Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
G |
T |
7: 120,119,184 (GRCm39) |
G975V |
probably damaging |
Het |
Abcg5 |
T |
A |
17: 84,978,575 (GRCm39) |
E294D |
probably benign |
Het |
Actl10 |
G |
A |
2: 154,394,153 (GRCm39) |
R35H |
probably damaging |
Het |
Adamts12 |
C |
T |
15: 11,310,665 (GRCm39) |
T974I |
probably damaging |
Het |
Ahctf1 |
C |
A |
1: 179,597,017 (GRCm39) |
R43L |
probably damaging |
Het |
Arhgef10 |
A |
G |
8: 14,984,820 (GRCm39) |
D200G |
probably damaging |
Het |
Arhgef38 |
T |
C |
3: 132,866,514 (GRCm39) |
K208E |
probably benign |
Het |
Arhgef7 |
A |
T |
8: 11,778,256 (GRCm39) |
N2I |
possibly damaging |
Het |
Blvra |
T |
G |
2: 126,928,817 (GRCm39) |
S102A |
probably damaging |
Het |
Btn1a1 |
A |
G |
13: 23,645,691 (GRCm39) |
L226P |
probably damaging |
Het |
C2cd4d |
G |
T |
3: 94,270,925 (GRCm39) |
E64* |
probably null |
Het |
Ccna2 |
A |
G |
3: 36,622,875 (GRCm39) |
V209A |
probably damaging |
Het |
Cd55 |
T |
A |
1: 130,387,354 (GRCm39) |
D148V |
possibly damaging |
Het |
Cdh2 |
G |
A |
18: 16,907,600 (GRCm39) |
P46L |
probably benign |
Het |
Cldn11 |
A |
G |
3: 31,217,300 (GRCm39) |
Y156C |
probably damaging |
Het |
Cmtm2a |
T |
C |
8: 105,019,655 (GRCm39) |
R12G |
possibly damaging |
Het |
Col4a3 |
T |
G |
1: 82,632,678 (GRCm39) |
F184V |
unknown |
Het |
Col4a4 |
T |
A |
1: 82,434,592 (GRCm39) |
D1406V |
unknown |
Het |
Col6a1 |
T |
C |
10: 76,557,332 (GRCm39) |
T207A |
probably benign |
Het |
Cyp2a12 |
A |
G |
7: 26,736,071 (GRCm39) |
*493W |
probably null |
Het |
Dcdc2a |
T |
G |
13: 25,303,268 (GRCm39) |
S266R |
possibly damaging |
Het |
Dmd |
G |
C |
X: 83,356,089 (GRCm39) |
A2257P |
probably benign |
Het |
Ecel1 |
A |
G |
1: 87,075,997 (GRCm39) |
S727P |
probably damaging |
Het |
Eif2ak4 |
T |
A |
2: 118,286,274 (GRCm39) |
V1063E |
probably damaging |
Het |
Enpp2 |
A |
T |
15: 54,761,188 (GRCm39) |
Y44* |
probably null |
Het |
Ep400 |
A |
T |
5: 110,856,716 (GRCm39) |
|
probably benign |
Het |
Exoc6b |
A |
G |
6: 84,598,464 (GRCm39) |
M779T |
probably benign |
Het |
F13a1 |
T |
A |
13: 37,209,653 (GRCm39) |
Y104F |
probably benign |
Het |
Fam78b |
G |
A |
1: 166,906,278 (GRCm39) |
V146M |
probably damaging |
Het |
Fgf18 |
A |
C |
11: 33,068,003 (GRCm39) |
F129C |
probably damaging |
Het |
Fscn3 |
A |
G |
6: 28,430,388 (GRCm39) |
D186G |
probably benign |
Het |
Gm5773 |
G |
A |
3: 93,680,624 (GRCm39) |
G99R |
possibly damaging |
Het |
Grk1 |
A |
T |
8: 13,455,221 (GRCm39) |
Y35F |
probably benign |
Het |
Heatr1 |
T |
C |
13: 12,418,145 (GRCm39) |
V359A |
probably benign |
Het |
Hfm1 |
A |
G |
5: 107,044,121 (GRCm39) |
S567P |
probably damaging |
Het |
Il1rap |
A |
T |
16: 26,529,315 (GRCm39) |
H379L |
probably damaging |
Het |
Kctd5 |
T |
C |
17: 24,274,940 (GRCm39) |
T212A |
probably benign |
Het |
Krtap5-5 |
A |
T |
7: 141,783,240 (GRCm39) |
C137S |
unknown |
Het |
Lrp2 |
T |
C |
2: 69,314,051 (GRCm39) |
T2227A |
probably damaging |
Het |
Ltbp1 |
T |
A |
17: 75,617,154 (GRCm39) |
V1031E |
possibly damaging |
Het |
Ltbr |
A |
G |
6: 125,286,440 (GRCm39) |
S249P |
probably benign |
Het |
Map1a |
T |
A |
2: 121,129,927 (GRCm39) |
Y248N |
probably damaging |
Het |
Mdc1 |
C |
T |
17: 36,158,835 (GRCm39) |
A405V |
probably benign |
Het |
Mfsd4b1 |
T |
C |
10: 39,878,647 (GRCm39) |
K417E |
possibly damaging |
Het |
Mroh2a |
T |
C |
1: 88,184,476 (GRCm39) |
V1453A |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,035,868 (GRCm39) |
E1027G |
probably damaging |
