg2 |
A |
T |
4: 137,265,800 (GRCm39) |
Y1837F |
probably damaging |
Het |
Ikzf1 |
G |
T |
11: 11,698,358 (GRCm39) |
A70S |
probably benign |
Het |
Il17ra |
T |
C |
6: 120,458,426 (GRCm39) |
Y526H |
probably damaging |
Het |
Il34 |
A |
T |
8: 111,469,375 (GRCm39) |
I186N |
possibly damaging |
Het |
Iqca1 |
G |
A |
1: 89,998,350 (GRCm39) |
|
probably benign |
Het |
Kntc1 |
A |
G |
5: 123,896,546 (GRCm39) |
Y136C |
probably damaging |
Het |
Man2b2 |
A |
T |
5: 36,971,681 (GRCm39) |
Y257* |
probably null |
Het |
Map3k19 |
A |
G |
1: 127,752,088 (GRCm39) |
F421S |
possibly damaging |
Het |
Melk |
A |
G |
4: 44,332,907 (GRCm39) |
T288A |
possibly damaging |
Het |
Mpp2 |
T |
C |
11: 101,954,135 (GRCm39) |
E187G |
probably damaging |
Het |
Mtf2 |
A |
G |
5: 108,252,323 (GRCm39) |
T394A |
probably benign |
Het |
Neil2 |
A |
G |
14: 63,429,177 (GRCm39) |
S39P |
probably damaging |
Het |
Or4e5 |
T |
A |
14: 52,727,624 (GRCm39) |
I266F |
probably benign |
Het |
Pcdh7 |
A |
G |
5: 58,286,566 (GRCm39) |
E1214G |
possibly damaging |
Het |
Pcdhb17 |
G |
T |
18: 37,620,548 (GRCm39) |
Q779H |
probably benign |
Het |
Pik3c2b |
A |
G |
1: 133,033,726 (GRCm39) |
I1577V |
probably benign |
Het |
Pkp3 |
C |
T |
7: 140,663,989 (GRCm39) |
P389S |
probably damaging |
Het |
Ppp4r2 |
T |
A |
6: 100,841,706 (GRCm39) |
Y92* |
probably null |
Het |
Rnf13 |
T |
C |
3: 57,714,508 (GRCm39) |
I189T |
probably benign |
Het |
Serpinf2 |
T |
C |
11: 75,328,871 (GRCm39) |
D53G |
probably benign |
Het |
Slc47a2 |
T |
A |
11: 61,220,607 (GRCm39) |
T184S |
probably benign |
Het |
Sned1 |
T |
C |
1: 93,210,936 (GRCm39) |
I1008T |
probably benign |
Het |
Sorcs3 |
A |
T |
19: 48,784,814 (GRCm39) |
E1079V |
probably damaging |
Het |
Trappc8 |
G |
A |
18: 20,999,176 (GRCm39) |
S318L |
probably benign |
Het |
Trappc9 |
A |
G |
15: 72,462,002 (GRCm39) |
S909P |
probably benign |
Het |
Ttn |
G |
A |
2: 76,560,483 (GRCm39) |
T29306I |
probably damaging |
Het |
Twnk |
G |
A |
19: 45,000,090 (GRCm39) |
R602Q |
possibly damaging |
Het |
Vmn2r15 |
A |
T |
5: 109,441,075 (GRCm39) |
I261K |
probably damaging |
Het |
Vmn2r77 |
G |
A |
7: 86,461,124 (GRCm39) |
A817T |
probably damaging |
Het |
|
Other mutations in 4930505A04Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01545:4930505A04Rik
|
APN |
11 |
30,376,228 (GRCm39) |
missense |
probably benign |
0.13 |
R0400:4930505A04Rik
|
UTSW |
11 |
30,376,360 (GRCm39) |
missense |
probably benign |
0.09 |
R1029:4930505A04Rik
|
UTSW |
11 |
30,396,389 (GRCm39) |
splice site |
probably benign |
|
R1029:4930505A04Rik
|
UTSW |
11 |
30,376,177 (GRCm39) |
missense |
probably damaging |
0.96 |
R1585:4930505A04Rik
|
UTSW |
11 |
30,377,175 (GRCm39) |
splice site |
probably benign |
|
R4708:4930505A04Rik
|
UTSW |
11 |
30,404,717 (GRCm39) |
missense |
probably damaging |
0.98 |
R4993:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R4994:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R4995:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R4996:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5187:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5189:4930505A04Rik
|
UTSW |
11 |
30,376,169 (GRCm39) |
missense |
probably damaging |
0.97 |
R5330:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5333:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5448:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5449:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5450:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5475:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5477:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5665:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5823:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5832:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5833:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5835:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R5873:4930505A04Rik
|
UTSW |
11 |
30,376,220 (GRCm39) |
nonsense |
probably null |
|
R6032:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R6032:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R6037:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R6037:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R6058:4930505A04Rik
|
UTSW |
11 |
30,376,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R6224:4930505A04Rik
|
UTSW |
11 |
30,404,815 (GRCm39) |
missense |
probably benign |
0.44 |
R8394:4930505A04Rik
|
UTSW |
11 |
30,404,880 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8536:4930505A04Rik
|
UTSW |
11 |
30,376,217 (GRCm39) |
missense |
probably benign |
0.19 |
R9149:4930505A04Rik
|
UTSW |
11 |
30,396,304 (GRCm39) |
missense |
probably benign |
0.39 |
R9765:4930505A04Rik
|
UTSW |
11 |
30,404,829 (GRCm39) |
missense |
probably benign |
0.01 |
RF046:4930505A04Rik
|
UTSW |
11 |
30,376,249 (GRCm39) |
frame shift |
probably null |
|
|