Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310061N02Rik |
A |
T |
16: 88,504,321 (GRCm39) |
S159T |
probably damaging |
Het |
2610028H24Rik |
T |
A |
10: 76,288,664 (GRCm39) |
M53K |
probably benign |
Het |
3425401B19Rik |
G |
A |
14: 32,383,632 (GRCm39) |
Q778* |
probably null |
Het |
Abhd16a |
T |
A |
17: 35,310,701 (GRCm39) |
|
probably benign |
Het |
Acp6 |
A |
G |
3: 97,075,810 (GRCm39) |
K226R |
probably benign |
Het |
Ankfy1 |
A |
G |
11: 72,650,811 (GRCm39) |
D998G |
probably damaging |
Het |
Apbb1 |
G |
T |
7: 105,223,432 (GRCm39) |
P60T |
probably damaging |
Het |
Apol9a |
T |
A |
15: 77,288,705 (GRCm39) |
I221F |
probably benign |
Het |
Arhgap29 |
A |
G |
3: 121,805,736 (GRCm39) |
E947G |
possibly damaging |
Het |
B430218F22Rik |
A |
T |
13: 118,523,934 (GRCm39) |
|
probably benign |
Het |
Carmil3 |
ACCCCC |
ACCCCCCC |
14: 55,741,456 (GRCm39) |
|
probably null |
Het |
Ccdc69 |
C |
T |
11: 54,943,716 (GRCm39) |
|
probably null |
Het |
Ccdc93 |
G |
T |
1: 121,390,849 (GRCm39) |
V274L |
possibly damaging |
Het |
Cdc25a |
A |
G |
9: 109,713,433 (GRCm39) |
D191G |
probably benign |
Het |
Cimip2a |
A |
T |
2: 25,110,578 (GRCm39) |
M129L |
probably benign |
Het |
Cmya5 |
A |
G |
13: 93,182,373 (GRCm39) |
|
probably null |
Het |
Crebzf |
TGGAGGAGGAGGAGGAGGA |
TGGAGGAGGAGGAGGA |
7: 90,092,479 (GRCm39) |
|
probably benign |
Het |
Csde1 |
T |
C |
3: 102,947,859 (GRCm39) |
|
probably benign |
Het |
Ctdp1 |
A |
G |
18: 80,502,003 (GRCm39) |
L177P |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,272,206 (GRCm39) |
H1003Q |
probably benign |
Het |
Epb41l2 |
T |
A |
10: 25,369,494 (GRCm39) |
N604K |
probably damaging |
Het |
Fig4 |
T |
A |
10: 41,130,881 (GRCm39) |
N465Y |
possibly damaging |
Het |
Gemin7 |
G |
A |
7: 19,299,223 (GRCm39) |
S124F |
probably damaging |
Het |
Gli3 |
G |
A |
13: 15,900,765 (GRCm39) |
R1384K |
probably benign |
Het |
Gm12258 |
G |
A |
11: 58,750,457 (GRCm39) |
C544Y |
probably damaging |
Het |
Grm1 |
C |
T |
10: 10,956,294 (GRCm39) |
|
probably benign |
Het |
H2-T15 |
T |
A |
17: 36,367,236 (GRCm39) |
M329L |
probably benign |
Het |
Hps4 |
C |
T |
5: 112,517,351 (GRCm39) |
T246I |
probably benign |
Het |
Ifngr2 |
A |
T |
16: 91,358,653 (GRCm39) |
E284D |
possibly damaging |
Het |
Impdh2 |
A |
G |
9: 108,441,165 (GRCm39) |
T148A |
probably benign |
Het |
Irx3 |
T |
C |
8: 92,527,763 (GRCm39) |
S36G |
probably benign |
Het |
Itga5 |
T |
A |
15: 103,259,514 (GRCm39) |
K667N |
probably benign |
Het |
Itgad |
G |
A |
7: 127,773,188 (GRCm39) |
C15Y |
probably benign |
Het |
Ly75 |
T |
G |
2: 60,213,490 (GRCm39) |
E29A |
probably benign |
Het |
Magi1 |
T |
A |
6: 93,685,180 (GRCm39) |
S506C |
probably damaging |
Het |
Map4 |
G |
A |
9: 109,901,702 (GRCm39) |
V781M |
possibly damaging |
Het |
Med23 |
T |
C |
10: 24,778,043 (GRCm39) |
L797P |
