Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,242,348 (GRCm39) |
I1404L |
possibly damaging |
Het |
Adra1b |
A |
G |
11: 43,726,057 (GRCm39) |
S287P |
probably damaging |
Het |
Atxn2 |
G |
T |
5: 121,952,406 (GRCm39) |
A1280S |
possibly damaging |
Het |
Bbip1 |
T |
C |
19: 53,920,639 (GRCm39) |
|
probably null |
Het |
Bbs2 |
A |
G |
8: 94,808,982 (GRCm39) |
|
probably null |
Het |
Bcl11b |
A |
T |
12: 107,932,031 (GRCm39) |
C180* |
probably null |
Het |
Bltp3a |
T |
C |
17: 28,105,580 (GRCm39) |
F702S |
probably benign |
Het |
Bod1l |
A |
G |
5: 41,977,816 (GRCm39) |
V1166A |
probably benign |
Het |
Bora |
C |
T |
14: 99,284,788 (GRCm39) |
P13S |
probably damaging |
Het |
C2cd4c |
T |
C |
10: 79,449,075 (GRCm39) |
E24G |
probably benign |
Het |
Ccne1 |
A |
T |
7: 37,799,996 (GRCm39) |
I196N |
probably damaging |
Het |
Chsy3 |
C |
T |
18: 59,542,647 (GRCm39) |
S595L |
probably benign |
Het |
Chsy3 |
T |
A |
18: 59,542,839 (GRCm39) |
I659N |
possibly damaging |
Het |
Cntrob |
T |
A |
11: 69,202,188 (GRCm39) |
|
probably null |
Het |
Col5a2 |
G |
A |
1: 45,428,618 (GRCm39) |
P983S |
possibly damaging |
Het |
Crat |
T |
A |
2: 30,297,148 (GRCm39) |
|
probably null |
Het |
Ctnnbl1 |
C |
T |
2: 157,678,473 (GRCm39) |
H359Y |
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,085,732 (GRCm39) |
V83A |
possibly damaging |
Het |
Dixdc1 |
A |
G |
9: 50,593,902 (GRCm39) |
S488P |
possibly damaging |
Het |
Dmrta1 |
T |
C |
4: 89,576,801 (GRCm39) |
C86R |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Fam171a1 |
G |
A |
2: 3,179,505 (GRCm39) |
|
probably null |
Het |
Fam222b |
T |
C |
11: 78,045,569 (GRCm39) |
C249R |
probably damaging |
Het |
Fbxw18 |
T |
A |
9: 109,531,719 (GRCm39) |
|
probably benign |
Het |
Fes |
T |
C |
7: 80,036,952 (GRCm39) |
Y44C |
probably damaging |
Het |
Gimap6 |
A |
G |
6: 48,684,933 (GRCm39) |
V51A |
probably benign |
Het |
Gpr75 |
C |
T |
11: 30,841,463 (GRCm39) |
L123F |
possibly damaging |
Het |
Gpr75 |
C |
A |
11: 30,841,462 (GRCm39) |
H122Q |
probably damaging |
Het |
Greb1 |
A |
G |
12: 16,774,762 (GRCm39) |
S212P |
probably damaging |
Het |
Grin3a |
T |
C |
4: 49,665,512 (GRCm39) |
H1041R |
probably benign |
Het |
Ifna5 |
A |
G |
4: 88,753,861 (GRCm39) |
N34D |
probably damaging |
Het |
Ift140 |
A |
T |
17: 25,255,968 (GRCm39) |
H221L |
probably damaging |
Het |
Igsf3 |
T |
C |
3: 101,342,983 (GRCm39) |
V540A |
probably benign |
Het |
Il10ra |
A |
G |
9: 45,180,357 (GRCm39) |
L5S |
probably damaging |
Het |
Klra2 |
A |
T |
6: 131,197,152 (GRCm39) |
D282E |
probably benign |
Het |
Lyst |
T |
A |
13: 13,900,539 (GRCm39) |
H3138Q |
probably damaging |
Het |
Malrd1 |
A |
G |
2: 16,046,940 (GRCm39) |
T1689A |
probably benign |
Het |
Mon2 |
A |
T |
10: 122,831,694 (GRCm39) |
L1671M |
probably damaging |
Het |
Mpped1 |
T |
C |
15: 83,720,528 (GRCm39) |
F71S |
probably damaging |
Het |
Mtpap |
C |
A |
18: 4,396,332 (GRCm39) |
H541Q |
probably benign |
Het |
Muc5ac |
T |
A |
7: 141,363,193 (GRCm39) |
|
probably benign |
Het |
Mybbp1a |
T |
C |
11: 72,336,040 (GRCm39) |
I451T |
probably damaging |
Het |
Myh7 |
T |
A |
14: 55,210,224 (GRCm39) |
E1827V |
probably damaging |
Het |
Or2h15 |
A |
T |
17: 38,441,468 (GRCm39) |
I205N |
probably damaging |
Het |
Or5p75-ps1 |
T |
A |
7: 108,107,855 (GRCm39) |
Y197* |
probably null |
Het |
Or8b8 |
C |
A |
9: 37,808,811 (GRCm39) |
T37N |
probably damaging |
Het |
Os9 |
C |
T |
10: 126,956,920 (GRCm39) |
R23H |
possibly damaging |
Het |
Otud6b |
A |
G |
4: 14,815,607 (GRCm39) |
L261P |
probably damaging |
Het |
Pcdhga2 |
A |
G |
18: 37,802,476 (GRCm39) |
N107D |
probably benign |
Het |
Pclo |
C |
T |
5: 14,729,308 (GRCm39) |
|
probably benign |
Het |
Peg10 |
T |
TCCG |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Phtf1 |
T |
A |
3: 103,906,024 (GRCm39) |
S524T |
