Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy2 |
A |
C |
13: 68,878,486 (GRCm39) |
I384S |
probably damaging |
Het |
Atxn7 |
T |
C |
14: 14,087,273 (GRCm38) |
|
probably benign |
Het |
Blm |
A |
T |
7: 80,143,895 (GRCm39) |
V848D |
probably damaging |
Het |
Cul1 |
G |
T |
6: 47,478,143 (GRCm39) |
L175F |
probably damaging |
Het |
Cyp4a29 |
A |
G |
4: 115,108,368 (GRCm39) |
H364R |
possibly damaging |
Het |
Ddx60 |
A |
G |
8: 62,465,483 (GRCm39) |
D1380G |
probably damaging |
Het |
Det1 |
A |
T |
7: 78,493,372 (GRCm39) |
C211S |
possibly damaging |
Het |
Dnaaf9 |
A |
G |
2: 130,559,200 (GRCm39) |
Y822H |
probably damaging |
Het |
F5 |
A |
C |
1: 164,020,801 (GRCm39) |
Q1092P |
probably damaging |
Het |
Fbxl13 |
A |
G |
5: 21,728,796 (GRCm39) |
|
probably null |
Het |
Galnt7 |
A |
G |
8: 57,979,212 (GRCm39) |
I637T |
probably benign |
Het |
H2-T24 |
T |
A |
17: 36,317,671 (GRCm39) |
K120N |
unknown |
Het |
Hes2 |
A |
G |
4: 152,244,269 (GRCm39) |
K18R |
probably damaging |
Het |
Icam5 |
A |
T |
9: 20,945,097 (GRCm39) |
Q220L |
probably benign |
Het |
Kdm8 |
G |
A |
7: 125,054,278 (GRCm39) |
A170T |
probably benign |
Het |
Krt40 |
G |
A |
11: 99,430,711 (GRCm39) |
A321V |
probably damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,828,979 (GRCm39) |
V45D |
probably damaging |
Het |
Mbip |
A |
G |
12: 56,382,597 (GRCm39) |
Y290H |
probably damaging |
Het |
Mical1 |
A |
G |
10: 41,354,195 (GRCm39) |
Y48C |
probably damaging |
Het |
Mslnl |
T |
C |
17: 25,963,051 (GRCm39) |
S300P |
probably benign |
Het |
Nanog |
T |
C |
6: 122,688,731 (GRCm39) |
L104P |
probably damaging |
Het |
Or10ak11 |
T |
C |
4: 118,687,238 (GRCm39) |
Y132C |
probably damaging |
Het |
Or4c113 |
A |
T |
2: 88,885,457 (GRCm39) |
H104Q |
probably damaging |
Het |
Or4f60 |
T |
A |
2: 111,902,007 (GRCm39) |
Y307F |
probably benign |
Het |
Or52n2c |
A |
T |
7: 104,574,580 (GRCm39) |
N130K |
probably benign |
Het |
Oxgr1 |
C |
A |
14: 120,260,199 (GRCm39) |
E3* |
probably null |
Het |
Pam16 |
A |
T |
16: 4,434,671 (GRCm39) |
|
probably benign |
Het |
Plcb1 |
A |
T |
2: 134,655,606 (GRCm39) |
|
probably benign |
Het |
Slc25a32 |
A |
T |
15: 38,969,359 (GRCm39) |
V58E |
probably benign |
Het |
Slc2a12 |
G |
T |
10: 22,541,134 (GRCm39) |
V330F |
probably damaging |
Het |
Slit1 |
T |
C |
19: 41,591,881 (GRCm39) |
E1247G |
possibly damaging |
Het |
Supt5 |
A |
T |
7: 28,019,508 (GRCm39) |
C519S |
possibly damaging |
Het |
Szt2 |
A |
G |
4: 118,221,922 (GRCm39) |
|
probably benign |
Het |
Tas2r118 |
A |
G |
6: 23,969,180 (GRCm39) |
W294R |
possibly damaging |
Het |
Tex21 |
A |
T |
12: 76,245,694 (GRCm39) |
M534K |
probably damaging |
Het |
Tmem132c |
T |
C |
5: 127,640,784 (GRCm39) |
I985T |
probably benign |
Het |
Tmem87b |
T |
C |
2: 128,665,019 (GRCm39) |
V61A |
probably benign |
Het |
Trhr2 |
G |
A |
8: 123,085,220 (GRCm39) |
|
probably benign |
Het |
Ttc28 |
A |
G |
5: 111,381,208 (GRCm39) |
D1209G |
probably benign |
Het |
Uchl5 |
A |
G |
1: 143,677,940 (GRCm39) |
E148G |
probably benign |
Het |
Wdr62 |
T |
C |
7: 29,970,199 (GRCm39) |
I203V |
possibly damaging |
Het |
Wnk1 |
T |
C |
6: 119,931,148 (GRCm39) |
I799V |
possibly damaging |
Het |
|
Other mutations in Fam117b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01128:Fam117b
|
APN |
1 |
60,008,177 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01596:Fam117b
|
APN |
1 |
59,992,130 (GRCm39) |
nonsense |
probably null |
|
IGL02104:Fam117b
|
APN |
1 |
59,988,278 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02129:Fam117b
|
APN |
1 |
60,020,582 (GRCm39) |
missense |
probably benign |
0.07 |
R0690:Fam117b
|
UTSW |
1 |
59,997,512 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1074:Fam117b
|
UTSW |
1 |
59,997,485 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1435:Fam117b
|
UTSW |
1 |
60,008,222 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2215:Fam117b
|
UTSW |
1 |
60,008,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R2267:Fam117b
|
UTSW |
1 |
59,952,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R2268:Fam117b
|
UTSW |
1 |
59,952,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R5765:Fam117b
|
UTSW |
1 |
60,009,631 (GRCm39) |
splice site |
probably null |
|
R6228:Fam117b
|
UTSW |
1 |
60,008,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R6439:Fam117b
|
UTSW |
1 |
60,020,731 (GRCm39) |
missense |
probably benign |
0.45 |
R6921:Fam117b
|
UTSW |
1 |
59,992,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R7633:Fam117b
|
UTSW |
1 |
60,020,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R7827:Fam117b
|
UTSW |
1 |
59,952,837 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7867:Fam117b
|
UTSW |
1 |
60,014,046 (GRCm39) |
missense |
probably damaging |
0.98 |
R8305:Fam117b
|
UTSW |
1 |
59,952,782 (GRCm39) |
missense |
probably benign |
0.18 |
R9116:Fam117b
|
UTSW |
1 |
60,018,456 (GRCm39) |
nonsense |
probably null |
|
R9368:Fam117b
|
UTSW |
1 |
60,020,740 (GRCm39) |
missense |
probably benign |
0.12 |
X0004:Fam117b
|
UTSW |
1 |
60,014,137 (GRCm39) |
missense |
probably damaging |
0.96 |
|