Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgra1 |
A |
G |
7: 139,455,860 (GRCm39) |
Q496R |
probably benign |
Het |
Ankrd17 |
A |
T |
5: 90,416,220 (GRCm39) |
S1151T |
probably damaging |
Het |
Ankrd55 |
A |
G |
13: 112,504,328 (GRCm39) |
K330R |
probably benign |
Het |
Anln |
A |
T |
9: 22,272,120 (GRCm39) |
Y666* |
probably null |
Het |
Atp1a2 |
A |
G |
1: 172,103,569 (GRCm39) |
W984R |
probably damaging |
Het |
Atp8b3 |
G |
T |
10: 80,361,998 (GRCm39) |
|
probably benign |
Het |
Casc3 |
A |
G |
11: 98,714,028 (GRCm39) |
E420G |
possibly damaging |
Het |
Cep250 |
G |
A |
2: 155,833,249 (GRCm39) |
D1724N |
probably benign |
Het |
Dhx15 |
T |
G |
5: 52,324,154 (GRCm39) |
E379D |
probably benign |
Het |
Dock1 |
T |
A |
7: 134,748,260 (GRCm39) |
|
probably benign |
Het |
Exph5 |
C |
T |
9: 53,288,006 (GRCm39) |
Q1696* |
probably null |
Het |
Fkbp6 |
C |
A |
5: 135,368,802 (GRCm39) |
A213S |
possibly damaging |
Het |
Fndc4 |
A |
G |
5: 31,450,840 (GRCm39) |
|
probably benign |
Het |
Gli3 |
A |
T |
13: 15,818,977 (GRCm39) |
T260S |
possibly damaging |
Het |
Glmp |
T |
A |
3: 88,233,169 (GRCm39) |
|
probably null |
Het |
H2ac22 |
G |
T |
13: 21,971,091 (GRCm39) |
R100S |
probably benign |
Het |
Hapstr1 |
T |
C |
16: 8,649,175 (GRCm39) |
|
probably benign |
Het |
Ighv1-19 |
G |
A |
12: 114,672,329 (GRCm39) |
T97I |
probably benign |
Het |
Kdm6b |
T |
C |
11: 69,297,132 (GRCm39) |
S407G |
possibly damaging |
Het |
Lrp1b |
T |
C |
2: 41,000,873 (GRCm39) |
Y2231C |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,884,188 (GRCm39) |
S2999T |
probably benign |
Het |
Lztr1 |
T |
C |
16: 17,335,314 (GRCm39) |
|
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,964,867 (GRCm39) |
V972A |
probably damaging |
Het |
Ncoa6 |
A |
T |
2: 155,248,128 (GRCm39) |
S1725R |
probably damaging |
Het |
Nfkbiz |
A |
G |
16: 55,638,272 (GRCm39) |
V396A |
probably benign |
Het |
Nup205 |
A |
G |
6: 35,191,737 (GRCm39) |
Q1074R |
probably damaging |
Het |
Pard3 |
T |
C |
8: 128,098,327 (GRCm39) |
V456A |
probably benign |
Het |
Peli1 |
T |
A |
11: 21,096,952 (GRCm39) |
V114E |
probably damaging |
Het |
Phf20l1 |
T |
G |
15: 66,487,482 (GRCm39) |
|
probably benign |
Het |
Pik3r1 |
A |
C |
13: 101,838,255 (GRCm39) |
I267S |
probably benign |
Het |
Polh |
C |
T |
17: 46,483,169 (GRCm39) |
|
probably benign |
Het |
Ppl |
A |
G |
16: 4,905,816 (GRCm39) |
I1493T |
probably benign |
Het |
Pramel19 |
T |
C |
4: 101,798,898 (GRCm39) |
F290L |
probably benign |
Het |
Pramel28 |
G |
A |
4: 143,693,184 (GRCm39) |
|
probably benign |
Het |
Prg3 |
A |
G |
2: 84,819,091 (GRCm39) |
I6V |
probably benign |
Het |
Ptprg |
T |
C |
14: 12,215,220 (GRCm38) |
V1069A |
probably damaging |
Het |
Rasal2 |
A |
T |
1: 157,001,745 (GRCm39) |
|
probably null |
Het |
Slc36a2 |
A |
T |
11: 55,053,614 (GRCm39) |
Y341* |
probably null |
Het |
Snapc3 |
A |
G |
4: 83,354,633 (GRCm39) |
I215V |
probably damaging |
Het |
Srrm2 |
T |
A |
17: 24,037,492 (GRCm39) |
S1475T |
probably benign |
Het |
Sycp2 |
A |
T |
2: 178,024,141 (GRCm39) |
D414E |
probably damaging |
