Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
T |
A |
19: 8,989,441 (GRCm39) |
V3575E |
probably damaging |
Het |
Arfgef3 |
G |
A |
10: 18,537,140 (GRCm39) |
|
probably benign |
Het |
Arhgap23 |
A |
G |
11: 97,345,123 (GRCm39) |
T631A |
probably benign |
Het |
Chka |
T |
A |
19: 3,942,112 (GRCm39) |
H355Q |
possibly damaging |
Het |
Ctsj |
C |
T |
13: 61,149,214 (GRCm39) |
A277T |
probably damaging |
Het |
Ddx49 |
T |
C |
8: 70,753,668 (GRCm39) |
D67G |
probably damaging |
Het |
Dennd4b |
T |
C |
3: 90,180,284 (GRCm39) |
S716P |
probably benign |
Het |
Enpp5 |
G |
T |
17: 44,393,766 (GRCm39) |
D321Y |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,205,253 (GRCm39) |
E17G |
probably benign |
Het |
Fam161b |
G |
A |
12: 84,400,688 (GRCm39) |
P428L |
probably benign |
Het |
Fbxw7 |
T |
C |
3: 84,872,586 (GRCm39) |
L256S |
probably damaging |
Het |
Fgfr2 |
G |
T |
7: 129,830,525 (GRCm39) |
|
probably null |
Het |
Foxred2 |
C |
T |
15: 77,831,362 (GRCm39) |
V484I |
probably benign |
Het |
Gm4744 |
T |
A |
6: 40,927,403 (GRCm39) |
|
probably benign |
Het |
H3c1 |
C |
T |
13: 23,946,231 (GRCm39) |
V36M |
probably benign |
Het |
Hipk2 |
T |
C |
6: 38,795,456 (GRCm39) |
N271S |
possibly damaging |
Het |
Ifna1 |
A |
G |
4: 88,768,496 (GRCm39) |
D58G |
possibly damaging |
Het |
Igkv4-80 |
A |
T |
6: 68,993,680 (GRCm39) |
Y70* |
probably null |
Het |
Ivns1abp |
G |
A |
1: 151,235,386 (GRCm39) |
R218H |
probably damaging |
Het |
Kng1 |
A |
T |
16: 22,898,595 (GRCm39) |
|
probably benign |
Het |
Lars1 |
T |
C |
18: 42,390,234 (GRCm39) |
D11G |
probably damaging |
Het |
Lgals12 |
T |
C |
19: 7,578,607 (GRCm39) |
|
probably benign |
Het |
Lpar4 |
T |
A |
X: 105,974,817 (GRCm39) |
F334I |
probably benign |
Het |
Muc5b |
G |
A |
7: 141,416,968 (GRCm39) |
G3305S |
probably benign |
Het |
Nalcn |
T |
C |
14: 123,555,291 (GRCm39) |
D864G |
probably benign |
Het |
Ndor1 |
T |
C |
2: 25,145,299 (GRCm39) |
E22G |
probably damaging |
Het |
Nt5c2 |
T |
A |
19: 46,912,749 (GRCm39) |
M69L |
probably benign |
Het |
Or52ab4 |
A |
C |
7: 102,987,636 (GRCm39) |
Y125S |
probably damaging |
Het |
Or8k22 |
T |
C |
2: 86,163,212 (GRCm39) |
I163V |
probably benign |
Het |
Pde12 |
A |
T |
14: 26,387,552 (GRCm39) |
H455Q |
probably damaging |
Het |
Pdia6 |
A |
G |
12: 17,324,422 (GRCm39) |
H91R |
probably benign |
Het |
Prl2c1 |
T |
C |
13: 28,041,480 (GRCm39) |
|
probably benign |
Het |
Rasgrf2 |
C |
T |
13: 92,267,900 (GRCm39) |
E35K |
probably damaging |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Sash1 |
T |
A |
10: 8,620,299 (GRCm39) |
M454L |
probably benign |
Het |
Secisbp2 |
C |
A |
13: 51,832,942 (GRCm39) |
T608K |
possibly damaging |
Het |
Slco1a7 |
T |
C |
6: 141,668,836 (GRCm39) |
Y532C |
probably damaging |
Het |
Slmap |
A |
G |
14: 26,143,586 (GRCm39) |
V750A |
possibly damaging |
Het |
Spaca6 |
T |
A |
17: 18,051,351 (GRCm39) |
L9Q |
probably damaging |
