Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,571,917 (GRCm39) |
D4826V |
probably damaging |
Het |
Acoxl |
G |
A |
2: 127,719,686 (GRCm39) |
C149Y |
probably benign |
Het |
Adamts3 |
G |
T |
5: 89,856,527 (GRCm39) |
H349N |
probably damaging |
Het |
Ap2b1 |
A |
G |
11: 83,227,256 (GRCm39) |
|
probably null |
Het |
Ap3m2 |
T |
C |
8: 23,293,877 (GRCm39) |
S58G |
possibly damaging |
Het |
Cacna1h |
T |
G |
17: 25,606,023 (GRCm39) |
D1092A |
probably damaging |
Het |
Cbfb |
A |
C |
8: 105,929,193 (GRCm39) |
Q170P |
probably damaging |
Het |
Ccdc73 |
A |
C |
2: 104,761,331 (GRCm39) |
K110N |
possibly damaging |
Het |
Cep350 |
C |
A |
1: 155,741,824 (GRCm39) |
R2149L |
probably damaging |
Het |
Cog2 |
A |
G |
8: 125,272,777 (GRCm39) |
T525A |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Fbxl5 |
A |
G |
5: 43,920,170 (GRCm39) |
I251T |
probably benign |
Het |
Fscn3 |
A |
G |
6: 28,430,030 (GRCm39) |
K67E |
possibly damaging |
Het |
Glmp |
T |
A |
3: 88,233,445 (GRCm39) |
N133K |
probably benign |
Het |
Gpr179 |
T |
C |
11: 97,242,232 (GRCm39) |
N204S |
probably damaging |
Het |
Gtf2ird1 |
C |
T |
5: 134,412,672 (GRCm39) |
R613Q |
probably damaging |
Het |
Hepacam |
A |
G |
9: 37,294,721 (GRCm39) |
D285G |
possibly damaging |
Het |
Hipk4 |
G |
A |
7: 27,227,841 (GRCm39) |
V196M |
probably damaging |
Het |
Hlx |
A |
T |
1: 184,463,754 (GRCm39) |
|
probably null |
Het |
Igf2r |
A |
T |
17: 12,936,254 (GRCm39) |
D597E |
probably benign |
Het |
Ighm |
T |
C |
12: 113,385,115 (GRCm39) |
T282A |
unknown |
Het |
Igsf9b |
T |
C |
9: 27,239,826 (GRCm39) |
C624R |
probably damaging |
Het |
Ksr2 |
T |
C |
5: 117,886,864 (GRCm39) |
V800A |
probably damaging |
Het |
Lyn |
A |
T |
4: 3,782,987 (GRCm39) |
I386F |
probably damaging |
Het |
Melk |
A |
G |
4: 44,310,333 (GRCm39) |
D102G |
probably damaging |
Het |
Mettl1 |
G |
T |
10: 126,877,863 (GRCm39) |
E4* |
probably null |
Het |
Mybl2 |
C |
T |
2: 162,910,203 (GRCm39) |
Q210* |
probably null |
Het |
Naga |
C |
T |
15: 82,219,054 (GRCm39) |
W231* |
probably null |
Het |
Or2y3 |
T |
C |
17: 38,393,347 (GRCm39) |
Y174C |
probably damaging |
Het |
Or4k2 |
C |
T |
14: 50,424,105 (GRCm39) |
V190I |
probably benign |
Het |
Or7g16 |
T |
C |
9: 18,727,125 (GRCm39) |
N155S |
possibly damaging |
Het |
Otud4 |
T |
C |
8: 80,400,090 (GRCm39) |
S935P |
probably benign |
Het |
P2rx7 |
C |
T |
5: 122,790,852 (GRCm39) |
T63I |
probably damaging |
Het |
Pga5 |
A |
T |
19: 10,647,024 (GRCm39) |
N260K |
probably benign |
Het |
Phka2 |
ACC |
AC |
X: 159,342,862 (GRCm39) |
|
probably null |
Het |
Plch1 |
T |
A |
3: 63,681,076 (GRCm39) |
R184W |
probably damaging |
Het |
Ppm1b |
T |
C |
17: 85,301,374 (GRCm39) |
F85L |
probably benign |
Het |
Prtg |
T |
A |
9: 72,819,288 (GRCm39) |
F1094I |
probably benign |
Het |
Ralgds |
G |
A |
2: 28,432,538 (GRCm39) |
|
probably benign |
Het |
Rgs17 |
A |
C |
10: 5,783,140 (GRCm39) |
V149G |
