Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1cf |
C |
A |
19: 31,870,507 (GRCm39) |
S3* |
probably null |
Het |
Adgrv1 |
C |
T |
13: 81,624,750 (GRCm39) |
V3740I |
probably benign |
Het |
Aida |
T |
C |
1: 183,079,127 (GRCm39) |
F22S |
probably damaging |
Het |
Ankrd65 |
A |
T |
4: 155,876,528 (GRCm39) |
D220V |
probably damaging |
Het |
Antxr2 |
A |
T |
5: 98,123,209 (GRCm39) |
C279* |
probably null |
Het |
Ap3b1 |
T |
C |
13: 94,545,320 (GRCm39) |
V191A |
probably damaging |
Het |
Arhgef28 |
T |
C |
13: 98,117,884 (GRCm39) |
K595E |
probably benign |
Het |
Atp12a |
A |
G |
14: 56,608,305 (GRCm39) |
T98A |
probably benign |
Het |
Cdcp1 |
A |
T |
9: 123,014,427 (GRCm39) |
S116T |
probably benign |
Het |
Chrm1 |
T |
C |
19: 8,656,582 (GRCm39) |
F429S |
possibly damaging |
Het |
Ckap5 |
C |
A |
2: 91,393,303 (GRCm39) |
Q395K |
possibly damaging |
Het |
Cntn4 |
T |
A |
6: 106,656,258 (GRCm39) |
I853K |
probably benign |
Het |
Cyp2g1 |
G |
A |
7: 26,509,107 (GRCm39) |
|
probably null |
Het |
Dhx57 |
C |
T |
17: 80,553,157 (GRCm39) |
V1257I |
possibly damaging |
Het |
Disp1 |
A |
T |
1: 182,869,306 (GRCm39) |
V1038D |
probably damaging |
Het |
Dmxl2 |
A |
T |
9: 54,358,314 (GRCm39) |
S462T |
possibly damaging |
Het |
Dnaaf10 |
A |
T |
11: 17,177,183 (GRCm39) |
E180D |
probably benign |
Het |
Exoc3l |
A |
G |
8: 106,019,692 (GRCm39) |
|
probably null |
Het |
Fam210a |
T |
C |
18: 68,409,167 (GRCm39) |
T48A |
probably benign |
Het |
Fbxw5 |
G |
A |
2: 25,393,286 (GRCm39) |
|
probably null |
Het |
Fkbp9 |
T |
C |
6: 56,850,434 (GRCm39) |
C437R |
probably damaging |
Het |
Gpc5 |
A |
G |
14: 115,636,691 (GRCm39) |
K458R |
probably benign |
Het |
Grik2 |
C |
A |
10: 49,120,439 (GRCm39) |
G56* |
probably null |
Het |
Igsf10 |
T |
C |
3: 59,238,706 (GRCm39) |
T492A |
probably damaging |
Het |
Kif1c |
C |
T |
11: 70,619,223 (GRCm39) |
L953F |
probably damaging |
Het |
Lrrc51 |
T |
C |
7: 101,562,645 (GRCm39) |
Y145C |
probably damaging |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Mapkbp1 |
A |
T |
2: 119,849,029 (GRCm39) |
I682F |
possibly damaging |
Het |
Mttp |
A |
T |
3: 137,808,954 (GRCm39) |
V718D |
probably damaging |
Het |
Myt1l |
T |
A |
12: 29,945,272 (GRCm39) |
D1012E |
unknown |
Het |
Nbn |
G |
A |
4: 15,971,771 (GRCm39) |
G301D |
probably benign |
Het |
Ncstn |
T |
A |
1: 171,894,339 (GRCm39) |
S677C |
possibly damaging |
Het |
Nod1 |
C |
A |
6: 54,921,218 (GRCm39) |
|
probably null |
Het |
Nos1ap |
A |
G |
1: 170,342,206 (GRCm39) |
V52A |
possibly damaging |
Het |
Or51f2 |
T |
G |
7: 102,526,863 (GRCm39) |
Y179D |
probably damaging |
Het |
Or5b98 |
T |
A |
19: 12,931,055 (GRCm39) |
I34N |
probably damaging |
Het |
Or5h23 |
T |
A |
16: 58,906,706 (GRCm39) |
I47F |
probably benign |
Het |
Phf13 |
T |
C |
4: 152,076,962 (GRCm39) |
I77V |
probably benign |
Het |
Pias2 |
A |
G |
18: 77,207,825 (GRCm39) |
K230E |
probably damaging |
Het |
Poli |
A |
G |
18: 70,642,535 (GRCm39) |
L469P |
probably damaging |
Het |
Prag1 |
A |
T |
8: 36,607,177 (GRCm39) |
T973S |
possibly damaging |
Het |
Prpf40b |
C |
A |
15: 99,203,442 (GRCm39) |
H101Q |
probably damaging |
Het |
Prss50 |
T |
C |
9: 110,691,557 (GRCm39) |
V287A |
possibly damaging |
Het |
Rbm25 |
C |
T |
12: 83,714,924 (GRCm39) |
|
probably benign |
Het |
Rcor2 |
T |
C |
19: 7,246,337 (GRCm39) |
V4A |
probably damaging |
Het |
Rnf180 |
T |
C |
13: 105,407,499 (GRCm39) |
T17A |
probably benign |
Het |
Robo3 |
A |
T |
9: 37,340,440 (GRCm39) |
V179E |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,446,458 (GRCm39) |
S2835T |
