Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
A |
7: 120,038,422 (GRCm39) |
L368Q |
probably damaging |
Het |
Abca2 |
T |
A |
2: 25,336,794 (GRCm39) |
|
probably null |
Het |
Ano7 |
T |
A |
1: 93,323,230 (GRCm39) |
V497D |
probably benign |
Het |
B4gat1 |
T |
C |
19: 5,090,037 (GRCm39) |
Y345H |
probably damaging |
Het |
Bckdha |
T |
A |
7: 25,358,132 (GRCm39) |
R12W |
possibly damaging |
Het |
Bcl7c |
T |
A |
7: 127,306,608 (GRCm39) |
N93Y |
probably damaging |
Het |
Cc2d2a |
C |
A |
5: 43,846,345 (GRCm39) |
T368K |
probably benign |
Het |
Chek1 |
G |
A |
9: 36,629,717 (GRCm39) |
Q210* |
probably null |
Het |
Chrdl2 |
A |
G |
7: 99,666,248 (GRCm39) |
Y56C |
probably damaging |
Het |
Cspg4 |
T |
A |
9: 56,805,872 (GRCm39) |
F2228I |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,473,205 (GRCm39) |
M3474V |
probably benign |
Het |
Dph7 |
T |
C |
2: 24,855,629 (GRCm39) |
S143P |
possibly damaging |
Het |
Ehbp1 |
T |
A |
11: 22,039,636 (GRCm39) |
K821N |
probably damaging |
Het |
Eomes |
T |
C |
9: 118,313,898 (GRCm39) |
S648P |
probably benign |
Het |
Fam20a |
A |
G |
11: 109,573,738 (GRCm39) |
V215A |
probably damaging |
Het |
Fer1l4 |
T |
A |
2: 155,862,259 (GRCm39) |
|
probably null |
Het |
Frem2 |
A |
G |
3: 53,448,459 (GRCm39) |
V2319A |
probably benign |
Het |
Gtf3c4 |
T |
C |
2: 28,723,584 (GRCm39) |
D575G |
probably benign |
Het |
Ifit1bl2 |
A |
G |
19: 34,596,404 (GRCm39) |
V404A |
probably benign |
Het |
Kcnf1 |
T |
C |
12: 17,225,349 (GRCm39) |
M291V |
probably benign |
Het |
Klra1 |
T |
A |
6: 130,341,224 (GRCm39) |
I250F |
probably benign |
Het |
Klra4 |
T |
A |
6: 130,038,985 (GRCm39) |
T136S |
probably benign |
Het |
Mcrs1 |
A |
T |
15: 99,141,266 (GRCm39) |
I399N |
probably damaging |
Het |
Neo1 |
T |
C |
9: 58,814,368 (GRCm39) |
E866G |
possibly damaging |
Het |
Notch3 |
T |
C |
17: 32,363,445 (GRCm39) |
D1206G |
probably damaging |
Het |
Or10ab4 |
A |
G |
7: 107,654,188 (GRCm39) |
|
probably benign |
Het |
Or14c43 |
T |
A |
7: 86,115,480 (GRCm39) |
I287N |
probably damaging |
Het |
Or4z4 |
A |
C |
19: 12,076,769 (GRCm39) |
V78G |
probably benign |
Het |
Or5ae1 |
T |
A |
7: 84,565,590 (GRCm39) |
V201E |
probably damaging |
Het |
Or5b95 |
A |
C |
19: 12,658,113 (GRCm39) |
I214L |
probably benign |
Het |
Pnkd |
A |
G |
1: 74,390,716 (GRCm39) |
N336D |
probably damaging |
Het |
Prag1 |
T |
C |
8: 36,571,088 (GRCm39) |
V557A |
probably benign |
Het |
Ptgfr |
A |
C |
3: 151,541,323 (GRCm39) |
S62A |
probably benign |
Het |
Smc2 |
A |
G |
4: 52,450,842 (GRCm39) |
Y220C |
probably damaging |
Het |
Sufu |
G |
A |
19: 46,439,382 (GRCm39) |
E246K |
probably damaging |
Het |
Sult2a1 |
T |
A |
7: 13,566,604 (GRCm39) |
R124* |
probably null |
Het |
Sult4a1 |
T |
A |
15: 83,970,817 (GRCm39) |
Y196F |
possibly damaging |
Het |
Trim15 |
G |
A |
17: 37,175,975 (GRCm39) |
R191W |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,773,319 (GRCm39) |
V2361A |
