Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030468B19Rik |
T |
C |
11: 117,697,112 (GRCm39) |
V237A |
probably benign |
Het |
Abca15 |
G |
A |
7: 120,006,631 (GRCm39) |
V1632M |
probably damaging |
Het |
Adamts18 |
G |
A |
8: 114,433,624 (GRCm39) |
P1037S |
probably damaging |
Het |
Apol7e |
T |
C |
15: 77,602,065 (GRCm39) |
V221A |
probably benign |
Het |
Aqp4 |
T |
G |
18: 15,533,048 (GRCm39) |
H15P |
probably benign |
Het |
Atp6v0d2 |
T |
A |
4: 19,910,649 (GRCm39) |
R80S |
probably benign |
Het |
Cdh15 |
A |
G |
8: 123,587,628 (GRCm39) |
D184G |
probably damaging |
Het |
Cers3 |
G |
A |
7: 66,435,850 (GRCm39) |
V270M |
probably damaging |
Het |
Ces3a |
A |
G |
8: 105,784,129 (GRCm39) |
H443R |
probably damaging |
Het |
Cntn1 |
T |
G |
15: 92,153,801 (GRCm39) |
F485V |
possibly damaging |
Het |
Cog6 |
A |
G |
3: 52,897,465 (GRCm39) |
L536P |
probably damaging |
Het |
Copa |
A |
G |
1: 171,947,081 (GRCm39) |
I1068M |
probably benign |
Het |
Ddx50 |
T |
C |
10: 62,452,021 (GRCm39) |
D734G |
unknown |
Het |
Dgkz |
T |
C |
2: 91,775,922 (GRCm39) |
T114A |
probably benign |
Het |
Dock2 |
A |
T |
11: 34,586,067 (GRCm39) |
D538E |
probably benign |
Het |
Drg1 |
T |
C |
11: 3,204,633 (GRCm39) |
S198G |
probably benign |
Het |
Epn3 |
C |
A |
11: 94,386,848 (GRCm39) |
G174V |
possibly damaging |
Het |
Ficd |
G |
T |
5: 113,876,575 (GRCm39) |
R250L |
probably damaging |
Het |
Fmo2 |
A |
G |
1: 162,708,005 (GRCm39) |
S377P |
probably benign |
Het |
Gm17027 |
T |
C |
14: 41,981,251 (GRCm39) |
I202V |
|
Het |
H6pd |
C |
T |
4: 150,066,758 (GRCm39) |
V551I |
probably benign |
Het |
Ighg1 |
A |
T |
12: 113,292,657 (GRCm39) |
L304* |
probably null |
Het |
Itga8 |
T |
C |
2: 12,266,940 (GRCm39) |
D165G |
probably damaging |
Het |
Lipt2 |
GGCGCCCGCGCGCG |
GGCG |
7: 99,808,888 (GRCm39) |
|
probably null |
Het |
Lrrc37a |
A |
G |
11: 103,348,766 (GRCm39) |
V2643A |
unknown |
Het |
Lyz3 |
T |
A |
10: 117,070,340 (GRCm39) |
I146F |
probably damaging |
Het |
Mast2 |
A |
T |
4: 116,292,757 (GRCm39) |
F71Y |
possibly damaging |
Het |
Mkrn1 |
C |
A |
6: 39,376,344 (GRCm39) |
E421* |
probably null |
Het |
Myo3a |
G |
T |
2: 22,448,319 (GRCm39) |
K969N |
possibly damaging |
Het |
Nr1d1 |
G |
C |
11: 98,660,073 (GRCm39) |
R484G |
probably damaging |
Het |
Nrg1 |
C |
A |
8: 32,308,103 (GRCm39) |
A686S |
probably damaging |
Het |
Or52e8 |
T |
C |
7: 104,624,325 (GRCm39) |
N293S |
probably damaging |
Het |
Plxna4 |
T |
A |
6: 32,169,276 (GRCm39) |
D1307V |
probably damaging |
Het |
Ppihl |
A |
T |
5: 44,070,999 (GRCm39) |
N119I |
probably benign |
Het |
Ppp1r13l |
G |
T |
7: 19,103,981 (GRCm39) |
G154V |
probably damaging |
Het |
Psmc5 |
A |
G |
