Incidental Mutation 'R1069:Tas2r131'
ID |
86126 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tas2r131
|
Ensembl Gene |
ENSMUSG00000057699 |
Gene Name |
taste receptor, type 2, member 131 |
Synonyms |
Tas2r31, mGR31, T2R31, mt2r61 |
MMRRC Submission |
039155-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1069 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
132933875-132934807 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 132934788 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Lysine
at position 7
(R7K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000080736
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000082085]
|
AlphaFold |
Q7M708 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000082085
AA Change: R7K
PolyPhen 2
Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
|
SMART Domains |
Protein: ENSMUSP00000080736 Gene: ENSMUSG00000057699 AA Change: R7K
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
1 |
293 |
1.2e-66 |
PFAM |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.8%
- 10x: 97.5%
- 20x: 95.4%
|
Validation Efficiency |
100% (33/33) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
A |
G |
18: 6,624,037 (GRCm39) |
N106S |
probably benign |
Het |
Akr1c21 |
C |
A |
13: 4,625,333 (GRCm39) |
|
probably benign |
Het |
Alpk2 |
G |
A |
18: 65,438,085 (GRCm39) |
R1570C |
probably benign |
Het |
Atp8b3 |
G |
A |
10: 80,366,852 (GRCm39) |
R249C |
probably damaging |
Het |
Cacnb4 |
C |
A |
2: 52,345,623 (GRCm39) |
R252I |
probably damaging |
Het |
Cars1 |
T |
C |
7: 143,123,844 (GRCm39) |
T480A |
probably benign |
Het |
Ccnf |
A |
T |
17: 24,442,971 (GRCm39) |
C745* |
probably null |
Het |
Ccr8 |
A |
G |
9: 119,923,283 (GRCm39) |
I133V |
probably benign |
Het |
Cndp1 |
G |
A |
18: 84,652,777 (GRCm39) |
|
probably benign |
Het |
Dgkq |
T |
C |
5: 108,803,903 (GRCm39) |
|
probably benign |
Het |
Ecd |
A |
G |
14: 20,383,504 (GRCm39) |
C312R |
probably damaging |
Het |
Eddm13 |
A |
T |
7: 6,258,921 (GRCm39) |
|
probably null |
Het |
Gstm1 |
T |
C |
3: 107,920,064 (GRCm39) |
S226G |
probably damaging |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Hacd4 |
T |
A |
4: 88,355,739 (GRCm39) |
I49L |
probably damaging |
Het |
Hid1 |
T |
C |
11: 115,247,591 (GRCm39) |
N269S |
probably damaging |
Het |
Ifitm3 |
A |
T |
7: 140,589,813 (GRCm39) |
|
probably benign |
Het |
Kctd9 |
C |
T |
14: 67,966,869 (GRCm39) |
|
probably benign |
Het |
Kif20b |
T |
C |
19: 34,928,251 (GRCm39) |
L1131P |
probably damaging |
Het |
Kif2c |
T |
C |
4: 117,035,350 (GRCm39) |
T33A |
probably damaging |
Het |
Lipc |
T |
C |
9: 70,730,819 (GRCm39) |
T38A |
probably benign |
Het |
Lrguk |
A |
C |
6: 34,025,818 (GRCm39) |
I205L |
possibly damaging |
Het |
Mir100hg |
G |
A |
9: 41,501,594 (GRCm39) |
R151H |
possibly damaging |
Het |
Ncapg |
T |
A |
5: 45,833,272 (GRCm39) |
|
probably benign |
Het |
Ptprd |
A |
G |
4: 75,916,724 (GRCm39) |
|
probably benign |
Het |
Ptprd |
T |
A |
4: 76,018,870 (GRCm39) |
K635* |
probably null |
Het |
Sap130 |
G |
A |
18: 31,844,682 (GRCm39) |
V898I |
probably damaging |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Svep1 |
C |
T |
4: 58,070,239 (GRCm39) |
G2516R |
probably damaging |
Het |
Tfpi |
A |
G |
2: 84,284,136 (GRCm39) |
|
probably benign |
Het |
Trim80 |
T |
C |
11: 115,338,909 (GRCm39) |
C580R |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,800,273 (GRCm39) |
I312F |
unknown |
Het |
|
Other mutations in Tas2r131 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00592:Tas2r131
|
APN |
6 |
132,934,159 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00795:Tas2r131
|
APN |
6 |
132,934,554 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01023:Tas2r131
|
APN |
6 |
132,934,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02439:Tas2r131
|
APN |
6 |
132,934,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R0335:Tas2r131
|
UTSW |
6 |
132,934,792 (GRCm39) |
missense |
probably benign |
|
R0523:Tas2r131
|
UTSW |
6 |
132,934,414 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1056:Tas2r131
|
UTSW |
6 |
132,934,030 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4073:Tas2r131
|
UTSW |
6 |
132,934,802 (GRCm39) |
nonsense |
probably null |
|
R4719:Tas2r131
|
UTSW |
6 |
132,933,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R5002:Tas2r131
|
UTSW |
6 |
132,934,114 (GRCm39) |
missense |
probably benign |
0.00 |
R5049:Tas2r131
|
UTSW |
6 |
132,934,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R5635:Tas2r131
|
UTSW |
6 |
132,934,571 (GRCm39) |
missense |
probably benign |
0.27 |
R5905:Tas2r131
|
UTSW |
6 |
132,934,639 (GRCm39) |
missense |
probably benign |
0.02 |
R6028:Tas2r131
|
UTSW |
6 |
132,934,639 (GRCm39) |
missense |
probably benign |
0.02 |
R6229:Tas2r131
|
UTSW |
6 |
132,933,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R7115:Tas2r131
|
UTSW |
6 |
132,934,567 (GRCm39) |
missense |
probably benign |
0.07 |
R7561:Tas2r131
|
UTSW |
6 |
132,933,921 (GRCm39) |
missense |
probably benign |
0.26 |
R7741:Tas2r131
|
UTSW |
6 |
132,934,438 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7810:Tas2r131
|
UTSW |
6 |
132,934,705 (GRCm39) |
missense |
probably benign |
0.11 |
R8878:Tas2r131
|
UTSW |
6 |
132,934,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R9506:Tas2r131
|
UTSW |
6 |
132,934,024 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0025:Tas2r131
|
UTSW |
6 |
132,934,501 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tas2r131
|
UTSW |
6 |
132,933,960 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GCAGGTGGCAAGCCATGTTGATAG -3'
(R):5'- ACAGAGTGCAGTGTTTCAGGTGAG -3'
Sequencing Primer
(F):5'- ATAGAAATGAGGCGCTAGTTCTTG -3'
(R):5'- CATCAATGGGAATTTTGAAGGCAC -3'
|
Posted On |
2013-11-18 |