probably damaging |
Het |
Naip1 |
C |
T |
13: 100,559,636 (GRCm39) |
G1123R |
probably benign |
Het |
Ncor1 |
G |
T |
11: 62,274,016 (GRCm39) |
P55Q |
probably damaging |
Het |
Odr4 |
A |
T |
1: 150,256,111 (GRCm39) |
N211K |
probably benign |
Het |
Ofcc1 |
T |
A |
13: 40,334,060 (GRCm39) |
I344F |
probably benign |
Het |
Or4d5 |
A |
T |
9: 40,012,189 (GRCm39) |
M199K |
probably damaging |
Het |
Or5d35 |
A |
G |
2: 87,855,465 (GRCm39) |
Y133C |
probably damaging |
Het |
Or5k1 |
G |
A |
16: 58,618,095 (GRCm39) |
T38I |
probably damaging |
Het |
Otub2 |
C |
T |
12: 103,369,687 (GRCm39) |
|
probably benign |
Het |
Parva |
A |
G |
7: 112,143,960 (GRCm39) |
M83V |
probably benign |
Het |
Pcdha8 |
T |
A |
18: 37,126,572 (GRCm39) |
N351K |
probably benign |
Het |
Pcdhb5 |
T |
A |
18: 37,455,732 (GRCm39) |
L704* |
probably null |
Het |
Pkd1l3 |
T |
A |
8: 110,353,468 (GRCm39) |
L683H |
probably damaging |
Het |
Plekhn1 |
C |
T |
4: 156,308,331 (GRCm39) |
R288H |
probably benign |
Het |
Polr2a |
A |
T |
11: 69,627,086 (GRCm39) |
N1457K |
probably damaging |
Het |
Ppp1r12b |
A |
G |
1: 134,693,719 (GRCm39) |
S981P |
probably damaging |
Het |
Ppp1r9a |
A |
G |
6: 5,159,648 (GRCm39) |
K1062E |
probably damaging |
Het |
Ptpre |
A |
T |
7: 135,276,007 (GRCm39) |
T498S |
probably benign |
Het |
Pus7l |
C |
T |
15: 94,427,332 (GRCm39) |
|
probably null |
Het |
Rptn |
C |
T |
3: 93,305,639 (GRCm39) |
Q991* |
probably null |
Het |
Rsu1 |
T |
G |
2: 13,229,170 (GRCm39) |
E76A |
probably damaging |
Het |
Septin11 |
T |
A |
5: 93,304,824 (GRCm39) |
F214I |
probably damaging |
Het |
Slc1a7 |
G |
T |
4: 107,869,587 (GRCm39) |
A551S |
probably benign |
Het |
Slc45a2 |
T |
A |
15: 11,000,941 (GRCm39) |
Y13* |
probably null |
Het |
Slc7a14 |
T |
G |
3: 31,311,719 (GRCm39) |
L100F |
probably damaging |
Het |
Slit3 |
A |
G |
11: 35,598,932 (GRCm39) |
E1512G |
probably damaging |
Het |
Stat5a |
A |
G |
11: 100,767,883 (GRCm39) |
Q458R |
possibly damaging |
Het |
Svep1 |
T |
C |
4: 58,084,906 (GRCm39) |
T1811A |
possibly damaging |
Het |
Tarbp1 |
A |
G |
8: 127,179,667 (GRCm39) |
F624L |
probably benign |
Het |
Tfeb |
T |
G |
17: 48,070,433 (GRCm39) |
|
probably null |
Het |
Tnxb |
G |
A |
17: 34,891,126 (GRCm39) |
G490R |
probably damaging |
Het |
Tra2b |
T |
C |
16: 22,077,953 (GRCm39) |
Y32C |
probably damaging |
Het |
Trpv4 |
C |
T |
5: 114,760,708 (GRCm39) |
|
probably benign |
Het |
Uvrag |
A |
T |
7: 98,637,414 (GRCm39) |
L138* |
probably null |
Het |
Vwf |
A |
T |
6: 125,655,725 (GRCm39) |
|
probably null |
Het |
Wdr47 |
G |
A |
3: 108,526,322 (GRCm39) |
D282N |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,340,290 (GRCm39) |
N844D |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,339,042 (GRCm39) |
M428V |
probably benign |
Het |
Znfx1 |
G |
A |
2: 166,880,920 (GRCm39) |
T288I |