probably damaging |
Het |
Serpinb3c |
T |
A |
1: 107,199,432 (GRCm39) |
H363L |
probably damaging |
Het |
Setd1a |
T |
C |
7: 127,395,841 (GRCm39) |
|
probably benign |
Het |
Skp2 |
A |
C |
15: 9,125,201 (GRCm39) |
V126G |
probably benign |
Het |
Snph |
G |
A |
2: 151,436,398 (GRCm39) |
Q108* |
probably null |
Het |
Snrpa1 |
T |
A |
7: 65,719,246 (GRCm39) |
V144E |
probably damaging |
Het |
Tifab |
T |
C |
13: 56,324,248 (GRCm39) |
E65G |
probably damaging |
Het |
Tmem201 |
A |
T |
4: 149,804,032 (GRCm39) |
Y468N |
probably damaging |
Het |
Tpcn1 |
T |
C |
5: 120,687,580 (GRCm39) |
N388S |
possibly damaging |
Het |
Tssk4 |
A |
G |
14: 55,888,029 (GRCm39) |
Q75R |
probably null |
Het |
Tuba4a |
T |
C |
1: 75,192,547 (GRCm39) |
N356D |
probably benign |
Het |
Ugt2b5 |
T |
A |
5: 87,287,477 (GRCm39) |
D230V |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,648,261 (GRCm39) |
V4622A |
probably benign |
Het |
Vmn2r11 |
T |
G |
5: 109,201,724 (GRCm39) |
Y260S |
possibly damaging |
Het |
Vmn2r89 |
C |
A |
14: 51,693,693 (GRCm39) |
H348N |
possibly damaging |
Het |
Vmn2r96 |
A |
T |
17: 18,817,988 (GRCm39) |
M714L |
probably benign |
Het |
Zbtb18 |
T |
C |
1: 177,275,329 (GRCm39) |
S221P |
probably benign |
Het |
Zfp418 |
A |
G |
7: 7,184,789 (GRCm39) |
T251A |
probably benign |
Het |
Zmynd15 |
A |
G |
11: 70,354,328 (GRCm39) |
Y267C |
probably damaging |
Het |
|
Other mutations in Or52z14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01610:Or52z14
|
APN |
7 |
103,253,274 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01806:Or52z14
|
APN |
7 |
103,253,548 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01934:Or52z14
|
APN |
7 |
103,253,182 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02269:Or52z14
|
APN |
7 |
103,253,089 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03049:Or52z14
|
APN |
7 |
103,253,298 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03165:Or52z14
|
APN |
7 |
103,253,218 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03338:Or52z14
|
APN |
7 |
103,253,615 (GRCm39) |
nonsense |
probably null |
|
R1378:Or52z14
|
UTSW |
7 |
103,253,145 (GRCm39) |
nonsense |
probably null |
|
R1975:Or52z14
|
UTSW |
7 |
103,253,219 (GRCm39) |
splice site |
probably null |
|
R1985:Or52z14
|
UTSW |
7 |
103,252,879 (GRCm39) |
missense |
probably benign |
|
R2249:Or52z14
|
UTSW |
7 |
103,252,943 (GRCm39) |
missense |
probably benign |
0.00 |
R2423:Or52z14
|
UTSW |
7 |
103,253,241 (GRCm39) |
missense |
probably benign |
0.14 |
R4005:Or52z14
|
UTSW |
7 |
103,253,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R4931:Or52z14
|
UTSW |
7 |
103,253,581 (GRCm39) |
missense |
probably benign |
0.01 |
R4939:Or52z14
|
UTSW |
7 |
103,253,458 (GRCm39) |
missense |
probably benign |
0.12 |
R4942:Or52z14
|
UTSW |
7 |
103,253,401 (GRCm39) |
missense |
probably benign |
|
R4970:Or52z14
|
UTSW |
7 |
103,253,197 (GRCm39) |
missense |
probably damaging |
0.98 |
R4993:Or52z14
|
UTSW |
7 |
103,252,863 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R5254:Or52z14
|
UTSW |
7 |
103,252,996 (GRCm39) |
missense |
probably benign |
0.19 |
R6001:Or52z14
|
UTSW |
7 |
103,253,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R6905:Or52z14
|
UTSW |
7 |
103,253,574 (GRCm39) |
missense |
probably benign |
|
R6985:Or52z14
|
UTSW |
7 |
103,252,875 (GRCm39) |
missense |
probably benign |
0.00 |
R8253:Or52z14
|
UTSW |
7 |
103,253,538 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9124:Or52z14
|
UTSW |
7 |
103,252,863 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
|