Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
T |
5: 77,030,902 (GRCm39) |
L566Q |
probably damaging |
Het |
Apbb1ip |
C |
T |
2: 22,764,972 (GRCm39) |
T551I |
probably benign |
Het |
Aqp5 |
A |
G |
15: 99,492,143 (GRCm39) |
E247G |
probably damaging |
Het |
Bdkrb1 |
T |
C |
12: 105,571,352 (GRCm39) |
F306S |
probably damaging |
Het |
Clca3a1 |
C |
T |
3: 144,465,021 (GRCm39) |
V71I |
probably benign |
Het |
Cog4 |
A |
G |
8: 111,577,994 (GRCm39) |
D36G |
probably damaging |
Het |
Ctbp1 |
A |
G |
5: 33,426,915 (GRCm39) |
|
probably benign |
Het |
Dync1li2 |
C |
T |
8: 105,169,396 (GRCm39) |
G13D |
probably benign |
Het |
F5 |
T |
C |
1: 164,022,037 (GRCm39) |
V1504A |
probably benign |
Het |
Fancm |
T |
C |
12: 65,144,203 (GRCm39) |
L555P |
probably damaging |
Het |
Fgfr2 |
A |
T |
7: 129,802,853 (GRCm39) |
S152T |
probably benign |
Het |
Fign |
A |
T |
2: 63,810,639 (GRCm39) |
H210Q |
possibly damaging |
Het |
Hbs1l |
A |
G |
10: 21,180,516 (GRCm39) |
N66S |
probably benign |
Het |
Ighv12-3 |
A |
T |
12: 114,330,435 (GRCm39) |
M20K |
probably benign |
Het |
Isoc2b |
T |
C |
7: 4,854,454 (GRCm39) |
K26E |
probably damaging |
Het |
Katnal1 |
C |
T |
5: 148,813,016 (GRCm39) |
A467T |
probably benign |
Het |
Loxl3 |
A |
G |
6: 83,025,147 (GRCm39) |
T292A |
probably benign |
Het |
Map3k9 |
A |
G |
12: 81,769,028 (GRCm39) |
S1007P |
possibly damaging |
Het |
Metrnl |
A |
C |
11: 121,593,704 (GRCm39) |
|
probably null |
Het |
Midn |
A |
G |
10: 79,992,418 (GRCm39) |
D490G |
probably damaging |
Het |
Mmp10 |
G |
A |
9: 7,506,513 (GRCm39) |
A330T |
probably benign |
Het |
Mto1 |
T |
A |
9: 78,364,510 (GRCm39) |
C281S |
possibly damaging |
Het |
Nek10 |
A |
G |
14: 14,999,108 (GRCm38) |
I1036V |
probably benign |
Het |
Odad1 |
G |
T |
7: 45,597,814 (GRCm39) |
A575S |
probably benign |
Het |
Or13c7c |
A |
C |
4: 43,835,686 (GRCm39) |
L268R |
probably benign |
Het |
Or1ab2 |
T |
C |
8: 72,863,715 (GRCm39) |
F102L |
probably damaging |
Het |
Or2b7 |
T |
C |
13: 21,739,677 (GRCm39) |
T172A |
probably damaging |
Het |
Or8b48 |
C |
A |
9: 38,450,733 (GRCm39) |
L181I |
probably benign |
Het |
Parp4 |
A |
C |
14: 56,885,339 (GRCm39) |
I1473L |
unknown |
Het |
Pcdhb9 |
A |
G |
18: 37,534,642 (GRCm39) |
Y212C |
probably damaging |
Het |
Pilra |
G |
T |
5: 137,820,237 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
A |
G |
1: 20,655,927 (GRCm39) |
I202T |
probably benign |
Het |
Ppfia2 |
A |
T |
10: 106,671,586 (GRCm39) |
E432D |
probably damaging |
Het |
Prom1 |
T |
C |
5: 44,194,851 (GRCm39) |
D298G |
possibly damaging |
Het |
Prr22 |
T |
A |
17: 57,077,527 (GRCm39) |
|
probably null |
Het |
Septin2 |
T |
A |
1: 93,425,188 (GRCm39) |
|
probably null |
Het |
Setdb1 |
C |
A |
3: 95,247,618 (GRCm39) |
V426L |
probably damaging |
Het |
Slc8b1 |
C |
T |
5: 120,667,582 (GRCm39) |
A405V |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,068,237 (GRCm39) |
R279* |
probably null |
Het |
Ssh2 |
C |
G |
11: 77,340,976 (GRCm39) |
D709E |
possibly damaging |
Het |
Tmprss9 |
A |
G |
10: 80,724,389 (GRCm39) |
D373G |
probably damaging |
Het |
Trpm3 |
T |
C |
19: 22,903,477 (GRCm39) |
L921S |
probably benign |
Het |
Ubqln3 |
T |
C |
7: 103,790,824 (GRCm39) |
N422S |
probably benign |
Het |
Vmn2r105 |
C |
T |
17: 20,448,803 (GRCm39) |
V125I |
probably benign |
Het |
Vmn2r69 |
A |
T |
7: 85,060,413 (GRCm39) |
Y390* |
probably null |
Het |
Zcwpw1 |
T |
C |
5: 137,810,282 (GRCm39) |
F353L |
probably damaging |
Het |
Zfp462 |
G |
A |
4: 55,023,433 (GRCm39) |
C987Y |
probably damaging |
Het |
Zkscan4 |
A |
G |
13: 21,668,508 (GRCm39) |
S320G |
probably damaging |
Het |
|
Other mutations in Mcur1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02428:Mcur1
|
APN |
13 |
43,695,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:Mcur1
|
UTSW |
13 |
43,699,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R0701:Mcur1
|
UTSW |
13 |
43,699,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R1085:Mcur1
|
UTSW |
13 |
43,708,480 (GRCm39) |
missense |
unknown |
|
R1793:Mcur1
|
UTSW |
13 |
43,713,491 (GRCm39) |
missense |
unknown |
|
R2418:Mcur1
|
UTSW |
13 |
43,703,013 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2419:Mcur1
|
UTSW |
13 |
43,703,013 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2508:Mcur1
|
UTSW |
13 |
43,697,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R4535:Mcur1
|
UTSW |
13 |
43,698,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R4817:Mcur1
|
UTSW |
13 |
43,705,147 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7137:Mcur1
|
UTSW |
13 |
43,697,931 (GRCm39) |
critical splice donor site |
probably null |
|
R7177:Mcur1
|
UTSW |
13 |
43,698,012 (GRCm39) |
missense |
probably damaging |
0.98 |
R7589:Mcur1
|
UTSW |
13 |
43,705,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Mcur1
|
UTSW |
13 |
43,697,959 (GRCm39) |
nonsense |
probably null |
|
R7859:Mcur1
|
UTSW |
13 |
43,713,485 (GRCm39) |
nonsense |
probably null |
|
R8686:Mcur1
|
UTSW |
13 |
43,695,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9572:Mcur1
|
UTSW |
13 |
43,713,433 (GRCm39) |
missense |
probably benign |
0.23 |
|