probably damaging |
Het |
|
Other mutations in Or4a74 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01101:Or4a74
|
APN |
2 |
89,440,191 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01337:Or4a74
|
APN |
2 |
89,439,720 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02537:Or4a74
|
APN |
2 |
89,439,739 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02651:Or4a74
|
APN |
2 |
89,439,842 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02734:Or4a74
|
APN |
2 |
89,440,303 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03177:Or4a74
|
APN |
2 |
89,439,826 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03184:Or4a74
|
APN |
2 |
89,439,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R0207:Or4a74
|
UTSW |
2 |
89,440,207 (GRCm39) |
missense |
probably damaging |
0.97 |
R0278:Or4a74
|
UTSW |
2 |
89,440,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R0278:Or4a74
|
UTSW |
2 |
89,440,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Or4a74
|
UTSW |
2 |
89,439,564 (GRCm39) |
missense |
probably benign |
0.00 |
R0633:Or4a74
|
UTSW |
2 |
89,439,718 (GRCm39) |
missense |
probably benign |
0.10 |
R1824:Or4a74
|
UTSW |
2 |
89,439,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R1863:Or4a74
|
UTSW |
2 |
89,440,053 (GRCm39) |
nonsense |
probably null |
|
R2073:Or4a74
|
UTSW |
2 |
89,439,822 (GRCm39) |
missense |
probably benign |
0.01 |
R2074:Or4a74
|
UTSW |
2 |
89,439,822 (GRCm39) |
missense |
probably benign |
0.01 |
R2075:Or4a74
|
UTSW |
2 |
89,439,822 (GRCm39) |
missense |
probably benign |
0.01 |
R3921:Or4a74
|
UTSW |
2 |
89,439,853 (GRCm39) |
missense |
probably benign |
0.00 |
R4559:Or4a74
|
UTSW |
2 |
89,440,043 (GRCm39) |
missense |
probably damaging |
0.99 |
R5128:Or4a74
|
UTSW |
2 |
89,439,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5140:Or4a74
|
UTSW |
2 |
89,439,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R5426:Or4a74
|
UTSW |
2 |
89,440,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Or4a74
|
UTSW |
2 |
89,439,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R6478:Or4a74
|
UTSW |
2 |
89,439,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R7143:Or4a74
|
UTSW |
2 |
89,440,363 (GRCm39) |
missense |
probably benign |
0.00 |
R7221:Or4a74
|
UTSW |
2 |
89,440,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R7599:Or4a74
|
UTSW |
2 |
89,439,571 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8709:Or4a74
|
UTSW |
2 |
89,440,366 (GRCm39) |
missense |
probably benign |
0.00 |
R8711:Or4a74
|
UTSW |
2 |
89,440,291 (GRCm39) |
missense |
probably benign |
0.05 |
R8721:Or4a74
|
UTSW |
2 |
89,440,186 (GRCm39) |
missense |
probably benign |
0.05 |
R9278:Or4a74
|
UTSW |
2 |
89,439,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R9630:Or4a74
|
UTSW |
2 |
89,440,349 (GRCm39) |
missense |
probably benign |
|
|