Incidental Mutation 'IGL02816:Tas2r144'
ID |
360798 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Tas2r144
|
Ensembl Gene |
ENSMUSG00000051917 |
Gene Name |
taste receptor, type 2, member 144 |
Synonyms |
mt2r33, Tas2r44 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.057)
|
Stock # |
IGL02816
|
Quality Score |
|
Status
|
|
Chromosome |
6 |
Chromosomal Location |
42192262-42193221 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 42192539 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Phenylalanine
at position 93
(Y93F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000067734
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000063489]
|
AlphaFold |
Q7TQB8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000063489
AA Change: Y93F
PolyPhen 2
Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000067734 Gene: ENSMUSG00000051917 AA Change: Y93F
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
12 |
314 |
9.6e-63 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Caskin1 |
C |
A |
17: 24,721,144 (GRCm39) |
P495T |
probably benign |
Het |
Clcn4 |
A |
G |
7: 7,298,087 (GRCm39) |
C41R |
probably damaging |
Het |
Etfdh |
G |
A |
3: 79,530,112 (GRCm39) |
T52M |
probably damaging |
Het |
Fam227a |
T |
C |
15: 79,510,497 (GRCm39) |
T386A |
possibly damaging |
Het |
Gabrr3 |
T |
C |
16: 59,260,830 (GRCm39) |
|
probably benign |
Het |
Krt25 |
G |
T |
11: 99,208,977 (GRCm39) |
D284E |
probably benign |
Het |
Map1b |
T |
C |
13: 99,578,263 (GRCm39) |
D130G |
probably damaging |
Het |
Nlrp3 |
T |
A |
11: 59,446,608 (GRCm39) |
F785I |
probably benign |
Het |
Nrn1 |
C |
A |
13: 36,914,080 (GRCm39) |
|
probably null |
Het |
Numa1 |
T |
A |
7: 101,645,307 (GRCm39) |
I311N |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,813,489 (GRCm39) |
C4010R |
probably benign |
Het |
Prph |
A |
G |
15: 98,955,301 (GRCm39) |
M423V |
probably damaging |
Het |
Rb1cc1 |
T |
A |
1: 6,333,052 (GRCm39) |
|
probably benign |
Het |
Ribc2 |
T |
G |
15: 85,017,106 (GRCm39) |
V48G |
probably damaging |
Het |
Scyl1 |
A |
T |
19: 5,820,410 (GRCm39) |
N141K |
probably damaging |
Het |
Sec23a |
T |
A |
12: 59,025,331 (GRCm39) |
M497L |
probably benign |
Het |
Strada |
C |
T |
11: 106,055,251 (GRCm39) |
|
probably benign |
Het |
Tmem94 |
T |
A |
11: 115,679,530 (GRCm39) |
|
probably null |
Het |
Trpc3 |
A |
G |
3: 36,705,851 (GRCm39) |
F448S |
probably damaging |
Het |
Ttc13 |
A |
G |
8: 125,439,415 (GRCm39) |
I113T |
possibly damaging |
Het |
Ttc27 |
T |
A |
17: 75,054,769 (GRCm39) |
|
probably benign |
Het |
Ttll13 |
G |
T |
7: 79,902,842 (GRCm39) |
C170F |
possibly damaging |
Het |
Yes1 |
C |
T |
5: 32,802,451 (GRCm39) |
T122M |
probably damaging |
Het |
|
Other mutations in Tas2r144 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02349:Tas2r144
|
APN |
6 |
42,193,010 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02644:Tas2r144
|
APN |
6 |
42,192,787 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0375:Tas2r144
|
UTSW |
6 |
42,193,058 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1526:Tas2r144
|
UTSW |
6 |
42,192,674 (GRCm39) |
missense |
probably benign |
|
R1543:Tas2r144
|
UTSW |
6 |
42,192,537 (GRCm39) |
missense |
probably benign |
0.00 |
R1678:Tas2r144
|
UTSW |
6 |
42,192,490 (GRCm39) |
missense |
probably benign |
0.44 |
R1868:Tas2r144
|
UTSW |
6 |
42,192,936 (GRCm39) |
missense |
probably benign |
0.01 |
R1880:Tas2r144
|
UTSW |
6 |
42,193,004 (GRCm39) |
missense |
probably benign |
0.02 |
R4060:Tas2r144
|
UTSW |
6 |
42,192,563 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5173:Tas2r144
|
UTSW |
6 |
42,193,048 (GRCm39) |
missense |
probably benign |
0.40 |
R6108:Tas2r144
|
UTSW |
6 |
42,192,691 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6249:Tas2r144
|
UTSW |
6 |
42,192,291 (GRCm39) |
nonsense |
probably null |
|
R6533:Tas2r144
|
UTSW |
6 |
42,192,280 (GRCm39) |
missense |
probably benign |
|
R6850:Tas2r144
|
UTSW |
6 |
42,192,857 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7237:Tas2r144
|
UTSW |
6 |
42,192,800 (GRCm39) |
missense |
probably damaging |
0.99 |
R7296:Tas2r144
|
UTSW |
6 |
42,192,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7431:Tas2r144
|
UTSW |
6 |
42,192,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R8206:Tas2r144
|
UTSW |
6 |
42,192,325 (GRCm39) |
missense |
probably damaging |
0.98 |
R9341:Tas2r144
|
UTSW |
6 |
42,193,066 (GRCm39) |
missense |
probably benign |
0.03 |
R9343:Tas2r144
|
UTSW |
6 |
42,193,066 (GRCm39) |
missense |
probably benign |
0.03 |
R9640:Tas2r144
|
UTSW |
6 |
42,192,428 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Tas2r144
|
UTSW |
6 |
42,193,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2015-12-18 |