probably damaging |
Het |
Rnf168 |
A |
G |
16: 32,101,192 (GRCm39) |
E124G |
probably damaging |
Het |
Sav1 |
T |
C |
12: 70,022,817 (GRCm39) |
E245G |
possibly damaging |
Het |
Slc25a19 |
T |
C |
11: 115,515,060 (GRCm39) |
I33V |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,095,941 (GRCm39) |
I318V |
probably damaging |
Het |
Tas2r136 |
A |
G |
6: 132,754,707 (GRCm39) |
L140P |
probably damaging |
Het |
Tbc1d9 |
A |
G |
8: 83,997,655 (GRCm39) |
I1071V |
probably benign |
Het |
Tecta |
G |
T |
9: 42,284,474 (GRCm39) |
N870K |
possibly damaging |
Het |
Tmem230 |
G |
A |
2: 132,086,048 (GRCm39) |
P38L |
possibly damaging |
Het |
Trpa1 |
G |
T |
1: 14,946,174 (GRCm39) |
H986N |
probably damaging |
Het |
Wdr41 |
A |
T |
13: 95,114,996 (GRCm39) |
I24L |
possibly damaging |
Het |
|
Other mutations in Bhmt2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Bhmt2
|
APN |
13 |
93,803,279 (GRCm39) |
splice site |
probably benign |
|
IGL01665:Bhmt2
|
APN |
13 |
93,799,661 (GRCm39) |
nonsense |
probably null |
|
IGL02059:Bhmt2
|
APN |
13 |
93,803,171 (GRCm39) |
missense |
probably benign |
|
IGL02239:Bhmt2
|
APN |
13 |
93,799,687 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02267:Bhmt2
|
APN |
13 |
93,805,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03148:Bhmt2
|
APN |
13 |
93,803,161 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1171:Bhmt2
|
UTSW |
13 |
93,798,837 (GRCm39) |
missense |
probably benign |
0.00 |
R1517:Bhmt2
|
UTSW |
13 |
93,798,847 (GRCm39) |
missense |
probably damaging |
0.97 |
R1886:Bhmt2
|
UTSW |
13 |
93,798,998 (GRCm39) |
missense |
probably benign |
0.02 |
R2167:Bhmt2
|
UTSW |
13 |
93,799,012 (GRCm39) |
missense |
probably benign |
0.29 |
R4024:Bhmt2
|
UTSW |
13 |
93,799,839 (GRCm39) |
splice site |
probably benign |
|
R4823:Bhmt2
|
UTSW |
13 |
93,799,798 (GRCm39) |
missense |
probably benign |
|
R5273:Bhmt2
|
UTSW |
13 |
93,803,086 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5333:Bhmt2
|
UTSW |
13 |
93,807,938 (GRCm39) |
missense |
probably benign |
0.00 |
R5955:Bhmt2
|
UTSW |
13 |
93,799,705 (GRCm39) |
missense |
probably benign |
0.00 |
R6281:Bhmt2
|
UTSW |
13 |
93,799,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R6858:Bhmt2
|
UTSW |
13 |
93,807,948 (GRCm39) |
missense |
probably damaging |
0.97 |
R6934:Bhmt2
|
UTSW |
13 |
93,798,819 (GRCm39) |
missense |
probably benign |
0.18 |
R6985:Bhmt2
|
UTSW |
13 |
93,799,830 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7185:Bhmt2
|
UTSW |
13 |
93,799,779 (GRCm39) |
missense |
probably benign |
0.22 |
R7639:Bhmt2
|
UTSW |
13 |
93,799,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R8412:Bhmt2
|
UTSW |
13 |
93,798,820 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9224:Bhmt2
|
UTSW |
13 |
93,805,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Bhmt2
|
UTSW |
13 |
93,799,833 (GRCm39) |
missense |
probably damaging |
0.99 |
|