Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
T |
A |
9: 55,907,186 (GRCm39) |
D180V |
possibly damaging |
Het |
Abat |
T |
C |
16: 8,421,618 (GRCm39) |
|
probably null |
Het |
Ankfn1 |
G |
A |
11: 89,282,576 (GRCm39) |
T357I |
probably benign |
Het |
Armc3 |
C |
T |
2: 19,290,790 (GRCm39) |
T423I |
probably benign |
Het |
Asb6 |
T |
C |
2: 30,714,472 (GRCm39) |
T213A |
possibly damaging |
Het |
Atp11a |
T |
C |
8: 12,882,575 (GRCm39) |
C488R |
probably benign |
Het |
Bag6 |
G |
A |
17: 35,363,368 (GRCm39) |
R736H |
probably benign |
Het |
Cela3a |
T |
A |
4: 137,132,950 (GRCm39) |
I101F |
probably damaging |
Het |
Cep170 |
A |
T |
1: 176,602,028 (GRCm39) |
D359E |
probably damaging |
Het |
Chfr |
T |
C |
5: 110,299,549 (GRCm39) |
V314A |
probably benign |
Het |
Clpb |
T |
C |
7: 101,371,935 (GRCm39) |
F224L |
possibly damaging |
Het |
Coro2a |
T |
C |
4: 46,539,188 (GRCm39) |
K527R |
probably benign |
Het |
Cpa5 |
A |
G |
6: 30,630,856 (GRCm39) |
T373A |
possibly damaging |
Het |
Ctsd |
A |
T |
7: 141,937,149 (GRCm39) |
|
probably null |
Het |
Dlx5 |
G |
A |
6: 6,878,340 (GRCm39) |
S230F |
possibly damaging |
Het |
Dlx5 |
A |
C |
6: 6,878,341 (GRCm39) |
S230A |
probably benign |
Het |
Dmc1 |
G |
T |
15: 79,486,621 (GRCm39) |
S11* |
probably null |
Het |
Dnah1 |
G |
A |
14: 31,037,079 (GRCm39) |
Q256* |
probably null |
Het |
Dnah3 |
A |
G |
7: 119,660,135 (GRCm39) |
F846L |
probably damaging |
Het |
Dnah5 |
A |
T |
15: 28,302,596 (GRCm39) |
I1618F |
probably damaging |
Het |
Emsy |
A |
G |
7: 98,279,538 (GRCm39) |
V267A |
possibly damaging |
Het |
Fgfr3 |
GGACCTCTCCGTG |
GG |
5: 33,892,766 (GRCm39) |
|
probably null |
Het |
Frem1 |
T |
C |
4: 82,924,007 (GRCm39) |
I317M |
probably damaging |
Het |
G6pc1 |
C |
A |
11: 101,267,520 (GRCm39) |
Y323* |
probably null |
Het |
Gm5114 |
A |
G |
7: 39,058,489 (GRCm39) |
C377R |
possibly damaging |
Het |
Gm7361 |
C |
A |
5: 26,466,188 (GRCm39) |
H183Q |
probably benign |
Het |
Hmbox1 |
A |
G |
14: 65,134,126 (GRCm39) |
V158A |
possibly damaging |
Het |
Hmg20a |
A |
G |
9: 56,396,227 (GRCm39) |
R340G |
unknown |
Het |
Ifi206 |
T |
A |
1: 173,309,607 (GRCm39) |
I130F |
|
Het |
Ifnb1 |
T |
C |
4: 88,440,911 (GRCm39) |
N34S |
probably benign |
Het |
Il16 |
T |
C |
7: 83,323,702 (GRCm39) |
K283E |
probably damaging |
Het |
Maf |
T |
C |
8: 116,419,920 (GRCm39) |
D374G |
probably benign |
Het |
Mettl14 |
A |
G |
3: 123,168,503 (GRCm39) |
I179T |
probably benign |
Het |
Mpped1 |
G |
A |
15: 83,684,251 (GRCm39) |
R91H |
probably damaging |
Het |
Nop2 |
C |
A |
6: 125,121,171 (GRCm39) |
P651Q |
possibly damaging |
Het |
Or5p62 |
A |
G |
7: 107,771,007 (GRCm39) |
*315Q |
probably null |
Het |
Phkg1 |
G |
A |
5: 129,902,109 (GRCm39) |
Q89* |
probably null |
Het |
Phykpl |
T |
A |
11: 51,482,285 (GRCm39) |
V133E |
probably damaging |
Het |
Polr3gl |
A |
T |
3: 96,487,137 (GRCm39) |
Y183N |
probably benign |
Het |
Rab13 |
A |
G |
3: 90,132,840 (GRCm39) |
T187A |
probably benign |
Het |
Ripor2 |
A |
G |
13: 24,877,755 (GRCm39) |
M252V |
probably damaging |
Het |
Sec61a2 |
T |
C |
2: 5,882,725 (GRCm39) |
N186S |
probably benign |
Het |
Serpinb5 |
T |
C |
1: 106,800,119 (GRCm39) |
|
probably null |
Het |
Serpine3 |
G |
A |
14: 62,902,476 (GRCm39) |
W29* |
probably null |
Het |
Sh2b3 |
T |
C |
5: 121,956,536 (GRCm39) |
R382G |
probably damaging |
Het |
Slc66a1 |
T |
