Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510039O18Rik |
C |
A |
4: 148,025,837 (GRCm39) |
T119K |
probably benign |
Het |
Abca13 |
T |
A |
11: 9,227,922 (GRCm39) |
L655* |
probably null |
Het |
Aifm2 |
A |
G |
10: 61,562,171 (GRCm39) |
Y69C |
probably damaging |
Het |
Atp2c1 |
C |
T |
9: 105,320,030 (GRCm39) |
V448I |
probably benign |
Het |
Barx2 |
A |
G |
9: 31,770,307 (GRCm39) |
S74P |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,978,498 (GRCm39) |
K939E |
probably damaging |
Het |
Cdh12 |
C |
A |
15: 21,358,949 (GRCm39) |
F124L |
probably benign |
Het |
Cdh12 |
T |
A |
15: 21,358,950 (GRCm39) |
Y125N |
probably damaging |
Het |
Cdx2 |
A |
G |
5: 147,243,477 (GRCm39) |
Y106H |
possibly damaging |
Het |
Chmp1a |
C |
T |
8: 123,932,980 (GRCm39) |
G158S |
probably damaging |
Het |
Cilp |
G |
A |
9: 65,186,286 (GRCm39) |
G794S |
probably damaging |
Het |
Cntnap1 |
A |
T |
11: 101,079,702 (GRCm39) |
Y1277F |
possibly damaging |
Het |
Csde1 |
A |
G |
3: 102,946,389 (GRCm39) |
|
probably benign |
Het |
Dennd4c |
A |
C |
4: 86,744,109 (GRCm39) |
D1317A |
probably benign |
Het |
Dgcr2 |
C |
T |
16: 17,676,242 (GRCm39) |
G176D |
probably benign |
Het |
Dock2 |
A |
T |
11: 34,260,362 (GRCm39) |
M993K |
possibly damaging |
Het |
Dpy19l1 |
G |
A |
9: 24,414,297 (GRCm39) |
P44S |
probably benign |
Het |
Dsg2 |
C |
T |
18: 20,708,121 (GRCm39) |
P74L |
probably benign |
Het |
Epg5 |
T |
A |
18: 78,065,894 (GRCm39) |
F2078Y |
probably damaging |
Het |
Fancl |
A |
G |
11: 26,349,642 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
C |
A |
2: 125,347,402 (GRCm39) |
R41L |
possibly damaging |
Het |
Gemin5 |
G |
A |
11: 58,042,420 (GRCm39) |
T467M |
probably damaging |
Het |
Hexb |
T |
C |
13: 97,330,707 (GRCm39) |
Q102R |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,286,127 (GRCm39) |
D2093G |
probably damaging |
Het |
Hmmr |
G |
A |
11: 40,612,499 (GRCm39) |
S206F |
probably damaging |
Het |
Igkv1-131 |
A |
G |
6: 67,743,051 (GRCm39) |
Y111H |
probably damaging |
Het |
Il6st |
G |
T |
13: 112,624,281 (GRCm39) |
G177V |
probably benign |
Het |
Kank4 |
G |
A |
4: 98,666,915 (GRCm39) |
Q511* |
probably null |
Het |
Krt90 |
A |
G |
15: 101,467,634 (GRCm39) |
L248P |
probably damaging |
Het |
Krtap5-2 |
A |
G |
7: 141,728,586 (GRCm39) |
C187R |
unknown |
Het |
Lonp1 |
C |
A |
17: 56,933,573 (GRCm39) |
A101S |
probably benign |
Het |
Nckap5l |
A |
G |
15: 99,321,058 (GRCm39) |
C1241R |
probably damaging |
Het |
Or1j11 |
A |
G |
2: 36,312,333 (GRCm39) |
T308A |
probably benign |
Het |
Or4c11c |
G |
A |
2: 88,661,633 (GRCm39) |
M57I |
possibly damaging |
Het |
Or6c203 |
T |
C |
10: 129,010,101 (GRCm39) |
D263G |
probably benign |
Het |
Pcdh15 |
T |
A |
10: 74,342,307 (GRCm39) |
C1131* |
probably null |
Het |
Pcdhgc3 |
A |
G |
18: 37,940,847 (GRCm39) |
D416G |
probably damaging |
Het |
Pikfyve |
T |
C |
1: 65,284,894 (GRCm39) |
M786T |
