Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930596D02Rik |
C |
T |
14: 35,532,170 (GRCm39) |
C135Y |
possibly damaging |
Het |
Afdn |
T |
A |
17: 14,072,575 (GRCm39) |
|
probably benign |
Het |
Akap10 |
A |
G |
11: 61,795,622 (GRCm39) |
V347A |
possibly damaging |
Het |
Ankrd11 |
A |
G |
8: 123,622,092 (GRCm39) |
S587P |
probably damaging |
Het |
Ces1g |
T |
C |
8: 94,029,660 (GRCm39) |
Y524C |
probably damaging |
Het |
Cimip2b |
A |
G |
4: 43,428,377 (GRCm39) |
L51P |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,283,219 (GRCm39) |
N3573S |
possibly damaging |
Het |
Cyp1a1 |
G |
T |
9: 57,607,990 (GRCm39) |
C206F |
probably damaging |
Het |
Fbxo30 |
T |
C |
10: 11,166,042 (GRCm39) |
Y255H |
probably benign |
Het |
Ggnbp2 |
T |
C |
11: 84,731,230 (GRCm39) |
I295V |
possibly damaging |
Het |
Gpatch8 |
A |
G |
11: 102,370,743 (GRCm39) |
Y932H |
unknown |
Het |
Heatr6 |
C |
T |
11: 83,650,135 (GRCm39) |
P197L |
probably damaging |
Het |
Helb |
T |
C |
10: 119,930,168 (GRCm39) |
D737G |
possibly damaging |
Het |
Helz |
A |
T |
11: 107,554,479 (GRCm39) |
I1226F |
possibly damaging |
Het |
Ipo11 |
A |
T |
13: 106,993,277 (GRCm39) |
I749N |
probably damaging |
Het |
Ipo13 |
T |
C |
4: 117,771,564 (GRCm39) |
E2G |
possibly damaging |
Het |
Jam3 |
A |
C |
9: 27,013,188 (GRCm39) |
D127E |
probably damaging |
Het |
Kif16b |
G |
T |
2: 142,553,664 (GRCm39) |
Q1045K |
probably benign |
Het |
Kin |
T |
C |
2: 10,095,159 (GRCm39) |
W121R |
possibly damaging |
Het |
Man1b1 |
T |
G |
2: 25,233,337 (GRCm39) |
S237A |
possibly damaging |
Het |
Mmel1 |
C |
T |
4: 154,972,289 (GRCm39) |
|
probably benign |
Het |
Morn4 |
T |
C |
19: 42,064,559 (GRCm39) |
N143S |
possibly damaging |
Het |
Nlrp4b |
A |
G |
7: 10,448,882 (GRCm39) |
T362A |
possibly damaging |
Het |
Ntpcr |
C |
T |
8: 126,474,501 (GRCm39) |
T153M |
probably damaging |
Het |
Or13p10 |
T |
A |
4: 118,523,475 (GRCm39) |
F254I |
probably damaging |
Het |
Pdzd2 |
A |
G |
15: 12,374,804 (GRCm39) |
L1777P |
probably benign |
Het |
Postn |
A |
G |
3: 54,276,697 (GRCm39) |
N192S |
possibly damaging |
Het |
Prkar1a |
A |
T |
11: 109,551,877 (GRCm39) |
Y122F |
probably benign |
Het |
Serpinb7 |
A |
G |
1: 107,355,976 (GRCm39) |
|
probably benign |
Het |
Setd3 |
A |
T |
12: 108,126,496 (GRCm39) |
I121N |
probably damaging |
Het |
Slamf7 |
T |
A |
1: 171,466,810 (GRCm39) |
I132L |
probably benign |
Het |
Syt4 |
T |
C |
18: 31,580,227 (GRCm39) |
|
probably benign |
Het |
Tesc |
G |
A |
5: 118,194,504 (GRCm39) |
|
probably null |
Het |
Tsc1 |
C |
A |
2: 28,560,952 (GRCm39) |
S270* |
probably null |
Het |
Wap |
C |
A |
11: 6,586,808 (GRCm39) |
C97F |
probably damaging |
Het |
Zfp451 |
A |
G |
1: 33,822,234 (GRCm39) |
S155P |
probably benign |
Het |
Zfp469 |
A |
G |
8: 122,996,472 (GRCm39) |
|
probably benign |
Het |
Zfp51 |
C |
T |
17: 21,683,844 (GRCm39) |
T153M |
probably benign |
Het |
Zfp579 |
A |
G |
7: 4,996,390 (GRCm39) |
I507T |
probably damaging |
Het |
|
Other mutations in Gvin-ps3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01125:Gvin-ps3
|
APN |
7 |
105,682,021 (GRCm39) |
missense |
unknown |
0.00 |
IGL01392:Gvin-ps3
|
APN |
7 |
105,682,962 (GRCm39) |
missense |
probably benign |
0.01 |
R1184:Gvin-ps3
|
UTSW |
7 |
105,683,159 (GRCm39) |
missense |
probably benign |
0.03 |
R1411:Gvin-ps3
|
UTSW |
7 |
105,682,686 (GRCm39) |
missense |
probably benign |
0.39 |
R2198:Gvin-ps3
|
UTSW |
7 |
105,682,758 (GRCm39) |
missense |
probably benign |
0.00 |
R2311:Gvin-ps3
|
UTSW |
7 |
105,682,797 (GRCm39) |
missense |
probably damaging |
0.99 |
R2380:Gvin-ps3
|
UTSW |
7 |
105,681,374 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3825:Gvin-ps3
|
UTSW |
7 |
105,682,780 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4397:Gvin-ps3
|
UTSW |
7 |
105,682,130 (GRCm39) |
exon |
noncoding transcript |
|
R4693:Gvin-ps3
|
UTSW |
7 |
105,681,585 (GRCm39) |
exon |
noncoding transcript |
|
R4787:Gvin-ps3
|
UTSW |
7 |
105,681,041 (GRCm39) |
exon |
noncoding transcript |
|
R4840:Gvin-ps3
|
UTSW |
7 |
105,680,627 (GRCm39) |
exon |
noncoding transcript |
|
R4972:Gvin-ps3
|
UTSW |
7 |
105,682,521 (GRCm39) |
exon |
noncoding transcript |
|
R5221:Gvin-ps3
|
UTSW |
7 |
105,683,181 (GRCm39) |
exon |
noncoding transcript |
|
R5296:Gvin-ps3
|
UTSW |
7 |
105,681,055 (GRCm39) |
exon |
noncoding transcript |
|
|