Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
A |
16: 4,667,187 (GRCm39) |
L220H |
unknown |
Het |
Amt |
T |
A |
9: 108,177,851 (GRCm39) |
L272Q |
probably damaging |
Het |
Ank2 |
G |
C |
3: 126,770,545 (GRCm39) |
Y894* |
probably null |
Het |
Ankzf1 |
T |
A |
1: 75,170,908 (GRCm39) |
F105I |
probably damaging |
Het |
Aox4 |
C |
A |
1: 58,298,236 (GRCm39) |
Y1067* |
probably null |
Het |
BC034090 |
T |
A |
1: 155,100,836 (GRCm39) |
Q476L |
probably damaging |
Het |
Bhmt |
G |
T |
13: 93,763,871 (GRCm39) |
R57S |
probably damaging |
Het |
Cacna1c |
A |
T |
6: 118,633,136 (GRCm39) |
F964L |
probably damaging |
Het |
Celsr3 |
A |
C |
9: 108,724,851 (GRCm39) |
S396R |
probably benign |
Het |
Cpne4 |
C |
A |
9: 104,799,755 (GRCm39) |
Q191K |
probably damaging |
Het |
D630003M21Rik |
A |
G |
2: 158,058,623 (GRCm39) |
S426P |
probably damaging |
Het |
Dennd10 |
T |
A |
19: 60,823,309 (GRCm39) |
F315I |
probably benign |
Het |
Dido1 |
G |
T |
2: 180,329,443 (GRCm39) |
N326K |
probably benign |
Het |
E2f2 |
T |
A |
4: 135,911,760 (GRCm39) |
I257N |
probably damaging |
Het |
Elfn1 |
T |
G |
5: 139,959,413 (GRCm39) |
F806V |
probably damaging |
Het |
Eml6 |
T |
A |
11: 29,783,204 (GRCm39) |
Y559F |
probably damaging |
Het |
Erich6 |
A |
G |
3: 58,543,480 (GRCm39) |
|
probably null |
Het |
Fam78a |
T |
C |
2: 31,972,617 (GRCm39) |
N101S |
probably damaging |
Het |
Fam83h |
A |
G |
15: 75,874,185 (GRCm39) |
S1051P |
probably benign |
Het |
Galns |
C |
T |
8: 123,330,195 (GRCm39) |
G112D |
probably damaging |
Het |
Gm9923 |
A |
G |
10: 72,145,524 (GRCm39) |
K125R |
probably damaging |
Het |
Hectd3 |
G |
A |
4: 116,854,415 (GRCm39) |
V326M |
probably damaging |
Het |
Iars2 |
A |
G |
1: 185,048,248 (GRCm39) |
S495P |
possibly damaging |
Het |
Ice1 |
T |
C |
13: 70,754,503 (GRCm39) |
R528G |
probably damaging |
Het |
Igkv12-38 |
T |
A |
6: 69,920,368 (GRCm39) |
Y50F |
possibly damaging |
Het |
Inpp5j |
T |
C |
11: 3,445,025 (GRCm39) |
S883G |
probably damaging |
Het |
Irf8 |
T |
C |
8: 121,480,178 (GRCm39) |
S139P |
probably damaging |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Kcnq4 |
G |
T |
4: 120,570,271 (GRCm39) |
D357E |
possibly damaging |
Het |
Klhl1 |
A |
G |
14: 96,517,584 (GRCm39) |
L364P |
probably damaging |
Het |
Krt7 |
A |
G |
15: 101,318,439 (GRCm39) |
I309V |
probably benign |
Het |
Krt76 |
G |
T |
15: 101,797,516 (GRCm39) |
A281D |
probably damaging |
Het |
Lancl2 |
T |
C |
6: 57,714,697 (GRCm39) |
F430L |
probably damaging |
Het |
Llgl2 |
T |
C |
11: 115,739,125 (GRCm39) |
V332A |
probably damaging |
Het |
Lrrc26 |
A |
T |
2: 25,180,076 (GRCm39) |
T26S |
probably benign |
Het |
Lrrk1 |
T |
A |
7: 65,912,041 (GRCm39) |
M1840L |
probably benign |
Het |
Lyst |
G |
A |
13: 13,812,486 (GRCm39) |
C966Y |
probably damaging |
Het |
Mad1l1 |
T |
A |
5: 140,247,266 (GRCm39) |
S354C |
possibly damaging |
Het |
Mbtps1 |
C |
T |
8: 120,252,159 (GRCm39) |
G577D |
probably damaging |
Het |
Mycbp2 |
C |
T |
14: 103,426,027 (GRCm39) |
R2366H |
probably damaging |
Het |
Myo18a |
T |
G |
11: 77,668,511 (GRCm39) |
|
probably null |
Het |
Naip5 |
G |
A |
13: 100,358,639 (GRCm39) |
R866C |
possibly damaging |
Het |
Nav2 |
T |
A |
7: 49,102,567 (GRCm39) |
V455E |
probably benign |
Het |
Neb |
A |
G |
2: 52,153,674 (GRCm39) |
I2417T |
possibly damaging |
Het |
Nme5 |
C |
T |
18: 34,702,890 (GRCm39) |
A133T |
probably benign |
Het |
Nradd |
T |
C |
9: 110,450,979 (GRCm39) |
D51G |
possibly damaging |
Het |
Pard3b |
A |
G |
1: 62,250,843 (GRCm39) |
R591G |
probably damaging |
Het |
Pcbp4 |
T |
C |
9: 106,337,929 (GRCm39) |
F73S |
probably damaging |
Het |
Pcdhb11 |
C |
T |
18: 37,555,419 (GRCm39) |
Q250* |
probably null |
Het |
Pde1c |
T |
A |
6: 56,049,194 (GRCm39) |
K766N |
probably damaging |
Het |
Phf21b |
G |
A |
15: 84,738,942 (GRCm39) |
Q40* |
probably null |
Het |
Prr14 |
A |
G |
7: 127,073,868 (GRCm39) |
D244G |
probably benign |
Het |
Rab11fip5 |
C |
T |
6: 85,351,249 (GRCm39) |
