Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
C |
T |
11: 109,969,481 (GRCm39) |
S365N |
probably damaging |
Het |
Baiap3 |
G |
A |
17: 25,462,814 (GRCm39) |
R1075C |
probably benign |
Het |
Baz2b |
A |
G |
2: 59,792,550 (GRCm39) |
L526P |
probably benign |
Het |
Bbs1 |
A |
T |
19: 4,945,043 (GRCm39) |
L376Q |
probably damaging |
Het |
Bcl9 |
T |
A |
3: 97,112,511 (GRCm39) |
M1315L |
possibly damaging |
Het |
Bcl9 |
T |
C |
3: 97,116,183 (GRCm39) |
Q837R |
probably damaging |
Het |
Cct2 |
A |
G |
10: 116,889,029 (GRCm39) |
V490A |
probably benign |
Het |
Cdh23 |
T |
C |
10: 60,148,378 (GRCm39) |
Y2663C |
possibly damaging |
Het |
Chit1 |
A |
G |
1: 134,078,229 (GRCm39) |
K346E |
possibly damaging |
Het |
Chl1 |
A |
G |
6: 103,683,517 (GRCm39) |
Y781C |
probably damaging |
Het |
Col12a1 |
A |
C |
9: 79,557,314 (GRCm39) |
L1938R |
possibly damaging |
Het |
Cpxm2 |
T |
A |
7: 131,681,813 (GRCm39) |
N239Y |
probably damaging |
Het |
Cyp3a41b |
A |
G |
5: 145,519,330 (GRCm39) |
Y54H |
probably benign |
Het |
Dclk1 |
A |
C |
3: 55,385,296 (GRCm39) |
D369A |
possibly damaging |
Het |
Dnai4 |
A |
G |
4: 102,919,610 (GRCm39) |
V498A |
probably damaging |
Het |
Dpy19l3 |
T |
C |
7: 35,449,190 (GRCm39) |
N71S |
possibly damaging |
Het |
Efcab3 |
T |
A |
11: 104,642,711 (GRCm39) |
N1111K |
probably benign |
Het |
Fer |
T |
A |
17: 64,228,683 (GRCm39) |
V186E |
possibly damaging |
Het |
Gm11042 |
T |
A |
12: 74,361,888 (GRCm39) |
H39L |
unknown |
Het |
Gm14325 |
A |
G |
2: 177,473,798 (GRCm39) |
I428T |
probably benign |
Het |
Gm47995 |
A |
G |
1: 151,074,404 (GRCm39) |
E69G |
possibly damaging |
Het |
Gm6176 |
T |
A |
7: 21,750,596 (GRCm39) |
I112F |
probably damaging |
Het |
Hivep2 |
T |
A |
10: 14,005,710 (GRCm39) |
D769E |
probably benign |
Het |
Hsdl1 |
C |
T |
8: 120,294,607 (GRCm39) |
V40I |
probably benign |
Het |
Ipmk |
A |
G |
10: 71,183,882 (GRCm39) |
H34R |
probably damaging |
Het |
Kcnd3 |
T |
C |
3: 105,366,856 (GRCm39) |
L242P |
probably damaging |
Het |
Kdm4d |
T |
C |
9: 14,375,316 (GRCm39) |
M181V |
probably damaging |
Het |
Lats2 |
A |
T |
14: 57,934,582 (GRCm39) |
I716N |
probably damaging |
Het |
Liph |
T |
C |
16: 21,784,772 (GRCm39) |
Y305C |
probably damaging |
Het |
Ltbp1 |
T |
C |
17: 75,533,962 (GRCm39) |
V150A |
possibly damaging |
Het |
Ly6d |
A |
T |
15: 74,634,384 (GRCm39) |
S69T |
probably benign |
Het |
Meltf |
A |
G |
16: 31,702,617 (GRCm39) |
R115G |
possibly damaging |
Het |
Msgn1 |
G |
T |
12: 11,258,902 (GRCm39) |
D16E |
probably benign |
Het |
Mthfd2l |
T |
A |
5: 91,094,705 (GRCm39) |
I58K |
probably damaging |
Het |
Mup18 |
G |
C |
4: 61,591,573 (GRCm39) |
|
probably null |
Het |
Nek10 |
T |
A |
14: 14,850,947 (GRCm38) |
W331R |
probably damaging |
Het |
Nphp3 |
A |
G |
9: 103,881,974 (GRCm39) |
Y148C |
probably damaging |
Het |
Or4a47 |
T |
C |
2: 89,666,076 (GRCm39) |
Y71C |
probably damaging |
Het |
Or6c33 |
T |
A |
10: 129,853,760 (GRCm39) |
C177S |
probably damaging |
Het |
Oscp1 |
A |
G |
4: 125,980,459 (GRCm39) |
T325A |
possibly damaging |
Het |
Pcdha4 |
T |
A |
18: 37,086,613 (GRCm39) |
N265K |
probably damaging |
Het |
Pigq |
C |
T |
17: 26,153,199 (GRCm39) |
V331I |
probably benign |
Het |
Plekhg4 |
A |
G |
8: 106,105,329 (GRCm39) |
E598G |
probably damaging |
Het |
Pou6f2 |
G |
A |
13: 18,303,748 (GRCm39) |
T120M |
probably damaging |
Het |
Psg27 |
T |
A |
7: 18,295,726 (GRCm39) |
T240S |
