Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
C |
17: 24,595,717 (GRCm39) |
S357P |
possibly damaging |
Het |
Arhgap28 |
T |
C |
17: 68,203,106 (GRCm39) |
R166G |
probably damaging |
Het |
Bcan |
T |
A |
3: 87,901,550 (GRCm39) |
E384V |
probably damaging |
Het |
Bcl9l |
A |
G |
9: 44,420,005 (GRCm39) |
N1137S |
probably benign |
Het |
Caprin1 |
A |
G |
2: 103,609,768 (GRCm39) |
L170S |
probably benign |
Het |
Card6 |
C |
T |
15: 5,129,354 (GRCm39) |
E681K |
probably benign |
Het |
Catsperb |
G |
A |
12: 101,447,243 (GRCm39) |
V248I |
probably benign |
Het |
Ccnj |
T |
A |
19: 40,825,477 (GRCm39) |
H62Q |
probably damaging |
Het |
Cd180 |
A |
C |
13: 102,842,936 (GRCm39) |
I661L |
probably benign |
Het |
Cdk11b |
A |
G |
4: 155,732,008 (GRCm39) |
R473G |
unknown |
Het |
Cep126 |
T |
C |
9: 8,099,799 (GRCm39) |
T912A |
possibly damaging |
Het |
Chek2 |
T |
A |
5: 111,021,380 (GRCm39) |
V530E |
probably benign |
Het |
Chga |
G |
T |
12: 102,529,100 (GRCm39) |
S359I |
probably damaging |
Het |
Cnrip1 |
T |
C |
11: 17,004,657 (GRCm39) |
V69A |
probably damaging |
Het |
Cyp2a5 |
A |
T |
7: 26,542,372 (GRCm39) |
Q458L |
probably damaging |
Het |
Cyp2j11 |
T |
A |
4: 96,195,524 (GRCm39) |
T391S |
possibly damaging |
Het |
Dhx16 |
T |
C |
17: 36,199,036 (GRCm39) |
L794P |
probably damaging |
Het |
Dscaml1 |
A |
G |
9: 45,585,802 (GRCm39) |
T580A |
probably benign |
Het |
Elmo1 |
A |
T |
13: 20,464,982 (GRCm39) |
I184L |
probably benign |
Het |
Gabra1 |
C |
T |
11: 42,073,121 (GRCm39) |
G51S |
unknown |
Het |
Gabrr3 |
C |
A |
16: 59,268,439 (GRCm39) |
L351I |
possibly damaging |
Het |
Gbp7 |
A |
T |
3: 142,243,786 (GRCm39) |
N111I |
probably damaging |
Het |
Gjd2 |
C |
T |
2: 113,841,583 (GRCm39) |
R298H |
probably damaging |
Het |
Gm5930 |
T |
C |
14: 44,573,914 (GRCm39) |
Y141C |
probably damaging |
Het |
Grin3a |
G |
T |
4: 49,771,238 (GRCm39) |
N511K |
probably benign |
Het |
Hdac7 |
T |
C |
15: 97,707,903 (GRCm39) |
D122G |
probably benign |
Het |
Ifi204 |
G |
A |
1: 173,587,703 (GRCm39) |
T152I |
possibly damaging |
Het |
Lrrc9 |
C |
T |
12: 72,510,305 (GRCm39) |
|
probably null |
Het |
Med21 |
T |
A |
6: 146,544,082 (GRCm39) |
|
probably benign |
Het |
Mmp19 |
A |
T |
10: 128,634,952 (GRCm39) |
T523S |
probably benign |
Het |
Nav3 |
G |
A |
10: 109,605,073 (GRCm39) |
T1000I |
probably benign |
Het |
Nherf2 |
T |
A |
17: 24,869,182 (GRCm39) |
|
probably benign |
Het |
Nin |
T |
C |
12: 70,090,838 (GRCm39) |
D859G |
|
Het |
Nip7 |
T |
G |
8: 107,783,916 (GRCm39) |
L52R |
possibly damaging |
Het |
Or10d1c |
A |
G |
9: 38,893,816 (GRCm39) |
Y175H |
probably damaging |
Het |
Or5al5 |
A |
T |
2: 85,961,726 (GRCm39) |
F94I |
probably damaging |
Het |
Otop1 |
T |
A |
5: 38,457,547 (GRCm39) |
Y435* |
probably null |
Het |
Pak4 |
A |
G |
7: 28,264,381 (GRCm39) |
S174P |
probably benign |
Het |
Pcsk7 |
G |
A |
9: 45,837,287 (GRCm39) |
R537Q |
probably benign |
Het |
Podxl |
G |
A |
6: 31,505,941 (GRCm39) |
S34F |
unknown |
Het |
Prr36 |
G |
A |
8: 4,266,212 (GRCm39) |
R113C |
probably damaging |
Het |
Ptk7 |
T |
C |
17: 46,890,525 (GRCm39) |
I436V |
probably benign |
Het |
Slc13a5 |
C |
T |
11: 72,157,310 (GRCm39) |
V28I |
probably benign |