possibly damaging |
Het |
Usp16 |
T |
C |
16: 87,263,164 (GRCm39) |
V122A |
possibly damaging |
Het |
Vmn1r122 |
T |
A |
7: 20,868,036 (GRCm39) |
K6N |
probably benign |
Het |
Vmn1r34 |
G |
A |
6: 66,613,899 (GRCm39) |
Q280* |
probably null |
Het |
Vmn2r45 |
T |
A |
7: 8,484,332 (GRCm39) |
H491L |
possibly damaging |
Het |
Wdpcp |
T |
C |
11: 21,661,949 (GRCm39) |
L407P |
probably damaging |
Het |
Zfp157 |
T |
C |
5: 138,445,840 (GRCm39) |
I65T |
probably benign |
Het |
|
Other mutations in Or6c210 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01915:Or6c210
|
APN |
10 |
129,496,519 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02458:Or6c210
|
APN |
10 |
129,496,475 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02721:Or6c210
|
APN |
10 |
129,495,824 (GRCm39) |
missense |
probably benign |
|
R0032:Or6c210
|
UTSW |
10 |
129,496,269 (GRCm39) |
missense |
probably benign |
0.05 |
R0442:Or6c210
|
UTSW |
10 |
129,495,693 (GRCm39) |
missense |
probably benign |
0.00 |
R1564:Or6c210
|
UTSW |
10 |
129,495,884 (GRCm39) |
missense |
probably benign |
0.22 |
R1580:Or6c210
|
UTSW |
10 |
129,496,184 (GRCm39) |
missense |
probably benign |
0.10 |
R1593:Or6c210
|
UTSW |
10 |
129,496,094 (GRCm39) |
nonsense |
probably null |
|
R1911:Or6c210
|
UTSW |
10 |
129,495,981 (GRCm39) |
missense |
probably benign |
0.07 |
R2001:Or6c210
|
UTSW |
10 |
129,496,290 (GRCm39) |
missense |
probably benign |
0.02 |
R2223:Or6c210
|
UTSW |
10 |
129,495,678 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R3876:Or6c210
|
UTSW |
10 |
129,496,143 (GRCm39) |
missense |
probably benign |
0.39 |
R3884:Or6c210
|
UTSW |
10 |
129,496,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R4366:Or6c210
|
UTSW |
10 |
129,496,400 (GRCm39) |
missense |
probably benign |
0.02 |
R4689:Or6c210
|
UTSW |
10 |
129,496,185 (GRCm39) |
missense |
probably benign |
0.01 |
R4909:Or6c210
|
UTSW |
10 |
129,496,589 (GRCm39) |
missense |
probably benign |
0.01 |
R5638:Or6c210
|
UTSW |
10 |
129,495,969 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5835:Or6c210
|
UTSW |
10 |
129,495,803 (GRCm39) |
missense |
probably benign |
0.39 |
R5838:Or6c210
|
UTSW |
10 |
129,495,907 (GRCm39) |
missense |
probably benign |
0.41 |
R6150:Or6c210
|
UTSW |
10 |
129,495,803 (GRCm39) |
missense |
probably benign |
0.39 |
R6248:Or6c210
|
UTSW |
10 |
129,496,532 (GRCm39) |
missense |
probably benign |
0.39 |
R8094:Or6c210
|
UTSW |
10 |
129,495,933 (GRCm39) |
missense |
probably damaging |
0.99 |
R9013:Or6c210
|
UTSW |
10 |
129,495,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Or6c210
|
UTSW |
10 |
129,496,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R9390:Or6c210
|
UTSW |
10 |
129,495,938 (GRCm39) |
missense |
probably benign |
0.01 |
R9726:Or6c210
|
UTSW |
10 |
129,495,920 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9777:Or6c210
|
UTSW |
10 |
129,495,705 (GRCm39) |
missense |
probably benign |
0.17 |
|