probably damaging |
Het |
Samd12 |
T |
A |
15: 53,723,649 (GRCm39) |
I15F |
probably damaging |
Het |
Scaf4 |
A |
T |
16: 90,049,318 (GRCm39) |
D256E |
unknown |
Het |
Scaf8 |
T |
A |
17: 3,213,373 (GRCm39) |
M154K |
unknown |
Het |
Slc27a1 |
T |
C |
8: 72,032,071 (GRCm39) |
V64A |
possibly damaging |
Het |
Smc5 |
G |
A |
19: 23,237,064 (GRCm39) |
R256* |
probably null |
Het |
Snx31 |
A |
G |
15: 36,555,455 (GRCm39) |
F31L |
probably benign |
Het |
Spag17 |
T |
C |
3: 100,002,888 (GRCm39) |
S1871P |
probably benign |
Het |
Tdpoz4 |
T |
G |
3: 93,704,662 (GRCm39) |
S320A |
probably benign |
Het |
Tmprss11c |
A |
T |
5: 86,379,691 (GRCm39) |
C406S |
probably damaging |
Het |
Tnip1 |
G |
A |
11: 54,808,630 (GRCm39) |
A519V |
probably benign |
Het |
Tssc4 |
T |
A |
7: 142,624,724 (GRCm39) |
|
probably null |
Het |
Uba3 |
A |
T |
6: 97,182,512 (GRCm39) |
M1K |
probably null |
Het |
Usp32 |
GAACAAGTCCACAACAA |
GAACAA |
11: 84,913,681 (GRCm39) |
|
probably null |
Het |
Wnt11 |
T |
C |
7: 98,496,588 (GRCm39) |
M176T |
possibly damaging |
Het |
Wrn |
C |
T |
8: 33,814,346 (GRCm39) |
G366D |
probably benign |
Het |
Xylt1 |
T |
A |
7: 117,255,807 (GRCm39) |
I793N |
probably damaging |
Het |
Zfp677 |
T |
G |
17: 21,618,679 (GRCm39) |
C579G |
probably damaging |
Het |
Zscan4-ps1 |
T |
A |
7: 10,799,626 (GRCm39) |
K421M |
probably damaging |
Het |
|
Other mutations in Or5h19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01333:Or5h19
|
APN |
16 |
58,856,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R0218:Or5h19
|
UTSW |
16 |
58,856,456 (GRCm39) |
missense |
probably benign |
0.00 |
R1023:Or5h19
|
UTSW |
16 |
58,856,178 (GRCm39) |
missense |
probably benign |
0.00 |
R1086:Or5h19
|
UTSW |
16 |
58,856,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Or5h19
|
UTSW |
16 |
58,856,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:Or5h19
|
UTSW |
16 |
58,856,638 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4738:Or5h19
|
UTSW |
16 |
58,856,558 (GRCm39) |
missense |
probably benign |
0.00 |
R5265:Or5h19
|
UTSW |
16 |
58,856,506 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6053:Or5h19
|
UTSW |
16 |
58,856,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R6704:Or5h19
|
UTSW |
16 |
58,856,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R6854:Or5h19
|
UTSW |
16 |
58,856,428 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7178:Or5h19
|
UTSW |
16 |
58,856,296 (GRCm39) |
missense |
probably benign |
0.06 |
R7404:Or5h19
|
UTSW |
16 |
58,856,603 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7462:Or5h19
|
UTSW |
16 |
58,856,379 (GRCm39) |
nonsense |
probably null |
|
R7938:Or5h19
|
UTSW |
16 |
58,856,325 (GRCm39) |
nonsense |
probably null |
|
R8785:Or5h19
|
UTSW |
16 |
58,856,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R8790:Or5h19
|
UTSW |
16 |
58,856,580 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8912:Or5h19
|
UTSW |
16 |
58,856,263 (GRCm39) |
missense |
probably benign |
0.21 |
R9198:Or5h19
|
UTSW |
16 |
58,856,263 (GRCm39) |
missense |
probably benign |
0.21 |
R9234:Or5h19
|
UTSW |
16 |
58,856,789 (GRCm39) |
missense |
probably benign |
0.05 |
R9368:Or5h19
|
UTSW |
16 |
58,856,678 (GRCm39) |
missense |
probably benign |
0.04 |
R9568:Or5h19
|
UTSW |
16 |
58,856,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R9679:Or5h19
|
UTSW |
16 |
58,856,521 (GRCm39) |
missense |
possibly damaging |
0.87 |
|