Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
T |
C |
14: 29,710,292 (GRCm39) |
L353S |
probably damaging |
Het |
Adgrf2 |
G |
A |
17: 43,021,049 (GRCm39) |
P592S |
probably damaging |
Het |
Aen |
G |
A |
7: 78,557,050 (GRCm39) |
M299I |
probably damaging |
Het |
Afap1l2 |
A |
C |
19: 56,901,843 (GRCm39) |
|
probably null |
Het |
Asnsd1 |
G |
A |
1: 53,387,436 (GRCm39) |
P64S |
probably damaging |
Het |
Bmt2 |
A |
G |
6: 13,663,270 (GRCm39) |
M76T |
probably damaging |
Het |
Clca3b |
A |
T |
3: 144,529,283 (GRCm39) |
V797D |
probably benign |
Het |
Cog2 |
T |
C |
8: 125,271,982 (GRCm39) |
S499P |
probably benign |
Het |
Cyp27a1 |
A |
T |
1: 74,771,097 (GRCm39) |
Y94F |
possibly damaging |
Het |
D630045J12Rik |
A |
G |
6: 38,113,898 (GRCm39) |
S1765P |
probably benign |
Het |
Fam149a |
A |
G |
8: 45,801,564 (GRCm39) |
L519P |
possibly damaging |
Het |
Fam171a2 |
G |
A |
11: 102,328,674 (GRCm39) |
A695V |
possibly damaging |
Het |
Fat1 |
T |
A |
8: 45,470,894 (GRCm39) |
V1566E |
probably damaging |
Het |
Flvcr1 |
T |
G |
1: 190,745,587 (GRCm39) |
N361H |
probably damaging |
Het |
Gm1110 |
T |
C |
9: 26,793,156 (GRCm39) |
N540S |
probably benign |
Het |
Katnip |
A |
G |
7: 125,394,485 (GRCm39) |
E187G |
probably damaging |
Het |
Kcns3 |
T |
A |
12: 11,141,572 (GRCm39) |
T376S |
possibly damaging |
Het |
Krt32 |
A |
G |
11: 99,978,605 (GRCm39) |
S150P |
probably benign |
Het |
Lrtm2 |
C |
T |
6: 119,297,753 (GRCm39) |
R96Q |
possibly damaging |
Het |
Mctp1 |
A |
G |
13: 77,168,917 (GRCm39) |
E838G |
probably damaging |
Het |
Mios |
T |
C |
6: 8,234,363 (GRCm39) |
|
probably null |
Het |
Or1j10 |
A |
T |
2: 36,267,178 (GRCm39) |
Y130F |
probably damaging |
Het |
Phldb1 |
T |
A |
9: 44,619,184 (GRCm39) |
K167* |
probably null |
Het |
Pkhd1l1 |
A |
G |
15: 44,347,265 (GRCm39) |
|
probably benign |
Het |
Plaa |
A |
G |
4: 94,462,284 (GRCm39) |
V531A |
probably benign |
Het |
Psmb2 |
A |
G |
4: 126,577,999 (GRCm39) |
Y59C |
probably damaging |
Het |
Ptprg |
A |
G |
14: 12,215,286 (GRCm38) |
H1091R |
probably damaging |
Het |
Rbm44 |
T |
A |
1: 91,096,419 (GRCm39) |
V926D |
possibly damaging |
Het |
Rgma |
G |
T |
7: 73,059,462 (GRCm39) |
V189L |
possibly damaging |
Het |
Sbf2 |
A |
T |
7: 109,948,169 (GRCm39) |
I1227K |
probably damaging |
Het |
Slc8a1 |
T |
C |
17: 81,955,710 (GRCm39) |
T443A |
probably damaging |
Het |
Slc8a1 |
A |
G |
17: 81,696,310 (GRCm39) |
V896A |
probably damaging |
Het |
Taf2 |
T |
C |
15: 54,879,977 (GRCm39) |
M1120V |
probably benign |
Het |
Ugt2b34 |
C |
T |
5: 87,054,185 (GRCm39) |
V199I |
probably benign |
Het |
Unc5c |
C |
A |
3: 141,523,963 (GRCm39) |
|
probably benign |
Het |
Usp37 |
G |
A |
1: 74,532,205 (GRCm39) |
R63* |
probably null |
Het |
|
Other mutations in Liat1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Liat1
|
APN |
11 |
75,894,192 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02112:Liat1
|
APN |
11 |
75,894,214 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02152:Liat1
|
APN |
11 |
75,894,051 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02189:Liat1
|
APN |
11 |
75,891,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Liat1
|
UTSW |
11 |
75,890,941 (GRCm39) |
small deletion |
probably benign |
|
R1562:Liat1
|
UTSW |
11 |
75,894,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R2068:Liat1
|
UTSW |
11 |
75,891,077 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5027:Liat1
|
UTSW |
11 |
75,891,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R5663:Liat1
|
UTSW |
11 |
75,891,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Liat1
|
UTSW |
11 |
75,890,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R7381:Liat1
|
UTSW |
11 |
75,893,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9092:Liat1
|
UTSW |
11 |
75,893,887 (GRCm39) |
missense |
possibly damaging |
0.48 |
|