Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933402J07Rik |
C |
T |
8: 88,312,691 (GRCm39) |
Q159* |
probably null |
Het |
Abca12 |
C |
A |
1: 71,302,647 (GRCm39) |
V2191L |
probably benign |
Het |
Adam34 |
A |
G |
8: 44,105,538 (GRCm39) |
Y36H |
probably benign |
Het |
Adprm |
A |
G |
11: 66,929,055 (GRCm39) |
V312A |
probably benign |
Het |
Anapc2 |
T |
C |
2: 25,162,682 (GRCm39) |
L52P |
probably benign |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
Apoc4 |
T |
A |
7: 19,412,560 (GRCm39) |
T62S |
probably damaging |
Het |
Arfgef1 |
C |
T |
1: 10,270,103 (GRCm39) |
A349T |
probably benign |
Het |
Arhgap32 |
A |
G |
9: 32,027,436 (GRCm39) |
E2G |
possibly damaging |
Het |
Atg4c |
C |
A |
4: 99,109,463 (GRCm39) |
N143K |
possibly damaging |
Het |
C1qtnf12 |
A |
G |
4: 156,050,922 (GRCm39) |
N297S |
probably benign |
Het |
Cadps2 |
G |
T |
6: 23,838,998 (GRCm39) |
|
probably benign |
Het |
Ccdc63 |
C |
G |
5: 122,265,628 (GRCm39) |
A71P |
possibly damaging |
Het |
Cdca2 |
T |
C |
14: 67,952,258 (GRCm39) |
K38E |
probably damaging |
Het |
Cyp2j11 |
G |
A |
4: 96,204,595 (GRCm39) |
T317I |
probably damaging |
Het |
Dab2 |
T |
C |
15: 6,446,398 (GRCm39) |
V5A |
probably benign |
Het |
Dennd3 |
A |
T |
15: 73,426,909 (GRCm39) |
H762L |
probably benign |
Het |
Disp1 |
A |
G |
1: 182,869,936 (GRCm39) |
F828S |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,406,587 (GRCm39) |
M552V |
probably benign |
Het |
Dock2 |
A |
G |
11: 34,179,472 (GRCm39) |
|
probably null |
Het |
Dsel |
A |
T |
1: 111,787,987 (GRCm39) |
N849K |
probably benign |
Het |
Fah |
A |
T |
7: 84,244,042 (GRCm39) |
I239N |
probably damaging |
Het |
Flt4 |
T |
C |
11: 49,536,824 (GRCm39) |
Y1265H |
probably benign |
Het |
Ghdc |
T |
C |
11: 100,660,018 (GRCm39) |
E243G |
probably benign |
Het |
Glb1 |
T |
C |
9: 114,279,716 (GRCm39) |
Y375H |
probably damaging |
Het |
Gm6619 |
A |
G |
6: 131,466,021 (GRCm39) |
I40V |
probably benign |
Het |
Gpld1 |
T |
C |
13: 25,146,630 (GRCm39) |
V225A |
probably benign |
Het |
Hectd4 |
T |
C |
5: 121,391,921 (GRCm39) |
|
probably benign |
Het |
Igdcc4 |
A |
G |
9: 65,032,617 (GRCm39) |
I542V |
possibly damaging |
Het |
Igsf9b |
T |
C |
9: 27,245,633 (GRCm39) |
L1200P |
probably damaging |
Het |
Itgb7 |
C |
T |
15: 102,130,553 (GRCm39) |
V378M |
probably damaging |
Het |
Krt84 |
T |
C |
15: 101,438,019 (GRCm39) |
E312G |
possibly damaging |
Het |
Man2a2 |
A |
G |
7: 80,017,532 (GRCm39) |
W250R |
probably damaging |
Het |
Mcam |
T |
C |
9: 44,047,932 (GRCm39) |
V59A |
probably damaging |
Het |
Mfrp |
T |
C |
9: 44,015,015 (GRCm39) |
L314P |
probably benign |
Het |
Mgat5 |
T |
C |
1: 127,396,987 (GRCm39) |
V578A |
probably damaging |
Het |
Mycbp2 |
G |
A |
14: 103,393,358 (GRCm39) |
H3068Y |
probably damaging |
Het |
Myh1 |
A |
C |
11: 67,113,234 (GRCm39) |
D1873A |
probably benign |
Het |
Nek9 |
A |
G |
12: 85,376,677 (GRCm39) |
W235R |
probably damaging |
Het |
Or9g19 |
T |
C |
2: 85,600,342 (GRCm39) |
S66P |
probably damaging |
Het |
Parvb |
A |
G |
15: 84,116,369 (GRCm39) |
K33E |
possibly damaging |
Het |
Pkhd1l1 |
T |
G |
15: 44,363,378 (GRCm39) |
|
probably null |
Het |
Plekha5 |
T |
C |
6: 140,516,129 (GRCm39) |
V270A |
