Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933405L10Rik |
A |
G |
8: 106,436,144 (GRCm39) |
S139G |
probably benign |
Het |
Abca2 |
T |
A |
2: 25,328,240 (GRCm39) |
|
probably benign |
Het |
Abcb1b |
A |
T |
5: 8,875,657 (GRCm39) |
N610I |
probably benign |
Het |
Ahnak |
T |
C |
19: 8,984,982 (GRCm39) |
F2089L |
probably benign |
Het |
Cacnb1 |
T |
C |
11: 97,895,843 (GRCm39) |
|
probably benign |
Het |
Cep57 |
T |
C |
9: 13,730,275 (GRCm39) |
I61V |
possibly damaging |
Het |
Ckap5 |
T |
C |
2: 91,380,974 (GRCm39) |
I110T |
probably benign |
Het |
Clasp2 |
T |
C |
9: 113,725,702 (GRCm39) |
|
probably benign |
Het |
Col11a1 |
A |
C |
3: 113,987,801 (GRCm39) |
E265A |
probably damaging |
Het |
Cst13 |
A |
G |
2: 148,672,251 (GRCm39) |
|
probably benign |
Het |
Cyp24a1 |
G |
A |
2: 170,333,537 (GRCm39) |
T272M |
probably damaging |
Het |
Cyp4a14 |
A |
C |
4: 115,347,193 (GRCm39) |
L415R |
probably damaging |
Het |
Dbnl |
T |
C |
11: 5,746,807 (GRCm39) |
F179S |
probably damaging |
Het |
Eepd1 |
T |
C |
9: 25,498,079 (GRCm39) |
L388P |
possibly damaging |
Het |
Exosc8 |
G |
T |
3: 54,640,159 (GRCm39) |
A55E |
probably damaging |
Het |
Fam72a |
G |
A |
1: 131,461,557 (GRCm39) |
V81I |
probably damaging |
Het |
Fasn |
C |
T |
11: 120,700,277 (GRCm39) |
M2182I |
probably benign |
Het |
Fras1 |
C |
T |
5: 96,862,322 (GRCm39) |
P2234S |
probably damaging |
Het |
Grn |
C |
A |
11: 102,323,896 (GRCm39) |
D33E |
possibly damaging |
Het |
Gsap |
A |
G |
5: 21,456,163 (GRCm39) |
|
probably benign |
Het |
H2bc15 |
T |
A |
13: 21,938,417 (GRCm39) |
V42E |
probably damaging |
Het |
Hook3 |
T |
C |
8: 26,562,378 (GRCm39) |
Q229R |
possibly damaging |
Het |
Itgb6 |
T |
C |
2: 60,480,412 (GRCm39) |
E308G |
probably damaging |
Het |
Kmo |
C |
T |
1: 175,479,184 (GRCm39) |
P240L |
possibly damaging |
Het |
Lrrc4c |
A |
G |
2: 97,460,330 (GRCm39) |
M319V |
probably benign |
Het |
Mia3 |
T |
C |
1: 183,138,698 (GRCm39) |
I672M |
probably benign |
Het |
Mib2 |
C |
T |
4: 155,743,917 (GRCm39) |
G42S |
probably damaging |
Het |
Mlc1 |
A |
G |
15: 88,849,664 (GRCm39) |
L223P |
probably damaging |
Het |
Mmp21 |
T |
C |
7: 133,276,182 (GRCm39) |
K554E |
probably benign |
Het |
Nup160 |
C |
T |
2: 90,524,246 (GRCm39) |
T383I |
probably damaging |
Het |
Opcml |
T |
A |
9: 28,814,595 (GRCm39) |
D290E |
probably damaging |
Het |
Or10a3b |
T |
A |
7: 108,445,191 (GRCm39) |
T9S |
probably benign |
Het |
Or4a27 |
T |
A |
2: 88,559,376 (GRCm39) |
D189V |
probably damaging |
Het |
Or5ac19 |
C |
T |
16: 59,089,307 (GRCm39) |
C241Y |
probably damaging |
Het |
Or5d38 |
A |
G |
2: 87,954,573 (GRCm39) |
I252T |
probably damaging |
Het |
Or5k14 |
T |
C |
16: 58,693,333 (GRCm39) |
