Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921513I03Rik |
G |
A |
10: 120,614,635 (GRCm39) |
|
probably benign |
Het |
Adcy10 |
T |
C |
1: 165,400,112 (GRCm39) |
V1507A |
probably damaging |
Het |
Ap3b2 |
T |
A |
7: 81,110,746 (GRCm39) |
M1010L |
unknown |
Het |
Bmp10 |
T |
C |
6: 87,411,130 (GRCm39) |
S308P |
probably benign |
Het |
Cnih3 |
C |
A |
1: 181,282,274 (GRCm39) |
Y169* |
probably null |
Het |
Cpsf4l |
A |
G |
11: 113,590,685 (GRCm39) |
S222P |
possibly damaging |
Het |
Cyp2d10 |
G |
A |
15: 82,288,808 (GRCm39) |
|
probably benign |
Het |
Dcstamp |
A |
T |
15: 39,617,928 (GRCm39) |
E112D |
probably damaging |
Het |
Fras1 |
C |
T |
5: 96,929,496 (GRCm39) |
Q3967* |
probably null |
Het |
Gcm1 |
C |
A |
9: 77,972,121 (GRCm39) |
P354H |
possibly damaging |
Het |
Gen1 |
A |
G |
12: 11,291,867 (GRCm39) |
S706P |
probably benign |
Het |
Glb1l3 |
G |
T |
9: 26,736,466 (GRCm39) |
T532N |
probably benign |
Het |
Gm5069 |
T |
A |
1: 180,154,872 (GRCm39) |
|
probably benign |
Het |
Gzmc |
A |
C |
14: 56,471,422 (GRCm39) |
F40V |
probably benign |
Het |
Itgb2 |
G |
T |
10: 77,385,895 (GRCm39) |
C286F |
probably damaging |
Het |
Jak3 |
A |
G |
8: 72,131,124 (GRCm39) |
Y48C |
probably damaging |
Het |
Lrp2 |
G |
A |
2: 69,367,960 (GRCm39) |
S184L |
probably benign |
Het |
Myo1f |
T |
A |
17: 33,798,945 (GRCm39) |
N203K |
probably benign |
Het |
Nrxn2 |
G |
A |
19: 6,522,306 (GRCm39) |
G182R |
probably damaging |
Het |
Or4k15c |
T |
C |
14: 50,321,943 (GRCm39) |
N65S |
probably damaging |
Het |
Or4p8 |
A |
G |
2: 88,727,503 (GRCm39) |
V146A |
probably benign |
Het |
Or5g23 |
A |
C |
2: 85,438,664 (GRCm39) |
L197V |
probably benign |
Het |
Otog |
C |
T |
7: 45,954,903 (GRCm39) |
S2692L |
probably damaging |
Het |
Pde9a |
C |
T |
17: 31,672,444 (GRCm39) |
T34I |
probably benign |
Het |
Phip |
T |
C |
9: 82,763,394 (GRCm39) |
T1295A |
possibly damaging |
Het |
Pik3cb |
A |
G |
9: 98,953,430 (GRCm39) |
V451A |
probably benign |
Het |
Psd2 |
T |
G |
18: 36,137,809 (GRCm39) |
|
probably benign |
Het |
Pycr2 |
T |
C |
1: 180,733,762 (GRCm39) |
I118T |
probably damaging |
Het |
Rnf17 |
T |
G |
14: 56,658,623 (GRCm39) |
M104R |
probably benign |
Het |
Rp1l1 |
T |
C |
14: 64,266,259 (GRCm39) |
V615A |
probably benign |
Het |
Sel1l3 |
T |
A |
5: 53,327,747 (GRCm39) |
R511W |
possibly damaging |
Het |
Sis |
T |
C |
3: 72,854,804 (GRCm39) |
N478D |
probably benign |
Het |
Trps1 |
T |
A |
15: 50,685,674 (GRCm39) |
S584C |
probably damaging |
Het |
Vmn2r124 |
T |
C |
17: 18,284,491 (GRCm39) |
|
probably benign |
Het |
Vmn2r9 |
G |
A |
5: 108,991,502 (GRCm39) |
L620F |
probably damaging |
Het |
Zc3h13 |
T |
C |
14: 75,567,787 (GRCm39) |
S1027P |
probably benign |
Het |
Zfp644 |
