Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
T |
G |
4: 53,092,806 (GRCm39) |
E326A |
probably damaging |
Het |
Aldh1a1 |
T |
A |
19: 20,614,100 (GRCm39) |
N423K |
probably benign |
Het |
Aldh4a1 |
T |
A |
4: 139,371,427 (GRCm39) |
I447N |
probably damaging |
Het |
Atg9b |
T |
C |
5: 24,596,406 (GRCm39) |
D170G |
possibly damaging |
Het |
Bnc2 |
C |
T |
4: 84,332,492 (GRCm39) |
V75M |
probably damaging |
Het |
Bnip3l |
G |
A |
14: 67,246,214 (GRCm39) |
P7L |
possibly damaging |
Het |
Ccdc162 |
C |
A |
10: 41,437,159 (GRCm39) |
C1750F |
probably benign |
Het |
Cdh10 |
T |
A |
15: 18,964,301 (GRCm39) |
N154K |
probably damaging |
Het |
Cdh22 |
T |
C |
2: 164,988,687 (GRCm39) |
I223V |
probably damaging |
Het |
Ces1b |
T |
A |
8: 93,806,534 (GRCm39) |
H4L |
probably benign |
Het |
Cfap46 |
A |
T |
7: 139,209,763 (GRCm39) |
F1806I |
unknown |
Het |
Cwh43 |
T |
A |
5: 73,565,486 (GRCm39) |
V17D |
possibly damaging |
Het |
Ddx3y |
C |
T |
Y: 1,263,599 (GRCm39) |
G623D |
probably benign |
Het |
Dtna |
A |
T |
18: 23,744,122 (GRCm39) |
I389L |
probably benign |
Het |
F830016B08Rik |
A |
G |
18: 60,432,956 (GRCm39) |
D13G |
probably benign |
Het |
Fam161b |
T |
C |
12: 84,403,187 (GRCm39) |
I148V |
probably benign |
Het |
Fhip1a |
T |
A |
3: 85,568,391 (GRCm39) |
N1043Y |
probably damaging |
Het |
Fli1 |
T |
C |
9: 32,388,020 (GRCm39) |
Y23C |
probably damaging |
Het |
Gimap6 |
A |
G |
6: 48,679,424 (GRCm39) |
V204A |
probably benign |
Het |
Ighv4-1 |
T |
G |
12: 113,911,904 (GRCm39) |
R116S |
probably damaging |
Het |
Isx |
T |
C |
8: 75,619,566 (GRCm39) |
L239P |
probably damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Krt81 |
T |
C |
15: 101,358,856 (GRCm39) |
T299A |
probably benign |
Het |
Lrrc30 |
A |
G |
17: 67,939,226 (GRCm39) |
L118P |
probably damaging |
Het |
Mapk8ip3 |
T |
C |
17: 25,118,023 (GRCm39) |
T1290A |
probably benign |
Het |
Mef2b |
ACCCTCACCC |
ACC |
8: 70,619,506 (GRCm39) |
|
probably null |
Het |
Meltf |
G |
A |
16: 31,706,409 (GRCm39) |
E298K |
possibly damaging |
Het |
Muc16 |
T |
A |
9: 18,550,626 (GRCm39) |
E5222D |
probably benign |
Het |
Nin |
T |
C |
12: 70,067,618 (GRCm39) |
N2003S |
|
Het |
Or1e23 |
A |
G |
11: 73,407,875 (GRCm39) |
I50T |
probably benign |
Het |
Or2b4 |
G |
A |
17: 38,116,509 (GRCm39) |
V158M |
probably damaging |
Het |
Palld |
A |
G |
8: 62,002,788 (GRCm39) |
V826A |
unknown |
Het |
Paxbp1 |
C |
A |
16: 90,831,881 (GRCm39) |
V336L |
probably benign |
Het |
Paxbp1 |
T |
A |
16: 90,831,882 (GRCm39) |
E335D |
probably benign |
Het |
Por |
C |
A |
5: 135,754,615 (GRCm39) |
Q12K |
unknown |
Het |
Pot1a |
G |
A |
6: 25,750,106 (GRCm39) |
Q519* |
probably null |
Het |
Psd |
GCC |
GC |
19: 46,301,841 (GRCm39) |
|
probably null |
Het |
Ptger4 |
A |
G |
15: 5,264,693 (GRCm39) |
F321S |
probably damaging |
Het |
Ptk7 |
A |
G |
17: 46,890,519 (GRCm39) |
Y438H |
possibly damaging |
Het |
Rimklb |
A |
T |
6: 122,433,558 (GRCm39) |
N254K |
probably benign |
Het |
Rpn2 |
A |
T |
