Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
A |
T |
5: 113,339,010 (GRCm39) |
M334K |
probably benign |
Het |
Abca1 |
A |
T |
4: 53,060,351 (GRCm39) |
I1525N |
probably benign |
Het |
Abca4 |
A |
T |
3: 121,879,275 (GRCm39) |
I398F |
|
Het |
Acbd3 |
A |
G |
1: 180,572,721 (GRCm39) |
D327G |
probably benign |
Het |
Acsm3 |
A |
G |
7: 119,383,166 (GRCm39) |
T544A |
probably damaging |
Het |
Atp11a |
C |
T |
8: 12,901,087 (GRCm39) |
T972M |
probably damaging |
Het |
Cbfb |
C |
T |
8: 105,929,123 (GRCm39) |
R147* |
probably null |
Het |
Ccdc17 |
G |
T |
4: 116,454,144 (GRCm39) |
R54L |
probably benign |
Het |
Cracdl |
T |
G |
1: 37,670,496 (GRCm39) |
E148A |
probably damaging |
Het |
Cuedc2 |
G |
T |
19: 46,319,399 (GRCm39) |
A223E |
probably benign |
Het |
Cul5 |
T |
C |
9: 53,532,474 (GRCm39) |
I787V |
probably benign |
Het |
D430041D05Rik |
T |
A |
2: 104,087,563 (GRCm39) |
H471L |
probably benign |
Het |
Ddx39a |
T |
C |
8: 84,448,916 (GRCm39) |
Y264H |
probably benign |
Het |
Dlgap3 |
C |
A |
4: 127,127,665 (GRCm39) |
R778S |
probably damaging |
Het |
Esrrg |
T |
C |
1: 187,930,848 (GRCm39) |
V313A |
probably damaging |
Het |
Fam124a |
T |
C |
14: 62,844,100 (GRCm39) |
I536T |
probably damaging |
Het |
Fbxo21 |
T |
C |
5: 118,127,272 (GRCm39) |
F275L |
possibly damaging |
Het |
Gabrg1 |
C |
A |
5: 70,999,558 (GRCm39) |
G2V |
possibly damaging |
Het |
Gcc1 |
G |
T |
6: 28,418,089 (GRCm39) |
A748D |
probably damaging |
Het |
Gjb6 |
T |
C |
14: 57,361,511 (GRCm39) |
D250G |
probably benign |
Het |
Gm44501 |
A |
T |
17: 40,889,872 (GRCm39) |
K129* |
probably null |
Het |
Hmcn2 |
T |
G |
2: 31,320,375 (GRCm39) |
L3952R |
|
Het |
Hpd |
A |
G |
5: 123,312,535 (GRCm39) |
I278T |
probably damaging |
Het |
Igsf3 |
T |
A |
3: 101,346,904 (GRCm39) |
F613Y |
probably damaging |
Het |
Igsf3 |
T |
C |
3: 101,346,817 (GRCm39) |
F584S |
probably damaging |
Het |
Ik |
A |
G |
18: 36,886,635 (GRCm39) |
D369G |
probably benign |
Het |
Ikbke |
A |
G |
1: 131,198,719 (GRCm39) |
L365P |
probably damaging |
Het |
Il22ra2 |
A |
T |
10: 19,508,542 (GRCm39) |
Q190L |
possibly damaging |
Het |
Itga6 |
T |
C |
2: 71,679,834 (GRCm39) |
V1033A |
probably benign |
Het |
Kif18a |
T |
C |
2: 109,120,032 (GRCm39) |
Y112H |
probably damaging |
Het |
Krt75 |
T |
C |
15: 101,482,238 (GRCm39) |
H10R |
probably benign |
Het |
L3mbtl1 |
T |
A |
2: 162,790,734 (GRCm39) |
L93H |
probably benign |
Het |
Lrfn1 |
G |
A |
7: 28,158,183 (GRCm39) |
C34Y |
probably damaging |
Het |
Lrrc47 |
A |
T |
4: 154,101,920 (GRCm39) |
I396F |
probably damaging |
Het |
Mgat3 |
T |
A |
15: 80,095,641 (GRCm39) |
V156E |
probably benign |
Het |
Mtus2 |
A |
G |
5: 148,232,300 (GRCm39) |
D1120G |
possibly damaging |
Het |
Muc5ac |
G |
T |
7: 141,365,465 (GRCm39) |
E2700* |
probably null |
Het |
Nxpe5 |
A |
T |
5: 138,228,591 (GRCm39) |
|
probably benign |
Het |
Or51v15-ps1 |
T |
C |
7: 103,278,931 (GRCm39) |
T79A |
probably damaging |
Het |
Or5aq6 |
A |
T |
2: 86,923,390 (GRCm39) |
M117K |
possibly damaging |
Het |
Pcdhga4 |
T |
A |
18: 37,819,746 (GRCm39) |
S432T |
possibly damaging |
Het |
Pdk4 |
T |
A |
6: 5,486,716 (GRCm39) |
M353L |
probably benign |
Het |
Ppp1r13b |
T |
A |
12: 111,800,210 (GRCm39) |
K645N |
probably benign |
Het |
Ppt1 |
A |
T |
4: 122,751,367 (GRCm39) |
D288V |
possibly damaging |
Het |
Prkcb |
A |
G |
7: 122,181,663 (GRCm39) |
Y417C |
probably damaging |
Het |
Prss22 |
A |
G |
17: 24,215,721 (GRCm39) |
I67T |
probably damaging |
Het |
Rab29 |
T |
C |
1: 131,795,508 (GRCm39) |
V40A |
possibly damaging |
Het |
Rae1 |
T |
C |
2: 172,849,941 (GRCm39) |
|
probably null |
Het |
Rasa3 |
C |
T |
8: 13,630,033 (GRCm39) |
|
probably null |
Het |
Rasgrp3 |
A |
G |
17: 75,807,717 (GRCm39) |
D258G |
probably benign |
Het |
Rcc1 |
T |
A |
4: 132,062,808 (GRCm39) |
T208S |
probably benign |
Het |
Rgs3 |
C |
A |
4: 62,575,354 (GRCm39) |
Y580* |
probably null |