Het |
Sycp1 |
T |
C |
3: 102,786,080 (GRCm39) |
|
probably benign |
Het |
Sycp2 |
A |
T |
2: 178,043,712 (GRCm39) |
D131E |
probably damaging |
Het |
Tc2n |
A |
T |
12: 101,659,404 (GRCm39) |
D176E |
probably damaging |
Het |
Thoc7 |
T |
C |
14: 13,953,154 (GRCm38) |
I83V |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,202,143 (GRCm39) |
V1590A |
possibly damaging |
Het |
Tyrp1 |
T |
C |
4: 80,758,994 (GRCm39) |
V289A |
possibly damaging |
Het |
Ube2dnl1 |
T |
A |
X: 113,815,483 (GRCm39) |
C119* |
probably null |
Het |
Vmn1r191 |
T |
A |
13: 22,363,431 (GRCm39) |
I108F |
possibly damaging |
Het |
Zfp710 |
T |
A |
7: 79,731,789 (GRCm39) |
I322N |
probably damaging |
Het |
|
Other mutations in Pdk4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01337:Pdk4
|
APN |
6 |
5,491,869 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01524:Pdk4
|
APN |
6 |
5,491,979 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01814:Pdk4
|
APN |
6 |
5,491,828 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02136:Pdk4
|
APN |
6 |
5,486,715 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02689:Pdk4
|
APN |
6 |
5,487,408 (GRCm39) |
missense |
probably benign |
0.44 |
R0277:Pdk4
|
UTSW |
6 |
5,491,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R0335:Pdk4
|
UTSW |
6 |
5,491,138 (GRCm39) |
missense |
probably benign |
0.00 |
R0990:Pdk4
|
UTSW |
6 |
5,485,577 (GRCm39) |
missense |
probably benign |
0.39 |
R1792:Pdk4
|
UTSW |
6 |
5,489,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R2043:Pdk4
|
UTSW |
6 |
5,485,502 (GRCm39) |
missense |
probably benign |
0.05 |
R2091:Pdk4
|
UTSW |
6 |
5,494,857 (GRCm39) |
intron |
probably benign |
|
R4074:Pdk4
|
UTSW |
6 |
5,491,865 (GRCm39) |
missense |
probably benign |
0.13 |
R4916:Pdk4
|
UTSW |
6 |
5,489,157 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5414:Pdk4
|
UTSW |
6 |
5,485,499 (GRCm39) |
missense |
probably benign |
|
R5867:Pdk4
|
UTSW |
6 |
5,487,452 (GRCm39) |
missense |
probably benign |
|
R6772:Pdk4
|
UTSW |
6 |
5,487,141 (GRCm39) |
missense |
probably benign |
|
R7146:Pdk4
|
UTSW |
6 |
5,491,068 (GRCm39) |
critical splice donor site |
probably null |
|
R7193:Pdk4
|
UTSW |
6 |
5,487,089 (GRCm39) |
missense |
probably benign |
|
R7774:Pdk4
|
UTSW |
6 |
5,492,757 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7873:Pdk4
|
UTSW |
6 |
5,487,086 (GRCm39) |
missense |
probably benign |
0.00 |
R7995:Pdk4
|
UTSW |
6 |
5,487,093 (GRCm39) |
missense |
probably benign |
0.42 |
R8782:Pdk4
|
UTSW |
6 |
5,494,962 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9483:Pdk4
|
UTSW |
6 |
5,486,716 (GRCm39) |
missense |
probably benign |
0.00 |
R9501:Pdk4
|
UTSW |
6 |
5,491,084 (GRCm39) |
missense |
probably damaging |
0.99 |
R9596:Pdk4
|
UTSW |
6 |
5,491,842 (GRCm39) |
missense |
probably benign |
|
Z1176:Pdk4
|
UTSW |
6 |
5,487,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|