2: 157,125,566 (GRCm39) |
T26S |
probably benign |
Het |
Rtn4rl2 |
A |
T |
2: 84,710,760 (GRCm39) |
L168H |
probably damaging |
Het |
Scel |
G |
T |
14: 103,779,409 (GRCm39) |
A127S |
possibly damaging |
Het |
Sema4a |
T |
A |
3: 88,357,066 (GRCm39) |
N302Y |
probably damaging |
Het |
Supt3 |
A |
G |
17: 45,234,133 (GRCm39) |
T50A |
possibly damaging |
Het |
Upf3a |
G |
A |
8: 13,848,343 (GRCm39) |
A380T |
probably benign |
Het |
Zbtb14 |
G |
A |
17: 69,695,375 (GRCm39) |
E358K |
probably damaging |
Het |
Zfp677 |
A |
T |
17: 21,618,056 (GRCm39) |
H371L |
probably damaging |
Het |
|
Other mutations in Or51f1d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02172:Or51f1d
|
APN |
7 |
102,700,582 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02200:Or51f1d
|
APN |
7 |
102,701,000 (GRCm39) |
missense |
probably benign |
|
IGL02412:Or51f1d
|
APN |
7 |
102,701,359 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02452:Or51f1d
|
APN |
7 |
102,701,138 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02859:Or51f1d
|
APN |
7 |
102,701,345 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03078:Or51f1d
|
APN |
7 |
102,701,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Or51f1d
|
UTSW |
7 |
102,700,909 (GRCm39) |
missense |
probably benign |
0.22 |
R1474:Or51f1d
|
UTSW |
7 |
102,701,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R1531:Or51f1d
|
UTSW |
7 |
102,700,795 (GRCm39) |
missense |
probably benign |
0.00 |
R1535:Or51f1d
|
UTSW |
7 |
102,700,576 (GRCm39) |
missense |
probably benign |
0.14 |
R1777:Or51f1d
|
UTSW |
7 |
102,700,583 (GRCm39) |
missense |
probably benign |
0.41 |
R1883:Or51f1d
|
UTSW |
7 |
102,701,189 (GRCm39) |
missense |
probably benign |
0.00 |
R1884:Or51f1d
|
UTSW |
7 |
102,701,189 (GRCm39) |
missense |
probably benign |
0.00 |
R2265:Or51f1d
|
UTSW |
7 |
102,701,344 (GRCm39) |
missense |
probably benign |
0.00 |
R2267:Or51f1d
|
UTSW |
7 |
102,701,344 (GRCm39) |
missense |
probably benign |
0.00 |
R2269:Or51f1d
|
UTSW |
7 |
102,701,344 (GRCm39) |
missense |
probably benign |
0.00 |
R2299:Or51f1d
|
UTSW |
7 |
102,700,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R3802:Or51f1d
|
UTSW |
7 |
102,701,372 (GRCm39) |
missense |
probably benign |
0.05 |
R4239:Or51f1d
|
UTSW |
7 |
102,701,003 (GRCm39) |
missense |
probably benign |
0.17 |
R4426:Or51f1d
|
UTSW |
7 |
102,701,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Or51f1d
|
UTSW |
7 |
102,700,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Or51f1d
|
UTSW |
7 |
102,700,526 (GRCm39) |
missense |
probably benign |
0.00 |
R6270:Or51f1d
|
UTSW |
7 |
102,700,538 (GRCm39) |
missense |
probably benign |
0.27 |
R6837:Or51f1d
|
UTSW |
7 |
102,700,929 (GRCm39) |
nonsense |
probably null |
|
R7257:Or51f1d
|
UTSW |
7 |
102,700,837 (GRCm39) |
missense |
probably benign |
0.39 |
R8506:Or51f1d
|
UTSW |
7 |
102,700,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R8947:Or51f1d
|
UTSW |
7 |
102,701,315 (GRCm39) |
missense |
probably damaging |
0.99 |
|