11: 106,153,687 (GRCm39) |
D382G |
probably benign |
Het |
Ptch2 |
T |
C |
4: 116,967,630 (GRCm39) |
L766P |
probably damaging |
Het |
Rev1 |
A |
C |
1: 38,098,353 (GRCm39) |
L730R |
probably damaging |
Het |
Rin3 |
G |
A |
12: 102,339,861 (GRCm39) |
V684I |
probably damaging |
Het |
Secisbp2 |
G |
A |
13: 51,833,869 (GRCm39) |
V670I |
possibly damaging |
Het |
Sema6d |
G |
A |
2: 124,497,134 (GRCm39) |
C136Y |
probably damaging |
Het |
Shprh |
T |
G |
10: 11,032,908 (GRCm39) |
V298G |
possibly damaging |
Het |
Slc37a4 |
C |
T |
9: 44,313,632 (GRCm39) |
T386I |
probably benign |
Het |
Slc4a3 |
T |
C |
1: 75,531,282 (GRCm39) |
I825T |
probably damaging |
Het |
Spta1 |
C |
T |
1: 174,040,940 (GRCm39) |
L1247F |
probably damaging |
Het |
Tigar |
A |
T |
6: 127,068,220 (GRCm39) |
I66K |
probably benign |
Het |
Tln2 |
T |
C |
9: 67,274,500 (GRCm39) |
Y376C |
probably damaging |
Het |
Tmem199 |
T |
A |
11: 78,398,633 (GRCm39) |
|
probably benign |
Het |
Tnc |
G |
A |
4: 63,924,501 (GRCm39) |
R1066C |
possibly damaging |
Het |
Ubqlnl |
T |
A |
7: 103,799,206 (GRCm39) |
H97L |
probably damaging |
Het |
Vmn1r13 |
A |
G |
6: 57,187,524 (GRCm39) |
T228A |
probably damaging |
Het |
Xab2 |
T |
C |
8: 3,661,672 (GRCm39) |
T594A |
probably benign |
Het |
Zc3h18 |
A |
G |
8: 123,138,124 (GRCm39) |
E687G |
unknown |
Het |
Zfp831 |
A |
G |
2: 174,487,874 (GRCm39) |
T850A |
probably benign |
Het |
|
Other mutations in 2310022B05Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01357:2310022B05Rik
|
APN |
8 |
125,366,072 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02141:2310022B05Rik
|
APN |
8 |
125,364,645 (GRCm39) |
utr 3 prime |
probably benign |
|
R0245:2310022B05Rik
|
UTSW |
8 |
125,378,168 (GRCm39) |
splice site |
probably benign |
|
R2038:2310022B05Rik
|
UTSW |
8 |
125,389,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R2157:2310022B05Rik
|
UTSW |
8 |
125,378,168 (GRCm39) |
splice site |
probably benign |
|
R4652:2310022B05Rik
|
UTSW |
8 |
125,366,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:2310022B05Rik
|
UTSW |
8 |
125,366,300 (GRCm39) |
missense |
probably benign |
0.01 |
R4867:2310022B05Rik
|
UTSW |
8 |
125,366,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6018:2310022B05Rik
|
UTSW |
8 |
125,365,853 (GRCm39) |
missense |
probably benign |
0.00 |
R6602:2310022B05Rik
|
UTSW |
8 |
125,365,993 (GRCm39) |
missense |
probably damaging |
0.98 |
R6849:2310022B05Rik
|
UTSW |
8 |
125,366,261 (GRCm39) |
missense |
probably damaging |
0.99 |
R7924:2310022B05Rik
|
UTSW |
8 |
125,390,051 (GRCm39) |
start gained |
probably benign |
|
R9778:2310022B05Rik
|
UTSW |
8 |
125,366,098 (GRCm39) |
missense |
probably damaging |
1.00 |
|