Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
T |
C |
16: 14,261,250 (GRCm39) |
V676A |
probably damaging |
Het |
Acvr1b |
T |
C |
15: 101,091,819 (GRCm39) |
L33P |
possibly damaging |
Het |
Adamts12 |
T |
G |
15: 11,256,980 (GRCm39) |
|
probably benign |
Het |
Ank1 |
T |
A |
8: 23,601,819 (GRCm39) |
|
probably benign |
Het |
Arhgef10 |
T |
A |
8: 14,990,225 (GRCm39) |
D233E |
probably damaging |
Het |
Cd209e |
T |
C |
8: 3,899,084 (GRCm39) |
*209W |
probably null |
Het |
Cebpz |
A |
G |
17: 79,230,742 (GRCm39) |
V825A |
probably benign |
Het |
Cep170 |
A |
G |
1: 176,563,290 (GRCm39) |
F1575L |
probably damaging |
Het |
Exoc2 |
A |
T |
13: 31,066,256 (GRCm39) |
Y473* |
probably null |
Het |
F3 |
A |
G |
3: 121,523,023 (GRCm39) |
T78A |
probably damaging |
Het |
Fanca |
G |
A |
8: 124,031,020 (GRCm39) |
|
probably benign |
Het |
Gga2 |
G |
A |
7: 121,598,138 (GRCm39) |
R319* |
probably null |
Het |
Gid8 |
A |
G |
2: 180,355,025 (GRCm39) |
I10M |
probably benign |
Het |
Glrb |
A |
G |
3: 80,769,311 (GRCm39) |
W139R |
probably damaging |
Het |
Hectd3 |
G |
T |
4: 116,854,367 (GRCm39) |
V310L |
probably null |
Het |
Insyn1 |
G |
T |
9: 58,406,263 (GRCm39) |
D58Y |
probably damaging |
Het |
Kif17 |
C |
A |
4: 138,005,305 (GRCm39) |
S290* |
probably null |
Het |
Kif26b |
A |
G |
1: 178,744,028 (GRCm39) |
N1375D |
probably damaging |
Het |
Lgr4 |
C |
G |
2: 109,821,480 (GRCm39) |
P121A |
probably damaging |
Het |
Ly75 |
A |
G |
2: 60,124,102 (GRCm39) |
|
probably null |
Het |
Mfsd13a |
C |
T |
19: 46,354,943 (GRCm39) |
T40I |
probably benign |
Het |
Nek3 |
T |
C |
8: 22,650,377 (GRCm39) |
|
probably benign |
Het |
Nin |
A |
T |
12: 70,090,703 (GRCm39) |
L904Q |
probably damaging |
Het |
Nlrp14 |
A |
G |
7: 106,782,018 (GRCm39) |
D405G |
probably benign |
Het |
Nuak1 |
C |
T |
10: 84,228,192 (GRCm39) |
|
probably benign |
Het |
Or5h23 |
T |
A |
16: 58,906,706 (GRCm39) |
I47F |
probably benign |
Het |
Plcg2 |
T |
A |
8: 118,341,977 (GRCm39) |
W1113R |
probably damaging |
Het |
Pms2 |
G |
A |
5: 143,862,731 (GRCm39) |
V613M |
probably damaging |
Het |
Prl3b1 |
G |
A |
13: 27,427,848 (GRCm39) |
A53T |
probably benign |
Het |
Pxk |
T |
G |
14: 8,150,915 (GRCm38) |
|
probably null |
Het |
Rasl10b |
G |
A |
11: 83,308,665 (GRCm39) |
|
probably null |
Het |
Rbm28 |
A |
T |
6: 29,137,639 (GRCm39) |
I438N |
probably damaging |
Het |
Rictor |
T |
C |
15: 6,820,119 (GRCm39) |
|
probably benign |
Het |
Slc41a1 |
A |
G |
1: 131,771,746 (GRCm39) |
T387A |
probably benign |
Het |
Slc44a2 |
T |
C |
9: 21,254,322 (GRCm39) |
V228A |
probably benign |
Het |
Slpi |
A |
G |
2: 164,196,787 (GRCm39) |
|
probably benign |
Het |
Tkfc |
A |
G |
19: 10,570,838 (GRCm39) |
S481P |
probably benign |
Het |
Tll2 |
G |
A |
19: 41,108,667 (GRCm39) |
R328C |
probably damaging |
Het |
Tns3 |
T |
C |
11: 8,398,704 (GRCm39) |
H1216R |
probably benign |
Het |
Ugt2b38 |
A |
T |
5: 87,571,973 (GRCm39) |
S20T |
probably benign |
Het |
Usp48 |
T |
A |
4: 137,366,606 (GRCm39) |
D921E |
possibly damaging |
Het |
Usp48 |
T |
A |
4: 137,371,774 (GRCm39) |
S967T |
probably damaging |
Het |
Vmn2r115 |
ATCTTCT |
ATCT |
17: 23,578,962 (GRCm39) |
|
probably benign |
Het |
Zdhhc23 |
A |
G |
16: 43,794,513 (GRCm39) |
S54P |
probably benign |
Het |
|
Other mutations in H2-M1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01147:H2-M1
|
APN |
17 |
36,982,199 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01671:H2-M1
|
APN |
17 |
36,981,330 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01870:H2-M1
|
APN |
17 |
36,980,955 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02032:H2-M1
|
APN |
17 |
36,982,768 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02383:H2-M1
|
APN |
17 |
36,981,141 (GRCm39) |
missense |
unknown |
|
IGL02417:H2-M1
|
APN |
17 |
36,983,026 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02700:H2-M1
|
APN |
17 |
36,982,161 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0193:H2-M1
|
UTSW |
17 |
36,982,224 (GRCm39) |
missense |
probably benign |
0.34 |
R0715:H2-M1
|
UTSW |
17 |
36,981,120 (GRCm39) |
splice site |
probably benign |
|
R1271:H2-M1
|
UTSW |
17 |
36,982,137 (GRCm39) |
missense |
probably benign |
0.33 |
R2120:H2-M1
|
UTSW |
17 |
36,980,929 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4854:H2-M1
|
UTSW |
17 |
36,980,950 (GRCm39) |
missense |
probably benign |
0.03 |
R4899:H2-M1
|
UTSW |
17 |
36,982,112 (GRCm39) |
missense |
probably benign |
0.09 |
R4963:H2-M1
|
UTSW |
17 |
36,982,630 (GRCm39) |
missense |
probably benign |
|
R5243:H2-M1
|
UTSW |
17 |
36,982,193 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6199:H2-M1
|
UTSW |
17 |
36,982,059 (GRCm39) |
missense |
probably benign |
0.00 |
R6276:H2-M1
|
UTSW |
17 |
36,982,602 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6395:H2-M1
|
UTSW |
17 |
36,982,701 (GRCm39) |
missense |
probably benign |
0.39 |
R6818:H2-M1
|
UTSW |
17 |
36,981,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R7913:H2-M1
|
UTSW |
17 |
36,981,129 (GRCm39) |
splice site |
probably null |
|
R9419:H2-M1
|
UTSW |
17 |
36,981,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R9640:H2-M1
|
UTSW |
17 |
36,983,031 (GRCm39) |
missense |
probably benign |
0.02 |
R9648:H2-M1
|
UTSW |
17 |
36,982,248 (GRCm39) |
missense |
probably benign |
0.01 |
R9746:H2-M1
|
UTSW |
17 |
36,980,997 (GRCm39) |
missense |
possibly damaging |
0.88 |
|