Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
G |
A |
4: 103,100,101 (GRCm39) |
T33I |
possibly damaging |
Het |
4930555F03Rik |
A |
G |
8: 49,948,474 (GRCm39) |
|
noncoding transcript |
Het |
Abcf3 |
T |
C |
16: 20,378,084 (GRCm39) |
L538P |
probably damaging |
Het |
Adamts6 |
T |
C |
13: 104,450,779 (GRCm39) |
S321P |
probably damaging |
Het |
Adgra2 |
G |
A |
8: 27,602,523 (GRCm39) |
R362H |
probably damaging |
Het |
AI597479 |
T |
G |
1: 43,150,330 (GRCm39) |
S147A |
probably benign |
Het |
Ajm1 |
A |
G |
2: 25,468,574 (GRCm39) |
S446P |
possibly damaging |
Het |
Ampd3 |
T |
C |
7: 110,399,904 (GRCm39) |
F340L |
probably damaging |
Het |
Atad3a |
A |
G |
4: 155,831,927 (GRCm39) |
V449A |
probably damaging |
Het |
Bmal2 |
T |
C |
6: 146,724,751 (GRCm39) |
|
probably benign |
Het |
Bpifa6 |
A |
T |
2: 153,834,192 (GRCm39) |
D328V |
probably benign |
Het |
Brca2 |
T |
C |
5: 150,483,658 (GRCm39) |
S2903P |
probably damaging |
Het |
Cct3 |
A |
T |
3: 88,206,652 (GRCm39) |
|
probably null |
Het |
Cdk4 |
A |
G |
10: 126,900,863 (GRCm39) |
T172A |
probably damaging |
Het |
Chd5 |
A |
G |
4: 152,468,616 (GRCm39) |
D1760G |
probably damaging |
Het |
Chd7 |
A |
G |
4: 8,801,310 (GRCm39) |
|
probably benign |
Het |
Crybb2 |
T |
C |
5: 113,210,037 (GRCm39) |
I109V |
probably benign |
Het |
Csmd3 |
A |
G |
15: 48,048,780 (GRCm39) |
|
probably benign |
Het |
Dach1 |
G |
T |
14: 98,406,051 (GRCm39) |
T232K |
possibly damaging |
Het |
Dnlz |
A |
G |
2: 26,241,485 (GRCm39) |
V81A |
possibly damaging |
Het |
Epb41l4b |
A |
G |
4: 57,086,003 (GRCm39) |
S191P |
probably damaging |
Het |
Eps15l1 |
C |
T |
8: 73,099,929 (GRCm39) |
D821N |
probably damaging |
Het |
Fam186a |
G |
A |
15: 99,839,893 (GRCm39) |
P2117L |
probably damaging |
Het |
Fam83d |
T |
A |
2: 158,621,808 (GRCm39) |
F173Y |
probably damaging |
Het |
Gm9116 |
A |
T |
3: 93,817,772 (GRCm39) |
R214S |
probably benign |
Het |
Gtpbp1 |
A |
G |
15: 79,600,401 (GRCm39) |
I445V |
probably damaging |
Het |
H2-M2 |
G |
A |
17: 37,793,640 (GRCm39) |
T122I |
probably damaging |
Het |
Hgd |
C |
T |
16: 37,448,971 (GRCm39) |
|
probably benign |
Het |
Hip1r |
A |
G |
5: 124,135,004 (GRCm39) |
Y380C |
probably benign |
Het |
Hspa8 |
G |
A |
9: 40,715,137 (GRCm39) |
G389R |
probably damaging |
Het |
Htt |
C |
A |
5: 34,975,097 (GRCm39) |
D622E |
probably benign |
Het |
Iqca1 |
C |
A |
1: 90,070,453 (GRCm39) |
G133V |
probably null |
Het |
Kdm4a |
A |
G |
4: 118,004,189 (GRCm39) |
|
probably null |
Het |
Map3k9 |
G |
A |
12: 81,769,043 (GRCm39) |
P1025S |
probably benign |
Het |
Pabpc1l |
C |
A |
2: 163,873,134 (GRCm39) |
H135N |
probably benign |
Het |
Pacsin2 |
A |
T |
15: 83,263,998 (GRCm39) |
S346R |
probably benign |
Het |
Pcdhb20 |
A |
G |
18: 37,638,938 (GRCm39) |
Y488C |
probably damaging |
Het |
Pkdcc |
G |
A |
17: 83,531,347 (GRCm39) |
C452Y |
probably damaging |
Het |
Poglut1 |
T |
C |
16: 38,355,083 (GRCm39) |
|
probably null |
Het |
Prss59 |
A |
G |
6: 40,905,533 (GRCm39) |
M41T |
probably damaging |
Het |
Pxk |
T |
C |
14: 8,148,123 (GRCm38) |
F409L |
probably benign |
Het |
Pygm |
G |
A |
19: 6,436,048 (GRCm39) |
|
probably benign |
Het |
