Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26b |
T |
A |
8: 43,973,637 (GRCm39) |
N455I |
probably damaging |
Het |
Alg12 |
A |
G |
15: 88,695,659 (GRCm39) |
F279S |
probably damaging |
Het |
Angpt4 |
A |
G |
2: 151,776,360 (GRCm39) |
D296G |
probably damaging |
Het |
Ank1 |
T |
A |
8: 23,586,204 (GRCm39) |
S437T |
probably damaging |
Het |
Arhgef38 |
T |
A |
3: 132,843,175 (GRCm39) |
Y465F |
probably damaging |
Het |
Atp8a2 |
T |
G |
14: 59,928,986 (GRCm39) |
T1023P |
probably benign |
Het |
Cdh20 |
C |
A |
1: 109,993,430 (GRCm39) |
A295E |
probably damaging |
Het |
Cela3b |
T |
C |
4: 137,152,181 (GRCm39) |
E92G |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,356,224 (GRCm39) |
S752P |
probably benign |
Het |
Dlx2 |
T |
C |
2: 71,376,585 (GRCm39) |
H51R |
probably damaging |
Het |
Dnm2 |
T |
C |
9: 21,415,874 (GRCm39) |
I736T |
probably damaging |
Het |
Dst |
A |
G |
1: 34,202,427 (GRCm39) |
T252A |
possibly damaging |
Het |
Fbxo40 |
T |
C |
16: 36,790,658 (GRCm39) |
R151G |
possibly damaging |
Het |
Gapdhs |
C |
T |
7: 30,431,410 (GRCm39) |
A357T |
probably benign |
Het |
Gon4l |
T |
A |
3: 88,807,319 (GRCm39) |
M1671K |
probably benign |
Het |
Gpi1 |
T |
C |
7: 33,907,113 (GRCm39) |
Y327C |
probably damaging |
Het |
Gucy2g |
T |
C |
19: 55,214,503 (GRCm39) |
R542G |
probably benign |
Het |
Hectd3 |
A |
G |
4: 116,854,361 (GRCm39) |
K308E |
possibly damaging |
Het |
Hip1 |
A |
G |
5: 135,478,675 (GRCm39) |
F178S |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,232,401 (GRCm39) |
D1640G |
probably damaging |
Het |
Il18r1 |
G |
A |
1: 40,520,227 (GRCm39) |
|
probably null |
Het |
Kdm3b |
T |
C |
18: 34,910,250 (GRCm39) |
S23P |
possibly damaging |
Het |
Lactb |
T |
C |
9: 66,882,426 (GRCm39) |
E83G |
probably benign |
Het |
Larp4 |
A |
T |
15: 99,903,171 (GRCm39) |
D414V |
probably damaging |
Het |
Map2k5 |
T |
C |
9: 63,164,296 (GRCm39) |
H336R |
probably benign |
Het |
Mast4 |
T |
C |
13: 102,887,071 (GRCm39) |
E1006G |
probably damaging |
Het |
Mbd5 |
T |
C |
2: 49,146,467 (GRCm39) |
S226P |
probably damaging |
Het |
Micall1 |
A |
T |
15: 79,007,034 (GRCm39) |
|
probably benign |
Het |
Mtpap |
T |
A |
18: 4,375,827 (GRCm39) |
|
probably benign |
Het |
Or52ae7 |
A |
T |
7: 103,119,488 (GRCm39) |
K81* |
probably null |
Het |
Or5p58 |
A |
G |
7: 107,694,522 (GRCm39) |
L85P |
probably damaging |
Het |
Pnrc1 |
G |
A |
4: 33,246,072 (GRCm39) |
Q296* |
probably null |
Het |
Poc1a |
G |
T |
9: 106,227,012 (GRCm39) |
|
probably benign |
Het |
Pramel28 |
A |
G |
4: 143,691,565 (GRCm39) |
V386A |
probably damaging |
Het |
Prkcsh |
T |
A |
9: 21,924,046 (GRCm39) |
L439Q |
probably damaging |
Het |
Prkdc |
T |
C |
16: 15,655,882 (GRCm39) |
L3970P |
probably damaging |
Het |
Ptcd1 |
G |
A |
5: 145,089,034 (GRCm39) |
P542L |
probably benign |
Het |
Rps6ka5 |
G |
A |
12: 100,520,634 (GRCm39) |
T631I |
probably damaging |
Het |
Rxfp1 |
T |
C |
3: 79,570,619 (GRCm39) |
N271S |
probably benign |
Het |
Taf6 |
A |
G |
5: 138,177,709 (GRCm39) |
M541T |
probably benign |
Het |
Tek |
T |
A |
4: 94,692,551 (GRCm39) |
C169S |
probably benign |
Het |
Tgfbr3l |
T |
A |
8: 4,299,343 (GRCm39) |
|
probably null |
Het |
Trpv3 |
A |
G |
11: 73,186,149 (GRCm39) |
N647D |
probably benign |
Het |
Ube3c |
A |
G |
5: 29,836,293 (GRCm39) |
K638R |
probably null |
Het |
Vmn1r191 |
G |
A |
13: 22,363,163 (GRCm39) |
A197V |
probably damaging |
Het |
Vmn2r6 |
T |
C |
3: 64,445,044 (GRCm39) |
T894A |
possibly damaging |
Het |
Vstm4 |
T |
G |
14: 32,585,687 (GRCm39) |
Y85D |
probably damaging |
Het |
Wnt7a |
A |
G |
6: 91,371,482 (GRCm39) |
I160T |
probably benign |
Het |
Zc3h7a |
TAGAGAG |
TAGAGAGAG |
16: 10,978,985 (GRCm39) |
|
probably null |
Het |
Zfp988 |
A |
T |
4: 147,416,372 (GRCm39) |
K269* |
probably null |
Het |
|
Other mutations in Apol7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01015:Apol7a
|
APN |
15 |
77,274,055 (GRCm39) |
unclassified |
probably benign |
|
IGL01408:Apol7a
|
APN |
15 |
77,273,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01702:Apol7a
|
APN |
15 |
77,273,886 (GRCm39) |
splice site |
probably null |
|
IGL02215:Apol7a
|
APN |
15 |
77,277,690 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02931:Apol7a
|
APN |
15 |
77,277,650 (GRCm39) |
nonsense |
probably null |
|
R0610:Apol7a
|
UTSW |
15 |
77,273,454 (GRCm39) |
missense |
probably benign |
0.06 |
R0652:Apol7a
|
UTSW |
15 |
77,274,055 (GRCm39) |
unclassified |
probably benign |
|
R1616:Apol7a
|
UTSW |
15 |
77,273,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R1756:Apol7a
|
UTSW |
15 |
77,277,671 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3034:Apol7a
|
UTSW |
15 |
77,273,923 (GRCm39) |
missense |
probably benign |
0.03 |
R4566:Apol7a
|
UTSW |
15 |
77,273,951 (GRCm39) |
nonsense |
probably null |
|
R6807:Apol7a
|
UTSW |
15 |
77,277,520 (GRCm39) |
splice site |
probably null |
|
R6995:Apol7a
|
UTSW |
15 |
77,274,176 (GRCm39) |
unclassified |
probably benign |
|
R7824:Apol7a
|
UTSW |
15 |
77,273,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R8364:Apol7a
|
UTSW |
15 |
77,273,820 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8375:Apol7a
|
UTSW |
15 |
77,273,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R9396:Apol7a
|
UTSW |
15 |
77,273,925 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9471:Apol7a
|
UTSW |
15 |
77,273,680 (GRCm39) |
missense |
possibly damaging |
0.95 |
|