Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930523C07Rik |
T |
C |
1: 159,902,865 (GRCm39) |
F45S |
possibly damaging |
Het |
Abca4 |
A |
G |
3: 121,913,714 (GRCm39) |
T897A |
probably benign |
Het |
Abhd5 |
A |
T |
9: 122,208,029 (GRCm39) |
T308S |
probably benign |
Het |
Abi2 |
G |
A |
1: 60,478,100 (GRCm39) |
|
probably null |
Het |
Abi3bp |
C |
A |
16: 56,409,046 (GRCm39) |
T283N |
possibly damaging |
Het |
Adcy2 |
A |
C |
13: 68,882,776 (GRCm39) |
N320K |
probably damaging |
Het |
Adcy3 |
T |
A |
12: 4,256,939 (GRCm39) |
M819K |
probably benign |
Het |
Anapc5 |
A |
G |
5: 122,940,209 (GRCm39) |
V354A |
probably benign |
Het |
Card14 |
A |
G |
11: 119,208,031 (GRCm39) |
I34V |
probably benign |
Het |
Ccdc153 |
A |
T |
9: 44,157,011 (GRCm39) |
T118S |
possibly damaging |
Het |
Champ1 |
G |
A |
8: 13,929,114 (GRCm39) |
G424D |
probably damaging |
Het |
Crybg3 |
A |
T |
16: 59,376,120 (GRCm39) |
|
probably benign |
Het |
Ctsr |
T |
A |
13: 61,307,295 (GRCm39) |
I334F |
possibly damaging |
Het |
Dlgap1 |
A |
T |
17: 70,823,964 (GRCm39) |
Q316H |
probably benign |
Het |
Dnajc18 |
A |
C |
18: 35,830,166 (GRCm39) |
C80G |
probably damaging |
Het |
Dthd1 |
G |
A |
5: 63,039,626 (GRCm39) |
R676H |
probably benign |
Het |
Fam186b |
G |
A |
15: 99,177,616 (GRCm39) |
A570V |
probably damaging |
Het |
Fancc |
T |
C |
13: 63,550,769 (GRCm39) |
K18E |
possibly damaging |
Het |
Fbxo46 |
G |
C |
7: 18,870,791 (GRCm39) |
R470P |
probably damaging |
Het |
Fbxw20 |
A |
C |
9: 109,050,399 (GRCm39) |
W409G |
probably damaging |
Het |
Gfy |
T |
C |
7: 44,827,251 (GRCm39) |
T282A |
probably benign |
Het |
Glb1l3 |
A |
G |
9: 26,761,351 (GRCm39) |
M227T |
probably damaging |
Het |
Gm8267 |
T |
C |
14: 44,960,346 (GRCm39) |
E133G |
probably damaging |
Het |
Hmcn1 |
A |
C |
1: 150,599,248 (GRCm39) |
I1556R |
possibly damaging |
Het |
Ifnl3 |
T |
C |
7: 28,223,287 (GRCm39) |
V102A |
probably damaging |
Het |
Kifc3 |
C |
T |
8: 95,830,622 (GRCm39) |
R548Q |
possibly damaging |
Het |
Lonrf1 |
T |
A |
8: 36,690,024 (GRCm39) |
Q678L |
probably benign |
Het |
Map2 |
A |
G |
1: 66,454,497 (GRCm39) |
E1129G |
probably damaging |
Het |
Mug2 |
C |
A |
6: 122,028,690 (GRCm39) |
D561E |
probably benign |
Het |
Myo3a |
G |
T |
2: 22,232,383 (GRCm39) |
|
probably benign |
Het |
N4bp1 |
A |
G |
8: 87,587,165 (GRCm39) |
V591A |
probably damaging |
Het |
Nckap5 |
C |
T |
1: 125,952,494 (GRCm39) |
G1353R |
probably benign |
Het |
Nek10 |
T |
A |
14: 14,937,766 (GRCm38) |
H828Q |
probably benign |
Het |
Or52n3 |
T |
A |
7: 104,530,050 (GRCm39) |
C45* |
probably null |
Het |
Or5k1b |
G |
T |
16: 58,581,202 (GRCm39) |
C112* |
probably null |
Het |
Pclo |
T |
C |
5: 14,816,830 (GRCm39) |
S1297P |
|
Het |
Pkhd1l1 |
T |
C |
15: 44,343,009 (GRCm39) |
I162T |
probably damaging |
Het |
Plaat5 |
A |
G |
19: 7,591,923 (GRCm39) |
E113G |
probably damaging |
Het |
Plekhg2 |
T |
C |
7: 28,062,297 (GRCm39) |
E541G |
probably damaging |
Het |
Ppp1r15a |
T |
C |
7: 45,174,149 (GRCm39) |
N220D |
possibly damaging |
Het |
Prss3l |
A |
G |
6: 41,420,486 (GRCm39) |
V80A |
probably benign |
Het |
Psmd4 |
A |
G |
3: 94,940,735 (GRCm39) |
S343P |
probably benign |
Het |
Rnf213 |
A |
T |
11: 119,354,406 (GRCm39) |
H4063L |
|
Het |
Rnf40 |
T |
C |
7: 127,190,954 (GRCm39) |
V313A |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,752,680 (GRCm39) |
E1880D |
probably benign |
Het |
Slc30a4 |
A |
T |
2: 122,527,200 (GRCm39) |
L398I |
probably damaging |
Het |
Sp100 |
A |
T |
1: 85,624,751 (GRCm39) |
N380I |
probably damaging |
Het |
Speer4d |
T |
G |
5: 15,828,393 (GRCm39) |
L175W |
probably damaging |
Het |
Srcap |
T |
A |
7: 127,137,273 (GRCm39) |
