Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300002M23Rik |
T |
C |
17: 35,878,845 (GRCm39) |
V61A |
probably benign |
Het |
Actr3b |
C |
T |
5: 26,030,137 (GRCm39) |
S67F |
probably damaging |
Het |
Ap3m1 |
T |
C |
14: 21,088,096 (GRCm39) |
M107V |
probably benign |
Het |
Ccdc27 |
C |
T |
4: 154,122,155 (GRCm39) |
G241D |
unknown |
Het |
Cit |
T |
G |
5: 116,046,734 (GRCm39) |
D382E |
probably damaging |
Het |
Clec3b |
G |
T |
9: 122,986,004 (GRCm39) |
G134V |
probably damaging |
Het |
Cntnap2 |
T |
A |
6: 47,026,307 (GRCm39) |
H44Q |
probably benign |
Het |
Dst |
T |
C |
1: 34,253,631 (GRCm39) |
S4300P |
probably damaging |
Het |
Ebna1bp2 |
C |
T |
4: 118,480,558 (GRCm39) |
R134* |
probably null |
Het |
Efcab14 |
T |
C |
4: 115,596,024 (GRCm39) |
S57P |
probably damaging |
Het |
Exosc2 |
T |
C |
2: 31,560,875 (GRCm39) |
|
probably null |
Het |
Hfm1 |
T |
C |
5: 107,043,145 (GRCm39) |
T630A |
probably damaging |
Het |
Hkdc1 |
A |
T |
10: 62,244,477 (GRCm39) |
I203N |
possibly damaging |
Het |
Hltf |
T |
A |
3: 20,137,996 (GRCm39) |
|
probably null |
Het |
Mslnl |
A |
G |
17: 25,965,047 (GRCm39) |
D471G |
probably damaging |
Het |
Msmo1 |
A |
G |
8: 65,172,061 (GRCm39) |
Y281H |
probably benign |
Het |
Nid1 |
A |
G |
13: 13,656,620 (GRCm39) |
T584A |
probably benign |
Het |
Olfr908 |
A |
G |
9: 38,427,561 (GRCm39) |
T78A |
probably damaging |
Het |
Or52a24 |
C |
T |
7: 103,381,691 (GRCm39) |
A186V |
probably damaging |
Het |
Otoa |
G |
A |
7: 120,721,173 (GRCm39) |
G396D |
probably damaging |
Het |
Prss45 |
G |
T |
9: 110,669,487 (GRCm39) |
A197S |
probably damaging |
Het |
Prxl2a |
T |
A |
14: 40,716,578 (GRCm39) |
H198L |
probably damaging |
Het |
Rpap2 |
T |
A |
5: 107,768,104 (GRCm39) |
I314N |
probably benign |
Het |
Sash1 |
A |
G |
10: 8,620,286 (GRCm39) |
M458T |
probably damaging |
Het |
Slc44a5 |
A |
G |
3: 153,945,714 (GRCm39) |
|
probably null |
Het |
Sorbs2 |
T |
C |
8: 46,225,651 (GRCm39) |
S254P |
probably damaging |
Het |
Sycp2 |
T |
C |
2: 178,016,144 (GRCm39) |
|
probably null |
Het |
Tedc1 |
A |
G |
12: 113,125,334 (GRCm39) |
D252G |
probably damaging |
Het |
Uty |
T |
C |
Y: 1,186,790 (GRCm39) |
H145R |
probably damaging |
Homo |
Vmn1r9 |
A |
G |
6: 57,048,291 (GRCm39) |
Y122C |
probably benign |
Het |
Wdfy4 |
T |
A |
14: 32,817,908 (GRCm39) |
N1491Y |
possibly damaging |
Het |
Wdr37 |
T |
C |
13: 8,899,684 (GRCm39) |
T140A |
probably benign |
Het |
|
Other mutations in Igkv3-2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01118:Igkv3-2
|
APN |
6 |
70,675,978 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02352:Igkv3-2
|
APN |
6 |
70,675,474 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02359:Igkv3-2
|
APN |
6 |
70,675,474 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02627:Igkv3-2
|
APN |
6 |
70,675,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3714:Igkv3-2
|
UTSW |
6 |
70,675,480 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4255:Igkv3-2
|
UTSW |
6 |
70,676,045 (GRCm39) |
missense |
probably benign |
0.00 |
R4449:Igkv3-2
|
UTSW |
6 |
70,675,825 (GRCm39) |
missense |
probably benign |
0.11 |
R4663:Igkv3-2
|
UTSW |
6 |
70,675,863 (GRCm39) |
missense |
probably benign |
0.02 |
R5361:Igkv3-2
|
UTSW |
6 |
70,676,011 (GRCm39) |
missense |
probably benign |
0.01 |
R6347:Igkv3-2
|
UTSW |
6 |
70,676,017 (GRCm39) |
missense |
probably benign |
0.01 |
R6466:Igkv3-2
|
UTSW |
6 |
70,676,023 (GRCm39) |
missense |
probably benign |
0.15 |
R6874:Igkv3-2
|
UTSW |
6 |
70,675,822 (GRCm39) |
nonsense |
probably null |
|
R8050:Igkv3-2
|
UTSW |
6 |
70,675,988 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Igkv3-2
|
UTSW |
6 |
70,676,030 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Igkv3-2
|
UTSW |
6 |
70,675,999 (GRCm39) |
nonsense |
probably null |
|
|