Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agap2 |
A |
G |
10: 126,923,175 (GRCm39) |
I670V |
unknown |
Het |
Bcan |
G |
T |
3: 87,904,405 (GRCm39) |
T117K |
probably damaging |
Het |
Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
Cbx8 |
C |
A |
11: 118,929,754 (GRCm39) |
V280F |
probably damaging |
Het |
Ccdc17 |
A |
T |
4: 116,456,823 (GRCm39) |
I509F |
probably damaging |
Het |
Cdon |
T |
C |
9: 35,403,163 (GRCm39) |
V1091A |
probably benign |
Het |
Cntnap5b |
C |
T |
1: 100,311,310 (GRCm39) |
T972I |
probably damaging |
Het |
Dlg2 |
T |
C |
7: 90,740,240 (GRCm39) |
L9P |
possibly damaging |
Het |
Dnah6 |
T |
A |
6: 73,051,634 (GRCm39) |
R3053S |
probably benign |
Het |
Dnah7a |
T |
A |
1: 53,512,112 (GRCm39) |
N2983I |
probably damaging |
Het |
Dnah7c |
T |
C |
1: 46,711,536 (GRCm39) |
Y2588H |
probably damaging |
Het |
Dpysl5 |
A |
G |
5: 30,902,811 (GRCm39) |
D81G |
probably damaging |
Het |
Dscaml1 |
A |
G |
9: 45,653,884 (GRCm39) |
D1387G |
probably benign |
Het |
Exd1 |
G |
T |
2: 119,369,348 (GRCm39) |
T89K |
possibly damaging |
Het |
Ezh2 |
T |
A |
6: 47,522,745 (GRCm39) |
R364* |
probably null |
Het |
Fam161b |
C |
T |
12: 84,404,369 (GRCm39) |
D104N |
probably benign |
Het |
Fbxw8 |
C |
A |
5: 118,215,763 (GRCm39) |
V416L |
probably benign |
Het |
Flnc |
A |
T |
6: 29,450,849 (GRCm39) |
D1499V |
probably benign |
Het |
Fmc1 |
A |
T |
6: 38,516,115 (GRCm39) |
R54* |
probably null |
Het |
Fzr1 |
A |
G |
10: 81,206,942 (GRCm39) |
F61S |
probably damaging |
Het |
Get4 |
T |
G |
5: 139,251,393 (GRCm39) |
C160G |
probably benign |
Het |
Gm32742 |
G |
A |
9: 51,055,675 (GRCm39) |
R1330* |
probably null |
Het |
Gnat3 |
G |
A |
5: 18,220,312 (GRCm39) |
A225T |
possibly damaging |
Het |
Gucy2c |
A |
G |
6: 136,704,892 (GRCm39) |
Y541H |
probably damaging |
Het |
Hand2 |
A |
G |
8: 57,775,461 (GRCm39) |
T174A |
probably benign |
Het |
Helb |
T |
C |
10: 119,927,522 (GRCm39) |
T863A |
probably damaging |
Het |
Hoxa7 |
A |
T |
6: 52,194,993 (GRCm39) |
V2D |
unknown |
Het |
Ifi44 |
G |
A |
3: 151,444,978 (GRCm39) |
R325* |
probably null |
Het |
Igfn1 |
C |
T |
1: 135,895,520 (GRCm39) |
G1682E |
probably damaging |
Het |
Itch |
A |
G |
2: 155,010,627 (GRCm39) |
N32D |
probably benign |
Het |
Kif26b |
T |
C |
1: 178,744,923 (GRCm39) |
V1673A |
probably benign |
Het |
Map1a |
A |
T |
2: 121,135,418 (GRCm39) |
D2078V |
probably benign |
Het |
Mgat4b |
G |
T |
11: 50,121,512 (GRCm39) |
V35L |
probably benign |
Het |
Micu3 |
G |
A |
8: 40,761,205 (GRCm39) |
M38I |
probably benign |
Het |
Myo15a |
A |
T |
11: 60,387,241 (GRCm39) |
H706L |
probably damaging |
Het |
Ndc1 |
A |
G |
4: 107,226,017 (GRCm39) |
T42A |
probably benign |
Het |
Nfat5 |
T |
A |
8: 108,095,152 (GRCm39) |
M1131K |
probably damaging |
Het |
Nop14 |
G |
A |
5: 34,798,784 (GRCm39) |
S648L |
probably damaging |
Het |
Or51k1 |
G |
T |
7: 103,661,632 (GRCm39) |
Y92* |
probably null |
Het |
Otogl |
A |
G |
10: 107,634,597 (GRCm39) |
V1413A |
probably damaging |
Het |
Palb2 |
T |
A |
7: 121,711,224 (GRCm39) |
M967L |
possibly damaging |
Het |
Pira12 |
G |
A |
7: 3,898,257 (GRCm39) |
T355I |
probably benign |