probably damaging |
Het |
Pkdrej |
A |
C |
15: 85,703,197 (GRCm39) |
L913R |
probably damaging |
Het |
Pld1 |
C |
A |
3: 28,085,447 (GRCm39) |
A201D |
probably damaging |
Het |
Rorb |
T |
A |
19: 18,955,052 (GRCm39) |
Q103L |
probably benign |
Het |
Sec24d |
C |
T |
3: 123,093,255 (GRCm39) |
T284M |
probably benign |
Het |
Serpinb3b |
T |
C |
1: 107,085,484 (GRCm39) |
I86V |
probably benign |
Het |
Serpinb6a |
A |
T |
13: 34,102,857 (GRCm39) |
M201K |
probably damaging |
Het |
Snx8 |
A |
G |
5: 140,337,989 (GRCm39) |
S219P |
probably benign |
Het |
Sp8 |
C |
T |
12: 118,812,160 (GRCm39) |
T5I |
probably damaging |
Het |
Tanc1 |
A |
G |
2: 59,630,287 (GRCm39) |
N749D |
probably damaging |
Het |
Tarm1 |
G |
C |
7: 3,537,612 (GRCm39) |
P284A |
probably damaging |
Het |
Tbx15 |
A |
T |
3: 99,161,390 (GRCm39) |
E65V |
probably benign |
Het |
Ticam1 |
T |
A |
17: 56,579,020 (GRCm39) |
H25L |
probably benign |
Het |
Tmprss11g |
T |
A |
5: 86,640,674 (GRCm39) |
L170F |
probably damaging |
Het |
Tnfsf9 |
A |
G |
17: 57,414,504 (GRCm39) |
*310W |
probably null |
Het |
Tsks |
C |
T |
7: 44,593,418 (GRCm39) |
T128I |
possibly damaging |
Het |
Vmn1r175 |
A |
T |
7: 23,508,494 (GRCm39) |
N44K |
possibly damaging |
Het |
Vmn1r45 |
A |
G |
6: 89,910,847 (GRCm39) |
I41T |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 45,004,532 (GRCm39) |
N1102S |
probably benign |
Het |
Zswim4 |
C |
T |
8: 84,953,296 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Or1j14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Or1j14
|
APN |
2 |
36,418,005 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01372:Or1j14
|
APN |
2 |
36,417,463 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01747:Or1j14
|
APN |
2 |
36,417,844 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01836:Or1j14
|
APN |
2 |
36,417,837 (GRCm39) |
nonsense |
probably null |
|
IGL02409:Or1j14
|
APN |
2 |
36,418,165 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02578:Or1j14
|
APN |
2 |
36,418,156 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03344:Or1j14
|
APN |
2 |
36,418,140 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03396:Or1j14
|
APN |
2 |
36,417,692 (GRCm39) |
missense |
probably benign |
0.00 |
R0086:Or1j14
|
UTSW |
2 |
36,417,462 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0427:Or1j14
|
UTSW |
2 |
36,417,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Or1j14
|
UTSW |
2 |
36,418,020 (GRCm39) |
missense |
probably benign |
0.13 |
R0973:Or1j14
|
UTSW |
2 |
36,418,020 (GRCm39) |
missense |
probably benign |
0.13 |
R0974:Or1j14
|
UTSW |
2 |
36,418,020 (GRCm39) |
missense |
probably benign |
0.13 |
R2183:Or1j14
|
UTSW |
2 |
36,417,723 (GRCm39) |
nonsense |
probably null |
|
R2437:Or1j14
|
UTSW |
2 |
36,418,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R4060:Or1j14
|
UTSW |
2 |
36,417,426 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R5070:Or1j14
|
UTSW |
2 |
36,417,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R6244:Or1j14
|
UTSW |
2 |
36,418,353 (GRCm39) |
missense |
probably benign |
0.00 |
R8350:Or1j14
|
UTSW |
2 |
36,418,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R8690:Or1j14
|
UTSW |
2 |
36,418,207 (GRCm39) |
missense |
probably benign |
0.22 |
R9105:Or1j14
|
UTSW |
2 |
36,418,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Or1j14
|
UTSW |
2 |
36,417,838 (GRCm39) |
missense |
probably benign |
0.00 |
R9249:Or1j14
|
UTSW |
2 |
36,417,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R9274:Or1j14
|
UTSW |
2 |
36,417,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R9465:Or1j14
|
UTSW |
2 |
36,417,898 (GRCm39) |
missense |
probably benign |
0.02 |
R9644:Or1j14
|
UTSW |
2 |
36,417,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R9700:Or1j14
|
UTSW |
2 |
36,418,313 (GRCm39) |
missense |
probably benign |
0.09 |
|