possibly damaging |
Het |
Pink1 |
A |
T |
4: 138,045,273 (GRCm39) |
M297K |
probably benign |
Het |
Pln |
T |
C |
10: 53,219,975 (GRCm39) |
Y6H |
unknown |
Het |
Ppp2r2c |
A |
G |
5: 37,104,430 (GRCm39) |
D270G |
probably damaging |
Het |
Prcd |
A |
T |
11: 116,550,199 (GRCm39) |
T76S |
possibly damaging |
Het |
Pxylp1 |
A |
G |
9: 96,721,137 (GRCm39) |
|
probably null |
Het |
Rab11fip4 |
A |
T |
11: 79,581,600 (GRCm39) |
N532Y |
possibly damaging |
Het |
Ralgapa1 |
C |
A |
12: 55,788,308 (GRCm39) |
V592L |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,753,498 (GRCm39) |
D793G |
probably damaging |
Het |
Sec14l1 |
G |
A |
11: 117,034,242 (GRCm39) |
|
probably null |
Het |
Srcap |
T |
A |
7: 127,124,541 (GRCm39) |
V237E |
probably damaging |
Het |
Srl |
A |
G |
16: 4,315,009 (GRCm39) |
I211T |
probably benign |
Het |
Tasor |
G |
T |
14: 27,193,622 (GRCm39) |
A941S |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,356,909 (GRCm39) |
V883A |
probably damaging |
Het |
Trim46 |
A |
G |
3: 89,151,223 (GRCm39) |
Y113H |
probably benign |
Het |
Trim58 |
G |
A |
11: 58,537,909 (GRCm39) |
A267T |
probably benign |
Het |
Tsks |
G |
A |
7: 44,607,086 (GRCm39) |
G140S |
|
Het |
Vmn2r110 |
C |
A |
17: 20,803,319 (GRCm39) |
V419L |
probably benign |
Het |
Vmn2r66 |
A |
G |
7: 84,656,270 (GRCm39) |
F249L |
probably benign |
Het |
Vps8 |
A |
C |
16: 21,314,652 (GRCm39) |
D584A |
probably benign |
Het |
Zfp605 |
T |
A |
5: 110,276,063 (GRCm39) |
C394S |
probably damaging |
Het |
Zscan4e |
A |
G |
7: 11,041,059 (GRCm39) |
I271T |
probably benign |
Het |
|
Other mutations in Pramel58 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02676:Pramel58
|
APN |
5 |
94,831,730 (GRCm39) |
missense |
possibly damaging |
0.64 |
PIT4469001:Pramel58
|
UTSW |
5 |
94,830,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Pramel58
|
UTSW |
5 |
94,831,277 (GRCm39) |
missense |
probably benign |
0.10 |
R6816:Pramel58
|
UTSW |
5 |
94,831,773 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7482:Pramel58
|
UTSW |
5 |
94,830,739 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7583:Pramel58
|
UTSW |
5 |
94,830,753 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7799:Pramel58
|
UTSW |
5 |
94,831,287 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8334:Pramel58
|
UTSW |
5 |
94,830,635 (GRCm39) |
missense |
probably benign |
0.04 |
R8459:Pramel58
|
UTSW |
5 |
94,830,742 (GRCm39) |
missense |
probably damaging |
0.97 |
R8460:Pramel58
|
UTSW |
5 |
94,831,790 (GRCm39) |
missense |
probably benign |
0.39 |
R8906:Pramel58
|
UTSW |
5 |
94,831,413 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9151:Pramel58
|
UTSW |
5 |
94,831,836 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9187:Pramel58
|
UTSW |
5 |
94,831,755 (GRCm39) |
missense |
probably benign |
0.21 |
Z1088:Pramel58
|
UTSW |
5 |
94,831,692 (GRCm39) |
missense |
probably benign |
0.01 |
|