probably damaging |
Het |
Prr14l |
T |
C |
5: 32,988,046 (GRCm39) |
D483G |
probably benign |
Het |
Rimkla |
T |
A |
4: 119,331,779 (GRCm39) |
M140L |
possibly damaging |
Het |
Senp1 |
C |
T |
15: 97,956,196 (GRCm39) |
V408I |
possibly damaging |
Het |
Stambpl1 |
T |
A |
19: 34,204,104 (GRCm39) |
Y65N |
probably damaging |
Het |
Tada2a |
T |
C |
11: 83,970,455 (GRCm39) |
D432G |
probably damaging |
Het |
Themis |
T |
A |
10: 28,544,723 (GRCm39) |
I23N |
probably damaging |
Het |
Thnsl1 |
T |
C |
2: 21,217,344 (GRCm39) |
I366T |
probably benign |
Het |
Tmem131 |
C |
A |
1: 36,851,690 (GRCm39) |
V938L |
probably benign |
Het |
Tmem178b |
A |
T |
6: 40,184,435 (GRCm39) |
Q111L |
probably damaging |
Het |
Vmn1r195 |
C |
G |
13: 22,462,934 (GRCm39) |
L135V |
possibly damaging |
Het |
Vmn2r-ps36 |
C |
T |
7: 7,431,539 (GRCm39) |
|
noncoding transcript |
Het |
Zfp956 |
G |
A |
6: 47,940,805 (GRCm39) |
R388H |
probably damaging |
Het |
Zfr2 |
T |
G |
10: 81,077,950 (GRCm39) |
V259G |
probably benign |
Het |
|
Other mutations in Pecr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03124:Pecr
|
APN |
1 |
72,316,499 (GRCm39) |
missense |
probably benign |
0.04 |
R1556:Pecr
|
UTSW |
1 |
72,298,542 (GRCm39) |
missense |
probably benign |
|
R1711:Pecr
|
UTSW |
1 |
72,316,568 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1882:Pecr
|
UTSW |
1 |
72,314,136 (GRCm39) |
splice site |
probably null |
|
R2507:Pecr
|
UTSW |
1 |
72,301,135 (GRCm39) |
missense |
probably benign |
0.11 |
R2516:Pecr
|
UTSW |
1 |
72,316,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R3774:Pecr
|
UTSW |
1 |
72,298,530 (GRCm39) |
missense |
probably benign |
0.00 |
R3775:Pecr
|
UTSW |
1 |
72,298,530 (GRCm39) |
missense |
probably benign |
0.00 |
R3968:Pecr
|
UTSW |
1 |
72,315,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R3969:Pecr
|
UTSW |
1 |
72,315,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R3970:Pecr
|
UTSW |
1 |
72,315,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R4171:Pecr
|
UTSW |
1 |
72,315,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R4773:Pecr
|
UTSW |
1 |
72,306,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Pecr
|
UTSW |
1 |
72,316,490 (GRCm39) |
missense |
probably benign |
0.35 |
R5191:Pecr
|
UTSW |
1 |
72,314,136 (GRCm39) |
splice site |
probably null |
|
R5259:Pecr
|
UTSW |
1 |
72,316,444 (GRCm39) |
critical splice donor site |
probably null |
|
R5331:Pecr
|
UTSW |
1 |
72,314,005 (GRCm39) |
intron |
probably benign |
|
R6828:Pecr
|
UTSW |
1 |
72,306,616 (GRCm39) |
nonsense |
probably null |
|
R7238:Pecr
|
UTSW |
1 |
72,298,592 (GRCm39) |
missense |
probably damaging |
0.99 |
R7358:Pecr
|
UTSW |
1 |
72,306,624 (GRCm39) |
missense |
probably benign |
0.01 |
R7745:Pecr
|
UTSW |
1 |
72,306,157 (GRCm39) |
splice site |
probably null |
|
R7997:Pecr
|
UTSW |
1 |
72,315,475 (GRCm39) |
nonsense |
probably null |
|
R8123:Pecr
|
UTSW |
1 |
72,314,094 (GRCm39) |
missense |
probably benign |
0.16 |
R8155:Pecr
|
UTSW |
1 |
72,309,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R8399:Pecr
|
UTSW |
1 |
72,306,624 (GRCm39) |
missense |
probably benign |
0.01 |
R8702:Pecr
|
UTSW |
1 |
72,306,661 (GRCm39) |
missense |
probably benign |
0.01 |
|