Het |
Rpe65 |
C |
T |
3: 159,328,318 (GRCm39) |
P405S |
probably damaging |
Het |
Rsf1 |
GGCGGC |
GGCGGCGGCAGCGGC |
7: 97,229,137 (GRCm39) |
|
probably benign |
Het |
Rsph4a |
A |
G |
10: 33,790,418 (GRCm39) |
E669G |
probably damaging |
Het |
Rusc1 |
A |
T |
3: 88,994,113 (GRCm39) |
V964E |
probably benign |
Het |
Rusc2 |
A |
G |
4: 43,415,897 (GRCm39) |
N401S |
probably damaging |
Het |
Slc10a1 |
G |
T |
12: 81,002,864 (GRCm39) |
T258K |
probably damaging |
Het |
Slc5a9 |
A |
G |
4: 111,747,418 (GRCm39) |
L323P |
probably damaging |
Het |
Slc6a17 |
T |
A |
3: 107,378,772 (GRCm39) |
I637F |
possibly damaging |
Het |
Slc8a2 |
A |
G |
7: 15,886,780 (GRCm39) |
E641G |
possibly damaging |
Het |
Sptbn2 |
G |
T |
19: 4,789,974 (GRCm39) |
A1321S |
probably damaging |
Het |
Ssh2 |
G |
T |
11: 77,283,976 (GRCm39) |
A77S |
possibly damaging |
Het |
St13 |
G |
T |
15: 81,250,587 (GRCm39) |
N316K |
probably damaging |
Het |
Taf10 |
A |
G |
7: 105,393,062 (GRCm39) |
M121T |
probably benign |
Het |
Tcta |
T |
C |
9: 108,182,942 (GRCm39) |
T68A |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,299,769 (GRCm39) |
E161G |
probably damaging |
Het |
Tmed10 |
T |
C |
12: 85,397,621 (GRCm39) |
I123V |
probably benign |
Het |
Ttf1 |
T |
C |
2: 28,969,492 (GRCm39) |
|
probably null |
Het |
Tubg1 |
A |
G |
11: 101,016,886 (GRCm39) |
D396G |
probably damaging |
Het |
Uhmk1 |
A |
G |
1: 170,034,913 (GRCm39) |
|
probably null |
Het |
Unc13a |
C |
T |
8: 72,103,221 (GRCm39) |
A922T |
probably benign |
Het |
Usp24 |
T |
A |
4: 106,219,379 (GRCm39) |
V525E |
probably damaging |
Het |
Usp28 |
C |
A |
9: 48,947,037 (GRCm39) |
Q823K |
probably damaging |
Het |
Vldlr |
A |
T |
19: 27,224,031 (GRCm39) |
I764F |
probably benign |
Het |
Vmn2r88 |
T |
C |
14: 51,648,641 (GRCm39) |
Y62H |
|
Het |
Zfp423 |
T |
A |
8: 88,507,725 (GRCm39) |
N873I |
possibly damaging |
Het |
|
Other mutations in Timd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01015:Timd2
|
APN |
11 |
46,567,170 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01289:Timd2
|
APN |
11 |
46,570,499 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02066:Timd2
|
APN |
11 |
46,569,050 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02439:Timd2
|
APN |
11 |
46,569,063 (GRCm39) |
splice site |
probably benign |
|
R2217:Timd2
|
UTSW |
11 |
46,577,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R2218:Timd2
|
UTSW |
11 |
46,577,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:Timd2
|
UTSW |
11 |
46,569,043 (GRCm39) |
missense |
probably benign |
0.01 |
R3621:Timd2
|
UTSW |
11 |
46,569,040 (GRCm39) |
missense |
probably benign |
0.00 |
R3876:Timd2
|
UTSW |
11 |
46,561,847 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4173:Timd2
|
UTSW |
11 |
46,561,787 (GRCm39) |
missense |
probably benign |
0.00 |
R4793:Timd2
|
UTSW |
11 |
46,578,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Timd2
|
UTSW |
11 |
46,568,094 (GRCm39) |
nonsense |
probably null |
|
R4963:Timd2
|
UTSW |
11 |
46,573,617 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5314:Timd2
|
UTSW |
11 |
46,568,087 (GRCm39) |
missense |
probably benign |
0.09 |
R5798:Timd2
|
UTSW |
11 |
46,568,064 (GRCm39) |
missense |
probably benign |
0.06 |
R6074:Timd2
|
UTSW |
11 |
46,577,999 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6090:Timd2
|
UTSW |
11 |
46,578,063 (GRCm39) |
missense |
probably benign |
0.11 |
R6694:Timd2
|
UTSW |
11 |
46,561,779 (GRCm39) |
nonsense |
probably null |
|
R7817:Timd2
|
UTSW |
11 |
46,561,781 (GRCm39) |
missense |
probably benign |
0.00 |
R8379:Timd2
|
UTSW |
11 |
46,568,027 (GRCm39) |
splice site |
probably null |
|
R9321:Timd2
|
UTSW |
11 |
46,577,916 (GRCm39) |
missense |
probably benign |
0.00 |
R9763:Timd2
|
UTSW |
11 |
46,573,540 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Timd2
|
UTSW |
11 |
46,570,506 (GRCm39) |
missense |
probably benign |
0.26 |
|