Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
G |
T |
17: 9,226,938 (GRCm39) |
|
probably benign |
Het |
Abca13 |
T |
A |
11: 9,242,775 (GRCm39) |
I1546N |
probably damaging |
Het |
Actrt3 |
A |
T |
3: 30,652,422 (GRCm39) |
M224K |
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,727,065 (GRCm39) |
N429S |
probably benign |
Het |
Appbp2 |
A |
C |
11: 85,105,129 (GRCm39) |
C146G |
possibly damaging |
Het |
Cabp2 |
A |
C |
19: 4,136,242 (GRCm39) |
D83A |
possibly damaging |
Het |
Ccl1 |
A |
G |
11: 82,068,843 (GRCm39) |
|
probably null |
Het |
Cdca8 |
T |
C |
4: 124,814,168 (GRCm39) |
T208A |
probably benign |
Het |
Dach1 |
C |
T |
14: 98,406,184 (GRCm39) |
G188R |
probably damaging |
Het |
Dcdc5 |
G |
A |
2: 106,187,541 (GRCm39) |
|
noncoding transcript |
Het |
Efr3b |
C |
A |
12: 4,043,003 (GRCm39) |
C89F |
probably damaging |
Het |
Enpp3 |
C |
T |
10: 24,675,051 (GRCm39) |
|
probably null |
Het |
Ep400 |
A |
T |
5: 110,821,395 (GRCm39) |
V2467E |
probably damaging |
Het |
Ermap |
T |
C |
4: 119,037,145 (GRCm39) |
|
probably benign |
Het |
Fig4 |
A |
G |
10: 41,149,003 (GRCm39) |
Y150H |
possibly damaging |
Het |
Fsip2 |
G |
A |
2: 82,822,416 (GRCm39) |
V6050M |
probably damaging |
Het |
Gnb1l |
T |
C |
16: 18,359,810 (GRCm39) |
W72R |
probably damaging |
Het |
Gpld1 |
A |
G |
13: 25,174,101 (GRCm39) |
D842G |
probably damaging |
Het |
Hmgcr |
A |
G |
13: 96,788,597 (GRCm39) |
|
probably benign |
Het |
Hrc |
A |
G |
7: 44,985,794 (GRCm39) |
H315R |
possibly damaging |
Het |
Ifit2 |
A |
T |
19: 34,550,973 (GRCm39) |
N171I |
probably damaging |
Het |
Ipo11 |
T |
A |
13: 107,023,238 (GRCm39) |
I416L |
probably benign |
Het |
Kcnab1 |
G |
A |
3: 65,264,527 (GRCm39) |
V259M |
probably damaging |
Het |
Kcng4 |
T |
C |
8: 120,360,259 (GRCm39) |
Y39C |
probably damaging |
Het |
Kif5c |
A |
G |
2: 49,622,725 (GRCm39) |
T526A |
probably benign |
Het |
Kntc1 |
A |
G |
5: 123,919,044 (GRCm39) |
Y805C |
probably damaging |
Het |
Mal |
A |
G |
2: 127,482,227 (GRCm39) |
S59P |
probably damaging |
Het |
Myh15 |
A |
G |
16: 48,983,423 (GRCm39) |
N1513D |
probably damaging |
Het |
Ncoa2 |
A |
G |
1: 13,244,976 (GRCm39) |
L574P |
probably damaging |
Het |
Nmd3 |
A |
G |
3: 69,643,425 (GRCm39) |
|
probably null |
Het |
Nucb2 |
A |
G |
7: 116,132,386 (GRCm39) |
D331G |
probably benign |
Het |
Nwd1 |
T |
C |
8: 73,436,053 (GRCm39) |
|
probably benign |
Het |
Nynrin |
T |
C |
14: 56,109,852 (GRCm39) |
F1653S |
probably damaging |
Het |
Or4a80 |
A |
C |
2: 89,582,365 (GRCm39) |
I269S |
possibly damaging |
Het |
Or8b12b |
T |
G |
9: 37,684,274 (GRCm39) |
F106L |
probably benign |
Het |
Pfdn6 |
T |
C |
17: 34,158,538 (GRCm39) |
R79G |
probably damaging |
Het |
Pkd1 |
G |
T |
17: 24,797,513 (GRCm39) |
|
probably null |
Het |
Pramel4 |
T |
G |
4: 143,794,914 (GRCm39) |
C434G |
probably benign |
Het |
Ptpn13 |
T |
C |
5: 103,634,638 (GRCm39) |
|
probably null |
Het |
Ptpro |
T |
C |
6: 137,393,825 (GRCm39) |
V831A |
probably benign |
Het |
Rabl6 |
A |
T |
2: 25,492,579 (GRCm39) |
|
probably benign |
Het |
Reg3b |
T |
A |
6: 78,349,844 (GRCm39) |
M128K |
possibly damaging |
Het |
Rif1 |
A |
G |
2: 52,006,686 (GRCm39) |
T2207A |
probably benign |
Het |
Rpa1 |
A |
C |
11: 75,205,687 (GRCm39) |
N223K |
probably null |
Het |
Rras2 |
T |
C |
7: 113,647,490 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
T |
A |
7: 28,746,967 (GRCm39) |
E3760V |
probably damaging |
Het |
Scyl3 |
T |
A |
1: 163,767,538 (GRCm39) |
I204N |
possibly damaging |