Rabep2 |
T |
C |
7: 126,037,896 (GRCm39) |
S223P |
probably damaging |
Het |
Rpp40 |
C |
T |
13: 36,086,034 (GRCm39) |
R109H |
probably benign |
Het |
Sbf2 |
T |
C |
7: 109,940,562 (GRCm39) |
Y1266C |
possibly damaging |
Het |
Slc5a4a |
T |
C |
10: 76,012,368 (GRCm39) |
V346A |
probably benign |
Het |
Smpd3 |
G |
T |
8: 106,991,421 (GRCm39) |
H377Q |
possibly damaging |
Het |
Sppl2a |
C |
A |
2: 126,762,227 (GRCm39) |
|
probably benign |
Het |
Tas2r134 |
T |
C |
2: 51,518,385 (GRCm39) |
I288T |
probably benign |
Het |
Trim35 |
T |
A |
14: 66,546,650 (GRCm39) |
H472Q |
probably damaging |
Het |
Trpm5 |
C |
A |
7: 142,632,088 (GRCm39) |
R907L |
probably damaging |
Het |
Ube2e2 |
G |
T |
14: 18,630,393 (GRCm38) |
S56* |
probably null |
Het |
Vmn2r88 |
A |
C |
14: 51,651,959 (GRCm39) |
R432S |
possibly damaging |
Het |
Wdr24 |
A |
G |
17: 26,045,102 (GRCm39) |
Y279C |
probably damaging |
Het |
Wdr90 |
A |
G |
17: 26,079,104 (GRCm39) |
V246A |
probably benign |
Het |
Xrn2 |
T |
A |
2: 146,871,818 (GRCm39) |
N385K |
probably benign |
Het |
Zfp28 |
T |
A |
7: 6,387,182 (GRCm39) |
S73T |
possibly damaging |
Het |
Zfp345 |
T |
C |
2: 150,314,271 (GRCm39) |
E422G |
probably benign |
Het |
Zhx2 |
A |
G |
15: 57,684,709 (GRCm39) |
E26G |
probably benign |
Het |
|
Other mutations in Or8b47 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01025:Or8b47
|
APN |
9 |
38,435,029 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02319:Or8b47
|
APN |
9 |
38,435,166 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02415:Or8b47
|
APN |
9 |
38,435,408 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02536:Or8b47
|
APN |
9 |
38,435,460 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02702:Or8b47
|
APN |
9 |
38,435,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02926:Or8b47
|
APN |
9 |
38,435,021 (GRCm39) |
utr 5 prime |
probably benign |
|
R0499:Or8b47
|
UTSW |
9 |
38,435,801 (GRCm39) |
missense |
probably benign |
0.01 |
R0662:Or8b47
|
UTSW |
9 |
38,435,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R1186:Or8b47
|
UTSW |
9 |
38,435,453 (GRCm39) |
missense |
probably damaging |
0.97 |
R1681:Or8b47
|
UTSW |
9 |
38,435,413 (GRCm39) |
missense |
probably benign |
0.03 |
R3522:Or8b47
|
UTSW |
9 |
38,435,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R5820:Or8b47
|
UTSW |
9 |
38,435,895 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6597:Or8b47
|
UTSW |
9 |
38,435,300 (GRCm39) |
missense |
probably benign |
0.00 |
R7721:Or8b47
|
UTSW |
9 |
38,435,013 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7846:Or8b47
|
UTSW |
9 |
38,435,675 (GRCm39) |
missense |
probably benign |
0.00 |
R7985:Or8b47
|
UTSW |
9 |
38,435,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R8339:Or8b47
|
UTSW |
9 |
38,435,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R8460:Or8b47
|
UTSW |
9 |
38,427,926 (GRCm39) |
unclassified |
probably benign |
|
R9143:Or8b47
|
UTSW |
9 |
38,427,917 (GRCm39) |
unclassified |
probably benign |
|
R9287:Or8b47
|
UTSW |
9 |
38,435,082 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Or8b47
|
UTSW |
9 |
38,435,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|