Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
T |
A |
12: 55,107,957 (GRCm39) |
T81S |
possibly damaging |
Het |
Ablim2 |
C |
T |
5: 36,030,518 (GRCm39) |
A581V |
possibly damaging |
Het |
Acbd5 |
T |
A |
2: 22,979,710 (GRCm39) |
S210T |
probably benign |
Het |
Adam10 |
T |
A |
9: 70,655,505 (GRCm39) |
F324L |
probably damaging |
Het |
Ak6 |
A |
G |
13: 100,791,857 (GRCm39) |
N100S |
possibly damaging |
Het |
Angptl3 |
G |
T |
4: 98,925,759 (GRCm39) |
V362L |
probably benign |
Het |
Ano9 |
C |
A |
7: 140,684,220 (GRCm39) |
W514L |
probably benign |
Het |
Asb8 |
T |
C |
15: 98,034,108 (GRCm39) |
Y149C |
probably damaging |
Het |
Bcl6b |
C |
A |
11: 70,117,447 (GRCm39) |
A392S |
probably damaging |
Het |
Cad |
T |
A |
5: 31,232,500 (GRCm39) |
I1855N |
possibly damaging |
Het |
Calm5 |
G |
A |
13: 3,904,277 (GRCm39) |
G4R |
probably damaging |
Het |
Carm1 |
T |
C |
9: 21,480,808 (GRCm39) |
V94A |
probably damaging |
Het |
Ccnl1 |
A |
T |
3: 65,855,165 (GRCm39) |
S399R |
possibly damaging |
Het |
Cdh17 |
T |
A |
4: 11,783,163 (GRCm39) |
I168N |
probably benign |
Het |
Ces2g |
C |
T |
8: 105,693,605 (GRCm39) |
R429C |
probably benign |
Het |
Chd3 |
T |
C |
11: 69,246,648 (GRCm39) |
|
probably benign |
Het |
Cmtr2 |
T |
A |
8: 110,948,977 (GRCm39) |
M429K |
probably benign |
Het |
Cnga1 |
T |
G |
5: 72,761,835 (GRCm39) |
I560L |
probably benign |
Het |
Col6a5 |
A |
G |
9: 105,759,796 (GRCm39) |
Y1975H |
probably damaging |
Het |
Copb1 |
T |
C |
7: 113,849,463 (GRCm39) |
I47V |
probably benign |
Het |
Crbn |
G |
A |
6: 106,777,010 (GRCm39) |
|
probably benign |
Het |
Ddx41 |
A |
G |
13: 55,680,939 (GRCm39) |
L324P |
probably damaging |
Het |
Dhx57 |
A |
G |
17: 80,577,794 (GRCm39) |
|
probably benign |
Het |
Dlgap2 |
A |
T |
8: 14,793,430 (GRCm39) |
I475F |
probably benign |
Het |
Dock2 |
T |
A |
11: 34,618,287 (GRCm39) |
K110* |
probably null |
Het |
Dpp7 |
T |
C |
2: 25,245,645 (GRCm39) |
D147G |
probably damaging |
Het |
Dync2h1 |
G |
T |
9: 7,075,824 (GRCm39) |
D3014E |
probably damaging |
Het |
Efcab5 |
A |
T |
11: 76,994,115 (GRCm39) |
F1291I |
probably damaging |
Het |
Endov |
T |
A |
11: 119,382,736 (GRCm39) |
V61D |
probably benign |
Het |
Etv3 |
C |
A |
3: 87,443,786 (GRCm39) |
P457T |
possibly damaging |
Het |
Fam185a |
T |
A |
5: 21,638,766 (GRCm39) |
H199Q |
probably benign |
Het |
Fat3 |
T |
A |
9: 15,878,397 (GRCm39) |
E3361D |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,186,015 (GRCm39) |
|
probably benign |
Het |
Gm17079 |
A |
T |
14: 51,932,787 (GRCm39) |
W37R |
|
Het |
Gpr68 |
T |
C |
12: 100,845,292 (GRCm39) |
H84R |
probably benign |
Het |
Gramd1b |
A |
T |
9: 40,215,674 (GRCm39) |
S725R |
probably damaging |
Het |
Greb1 |
T |
A |
12: 16,746,548 (GRCm39) |
T1241S |
probably benign |
Het |
Hcn4 |
T |
C |
9: 58,751,193 (GRCm39) |
M273T |
probably benign |
Het |
Hdlbp |
A |
G |
1: 93,341,640 (GRCm39) |
V973A |
probably damaging |
Het |
Ighv8-11 |
A |
T |
12: 115,531,164 (GRCm39) |
|
probably benign |
Het |
Itpkb |
A |
T |
1: 180,249,346 (GRCm39) |
Q907L |
probably benign |
Het |
Lmo7 |
T |
A |
14: 102,168,644 (GRCm39) |
N1634K |
unknown |
Het |
Lrrk1 |
C |
A |
7: 65,952,477 (GRCm39) |
L486F |
probably benign |
Het |
Mdfic |
G |
A |
6: 15,799,653 (GRCm39) |
C260Y |
probably damaging |
Het |
Mdh2 |
T |
C |
5: 135,814,882 (GRCm39) |
I140T |
probably benign |
Het |
Myo9a |
T |
C |
9: 59,782,657 (GRCm39) |
V1775A |
probably benign |
Het |
Or1j14 |
T |
C |
2: 36,418,207 (GRCm39) |
V261A |
probably benign |
Het |
Or51d1 |
C |
A |
7: 102,348,028 (GRCm39) |
D194E |
probably damaging |
Het |
Or52n3 |
T |
C |
7: 104,530,762 (GRCm39) |
Y283H |
probably damaging |