Het |
Serpinb9h |
A |
C |
13: 33,588,494 (GRCm39) |
I360L |
probably damaging |
Het |
Slc16a12 |
A |
G |
19: 34,650,098 (GRCm39) |
|
probably benign |
Het |
Slc22a1 |
A |
G |
17: 12,878,646 (GRCm39) |
F356L |
probably damaging |
Het |
Slc22a29 |
A |
G |
19: 8,195,630 (GRCm39) |
|
probably benign |
Het |
Slc45a1 |
C |
A |
4: 150,714,023 (GRCm39) |
D741Y |
possibly damaging |
Het |
Slco1a5 |
A |
T |
6: 142,182,061 (GRCm39) |
|
probably benign |
Het |
Smg5 |
G |
T |
3: 88,258,412 (GRCm39) |
R461L |
probably damaging |
Het |
Snrk |
T |
C |
9: 121,995,306 (GRCm39) |
S362P |
probably damaging |
Het |
Spata31d1b |
A |
G |
13: 59,863,883 (GRCm39) |
S344G |
probably benign |
Het |
Sync |
G |
A |
4: 129,187,537 (GRCm39) |
V190M |
probably damaging |
Het |
Taf5l |
T |
C |
8: 124,730,383 (GRCm39) |
Y67C |
probably damaging |
Het |
Tbkbp1 |
A |
G |
11: 97,037,115 (GRCm39) |
|
probably benign |
Het |
Tshr |
A |
T |
12: 91,504,660 (GRCm39) |
I533F |
possibly damaging |
Het |
Tsn |
T |
C |
1: 118,228,589 (GRCm39) |
D211G |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,621,988 (GRCm39) |
T15518I |
probably benign |
Het |
Unc13c |
T |
C |
9: 73,600,583 (GRCm39) |
D1387G |
probably benign |
Het |
Vapb |
A |
G |
2: 173,613,397 (GRCm39) |
T99A |
probably benign |
Het |
Vmn2r127 |
A |
G |
17: 19,373,879 (GRCm39) |
|
noncoding transcript |
Het |
Zfp280d |
A |
T |
9: 72,246,292 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Or7c19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01104:Or7c19
|
APN |
8 |
85,957,813 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01380:Or7c19
|
APN |
8 |
85,957,775 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01380:Or7c19
|
APN |
8 |
85,957,958 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01680:Or7c19
|
APN |
8 |
85,957,308 (GRCm39) |
missense |
probably benign |
|
IGL01880:Or7c19
|
APN |
8 |
85,957,712 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02194:Or7c19
|
APN |
8 |
85,957,262 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02416:Or7c19
|
APN |
8 |
85,957,662 (GRCm39) |
nonsense |
probably null |
|
IGL02494:Or7c19
|
APN |
8 |
85,957,312 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03072:Or7c19
|
APN |
8 |
85,957,139 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03130:Or7c19
|
APN |
8 |
85,957,258 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1157:Or7c19
|
UTSW |
8 |
85,957,889 (GRCm39) |
missense |
probably damaging |
0.98 |
R1165:Or7c19
|
UTSW |
8 |
85,957,400 (GRCm39) |
missense |
probably damaging |
0.98 |
R1730:Or7c19
|
UTSW |
8 |
85,957,477 (GRCm39) |
missense |
probably benign |
0.16 |
R2017:Or7c19
|
UTSW |
8 |
85,957,373 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2426:Or7c19
|
UTSW |
8 |
85,957,693 (GRCm39) |
missense |
probably damaging |
0.97 |
R4447:Or7c19
|
UTSW |
8 |
85,957,995 (GRCm39) |
nonsense |
probably null |
|
R4703:Or7c19
|
UTSW |
8 |
85,957,237 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4797:Or7c19
|
UTSW |
8 |
85,957,567 (GRCm39) |
missense |
probably benign |
|
R5029:Or7c19
|
UTSW |
8 |
85,957,835 (GRCm39) |
missense |
probably benign |
0.00 |
R5173:Or7c19
|
UTSW |
8 |
85,957,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R6349:Or7c19
|
UTSW |
8 |
85,957,787 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7754:Or7c19
|
UTSW |
8 |
85,957,427 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8955:Or7c19
|
UTSW |
8 |
85,957,913 (GRCm39) |
missense |
probably benign |
0.00 |
|