Het |
Slco6d1 |
A |
T |
1: 98,349,097 (GRCm39) |
D56V |
probably benign |
Het |
Spg11 |
G |
A |
2: 121,885,858 (GRCm39) |
R2317W |
probably damaging |
Het |
Stom |
T |
A |
2: 35,213,760 (GRCm39) |
|
probably null |
Het |
Svs5 |
T |
C |
2: 164,174,728 (GRCm39) |
L8P |
possibly damaging |
Het |
Tmem141 |
C |
A |
2: 25,511,626 (GRCm39) |
V39F |
probably damaging |
Het |
Tmprss6 |
A |
G |
15: 78,344,019 (GRCm39) |
L181P |
probably damaging |
Het |
Tnni3 |
A |
G |
7: 4,524,379 (GRCm39) |
S40P |
probably benign |
Het |
Tubgcp4 |
A |
G |
2: 121,024,465 (GRCm39) |
I548V |
probably benign |
Het |
Twf2 |
A |
G |
9: 106,081,138 (GRCm39) |
|
probably benign |
Het |
Wnt5b |
C |
A |
6: 119,425,092 (GRCm39) |
|
probably null |
Het |
Wrap73 |
A |
G |
4: 154,237,043 (GRCm39) |
D210G |
probably benign |
Het |
Yipf4 |
T |
G |
17: 74,796,771 (GRCm39) |
S21A |
probably benign |
Het |
Zscan20 |
A |
G |
4: 128,481,943 (GRCm39) |
M573T |
probably benign |
Het |
|
Other mutations in Or6b13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01991:Or6b13
|
APN |
7 |
139,782,345 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01999:Or6b13
|
APN |
7 |
139,782,345 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02005:Or6b13
|
APN |
7 |
139,782,345 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02030:Or6b13
|
APN |
7 |
139,782,545 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02474:Or6b13
|
APN |
7 |
139,782,500 (GRCm39) |
missense |
probably damaging |
1.00 |
H8441:Or6b13
|
UTSW |
7 |
139,781,871 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0426:Or6b13
|
UTSW |
7 |
139,782,029 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0704:Or6b13
|
UTSW |
7 |
139,782,548 (GRCm39) |
missense |
probably benign |
0.00 |
R0891:Or6b13
|
UTSW |
7 |
139,782,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R1624:Or6b13
|
UTSW |
7 |
139,781,864 (GRCm39) |
missense |
probably damaging |
0.96 |
R1865:Or6b13
|
UTSW |
7 |
139,782,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Or6b13
|
UTSW |
7 |
139,782,144 (GRCm39) |
missense |
probably benign |
0.30 |
R2105:Or6b13
|
UTSW |
7 |
139,782,656 (GRCm39) |
missense |
probably benign |
0.02 |
R3009:Or6b13
|
UTSW |
7 |
139,782,669 (GRCm39) |
missense |
probably benign |
|
R3546:Or6b13
|
UTSW |
7 |
139,782,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R4849:Or6b13
|
UTSW |
7 |
139,782,340 (GRCm39) |
nonsense |
probably null |
|
R5009:Or6b13
|
UTSW |
7 |
139,781,751 (GRCm39) |
missense |
probably benign |
|
R5105:Or6b13
|
UTSW |
7 |
139,782,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R5413:Or6b13
|
UTSW |
7 |
139,782,635 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5422:Or6b13
|
UTSW |
7 |
139,782,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R7314:Or6b13
|
UTSW |
7 |
139,782,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R7921:Or6b13
|
UTSW |
7 |
139,782,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8438:Or6b13
|
UTSW |
7 |
139,782,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R9261:Or6b13
|
UTSW |
7 |
139,782,563 (GRCm39) |
missense |
probably benign |
0.29 |
V1662:Or6b13
|
UTSW |
7 |
139,781,871 (GRCm39) |
missense |
possibly damaging |
0.81 |
|