Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anpep |
A |
G |
7: 79,491,953 (GRCm39) |
I16T |
possibly damaging |
Het |
Ap1s1 |
T |
C |
5: 137,066,240 (GRCm39) |
|
probably benign |
Het |
Atp1a2 |
T |
C |
1: 172,106,459 (GRCm39) |
S848G |
probably damaging |
Het |
Ccdc148 |
T |
A |
2: 58,713,645 (GRCm39) |
Y502F |
probably damaging |
Het |
Ccdc88c |
T |
C |
12: 100,919,642 (GRCm39) |
M416V |
probably damaging |
Het |
Cdk17 |
T |
C |
10: 93,071,331 (GRCm39) |
S351P |
probably benign |
Het |
Cfap100 |
T |
C |
6: 90,392,768 (GRCm39) |
E114G |
probably benign |
Het |
Clec4a4 |
T |
C |
6: 122,968,833 (GRCm39) |
I66T |
possibly damaging |
Het |
Cpeb4 |
T |
C |
11: 31,870,584 (GRCm39) |
|
probably null |
Het |
Cybrd1 |
T |
C |
2: 70,948,618 (GRCm39) |
V52A |
probably damaging |
Het |
Decr1 |
G |
A |
4: 15,924,347 (GRCm39) |
A191V |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,378,489 (GRCm39) |
I2942L |
probably benign |
Het |
Ehd4 |
C |
T |
2: 119,932,689 (GRCm39) |
V246I |
possibly damaging |
Het |
Ercc6l2 |
A |
G |
13: 64,020,158 (GRCm39) |
|
probably benign |
Het |
Exoc4 |
T |
A |
6: 33,309,218 (GRCm39) |
M280K |
probably damaging |
Het |
Fmo1 |
T |
G |
1: 162,678,979 (GRCm39) |
E89A |
probably benign |
Het |
Foxm1 |
A |
G |
6: 128,350,898 (GRCm39) |
D733G |
probably benign |
Het |
Garin5b |
T |
C |
7: 4,773,677 (GRCm39) |
T73A |
probably damaging |
Het |
Gulp1 |
A |
C |
1: 44,793,511 (GRCm39) |
R57S |
probably damaging |
Het |
Hdac1-ps |
T |
C |
17: 78,799,716 (GRCm39) |
S236P |
probably damaging |
Het |
Hdac4 |
G |
T |
1: 91,957,876 (GRCm39) |
A46E |
probably benign |
Het |
Hspg2 |
T |
C |
4: 137,241,966 (GRCm39) |
S567P |
possibly damaging |
Het |
Insyn1 |
C |
A |
9: 58,406,530 (GRCm39) |
P147T |
probably damaging |
Het |
Iqgap1 |
A |
C |
7: 80,458,854 (GRCm39) |
C21W |
unknown |
Het |
Isoc2a |
T |
C |
7: 4,894,488 (GRCm39) |
L57P |
probably damaging |
Het |
Krt34 |
G |
A |
11: 99,929,272 (GRCm39) |
Q313* |
probably null |
Het |
Krt6a |
C |
T |
15: 101,601,008 (GRCm39) |
V263I |
probably damaging |
Het |
Man2a1 |
A |
G |
17: 65,040,719 (GRCm39) |
I106V |
possibly damaging |
Het |
Muc16 |
T |
C |
9: 18,469,675 (GRCm39) |
D7300G |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,417,082 (GRCm39) |
S3343C |
possibly damaging |
Het |
Mup11 |
C |
T |
4: 60,618,239 (GRCm39) |
E21K |
possibly damaging |
Het |
Myo3b |
T |
A |
2: 70,075,754 (GRCm39) |
|
probably null |
Het |
Nlrp4c |
T |
C |
7: 6,095,507 (GRCm39) |
L795P |
probably damaging |
Het |
Nup160 |
T |
A |
2: 90,548,220 (GRCm39) |
Y984* |
probably null |
Het |
Nwd1 |
C |
T |
8: 73,388,814 (GRCm39) |
R81W |
probably damaging |
Het |
Or2d3 |
G |
T |
7: 106,491,135 (GRCm39) |
Y60* |
probably null |
Het |
Or5p52 |
A |
G |
7: 107,502,595 (GRCm39) |
T224A |
probably benign |
Het |
Osmr |
A |
G |
15: 6,889,833 (GRCm39) |
V5A |
probably benign |
Het |
Pabir1 |
T |
A |
19: 24,454,450 (GRCm39) |
M91L |
probably benign |
Het |
Pcsk5 |
A |
G |
19: 17,814,317 (GRCm39) |
|
probably null |
Het |
Pex11a |
G |
A |
7: 79,387,127 (GRCm39) |
T235M |
probably damaging |
Het |
Pik3r6 |
A |
G |
11: 68,442,799 (GRCm39) |
T730A |
probably benign |
Het |
Ppp1r9a |
C |
T |
6: 5,110,715 (GRCm39) |
|
probably benign |
Het |
Ppp2r2d |
T |
C |
7: 138,474,742 (GRCm39) |
I41T |
probably damaging |
Het |
Prdm1 |
C |
T |
10: 44,326,191 (GRCm39) |
R126H |
probably damaging |
Het |
Primpol |
C |
T |
8: 47,039,477 (GRCm39) |
R381H |
probably benign |
Het |
Prl7a1 |
C |
A |
13: 27,821,626 (GRCm39) |
Q102H |
probably benign |
Het |
Rbpjl |
T |
C |
2: 164,252,799 (GRCm39) |
L284P |
probably damaging |
Het |
Rgs21 |
A |
T |
1: 144,417,035 (GRCm39) |
C6S |
probably benign |
Het |
Rnasel |
T |
C |
1: 153,630,138 (GRCm39) |
V218A |
probably benign |
Het |
Sag |
G |
T |
1: 87,752,175 (GRCm39) |
V223L |
probably damaging |
Het |
Sdk1 |
C |
T |
5: 142,117,824 (GRCm39) |
T1574M |
probably damaging |
Het |
Secisbp2 |
G |
A |
13: 51,833,896 (GRCm39) |
V679M |
probably damaging |
Het |
Sele |
T |
A |
1: 163,879,386 (GRCm39) |
|
probably null |
Het |
Senp7 |
T |
A |
16: 55,990,117 (GRCm39) |
L622M |
probably damaging |
Het |
Sgo1 |
G |
A |
17: 53,983,981 (GRCm39) |
R466C |
probably damaging |
Het |
Sh3tc1 |
C |
A |
5: 35,863,590 (GRCm39) |
V866L |
probably benign |
Het |
Snrnp25 |
T |
A |
11: 32,157,647 (GRCm39) |
V75D |
probably benign |
Het |
Syne1 |
C |
T |
10: 5,011,429 (GRCm39) |
C7899Y |
probably damaging |
Het |
U2af1l4 |
T |
C |
7: 30,264,007 (GRCm39) |
S55P |
probably damaging |
Het |
Vmn1r23 |
A |
G |
6: 57,903,040 (GRCm39) |
I246T |
possibly damaging |
Het |
Vmn1r66 |
T |
A |
7: 10,008,329 (GRCm39) |
R235* |
probably null |
Het |
Wnk4 |
C |
T |
11: 101,165,894 (GRCm39) |
A807V |
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 |
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 |
R7499:Bche
|
UTSW |
3 |
73,609,231 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|