Het |
P2rx2 |
C |
T |
5: 110,490,380 (GRCm39) |
V112I |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,787,319 (GRCm39) |
V1038E |
probably benign |
Het |
Rab25 |
T |
A |
3: 88,452,388 (GRCm39) |
R73S |
probably damaging |
Het |
Rab8a |
TA |
TAA |
8: 72,925,130 (GRCm39) |
|
probably null |
Het |
Rnf213 |
T |
C |
11: 119,308,955 (GRCm39) |
Y729H |
|
Het |
Rnf213 |
A |
G |
11: 119,332,038 (GRCm39) |
T2417A |
|
Het |
Rnft2 |
C |
A |
5: 118,366,935 (GRCm39) |
A268S |
probably benign |
Het |
Samhd1 |
T |
C |
2: 156,971,794 (GRCm39) |
D116G |
probably benign |
Het |
Sema6d |
T |
A |
2: 124,506,937 (GRCm39) |
V915E |
probably benign |
Het |
Sp140l2 |
G |
A |
1: 85,235,170 (GRCm39) |
H130Y |
probably benign |
Het |
Srcin1 |
C |
A |
11: 97,414,368 (GRCm39) |
R1045L |
probably damaging |
Het |
St18 |
T |
A |
1: 6,872,788 (GRCm39) |
N174K |
probably benign |
Het |
Stac3 |
G |
A |
10: 127,339,494 (GRCm39) |
C130Y |
probably damaging |
Het |
Stum |
G |
C |
1: 180,310,740 (GRCm39) |
P52R |
probably damaging |
Het |
Tbc1d2 |
C |
T |
4: 46,615,106 (GRCm39) |
E526K |
possibly damaging |
Het |
Tiam1 |
A |
G |
16: 89,694,900 (GRCm39) |
S186P |
probably damaging |
Het |
Tiparp |
G |
C |
3: 65,460,963 (GRCm39) |
V651L |
probably benign |
Het |
Tmem19 |
C |
T |
10: 115,179,765 (GRCm39) |
G244S |
probably damaging |
Het |
Trip11 |
A |
T |
12: 101,839,656 (GRCm39) |
V1658D |
possibly damaging |
Het |
Ube2h |
C |
T |
6: 30,262,338 (GRCm39) |
|
probably benign |
Het |
Zbtb4 |
T |
C |
11: 69,667,618 (GRCm39) |
S308P |
probably damaging |
Het |
Zfyve1 |
T |
C |
12: 83,597,681 (GRCm39) |
E672G |
probably damaging |
Het |
Zswim5 |
G |
A |
4: 116,842,002 (GRCm39) |
D861N |
probably damaging |
Het |
|
Other mutations in Ttyh3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01285:Ttyh3
|
APN |
5 |
140,615,167 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01324:Ttyh3
|
APN |
5 |
140,617,268 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01982:Ttyh3
|
APN |
5 |
140,621,829 (GRCm39) |
splice site |
probably benign |
|
IGL02002:Ttyh3
|
APN |
5 |
140,615,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02218:Ttyh3
|
APN |
5 |
140,612,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02385:Ttyh3
|
APN |
5 |
140,619,060 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02510:Ttyh3
|
APN |
5 |
140,615,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R0843:Ttyh3
|
UTSW |
5 |
140,612,201 (GRCm39) |
splice site |
probably null |
|
R3037:Ttyh3
|
UTSW |
5 |
140,634,597 (GRCm39) |
start gained |
probably benign |
|
R3774:Ttyh3
|
UTSW |
5 |
140,634,489 (GRCm39) |
missense |
probably damaging |
0.99 |
R4795:Ttyh3
|
UTSW |
5 |
140,620,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Ttyh3
|
UTSW |
5 |
140,620,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R4868:Ttyh3
|
UTSW |
5 |
140,615,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Ttyh3
|
UTSW |
5 |
140,617,307 (GRCm39) |
missense |
probably benign |
0.02 |
R6107:Ttyh3
|
UTSW |
5 |
140,619,317 (GRCm39) |
critical splice donor site |
probably null |
|
R6363:Ttyh3
|
UTSW |
5 |
140,620,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R7104:Ttyh3
|
UTSW |
5 |
140,615,540 (GRCm39) |
missense |
probably benign |
0.00 |
R7454:Ttyh3
|
UTSW |
5 |
140,615,180 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7798:Ttyh3
|
UTSW |
5 |
140,620,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R7810:Ttyh3
|
UTSW |
5 |
140,610,896 (GRCm39) |
missense |
|
|
R8690:Ttyh3
|
UTSW |
5 |
140,612,945 (GRCm39) |
missense |
probably benign |
0.02 |
R9162:Ttyh3
|
UTSW |
5 |
140,621,820 (GRCm39) |
missense |
possibly damaging |
0.91 |
|