Y60C |
probably damaging |
Het |
Palm3 |
C |
A |
8: 84,755,901 (GRCm39) |
T471K |
probably benign |
Het |
Prl2c5 |
T |
A |
13: 13,360,492 (GRCm39) |
L50* |
probably null |
Het |
Pzp |
T |
C |
6: 128,496,389 (GRCm39) |
N281S |
probably benign |
Het |
Qser1 |
T |
C |
2: 104,590,900 (GRCm39) |
Y1722C |
probably damaging |
Het |
Ryr3 |
A |
G |
2: 112,699,453 (GRCm39) |
V879A |
probably benign |
Het |
Sbno1 |
A |
G |
5: 124,531,975 (GRCm39) |
S736P |
possibly damaging |
Het |
Septin5 |
G |
A |
16: 18,441,844 (GRCm39) |
|
probably benign |
Het |
Slc17a6 |
A |
G |
7: 51,298,996 (GRCm39) |
|
probably benign |
Het |
Spag17 |
A |
T |
3: 100,010,433 (GRCm39) |
T1976S |
probably benign |
Het |
Swt1 |
A |
T |
1: 151,246,320 (GRCm39) |
|
probably benign |
Het |
Tenm4 |
T |
C |
7: 96,446,688 (GRCm39) |
W853R |
probably damaging |
Het |
Thbs1 |
A |
T |
2: 117,953,532 (GRCm39) |
Q983L |
probably damaging |
Het |
Tmem191 |
A |
G |
16: 17,094,347 (GRCm39) |
|
probably benign |
Het |
Tmprss11g |
A |
T |
5: 86,638,606 (GRCm39) |
V294D |
probably damaging |
Het |
Tor1aip2 |
A |
G |
1: 155,941,082 (GRCm39) |
S463G |
probably benign |
Het |
Trim36 |
A |
G |
18: 46,329,385 (GRCm39) |
|
probably benign |
Het |
Uckl1 |
C |
T |
2: 181,214,278 (GRCm39) |
R303H |
possibly damaging |
Het |
Vwa8 |
C |
A |
14: 79,324,094 (GRCm39) |
C1132* |
probably null |
Het |
|
Other mutations in Ttc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01017:Ttc1
|
APN |
11 |
43,621,320 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01449:Ttc1
|
APN |
11 |
43,629,630 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01980:Ttc1
|
APN |
11 |
43,621,291 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02414:Ttc1
|
APN |
11 |
43,630,664 (GRCm39) |
splice site |
probably benign |
|
IGL02541:Ttc1
|
APN |
11 |
43,629,648 (GRCm39) |
missense |
probably benign |
|
IGL03006:Ttc1
|
APN |
11 |
43,636,147 (GRCm39) |
missense |
probably benign |
|
IGL03253:Ttc1
|
APN |
11 |
43,629,650 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4434001:Ttc1
|
UTSW |
11 |
43,635,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0113:Ttc1
|
UTSW |
11 |
43,636,115 (GRCm39) |
missense |
probably benign |
0.25 |
R0391:Ttc1
|
UTSW |
11 |
43,629,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Ttc1
|
UTSW |
11 |
43,636,144 (GRCm39) |
missense |
probably benign |
0.01 |
R7493:Ttc1
|
UTSW |
11 |
43,636,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7956:Ttc1
|
UTSW |
11 |
43,627,240 (GRCm39) |
critical splice donor site |
probably null |
|
R8032:Ttc1
|
UTSW |
11 |
43,628,806 (GRCm39) |
missense |
probably damaging |
0.98 |
R9515:Ttc1
|
UTSW |
11 |
43,621,305 (GRCm39) |
missense |
|
|
|