Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
T |
A |
4: 103,099,978 (GRCm39) |
N74I |
probably benign |
Het |
Abr |
T |
C |
11: 76,369,990 (GRCm39) |
K75R |
probably damaging |
Het |
Adcy10 |
A |
C |
1: 165,347,087 (GRCm39) |
D368A |
possibly damaging |
Het |
Alas1 |
A |
G |
9: 106,118,309 (GRCm39) |
|
probably benign |
Het |
Alms1 |
T |
A |
6: 85,576,949 (GRCm39) |
D168E |
probably benign |
Het |
Ankar |
C |
T |
1: 72,729,444 (GRCm39) |
A82T |
possibly damaging |
Het |
Atp2c2 |
C |
T |
8: 120,457,013 (GRCm39) |
T205I |
probably benign |
Het |
Atp9a |
A |
T |
2: 168,494,588 (GRCm39) |
L639Q |
probably damaging |
Het |
Btf3l4 |
T |
C |
4: 108,675,411 (GRCm39) |
D134G |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,007,257 (GRCm39) |
C425R |
probably damaging |
Het |
Cct6b |
G |
T |
11: 82,627,271 (GRCm39) |
T322N |
probably damaging |
Het |
Col19a1 |
G |
A |
1: 24,573,197 (GRCm39) |
R192* |
probably null |
Het |
Cyp8b1 |
A |
T |
9: 121,744,801 (GRCm39) |
F177Y |
probably damaging |
Het |
Dnajc11 |
T |
A |
4: 152,063,941 (GRCm39) |
N474K |
probably benign |
Het |
Dusp16 |
T |
C |
6: 134,737,999 (GRCm39) |
E13G |
probably damaging |
Het |
Ephx2 |
T |
C |
14: 66,323,741 (GRCm39) |
N397S |
probably damaging |
Het |
Fancm |
T |
C |
12: 65,122,913 (GRCm39) |
V145A |
possibly damaging |
Het |
Fiz1 |
A |
G |
7: 5,012,158 (GRCm39) |
L120P |
possibly damaging |
Het |
Galnt6 |
C |
T |
15: 100,612,100 (GRCm39) |
V181M |
probably damaging |
Het |
Gja10 |
T |
G |
4: 32,601,509 (GRCm39) |
I292L |
probably benign |
Het |
Gnb3 |
T |
C |
6: 124,814,378 (GRCm39) |
S136G |
probably benign |
Het |
Gramd1a |
A |
T |
7: 30,833,940 (GRCm39) |
V495E |
probably damaging |
Het |
Il1rn |
G |
T |
2: 24,235,462 (GRCm39) |
|
probably benign |
Het |
Itpr3 |
A |
G |
17: 27,333,486 (GRCm39) |
|
probably benign |
Het |
Kctd1 |
A |
G |
18: 15,195,937 (GRCm39) |
S229P |
possibly damaging |
Het |
Kdm4a |
T |
C |
4: 118,017,486 (GRCm39) |
T527A |
probably benign |
Het |
Kif14 |
C |
T |
1: 136,424,331 (GRCm39) |
A982V |
probably damaging |
Het |
Klf6 |
A |
G |
13: 5,916,734 (GRCm39) |
K293R |
probably damaging |
Het |
Letmd1 |
A |
G |
15: 100,372,972 (GRCm39) |
D92G |
probably damaging |
Het |
Lmod1 |
G |
A |
1: 135,292,218 (GRCm39) |
V358M |
probably benign |
Het |
Ndufs1 |
A |
T |
1: 63,199,011 (GRCm39) |
D295E |
probably damaging |
Het |
Nek4 |
A |
G |
14: 30,685,916 (GRCm39) |
N283S |
probably benign |
Het |
Nhsl1 |
A |
G |
10: 18,387,385 (GRCm39) |
T220A |
probably damaging |
Het |
Nucks1 |
T |
A |
1: 131,852,363 (GRCm39) |
D71E |
probably damaging |
Het |
Or4n4 |
T |
C |
14: 50,519,530 (GRCm39) |
Y60C |
probably damaging |
Het |
Or8g18 |
C |
A |
9: 39,149,490 (GRCm39) |
V77F |
probably damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,452,852 (GRCm39) |
T3926A |
probably benign |
Het |
Pptc7 |
