Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdhppt |
A |
G |
9: 4,308,732 (GRCm39) |
V124A |
probably benign |
Het |
Abca4 |
A |
G |
3: 121,904,186 (GRCm39) |
M746V |
possibly damaging |
Het |
Aldh18a1 |
G |
T |
19: 40,562,226 (GRCm39) |
S266* |
probably null |
Het |
Aldh1b1 |
C |
A |
4: 45,802,968 (GRCm39) |
H169N |
probably benign |
Het |
Anpep |
A |
G |
7: 79,476,709 (GRCm39) |
I756T |
possibly damaging |
Het |
Asb16 |
A |
T |
11: 102,168,739 (GRCm39) |
E405V |
probably benign |
Het |
B4galnt1 |
T |
A |
10: 127,007,490 (GRCm39) |
F464I |
probably damaging |
Het |
Bpifb5 |
A |
G |
2: 154,070,975 (GRCm39) |
I225V |
probably benign |
Het |
Brox |
T |
C |
1: 183,062,484 (GRCm39) |
E290G |
probably damaging |
Het |
Cacna1s |
T |
A |
1: 136,020,333 (GRCm39) |
V790D |
possibly damaging |
Het |
Cacng6 |
G |
T |
7: 3,473,384 (GRCm39) |
K69N |
possibly damaging |
Het |
Catsperg1 |
A |
G |
7: 28,895,344 (GRCm39) |
I503T |
possibly damaging |
Het |
Cdcp3 |
A |
G |
7: 130,852,205 (GRCm39) |
N814D |
probably damaging |
Het |
Celsr3 |
A |
C |
9: 108,706,840 (GRCm39) |
M1108L |
probably benign |
Het |
Chd2 |
T |
C |
7: 73,149,373 (GRCm39) |
N449S |
probably benign |
Het |
Cpne6 |
T |
C |
14: 55,750,066 (GRCm39) |
C66R |
possibly damaging |
Het |
Ctnna2 |
T |
C |
6: 76,919,270 (GRCm39) |
E656G |
probably damaging |
Het |
Dnah17 |
A |
T |
11: 118,018,048 (GRCm39) |
M149K |
probably benign |
Het |
Dpp8 |
A |
T |
9: 64,944,262 (GRCm39) |
M10L |
possibly damaging |
Het |
Dst |
T |
C |
1: 34,329,486 (GRCm39) |
L4838P |
probably damaging |
Het |
Eif4g3 |
T |
A |
4: 137,824,082 (GRCm39) |
I55N |
probably damaging |
Het |
Gm10750 |
A |
G |
2: 148,858,017 (GRCm39) |
L78P |
unknown |
Het |
Gulo |
T |
G |
14: 66,237,288 (GRCm39) |
K200Q |
probably benign |
Het |
Jmjd8 |
T |
A |
17: 26,048,071 (GRCm39) |
L56Q |
probably benign |
Het |
Kansl1 |
G |
T |
11: 104,315,112 (GRCm39) |
Q309K |
probably damaging |
Het |
Kcns3 |
A |
C |
12: 11,141,718 (GRCm39) |
L327R |
probably damaging |
Het |
Mapk10 |
A |
G |
5: 103,139,792 (GRCm39) |
I153T |
possibly damaging |
Het |
Muc5b |
G |
T |
7: 141,400,569 (GRCm39) |
M513I |
unknown |
Het |
Nbea |
A |
G |
3: 55,966,086 (GRCm39) |
F459L |
probably damaging |
Het |
Nrcam |
G |
A |
12: 44,631,644 (GRCm39) |
V1066I |
possibly damaging |
Het |
Numa1 |
A |
G |
7: 101,651,538 (GRCm39) |
K178E |
probably damaging |
Het |
Or4b1 |
C |
T |
2: 89,979,928 (GRCm39) |
V141M |
probably benign |
Het |
Or5au1 |
T |
C |
14: 52,272,645 (GRCm39) |
K308E |
probably benign |
Het |
Or5d14 |
G |
A |
2: 87,880,290 (GRCm39) |
T226M |
probably damaging |
Het |
Pabpc4 |
C |
T |
4: 123,191,837 (GRCm39) |
A649V |
probably benign |
Het |
Parp12 |
C |
A |
6: 39,079,612 (GRCm39) |
K299N |
possibly damaging |
Het |
Pcdhga7 |
A |
G |
18: 37,849,562 (GRCm39) |
D523G |
possibly damaging |
Het |
Polr2a |
T |
C |
11: 69,638,330 (GRCm39) |
T79A |
probably benign |
Het |
Ppp1r7 |
