Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,212,139 (GRCm39) |
|
probably null |
Het |
Abcf1 |
C |
A |
17: 36,272,890 (GRCm39) |
K252N |
probably damaging |
Het |
Abi3 |
C |
T |
11: 95,724,851 (GRCm39) |
A211T |
possibly damaging |
Het |
Acaca |
A |
T |
11: 84,140,350 (GRCm39) |
D608V |
possibly damaging |
Het |
Akap10 |
A |
G |
11: 61,791,272 (GRCm39) |
Y396H |
probably damaging |
Het |
Ap3b1 |
C |
G |
13: 94,619,771 (GRCm39) |
S778W |
unknown |
Het |
Arb2a |
T |
C |
13: 78,050,837 (GRCm39) |
M165T |
probably benign |
Het |
Baat |
G |
A |
4: 49,502,925 (GRCm39) |
L66F |
probably benign |
Het |
Cachd1 |
A |
G |
4: 100,845,759 (GRCm39) |
N981S |
probably damaging |
Het |
Cacna1c |
C |
T |
6: 118,753,407 (GRCm39) |
R243H |
|
Het |
Cdh23 |
T |
A |
10: 60,150,390 (GRCm39) |
I2527F |
probably damaging |
Het |
Cinp |
A |
G |
12: 110,840,557 (GRCm39) |
V198A |
probably benign |
Het |
Clec4d |
T |
C |
6: 123,244,123 (GRCm39) |
|
probably null |
Het |
Cnn3 |
A |
G |
3: 121,248,704 (GRCm39) |
I204V |
probably benign |
Het |
Cpxm2 |
C |
A |
7: 131,650,800 (GRCm39) |
G620V |
probably damaging |
Het |
Ctrl |
A |
C |
8: 106,659,497 (GRCm39) |
S93A |
probably benign |
Het |
Cyp2d34 |
A |
G |
15: 82,501,425 (GRCm39) |
V301A |
possibly damaging |
Het |
Dnaaf5 |
G |
T |
5: 139,147,565 (GRCm39) |
K376N |
probably damaging |
Het |
Eno2 |
C |
T |
6: 124,740,137 (GRCm39) |
D300N |
probably damaging |
Het |
Entrep3 |
T |
A |
3: 89,093,083 (GRCm39) |
Y280* |
probably null |
Het |
Fam131a |
A |
G |
16: 20,514,584 (GRCm39) |
S62G |
probably benign |
Het |
Fancm |
T |
A |
12: 65,163,240 (GRCm39) |
|
probably null |
Het |
Fancm |
A |
G |
12: 65,165,173 (GRCm39) |
D1506G |
probably benign |
Het |
Fhad1 |
C |
A |
4: 141,632,902 (GRCm39) |
V1201L |
probably benign |
Het |
Gdpd4 |
T |
A |
7: 97,623,185 (GRCm39) |
C265* |
probably null |
Het |
Gm3127 |
A |
T |
14: 15,425,888 (GRCm39) |
T98S |
probably null |
Het |
Gpsm1 |
A |
T |
2: 26,230,448 (GRCm39) |
D466V |
probably benign |
Het |
Gramd1a |
T |
G |
7: 30,842,992 (GRCm39) |
K76Q |
probably damaging |
Het |
Gstp3 |
T |
C |
19: 4,108,808 (GRCm39) |
D24G |
probably damaging |
Het |
Kalrn |
G |
A |
16: 33,810,161 (GRCm39) |
T2531I |
possibly damaging |
Het |
Klk7 |
C |
A |
7: 43,462,333 (GRCm39) |
D108E |
probably damaging |
Het |
Klkb1 |
A |
G |
8: 45,740,002 (GRCm39) |
S97P |
probably damaging |
Het |
Krt13 |
T |
C |
11: 100,012,008 (GRCm39) |
D105G |
probably damaging |
Het |
Lingo2 |
T |
A |
4: 35,709,302 (GRCm39) |
H226L |
probably benign |
Het |
Lrba |
T |
C |
3: 86,275,896 (GRCm39) |
S1755P |
probably damaging |
Het |
Marf1 |
A |
G |
16: 13,946,470 (GRCm39) |
V1217A |
probably damaging |