Het |
Nudt6 |
A |
C |
3: 37,466,554 (GRCm39) |
F80L |
probably benign |
Het |
Nxph1 |
A |
G |
6: 9,247,791 (GRCm39) |
K254R |
probably damaging |
Het |
Obsl1 |
C |
T |
1: 75,470,527 (GRCm39) |
R1043H |
probably benign |
Het |
Or10a4 |
A |
T |
7: 106,697,316 (GRCm39) |
I215F |
probably damaging |
Het |
Pde6d |
A |
G |
1: 86,473,524 (GRCm39) |
F91L |
probably benign |
Het |
Phldb2 |
T |
A |
16: 45,583,304 (GRCm39) |
I1065F |
probably damaging |
Het |
Ppp1r3a |
A |
T |
6: 14,721,874 (GRCm39) |
N317K |
possibly damaging |
Het |
Psmd1 |
T |
A |
1: 86,006,422 (GRCm39) |
S263T |
possibly damaging |
Het |
Pum1 |
C |
A |
4: 130,396,581 (GRCm39) |
T112K |
possibly damaging |
Het |
Rasgrp2 |
T |
A |
19: 6,454,425 (GRCm39) |
M156K |
probably benign |
Het |
Reg3a |
T |
C |
6: 78,358,119 (GRCm39) |
C17R |
possibly damaging |
Het |
Ripor2 |
A |
G |
13: 24,897,701 (GRCm39) |
S800G |
probably damaging |
Het |
Rnf168 |
T |
G |
16: 32,097,036 (GRCm39) |
L37R |
probably damaging |
Het |
Rnf31 |
A |
G |
14: 55,833,654 (GRCm39) |
D554G |
probably damaging |
Het |
Rpe |
T |
C |
1: 66,754,387 (GRCm39) |
M153T |
probably damaging |
Het |
Sacs |
A |
T |
14: 61,449,765 (GRCm39) |
Q3937L |
probably damaging |
Het |
Sap18 |
T |
A |
14: 58,036,011 (GRCm39) |
S66T |
probably damaging |
Het |
Slc20a1 |
T |
G |
2: 129,041,739 (GRCm39) |
I34S |
possibly damaging |
Het |
Slc25a30 |
A |
G |
14: 76,007,658 (GRCm39) |
S116P |
possibly damaging |
Het |
Speer4c1 |
T |
A |
5: 15,919,115 (GRCm39) |
D29V |
possibly damaging |
Het |
Stk40 |
C |
T |
4: 126,022,640 (GRCm39) |
T138I |
probably benign |
Het |
Susd3 |
A |
G |
13: 49,384,626 (GRCm39) |
Y254H |
probably damaging |
Het |
Tanc2 |
T |
C |
11: 105,786,775 (GRCm39) |
L858P |
probably damaging |
Het |
Tas2r106 |
A |
T |
6: 131,655,317 (GRCm39) |
L178H |
probably damaging |
Het |
Tfpt |
C |
T |
7: 3,631,930 (GRCm39) |
R60Q |
probably damaging |
Het |
Tmem44 |
T |
A |
16: 30,366,262 (GRCm39) |
K55* |
probably null |
Het |
Tnfsf9 |
A |
T |
17: 57,414,316 (GRCm39) |
|
probably null |
Het |
Ube3c |
T |
C |
5: 29,824,604 (GRCm39) |
I543T |
probably benign |
Het |
Ugt1a2 |
C |
A |
1: 88,128,735 (GRCm39) |
S126Y |
possibly damaging |
Het |
Vmn1r180 |
T |
A |
7: 23,652,566 (GRCm39) |
L243Q |
probably damaging |
Het |
Vmn2r15 |
A |
C |
5: 109,434,322 (GRCm39) |
V794G |
probably damaging |
Het |
Vmn2r24 |
A |
G |
6: 123,792,353 (GRCm39) |
D560G |
possibly damaging |
Het |
Wdr11 |
G |
A |
7: 129,233,490 (GRCm39) |
C1028Y |
probably damaging |
Het |
Zfp318 |
A |
G |
17: 46,724,297 (GRCm39) |
D2100G |
probably benign |
Het |
Zfyve16 |
A |
T |
13: 92,655,991 (GRCm39) |
Y789* |
probably null |
Het |
|
Other mutations in Cog2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01089:Cog2
|
APN |
8 |
125,271,982 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01092:Cog2
|
APN |
8 |
125,272,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01150:Cog2
|
APN |
8 |
125,269,630 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02052:Cog2
|
APN |
8 |
125,269,627 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02308:Cog2
|
APN |
8 |
125,259,951 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02543:Cog2
|
APN |
8 |
125,256,698 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02978:Cog2
|
APN |
8 |
125,277,075 (GRCm39) |
missense |
probably benign |
|
IGL03008:Cog2
|
APN |
8 |
125,262,131 (GRCm39) |
splice site |
probably benign |
|
IGL03144:Cog2
|
APN |
8 |
125,267,763 (GRCm39) |
missense |
probably damaging |