T |
C |
1: 93,273,904 (GRCm39) |
S27P |
probably damaging |
Het |
Pramel42 |
G |
T |
5: 94,685,440 (GRCm39) |
D367Y |
probably damaging |
Het |
Prol1 |
T |
G |
5: 88,475,874 (GRCm39) |
L88R |
probably damaging |
Het |
Ptpn6 |
T |
C |
6: 124,709,425 (GRCm39) |
Q57R |
possibly damaging |
Het |
Rock2 |
T |
A |
12: 16,998,558 (GRCm39) |
C275S |
probably damaging |
Het |
Rp1l1 |
G |
T |
14: 64,268,674 (GRCm39) |
R1420L |
probably damaging |
Het |
Sav1 |
A |
G |
12: 70,033,481 (GRCm39) |
Y21H |
probably damaging |
Het |
Sec24a |
T |
C |
11: 51,612,749 (GRCm39) |
N536S |
probably benign |
Het |
Serpina9 |
A |
C |
12: 103,964,421 (GRCm39) |
F339V |
probably damaging |
Het |
Slc6a13 |
T |
G |
6: 121,311,450 (GRCm39) |
L369V |
possibly damaging |
Het |
Smarcd3 |
A |
T |
5: 24,801,024 (GRCm39) |
F128I |
probably damaging |
Het |
Smok2a |
A |
T |
17: 13,444,599 (GRCm39) |
I59F |
probably damaging |
Het |
Spaca9 |
A |
G |
2: 28,583,634 (GRCm39) |
|
probably null |
Het |
Ssx2ip |
A |
T |
3: 146,124,928 (GRCm39) |
E84D |
probably benign |
Het |
Syt12 |
A |
T |
19: 4,497,830 (GRCm39) |
V384E |
probably benign |
Het |
Ticrr |
T |
A |
7: 79,331,584 (GRCm39) |
L727Q |
probably damaging |
Het |
Tmem170b |
A |
G |
13: 41,781,463 (GRCm39) |
Y36C |
probably damaging |
Het |
Tpd52l1 |
T |
C |
10: 31,214,201 (GRCm39) |
T161A |
probably damaging |
Het |
Zan |
T |
A |
5: 137,461,841 (GRCm39) |
T1113S |
unknown |
Het |
Zfp512b |
T |
C |
2: 181,231,689 (GRCm39) |
T164A |
probably damaging |
Het |
Zfp521 |
G |
A |
18: 13,977,549 (GRCm39) |
P955S |
probably damaging |
Het |
Zfp770 |
C |
T |
2: 114,027,305 (GRCm39) |
V255I |
probably benign |
Het |
Zfp942 |
A |
T |
17: 22,148,208 (GRCm39) |
C140* |
probably null |
Het |
|
Other mutations in Rdh16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01304:Rdh16
|
APN |
10 |
127,649,365 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01618:Rdh16
|
APN |
10 |
127,637,176 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02125:Rdh16
|
APN |
10 |
127,647,188 (GRCm39) |
intron |
probably benign |
|
IGL02820:Rdh16
|
APN |
10 |
127,649,470 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03091:Rdh16
|
APN |
10 |
127,649,502 (GRCm39) |
utr 3 prime |
probably benign |
|
R1674:Rdh16
|
UTSW |
10 |
127,637,226 (GRCm39) |
missense |
probably benign |
0.25 |
R4616:Rdh16
|
UTSW |
10 |
127,637,382 (GRCm39) |
splice site |
probably null |
|
R4675:Rdh16
|
UTSW |
10 |
127,637,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R5324:Rdh16
|
UTSW |
10 |
127,637,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R7191:Rdh16
|
UTSW |
10 |
127,649,287 (GRCm39) |
missense |
probably benign |
0.00 |
R9263:Rdh16
|
UTSW |
10 |
127,649,306 (GRCm39) |
missense |
probably benign |
|
X0013:Rdh16
|
UTSW |
10 |
127,637,199 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Rdh16
|
UTSW |
10 |
127,637,199 (GRCm39) |
missense |
probably damaging |
1.00 |
|