Het |
Mtss1 |
A |
T |
15: 58,842,858 (GRCm39) |
V118E |
possibly damaging |
Het |
Mug1 |
T |
A |
6: 121,850,593 (GRCm39) |
D696E |
probably benign |
Het |
Ndufa3 |
C |
T |
7: 3,623,003 (GRCm39) |
P56L |
probably damaging |
Het |
Nop56 |
T |
A |
2: 130,120,205 (GRCm39) |
C471S |
possibly damaging |
Het |
Obscn |
T |
A |
11: 58,891,652 (GRCm39) |
H6960L |
unknown |
Het |
Or13a22 |
C |
T |
7: 140,073,049 (GRCm39) |
T166I |
probably benign |
Het |
Pcdhb10 |
A |
C |
18: 37,546,619 (GRCm39) |
Q565P |
probably benign |
Het |
Pde6g |
T |
A |
11: 120,338,953 (GRCm39) |
H79L |
possibly damaging |
Het |
Phrf1 |
G |
T |
7: 140,836,524 (GRCm39) |
M265I |
unknown |
Het |
Pkd2 |
T |
C |
5: 104,630,986 (GRCm39) |
F470S |
probably damaging |
Het |
Plekhm1 |
T |
A |
11: 103,271,153 (GRCm39) |
D446V |
probably damaging |
Het |
Prkaca |
A |
T |
8: 84,721,963 (GRCm39) |
T325S |
probably benign |
Het |
Proz |
A |
T |
8: 13,111,027 (GRCm39) |
|
probably benign |
Het |
Pten |
T |
C |
19: 32,792,894 (GRCm39) |
F238L |
probably benign |
Het |
Ptpn21 |
G |
A |
12: 98,671,435 (GRCm39) |
L198F |
probably damaging |
Het |
Rbm5 |
A |
T |
9: 107,628,930 (GRCm39) |
S394T |
probably benign |
Het |
Scaf8 |
T |
G |
17: 3,227,994 (GRCm39) |
S408A |
unknown |
Het |
Slc41a3 |
T |
A |
6: 90,617,909 (GRCm39) |
F312I |
probably damaging |
Het |
Soat2 |
T |
A |
15: 102,059,598 (GRCm39) |
|
probably null |
Het |
Sorcs1 |
C |
A |
19: 50,218,698 (GRCm39) |
G595* |
probably null |
Het |
Spopfm1 |
G |
C |
3: 94,173,154 (GRCm39) |
S50T |
probably benign |
Het |
Stox1 |
G |
T |
10: 62,500,723 (GRCm39) |
D612E |
probably benign |
Het |
Suco |
T |
C |
1: 161,665,365 (GRCm39) |
I530M |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,030,501 (GRCm39) |
|
probably null |
Het |
Thbd |
G |
A |
2: 148,249,664 (GRCm39) |
A68V |
probably damaging |
Het |
Tmem109 |
A |
T |
19: 10,855,466 (GRCm39) |
M4K |
unknown |
Het |
Tmub1 |
G |
C |
5: 24,651,664 (GRCm39) |
P85R |
possibly damaging |
Het |
Tnk2 |
A |
C |
16: 32,500,053 (GRCm39) |
Q1039H |
probably damaging |
Het |
Tpm3 |
T |
C |
3: 89,993,775 (GRCm39) |
L89S |
probably damaging |
Het |
Unc13b |
C |
T |
4: 43,232,573 (GRCm39) |
R432* |
probably null |
Het |
Vmn2r59 |
T |
A |
7: 41,661,707 (GRCm39) |
I703F |
probably damaging |
Het |
Xylt1 |
T |
A |
7: 117,074,749 (GRCm39) |
I122N |
probably benign |
Het |
Zc3h12c |
T |
C |
9: 52,055,248 (GRCm39) |
E187G |
probably 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 |
IGL03387:Fam117b
|
APN |
1 |
59,992,119 (GRCm39) |
missense |
probably benign |
0.26 |
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 |
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 |
|