Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef4 |
T |
C |
1: 34,762,162 (GRCm39) |
S473P |
unknown |
Het |
Azin1 |
A |
T |
15: 38,493,849 (GRCm39) |
I258N |
probably benign |
Het |
Bod1l |
G |
A |
5: 41,989,574 (GRCm39) |
A383V |
probably benign |
Het |
Carmil3 |
GGACGA |
GGA |
14: 55,736,933 (GRCm39) |
|
probably benign |
Het |
Cd200r3 |
T |
A |
16: 44,774,552 (GRCm39) |
D188E |
probably benign |
Het |
Cd4 |
A |
T |
6: 124,847,414 (GRCm39) |
F250Y |
probably benign |
Het |
Clcn4 |
T |
A |
7: 7,290,813 (GRCm39) |
Y662F |
probably benign |
Het |
Cpa2 |
T |
C |
6: 30,552,020 (GRCm39) |
V249A |
probably benign |
Het |
Depdc5 |
CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT |
CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT |
5: 33,067,751 (GRCm39) |
|
probably benign |
Het |
Dhx57 |
A |
G |
17: 80,582,511 (GRCm39) |
Y365H |
probably damaging |
Het |
Dsg1c |
A |
G |
18: 20,408,322 (GRCm39) |
E457G |
probably benign |
Het |
Eef2k |
T |
A |
7: 120,457,822 (GRCm39) |
Y60* |
probably null |
Het |
Efcc1 |
A |
G |
6: 87,730,133 (GRCm39) |
D482G |
probably null |
Het |
Exoc4 |
C |
T |
6: 33,254,179 (GRCm39) |
R112C |
probably damaging |
Het |
Fam178b |
A |
T |
1: 36,639,606 (GRCm39) |
D293E |
probably benign |
Het |
Fbxl21 |
G |
A |
13: 56,674,873 (GRCm39) |
V49I |
probably damaging |
Het |
Fyco1 |
A |
G |
9: 123,667,953 (GRCm39) |
V91A |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,439,531 (GRCm39) |
I5434T |
probably damaging |
Het |
Hormad1 |
T |
C |
3: 95,492,452 (GRCm39) |
V343A |
probably benign |
Het |
Incenp |
T |
C |
19: 9,861,303 (GRCm39) |
N450S |
unknown |
Het |
Iqsec3 |
T |
C |
6: 121,356,977 (GRCm39) |
K1035E |
possibly damaging |
Het |
Ltn1 |
A |
T |
16: 87,223,174 (GRCm39) |
V102D |
probably damaging |
Het |
Mcur1 |
T |
C |
13: 43,698,016 (GRCm39) |
T295A |
probably damaging |
Het |
Pals1 |
A |
T |
12: 78,871,611 (GRCm39) |
D397V |
possibly damaging |
Het |
Pcdha3 |
T |
C |
18: 37,081,013 (GRCm39) |
V585A |
probably damaging |
Het |
Plcd4 |
A |
G |
1: 74,602,627 (GRCm39) |
T594A |
probably damaging |
Het |
Ppp1r3c |
T |
C |
19: 36,711,522 (GRCm39) |
K83E |
probably damaging |
Het |
Sesn3 |
C |
A |
9: 14,233,954 (GRCm39) |
T309K |
probably benign |
Het |
Slc38a3 |
T |
C |
9: 107,533,405 (GRCm39) |
N251S |
probably benign |
Het |
Sptbn4 |
A |
G |
7: 27,067,127 (GRCm39) |
V614A |
probably damaging |
Het |
Srsf4 |
A |
G |
4: 131,601,175 (GRCm39) |
K34R |
probably damaging |
Het |
Tfpi2 |
T |
C |
6: 3,968,044 (GRCm39) |
N32S |
possibly damaging |
Het |
Ttll2 |
A |
T |
17: 7,619,120 (GRCm39) |
I269N |
probably benign |
Het |
Utp3 |
T |
C |
5: 88,703,458 (GRCm39) |
V329A |
probably benign |
Het |
Vmn2r102 |
A |
G |
17: 19,914,975 (GRCm39) |
T847A |
probably benign |
Het |
Vmn2r70 |
A |
T |
7: 85,214,541 (GRCm39) |
W204R |
probably damaging |
Het |
Xrcc3 |
A |
G |
12: 111,770,966 (GRCm39) |
L321P |
probably damaging |
Het |
|
Other mutations in H2-M10.4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02329:H2-M10.4
|
APN |
17 |
36,771,359 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02651:H2-M10.4
|
APN |
17 |
36,771,548 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02821:H2-M10.4
|
APN |
17 |
36,771,323 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03123:H2-M10.4
|
APN |
17 |
36,772,812 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03171:H2-M10.4
|
APN |
17 |
36,772,142 (GRCm39) |
missense |
probably damaging |
0.98 |
R0206:H2-M10.4
|
UTSW |
17 |
36,771,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:H2-M10.4
|
UTSW |
17 |
36,771,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:H2-M10.4
|
UTSW |
17 |
36,772,877 (GRCm39) |
missense |
probably benign |
0.23 |
R4685:H2-M10.4
|
UTSW |
17 |
36,772,688 (GRCm39) |
missense |
probably benign |
0.23 |
R4702:H2-M10.4
|
UTSW |
17 |
36,772,874 (GRCm39) |
missense |
probably benign |
0.25 |
R5390:H2-M10.4
|
UTSW |
17 |
36,771,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R5945:H2-M10.4
|
UTSW |
17 |
36,771,518 (GRCm39) |
missense |
probably benign |
0.01 |
R8135:H2-M10.4
|
UTSW |
17 |
36,772,662 (GRCm39) |
missense |
probably benign |
|
R8956:H2-M10.4
|
UTSW |
17 |
36,772,245 (GRCm39) |
missense |
probably benign |
0.08 |
R9342:H2-M10.4
|
UTSW |
17 |
36,771,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:H2-M10.4
|
UTSW |
17 |
36,771,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|