0.98 |
kugge
|
UTSW |
8 |
125,276,971 (GRCm39) |
missense |
probably damaging |
1.00 |
Pelota
|
UTSW |
8 |
125,277,045 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4677001:Cog2
|
UTSW |
8 |
125,272,010 (GRCm39) |
missense |
probably benign |
0.22 |
R0071:Cog2
|
UTSW |
8 |
125,275,407 (GRCm39) |
splice site |
probably benign |
|
R0071:Cog2
|
UTSW |
8 |
125,275,407 (GRCm39) |
splice site |
probably benign |
|
R0110:Cog2
|
UTSW |
8 |
125,255,797 (GRCm39) |
critical splice donor site |
probably null |
|
R0436:Cog2
|
UTSW |
8 |
125,275,253 (GRCm39) |
splice site |
probably benign |
|
R0450:Cog2
|
UTSW |
8 |
125,255,797 (GRCm39) |
critical splice donor site |
probably null |
|
R1365:Cog2
|
UTSW |
8 |
125,267,713 (GRCm39) |
missense |
probably damaging |
0.97 |
R1661:Cog2
|
UTSW |
8 |
125,269,629 (GRCm39) |
missense |
probably benign |
0.20 |
R1698:Cog2
|
UTSW |
8 |
125,252,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Cog2
|
UTSW |
8 |
125,278,142 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2398:Cog2
|
UTSW |
8 |
125,256,665 (GRCm39) |
missense |
probably benign |
0.07 |
R3855:Cog2
|
UTSW |
8 |
125,256,742 (GRCm39) |
critical splice donor site |
probably null |
|
R4580:Cog2
|
UTSW |
8 |
125,271,875 (GRCm39) |
missense |
probably benign |
0.01 |
R4803:Cog2
|
UTSW |
8 |
125,262,190 (GRCm39) |
missense |
probably damaging |
0.96 |
R5316:Cog2
|
UTSW |
8 |
125,255,779 (GRCm39) |
missense |
probably benign |
0.14 |
R5346:Cog2
|
UTSW |
8 |
125,273,370 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5394:Cog2
|
UTSW |
8 |
125,259,268 (GRCm39) |
missense |
probably benign |
0.00 |
R5395:Cog2
|
UTSW |
8 |
125,271,960 (GRCm39) |
missense |
probably benign |
0.00 |
R5738:Cog2
|
UTSW |
8 |
125,272,777 (GRCm39) |
missense |
probably benign |
0.03 |
R5861:Cog2
|
UTSW |
8 |
125,264,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Cog2
|
UTSW |
8 |
125,272,006 (GRCm39) |
missense |
probably benign |
0.00 |
R5941:Cog2
|
UTSW |
8 |
125,272,825 (GRCm39) |
missense |
probably benign |
|
R6186:Cog2
|
UTSW |
8 |
125,273,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R6400:Cog2
|
UTSW |
8 |
125,277,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R6518:Cog2
|
UTSW |
8 |
125,253,842 (GRCm39) |
nonsense |
probably null |
|
R6558:Cog2
|
UTSW |
8 |
125,276,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R6717:Cog2
|
UTSW |
8 |
125,252,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R6902:Cog2
|
UTSW |
8 |
125,273,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R6914:Cog2
|
UTSW |
8 |
125,271,875 (GRCm39) |
missense |
probably benign |
0.00 |
R6942:Cog2
|
UTSW |
8 |
125,271,875 (GRCm39) |
missense |
probably benign |
0.00 |
R7103:Cog2
|
UTSW |
8 |
125,267,853 (GRCm39) |
critical splice donor site |
probably null |
|
R7274:Cog2
|
UTSW |
8 |
125,262,258 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7641:Cog2
|
UTSW |
8 |
125,264,621 (GRCm39) |
missense |
probably damaging |
0.96 |
R7674:Cog2
|
UTSW |
8 |
125,264,621 (GRCm39) |
missense |
probably damaging |
0.96 |
R8559:Cog2
|
UTSW |
8 |
125,269,647 (GRCm39) |
missense |
probably benign |
0.25 |
R9190:Cog2
|
UTSW |
8 |
125,260,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Cog2
|
UTSW |
8 |
125,253,837 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9629:Cog2
|
UTSW |
8 |
125,260,125 (GRCm39) |
missense |
possibly damaging |
0.67 |
X0026:Cog2
|
UTSW |
8 |
125,272,759 (GRCm39) |
missense |
possibly damaging |
0.88 |
|