A |
T |
5: 106,783,760 (GRCm39) |
I929K |
probably benign |
Het |
|
Other mutations in 4930432E11Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01121:4930432E11Rik
|
APN |
7 |
29,273,426 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL01955:4930432E11Rik
|
APN |
7 |
29,273,420 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL01971:4930432E11Rik
|
APN |
7 |
29,273,987 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02484:4930432E11Rik
|
APN |
7 |
29,262,777 (GRCm39) |
unclassified |
noncoding transcript |
|
P0016:4930432E11Rik
|
UTSW |
7 |
29,262,537 (GRCm39) |
unclassified |
noncoding transcript |
|
R0051:4930432E11Rik
|
UTSW |
7 |
29,278,526 (GRCm39) |
exon |
noncoding transcript |
|
R0060:4930432E11Rik
|
UTSW |
7 |
29,273,595 (GRCm39) |
unclassified |
noncoding transcript |
|
R0094:4930432E11Rik
|
UTSW |
7 |
29,260,236 (GRCm39) |
exon |
noncoding transcript |
|
R0268:4930432E11Rik
|
UTSW |
7 |
29,274,027 (GRCm39) |
unclassified |
noncoding transcript |
|
R0423:4930432E11Rik
|
UTSW |
7 |
29,261,825 (GRCm39) |
exon |
noncoding transcript |
|
R0478:4930432E11Rik
|
UTSW |
7 |
29,262,014 (GRCm39) |
exon |
noncoding transcript |
|
R0646:4930432E11Rik
|
UTSW |
7 |
29,260,710 (GRCm39) |
exon |
noncoding transcript |
|
R1208:4930432E11Rik
|
UTSW |
7 |
29,260,708 (GRCm39) |
exon |
noncoding transcript |
|
R1778:4930432E11Rik
|
UTSW |
7 |
29,260,131 (GRCm39) |
exon |
noncoding transcript |
|
R1779:4930432E11Rik
|
UTSW |
7 |
29,278,591 (GRCm39) |
exon |
noncoding transcript |
|
R1918:4930432E11Rik
|
UTSW |
7 |
29,273,514 (GRCm39) |
unclassified |
noncoding transcript |
|
R2360:4930432E11Rik
|
UTSW |
7 |
29,274,214 (GRCm39) |
unclassified |
noncoding transcript |
|
R3736:4930432E11Rik
|
UTSW |
7 |
29,273,996 (GRCm39) |
unclassified |
noncoding transcript |
|
R3780:4930432E11Rik
|
UTSW |
7 |
29,260,263 (GRCm39) |
exon |
noncoding transcript |
|
R4427:4930432E11Rik
|
UTSW |
7 |
29,278,678 (GRCm39) |
exon |
noncoding transcript |
|
R4835:4930432E11Rik
|
UTSW |
7 |
29,274,326 (GRCm39) |
unclassified |
noncoding transcript |
|
R4929:4930432E11Rik
|
UTSW |
7 |
29,273,467 (GRCm39) |
unclassified |
noncoding transcript |
|
R5042:4930432E11Rik
|
UTSW |
7 |
29,273,927 (GRCm39) |
unclassified |
noncoding transcript |
|
R5129:4930432E11Rik
|
UTSW |
7 |
29,260,786 (GRCm39) |
exon |
noncoding transcript |
|
R5371:4930432E11Rik
|
UTSW |
7 |
29,261,918 (GRCm39) |
exon |
noncoding transcript |
|
R5381:4930432E11Rik
|
UTSW |
7 |
29,262,393 (GRCm39) |
unclassified |
noncoding transcript |
|
R5586:4930432E11Rik
|
UTSW |
7 |
29,277,153 (GRCm39) |
unclassified |
noncoding transcript |
|
R5874:4930432E11Rik
|
UTSW |
7 |
29,280,610 (GRCm39) |
exon |
noncoding transcript |
|
|