Het |
Ppa2 |
A |
G |
3: 133,053,904 (GRCm39) |
K198R |
probably damaging |
Het |
Prokr1 |
T |
C |
6: 87,565,756 (GRCm39) |
T30A |
probably benign |
Het |
Prss50 |
C |
T |
9: 110,687,128 (GRCm39) |
R24C |
unknown |
Het |
Rbm17 |
T |
C |
2: 11,605,441 (GRCm39) |
T38A |
possibly damaging |
Het |
Rps6ka5 |
G |
A |
12: 100,541,500 (GRCm39) |
Q420* |
probably null |
Het |
Senp6 |
G |
T |
9: 80,025,794 (GRCm39) |
R448L |
probably damaging |
Het |
Senp7 |
T |
C |
16: 55,999,391 (GRCm39) |
I838T |
probably damaging |
Het |
Sf3b2 |
C |
T |
19: 5,337,242 (GRCm39) |
S329N |
possibly damaging |
Het |
Slc13a4 |
A |
T |
6: 35,245,814 (GRCm39) |
D610E |
probably benign |
Het |
Slc24a2 |
A |
G |
4: 87,145,337 (GRCm39) |
L239P |
probably damaging |
Het |
Slc39a5 |
T |
A |
10: 128,232,884 (GRCm39) |
H389L |
probably damaging |
Het |
Syt4 |
A |
G |
18: 31,577,072 (GRCm39) |
L94P |
probably damaging |
Het |
Tgm5 |
A |
G |
2: 120,879,356 (GRCm39) |
V560A |
probably benign |
Het |
Thoc5 |
A |
G |
11: 4,876,115 (GRCm39) |
T623A |
probably damaging |
Het |
Tm7sf2 |
C |
T |
19: 6,113,074 (GRCm39) |
V376I |
probably benign |
Het |
Tmem268 |
T |
A |
4: 63,496,141 (GRCm39) |
V194E |
probably damaging |
Het |
Tpr |
C |
A |
1: 150,290,564 (GRCm39) |
R798S |
probably damaging |
Het |
Trpv5 |
G |
T |
6: 41,630,182 (GRCm39) |
T685K |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,584,774 (GRCm39) |
N22141K |
probably damaging |
Het |
Txnrd2 |
T |
C |
16: 18,275,048 (GRCm39) |
I353T |
unknown |
Het |
Upk1a |
A |
G |
7: 30,303,043 (GRCm39) |
Y252H |
probably damaging |
Het |
Vmn2r118 |
A |
G |
17: 55,915,642 (GRCm39) |
I436T |
probably benign |
Het |
Vmn2r76 |
T |
A |
7: 85,874,479 (GRCm39) |
I833F |
possibly damaging |
Het |
Zfp277 |
T |
C |
12: 40,379,577 (GRCm39) |
H319R |
probably damaging |
Het |
|
Other mutations in Ccdc117 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01160:Ccdc117
|
APN |
11 |
5,481,532 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01455:Ccdc117
|
APN |
11 |
5,484,297 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02167:Ccdc117
|
APN |
11 |
5,481,333 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5029_Ccdc117_570
|
UTSW |
11 |
5,484,897 (GRCm39) |
missense |
possibly damaging |
0.53 |
D6062:Ccdc117
|
UTSW |
11 |
5,475,039 (GRCm39) |
unclassified |
probably benign |
|
R0645:Ccdc117
|
UTSW |
11 |
5,484,385 (GRCm39) |
splice site |
probably benign |
|
R2697:Ccdc117
|
UTSW |
11 |
5,484,888 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5029:Ccdc117
|
UTSW |
11 |
5,484,897 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6191:Ccdc117
|
UTSW |
11 |
5,484,242 (GRCm39) |
critical splice donor site |
probably null |
|
R6395:Ccdc117
|
UTSW |
11 |
5,484,762 (GRCm39) |
splice site |
probably null |
|
R6924:Ccdc117
|
UTSW |
11 |
5,484,255 (GRCm39) |
missense |
probably benign |
0.05 |
R7982:Ccdc117
|
UTSW |
11 |
5,481,460 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8959:Ccdc117
|
UTSW |
11 |
5,491,421 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9772:Ccdc117
|
UTSW |
11 |
5,492,042 (GRCm39) |
missense |
possibly damaging |
0.53 |
|