I985K |
possibly damaging |
Het |
Tesk2 |
T |
C |
4: 116,658,443 (GRCm39) |
|
probably null |
Het |
Tgfbrap1 |
A |
G |
1: 43,114,608 (GRCm39) |
V164A |
probably damaging |
Het |
Tlk1 |
T |
C |
2: 70,544,341 (GRCm39) |
T765A |
probably benign |
Het |
Tmem207 |
A |
T |
16: 26,345,413 (GRCm39) |
C18S |
|
Het |
Tph2 |
A |
T |
10: 114,915,992 (GRCm39) |
C394S |
probably benign |
Het |
Trrap |
C |
A |
5: 144,763,517 (GRCm39) |
H2470N |
probably damaging |
Het |
Ttc21b |
T |
C |
2: 66,053,866 (GRCm39) |
Y771C |
probably damaging |
Het |
Uchl3 |
T |
C |
14: 101,904,451 (GRCm39) |
F122L |
probably damaging |
Het |
Vipr1 |
G |
A |
9: 121,471,993 (GRCm39) |
|
probably null |
Het |
Vmn2r117 |
G |
T |
17: 23,696,578 (GRCm39) |
D276E |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,858,674 (GRCm39) |
L2708P |
probably damaging |
Het |
Vwa3a |
T |
A |
7: 120,385,682 (GRCm39) |
S675T |
possibly damaging |
Het |
Zfp473 |
A |
G |
7: 44,383,766 (GRCm39) |
L189P |
probably benign |
Het |
Zfp956 |
T |
A |
6: 47,941,041 (GRCm39) |
C467S |
probably damaging |
Het |
Zgrf1 |
T |
A |
3: 127,377,741 (GRCm39) |
N995K |
probably benign |
Het |
|
Other mutations in Gcnt4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00950:Gcnt4
|
APN |
13 |
97,083,064 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02677:Gcnt4
|
APN |
13 |
97,083,741 (GRCm39) |
missense |
probably benign |
|
IGL02936:Gcnt4
|
APN |
13 |
97,082,919 (GRCm39) |
missense |
probably benign |
0.00 |
R0332:Gcnt4
|
UTSW |
13 |
97,083,018 (GRCm39) |
missense |
probably benign |
0.01 |
R0741:Gcnt4
|
UTSW |
13 |
97,082,940 (GRCm39) |
nonsense |
probably null |
|
R0853:Gcnt4
|
UTSW |
13 |
97,083,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R2156:Gcnt4
|
UTSW |
13 |
97,082,974 (GRCm39) |
missense |
probably damaging |
0.99 |
R3837:Gcnt4
|
UTSW |
13 |
97,083,522 (GRCm39) |
nonsense |
probably null |
|
R3838:Gcnt4
|
UTSW |
13 |
97,083,522 (GRCm39) |
nonsense |
probably null |
|
R3839:Gcnt4
|
UTSW |
13 |
97,083,522 (GRCm39) |
nonsense |
probably null |
|
R4434:Gcnt4
|
UTSW |
13 |
97,082,850 (GRCm39) |
missense |
probably benign |
0.00 |
R4611:Gcnt4
|
UTSW |
13 |
97,082,990 (GRCm39) |
missense |
probably benign |
|
R4782:Gcnt4
|
UTSW |
13 |
97,083,914 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5853:Gcnt4
|
UTSW |
13 |
97,083,160 (GRCm39) |
missense |
probably benign |
0.01 |
R6013:Gcnt4
|
UTSW |
13 |
97,083,786 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6139:Gcnt4
|
UTSW |
13 |
97,083,360 (GRCm39) |
missense |
probably benign |
0.16 |
R6329:Gcnt4
|
UTSW |
13 |
97,083,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Gcnt4
|
UTSW |
13 |
97,083,027 (GRCm39) |
missense |
probably damaging |
0.98 |
R7217:Gcnt4
|
UTSW |
13 |
97,082,818 (GRCm39) |
missense |
probably damaging |
0.98 |
R7497:Gcnt4
|
UTSW |
13 |
97,083,468 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7509:Gcnt4
|
UTSW |
13 |
97,083,678 (GRCm39) |
missense |
probably benign |
0.28 |
R7592:Gcnt4
|
UTSW |
13 |
97,083,669 (GRCm39) |
missense |
probably benign |
0.02 |
R8673:Gcnt4
|
UTSW |
13 |
97,082,997 (GRCm39) |
missense |
probably benign |
0.24 |
R8907:Gcnt4
|
UTSW |
13 |
97,083,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R9036:Gcnt4
|
UTSW |
13 |
97,083,042 (GRCm39) |
missense |
probably benign |
|
R9371:Gcnt4
|
UTSW |
13 |
97,083,634 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9780:Gcnt4
|
UTSW |
13 |
97,083,948 (GRCm39) |
missense |
probably benign |
0.17 |
R9789:Gcnt4
|
UTSW |
13 |
97,083,429 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Gcnt4
|
UTSW |
13 |
97,082,961 (GRCm39) |
missense |
probably damaging |
0.98 |
|