Het |
Tanc1 |
A |
G |
2: 59,623,520 (GRCm39) |
T468A |
probably benign |
Het |
Tgfbr2 |
T |
A |
9: 115,987,357 (GRCm39) |
I51F |
probably benign |
Het |
Trip11 |
A |
T |
12: 101,851,570 (GRCm39) |
C546* |
probably null |
Het |
Ttbk2 |
C |
T |
2: 120,604,367 (GRCm39) |
W210* |
probably null |
Het |
Upk1b |
T |
G |
16: 38,600,378 (GRCm39) |
N201H |
possibly damaging |
Het |
Uqcc5 |
T |
A |
14: 30,810,879 (GRCm39) |
|
probably benign |
Het |
Ush2a |
A |
T |
1: 188,514,710 (GRCm39) |
T3180S |
probably benign |
Het |
Vps13d |
T |
G |
4: 144,853,145 (GRCm39) |
Q2323P |
probably benign |
Het |
Zfp810 |
A |
T |
9: 22,189,605 (GRCm39) |
Y434* |
probably null |
Het |
|
Other mutations in Tfap2d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00837:Tfap2d
|
APN |
1 |
19,189,430 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01370:Tfap2d
|
APN |
1 |
19,175,009 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01470:Tfap2d
|
APN |
1 |
19,218,620 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01757:Tfap2d
|
APN |
1 |
19,174,804 (GRCm39) |
missense |
probably benign |
|
IGL01986:Tfap2d
|
APN |
1 |
19,189,383 (GRCm39) |
splice site |
probably benign |
|
IGL02613:Tfap2d
|
APN |
1 |
19,189,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Tfap2d
|
APN |
1 |
19,174,979 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02812:Tfap2d
|
APN |
1 |
19,213,151 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02900:Tfap2d
|
APN |
1 |
19,189,474 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03184:Tfap2d
|
APN |
1 |
19,189,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R0389:Tfap2d
|
UTSW |
1 |
19,174,591 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0443:Tfap2d
|
UTSW |
1 |
19,174,591 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3962:Tfap2d
|
UTSW |
1 |
19,189,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R3977:Tfap2d
|
UTSW |
1 |
19,174,718 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3980:Tfap2d
|
UTSW |
1 |
19,236,187 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4721:Tfap2d
|
UTSW |
1 |
19,174,984 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6281:Tfap2d
|
UTSW |
1 |
19,174,702 (GRCm39) |
missense |
probably benign |
0.12 |
R6283:Tfap2d
|
UTSW |
1 |
19,174,702 (GRCm39) |
missense |
probably benign |
0.12 |
R6492:Tfap2d
|
UTSW |
1 |
19,174,702 (GRCm39) |
missense |
probably benign |
0.12 |
R6493:Tfap2d
|
UTSW |
1 |
19,174,702 (GRCm39) |
missense |
probably benign |
0.12 |
R6751:Tfap2d
|
UTSW |
1 |
19,173,507 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7288:Tfap2d
|
UTSW |
1 |
19,189,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R7400:Tfap2d
|
UTSW |
1 |
19,213,150 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8156:Tfap2d
|
UTSW |
1 |
19,173,486 (GRCm39) |
missense |
probably benign |
|
R8551:Tfap2d
|
UTSW |
1 |
19,175,024 (GRCm39) |
missense |
probably benign |
0.08 |
R8686:Tfap2d
|
UTSW |
1 |
19,178,508 (GRCm39) |
missense |
probably benign |
0.06 |
R8838:Tfap2d
|
UTSW |
1 |
19,175,036 (GRCm39) |
missense |
possibly damaging |
0.83 |
|