T |
A |
5: 122,451,651 (GRCm39) |
|
probably benign |
Het |
Prdm11 |
A |
G |
2: 92,805,948 (GRCm39) |
V334A |
probably benign |
Het |
Ptdss2 |
C |
A |
7: 140,732,911 (GRCm39) |
C231* |
probably null |
Het |
R3hdm1 |
C |
T |
1: 128,118,456 (GRCm39) |
P570S |
probably benign |
Het |
Rlbp1 |
T |
C |
7: 79,027,037 (GRCm39) |
T208A |
possibly damaging |
Het |
Rnaseh2a |
T |
G |
8: 85,686,723 (GRCm39) |
D142A |
probably damaging |
Het |
Rufy4 |
C |
T |
1: 74,172,509 (GRCm39) |
|
probably benign |
Het |
Tektl1 |
A |
G |
10: 78,584,300 (GRCm39) |
Y372H |
probably benign |
Het |
Tlcd4 |
G |
T |
3: 121,022,013 (GRCm39) |
D128E |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,646,565 (GRCm39) |
I11081T |
possibly damaging |
Het |
Ubap2l |
A |
T |
3: 89,945,735 (GRCm39) |
S173R |
probably damaging |
Het |
Vmn1r80 |
A |
G |
7: 11,926,959 (GRCm39) |
N23S |
probably damaging |
Het |
Vwce |
C |
A |
19: 10,632,712 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ginm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Ginm1
|
APN |
10 |
7,668,460 (GRCm39) |
unclassified |
probably benign |
|
IGL02474:Ginm1
|
APN |
10 |
7,653,532 (GRCm39) |
splice site |
probably benign |
|
Juniper
|
UTSW |
10 |
7,655,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Ginm1
|
UTSW |
10 |
7,651,138 (GRCm39) |
splice site |
probably benign |
|
R0010:Ginm1
|
UTSW |
10 |
7,651,138 (GRCm39) |
splice site |
probably benign |
|
R0052:Ginm1
|
UTSW |
10 |
7,655,070 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0052:Ginm1
|
UTSW |
10 |
7,655,070 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1901:Ginm1
|
UTSW |
10 |
7,650,980 (GRCm39) |
critical splice donor site |
probably null |
|
R2106:Ginm1
|
UTSW |
10 |
7,651,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5374:Ginm1
|
UTSW |
10 |
7,655,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R5929:Ginm1
|
UTSW |
10 |
7,649,814 (GRCm39) |
missense |
probably benign |
0.16 |
R6062:Ginm1
|
UTSW |
10 |
7,651,097 (GRCm39) |
missense |
probably benign |
0.00 |
R6102:Ginm1
|
UTSW |
10 |
7,644,260 (GRCm39) |
missense |
probably benign |
0.00 |
R6792:Ginm1
|
UTSW |
10 |
7,649,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Ginm1
|
UTSW |
10 |
7,653,614 (GRCm39) |
nonsense |
probably null |
|
R7417:Ginm1
|
UTSW |
10 |
7,649,844 (GRCm39) |
missense |
probably damaging |
0.99 |
R7663:Ginm1
|
UTSW |
10 |
7,651,126 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7757:Ginm1
|
UTSW |
10 |
7,655,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Ginm1
|
UTSW |
10 |
7,668,419 (GRCm39) |
missense |
unknown |
|
R8437:Ginm1
|
UTSW |
10 |
7,646,130 (GRCm39) |
missense |
probably benign |
|
R9004:Ginm1
|
UTSW |
10 |
7,651,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R9239:Ginm1
|
UTSW |
10 |
7,649,825 (GRCm39) |
missense |
possibly damaging |
0.93 |
|