Incidental Mutation 'IGL01777:Tas2r114'
| ID |
154133 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Tas2r114
|
| Ensembl Gene |
ENSMUSG00000063478 |
| Gene Name |
taste receptor, type 2, member 114 |
| Synonyms |
mt2r46, mGR14, T2R14, Tas2r14 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.053)
|
| Stock # |
IGL01777
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
6 |
| Chromosomal Location |
131666097-131667026 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to T
at 131666664 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tryptophan to Stop codon
at position 121
(W121*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000079453
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053652]
[ENSMUST00000072404]
[ENSMUST00000080619]
|
| AlphaFold |
Q7M722 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000053652
|
| SMART Domains |
Protein: ENSMUSP00000058006
Gene: ENSMUSG00000051153
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TAS2R
|
1 |
298 |
9.4e-109 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000072404
|
| SMART Domains |
Protein: ENSMUSP00000072237
Gene: ENSMUSG00000061977
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TAS2R
|
1 |
298 |
8.3e-102 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000080619
AA Change: W121*
|
| SMART Domains |
Protein: ENSMUSP00000079453
Gene: ENSMUSG00000063478
AA Change: W121*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TAS2R
|
1 |
298 |
8.1e-104 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aadacl2 |
T |
C |
3: 59,932,205 (GRCm39) |
V240A |
possibly damaging |
Het |
| Aftph |
A |
T |
11: 20,676,554 (GRCm39) |
C352S |
possibly damaging |
Het |
| Cand2 |
T |
C |
6: 115,769,818 (GRCm39) |
V876A |
probably damaging |
Het |
| Ccar1 |
T |
C |
10: 62,616,356 (GRCm39) |
I125V |
possibly damaging |
Het |
| Celsr3 |
A |
T |
9: 108,713,141 (GRCm39) |
M1858L |
probably benign |
Het |
| Csmd3 |
A |
T |
15: 47,561,594 (GRCm39) |
N2134K |
probably benign |
Het |
| Dhx29 |
A |
G |
13: 113,067,406 (GRCm39) |
I96V |
probably benign |
Het |
| Dst |
A |
G |
1: 34,238,478 (GRCm39) |
T3727A |
probably benign |
Het |
| Elavl4 |
T |
A |
4: 110,063,858 (GRCm39) |
|
probably null |
Het |
| Eno2 |
C |
T |
6: 124,743,600 (GRCm39) |
G113D |
probably damaging |
Het |
| Esf1 |
A |
C |
2: 139,999,092 (GRCm39) |
|
probably null |
Het |
| Frmd4b |
T |
C |
6: 97,272,905 (GRCm39) |
D783G |
probably benign |
Het |
| Grin2a |
C |
T |
16: 9,461,994 (GRCm39) |
V713I |
probably benign |
Het |
| Impa1 |
C |
T |
3: 10,388,008 (GRCm39) |
G138D |
probably damaging |
Het |
| Kcnt2 |
A |
G |
1: 140,523,736 (GRCm39) |
T1079A |
probably benign |
Het |
| Kmt2a |
A |
G |
9: 44,760,302 (GRCm39) |
S549P |
probably damaging |
Het |
| Magoh |
C |
A |
4: 107,740,373 (GRCm39) |
Q86K |
probably benign |
Het |
| Moxd1 |
C |
A |
10: 24,128,494 (GRCm39) |
T182K |
probably benign |
Het |
| Or5p55 |
A |
G |
7: 107,566,709 (GRCm39) |
Y35C |
probably damaging |
Het |
| Pramel25 |
T |
G |
4: 143,521,688 (GRCm39) |
C435G |
possibly damaging |
Het |
| Rab3b |
A |
T |
4: 108,786,607 (GRCm39) |
Q119L |
probably damaging |
Het |
| Snap47 |
T |
A |
11: 59,312,477 (GRCm39) |
|
probably null |
Het |
| Taar3 |
A |
G |
10: 23,825,903 (GRCm39) |
R150G |
probably benign |
Het |
| Tas2r102 |
C |
T |
6: 132,739,815 (GRCm39) |
T241I |
probably damaging |
Het |
| Trak1 |
G |
A |
9: 121,260,626 (GRCm39) |
|
probably null |
Het |
| Ubn1 |
T |
C |
16: 4,890,013 (GRCm39) |
V426A |
possibly damaging |
Het |
| Vmn1r40 |
T |
C |
6: 89,691,204 (GRCm39) |
L7P |
probably benign |
Het |
| Vmn2r43 |
T |
C |
7: 8,258,272 (GRCm39) |
I314V |
probably damaging |
Het |
| Vrtn |
T |
G |
12: 84,695,696 (GRCm39) |
S149A |
probably benign |
Het |
|
| Other mutations in Tas2r114 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02971:Tas2r114
|
APN |
6 |
131,666,243 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0561:Tas2r114
|
UTSW |
6 |
131,666,758 (GRCm39) |
missense |
probably benign |
0.30 |
|
R3034:Tas2r114
|
UTSW |
6 |
131,666,611 (GRCm39) |
missense |
probably benign |
0.15 |
|
R3687:Tas2r114
|
UTSW |
6 |
131,666,231 (GRCm39) |
missense |
probably benign |
0.25 |
|
R4411:Tas2r114
|
UTSW |
6 |
131,666,585 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4826:Tas2r114
|
UTSW |
6 |
131,666,800 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4889:Tas2r114
|
UTSW |
6 |
131,666,758 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5084:Tas2r114
|
UTSW |
6 |
131,666,251 (GRCm39) |
nonsense |
probably null |
|
|
R5258:Tas2r114
|
UTSW |
6 |
131,666,504 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6038:Tas2r114
|
UTSW |
6 |
131,666,444 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R6038:Tas2r114
|
UTSW |
6 |
131,666,444 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R6499:Tas2r114
|
UTSW |
6 |
131,666,099 (GRCm39) |
makesense |
probably null |
|
|
R7164:Tas2r114
|
UTSW |
6 |
131,666,728 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R7276:Tas2r114
|
UTSW |
6 |
131,666,310 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7745:Tas2r114
|
UTSW |
6 |
131,666,401 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7851:Tas2r114
|
UTSW |
6 |
131,666,888 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8002:Tas2r114
|
UTSW |
6 |
131,666,102 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8901:Tas2r114
|
UTSW |
6 |
131,666,914 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9297:Tas2r114
|
UTSW |
6 |
131,666,287 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9380:Tas2r114
|
UTSW |
6 |
131,666,381 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9402:Tas2r114
|
UTSW |
6 |
131,666,894 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R9473:Tas2r114
|
UTSW |
6 |
131,666,104 (GRCm39) |
missense |
probably benign |
|
|
R9513:Tas2r114
|
UTSW |
6 |
131,666,746 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Posted On |
2014-02-04 |
Incidental Mutation