A |
4: 139,033,823 (GRCm39) |
D32V |
probably damaging |
Het |
Slc7a5 |
A |
G |
8: 122,610,461 (GRCm39) |
L451P |
probably damaging |
Het |
Slco1a5 |
T |
C |
6: 142,208,257 (GRCm39) |
|
probably null |
Het |
Tep1 |
G |
A |
14: 51,091,047 (GRCm39) |
A695V |
probably damaging |
Het |
Tnik |
T |
C |
3: 28,684,743 (GRCm39) |
V857A |
possibly damaging |
Het |
Trdn |
A |
T |
10: 33,072,097 (GRCm39) |
M255L |
probably benign |
Het |
Tsc22d4 |
G |
A |
5: 137,745,985 (GRCm39) |
S203N |
probably benign |
Het |
Tsfm |
T |
C |
10: 126,858,417 (GRCm39) |
E316G |
possibly damaging |
Het |
Tvp23b |
T |
C |
11: 62,770,289 (GRCm39) |
|
probably benign |
Het |
Vgf |
C |
A |
5: 137,061,099 (GRCm39) |
D420E |
probably damaging |
Het |
Zan |
G |
A |
5: 137,462,618 (GRCm39) |
P854S |
probably benign |
Het |
Zfp831 |
T |
C |
2: 174,485,816 (GRCm39) |
S164P |
possibly damaging |
Het |
|
Other mutations in Bche |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00338:Bche
|
APN |
3 |
73,608,640 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01420:Bche
|
APN |
3 |
73,609,342 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02433:Bche
|
APN |
3 |
73,609,262 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02734:Bche
|
APN |
3 |
73,609,409 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03095:Bche
|
APN |
3 |
73,609,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03227:Bche
|
APN |
3 |
73,608,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R0056:Bche
|
UTSW |
3 |
73,608,654 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1780:Bche
|
UTSW |
3 |
73,607,953 (GRCm39) |
missense |
probably benign |
0.00 |
R1984:Bche
|
UTSW |
3 |
73,609,160 (GRCm39) |
missense |
probably benign |
|
R1984:Bche
|
UTSW |
3 |
73,609,159 (GRCm39) |
missense |
probably benign |
0.03 |
R2403:Bche
|
UTSW |
3 |
73,608,805 (GRCm39) |
missense |
probably damaging |
0.96 |
R4989:Bche
|
UTSW |
3 |
73,609,177 (GRCm39) |
missense |
probably benign |
0.02 |
R5231:Bche
|
UTSW |
3 |
73,608,194 (GRCm39) |
missense |
probably benign |
0.07 |
R5363:Bche
|
UTSW |
3 |
73,607,972 (GRCm39) |
missense |
probably damaging |
0.98 |
R5987:Bche
|
UTSW |
3 |
73,556,011 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6164:Bche
|
UTSW |
3 |
73,608,389 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6381:Bche
|
UTSW |
3 |
73,609,132 (GRCm39) |
missense |
probably benign |
0.00 |
R6571:Bche
|
UTSW |
3 |
73,608,824 (GRCm39) |
missense |
probably benign |
0.08 |
R6801:Bche
|
UTSW |
3 |
73,609,133 (GRCm39) |
missense |
probably benign |
|
R6935:Bche
|
UTSW |
3 |
73,609,133 (GRCm39) |
missense |
probably benign |
|
R7275:Bche
|
UTSW |
3 |
73,607,969 (GRCm39) |
missense |
probably benign |
0.19 |
R7543:Bche
|
UTSW |
3 |
73,609,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R7757:Bche
|
UTSW |
3 |
73,608,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Bche
|
UTSW |
3 |
73,609,149 (GRCm39) |
missense |
probably damaging |
0.98 |
R8878:Bche
|
UTSW |
3 |
73,608,506 (GRCm39) |
missense |
probably benign |
|
R8944:Bche
|
UTSW |
3 |
73,608,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R8947:Bche
|
UTSW |
3 |
73,608,761 (GRCm39) |
missense |
probably damaging |
0.97 |
R8964:Bche
|
UTSW |
3 |
73,608,406 (GRCm39) |
missense |
probably benign |
0.00 |
R9402:Bche
|
UTSW |
3 |
73,608,656 (GRCm39) |
missense |
probably benign |
0.06 |
|