A88T |
probably damaging |
Het |
Rad54l2 |
A |
T |
9: 106,593,317 (GRCm39) |
S428T |
probably benign |
Het |
Rdh9 |
A |
G |
10: 127,612,621 (GRCm39) |
I90V |
probably benign |
Het |
Rhag |
G |
T |
17: 41,139,292 (GRCm39) |
G76C |
probably damaging |
Het |
Riok3 |
T |
A |
18: 12,261,984 (GRCm39) |
V6E |
possibly damaging |
Het |
Rnf7l |
A |
T |
10: 63,257,244 (GRCm39) |
V92E |
probably damaging |
Het |
Scn10a |
A |
G |
9: 119,500,592 (GRCm39) |
I229T |
probably damaging |
Het |
Slco1a1 |
G |
T |
6: 141,854,695 (GRCm39) |
T652K |
probably benign |
Het |
Slit1 |
T |
A |
19: 41,635,459 (GRCm39) |
I345F |
probably damaging |
Het |
Snrnp200 |
A |
T |
2: 127,074,857 (GRCm39) |
I1477F |
probably damaging |
Het |
Snx31 |
G |
A |
15: 36,523,698 (GRCm39) |
T328I |
possibly damaging |
Het |
Strn |
A |
G |
17: 78,965,390 (GRCm39) |
F634S |
probably damaging |
Het |
Tmem101 |
C |
T |
11: 102,047,155 (GRCm39) |
G6R |
probably benign |
Het |
Tmem199 |
C |
G |
11: 78,399,506 (GRCm39) |
G131R |
probably benign |
Het |
Trim66 |
A |
G |
7: 109,055,267 (GRCm39) |
|
probably null |
Het |
Ttn |
G |
T |
2: 76,681,929 (GRCm39) |
|
probably benign |
Het |
Upk3bl |
T |
C |
5: 136,086,247 (GRCm39) |
L61P |
probably benign |
Het |
Vmn2r108 |
A |
G |
17: 20,692,632 (GRCm39) |
Y75H |
probably damaging |
Het |
Vmn2r91 |
T |
A |
17: 18,327,906 (GRCm39) |
I500K |
probably damaging |
Het |
Vps18 |
C |
T |
2: 119,124,272 (GRCm39) |
R400C |
probably damaging |
Het |
Zeb1 |
C |
T |
18: 5,767,286 (GRCm39) |
P599L |
probably damaging |
Het |
Zfhx4 |
G |
T |
3: 5,464,557 (GRCm39) |
A1572S |
probably damaging |
Het |
Zfp677 |
T |
A |
17: 21,617,680 (GRCm39) |
C246S |
possibly damaging |
Het |
Zfp719 |
T |
A |
7: 43,239,834 (GRCm39) |
I474N |
probably damaging |
Het |
|
Other mutations in Csnk1g2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01066:Csnk1g2
|
APN |
10 |
80,470,481 (GRCm39) |
unclassified |
probably benign |
|
IGL01657:Csnk1g2
|
APN |
10 |
80,475,463 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01920:Csnk1g2
|
APN |
10 |
80,474,262 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02887:Csnk1g2
|
APN |
10 |
80,474,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2845:Csnk1g2
|
UTSW |
10 |
80,474,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R4135:Csnk1g2
|
UTSW |
10 |
80,474,130 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4626:Csnk1g2
|
UTSW |
10 |
80,475,648 (GRCm39) |
missense |
probably damaging |
0.98 |
R4717:Csnk1g2
|
UTSW |
10 |
80,473,749 (GRCm39) |
missense |
probably benign |
0.36 |
R5546:Csnk1g2
|
UTSW |
10 |
80,474,232 (GRCm39) |
missense |
probably benign |
0.36 |
R6000:Csnk1g2
|
UTSW |
10 |
80,474,778 (GRCm39) |
missense |
probably damaging |
0.99 |
R6415:Csnk1g2
|
UTSW |
10 |
80,474,130 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6449:Csnk1g2
|
UTSW |
10 |
80,475,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Csnk1g2
|
UTSW |
10 |
80,473,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7263:Csnk1g2
|
UTSW |
10 |
80,470,332 (GRCm39) |
missense |
probably damaging |
0.97 |
R7316:Csnk1g2
|
UTSW |
10 |
80,475,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8169:Csnk1g2
|
UTSW |
10 |
80,475,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Csnk1g2
|
UTSW |
10 |
80,475,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Csnk1g2
|
UTSW |
10 |
80,474,463 (GRCm39) |
critical splice donor site |
probably null |
|
R8724:Csnk1g2
|
UTSW |
10 |
80,474,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R8816:Csnk1g2
|
UTSW |
10 |
80,474,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R8960:Csnk1g2
|
UTSW |
10 |
80,474,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R9243:Csnk1g2
|
UTSW |
10 |
80,475,648 (GRCm39) |
missense |
probably damaging |
0.98 |
R9322:Csnk1g2
|
UTSW |
10 |
80,474,978 (GRCm39) |
missense |
probably damaging |
0.96 |
R9751:Csnk1g2
|
UTSW |
10 |
80,473,745 (GRCm39) |
missense |
possibly damaging |
0.80 |
|