Mutagenetix > Incidental Mutation

Incidental Mutation 'R4073:Tas2r131'

316392

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

041621-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4073 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

132933875-132934807 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 132934802 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 2 (Y2*)

Ref Sequence

ENSEMBL: ENSMUSP00000080736 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000082085]

AlphaFold

Q7M708

Predicted Effect

probably null
Transcript: ENSMUST00000082085
AA Change: Y2*

SMART Domains

Protein: ENSMUSP00000080736
Gene: ENSMUSG00000057699
AA Change: Y2*

Domain	Start	End	E-Value	Type
Pfam:TAS2R	1	293	1.2e-66	PFAM

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.4%

Validation Efficiency

96% (67/70)

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932415M13Rik	C	T	17: 54,031,494 (GRCm39)		noncoding transcript	Het
Alox12	T	C	11: 70,138,136 (GRCm39)	N400D	probably damaging	Het
Axl	A	G	7: 25,463,336 (GRCm39)		probably benign	Het
Cbs	C	T	17: 31,851,979 (GRCm39)	C8Y	possibly damaging	Het
Ccdc103	C	T	11: 102,774,925 (GRCm39)	R175W	probably damaging	Het
Clasp1	T	C	1: 118,431,578 (GRCm39)	F171L	probably damaging	Het
Cnot10	A	G	9: 114,452,015 (GRCm39)	F254L	possibly damaging	Het
Cytl1	A	G	5: 37,892,940 (GRCm39)	I17V	unknown	Het
Dnah11	A	G	12: 118,009,413 (GRCm39)	M2083T	probably benign	Het
Dock7	A	T	4: 98,896,296 (GRCm39)	S768R	probably benign	Het
Egf	C	T	3: 129,529,618 (GRCm39)	R264Q	probably benign	Het
Ehhadh	T	C	16: 21,585,257 (GRCm39)	D208G	probably benign	Het
Eqtn	A	G	4: 94,808,199 (GRCm39)	I201T	possibly damaging	Het
Erbin	T	C	13: 103,996,619 (GRCm39)	E211G	probably damaging	Het
Ercc4	G	A	16: 12,948,549 (GRCm39)	V499I	probably damaging	Het
Gpd2	A	G	2: 57,180,025 (GRCm39)	R91G	probably damaging	Het
Herc1	A	G	9: 66,325,774 (GRCm39)	D1416G	probably benign	Het
Ighv1-30	C	T	12: 114,781,021 (GRCm39)		noncoding transcript	Het
Il23r	A	G	6: 67,463,106 (GRCm39)	I129T	probably damaging	Het
Jph4	T	C	14: 55,352,497 (GRCm39)	S79G	probably benign	Het
Lamp3	A	G	16: 19,519,466 (GRCm39)	L239P	possibly damaging	Het
Lrig3	C	T	10: 125,849,277 (GRCm39)	T999I	probably benign	Het
Lrrc71	G	A	3: 87,652,569 (GRCm39)	T185I	probably benign	Het
Mroh1	A	G	15: 76,292,185 (GRCm39)	D219G	probably benign	Het
Mtor	T	A	4: 148,633,832 (GRCm39)	S2342T	probably damaging	Het
Nf2	T	C	11: 4,798,958 (GRCm39)	S10G	probably benign	Het
Nlrp4c	A	G	7: 6,075,709 (GRCm39)	K667E	probably benign	Het
Nrm	T	A	17: 36,172,424 (GRCm39)		probably benign	Het
Nsd1	T	A	13: 55,395,541 (GRCm39)	H1047Q	probably benign	Het
Obox3	G	T	7: 15,359,724 (GRCm39)	T315N	possibly damaging	Het
Or2t47	T	C	11: 58,442,888 (GRCm39)	Y59C	probably damaging	Het
Or4k5	A	G	14: 50,385,500 (GRCm39)	V277A	possibly damaging	Het
Or4x13	T	C	2: 90,231,337 (GRCm39)	F111L	probably benign	Het
Or5b3	G	A	19: 13,388,299 (GRCm39)	R122H	possibly damaging	Het
Or6aa1	T	A	7: 86,044,155 (GRCm39)	I184F	probably damaging	Het
Or8b38	T	C	9: 37,973,165 (GRCm39)	L183P	probably damaging	Het
Pbx3	T	C	2: 34,114,424 (GRCm39)	Y112C	probably damaging	Het
Pde11a	C	T	2: 76,168,242 (GRCm39)	R237H	probably damaging	Het
Phactr1	ACTT	A	13: 43,213,245 (GRCm39)		probably benign	Het
Pidd1	A	G	7: 141,020,739 (GRCm39)	F453L	probably damaging	Het
Ptgs1	C	T	2: 36,127,788 (GRCm39)	R116C	probably damaging	Het
Rab39b	T	C	X: 74,618,658 (GRCm39)		probably benign	Het
Rpp25	T	C	9: 57,411,592 (GRCm39)	S25P	probably benign	Het
Rrbp1	T	G	2: 143,805,030 (GRCm39)	Q1045P	probably benign	Het
Sbk3	G	T	7: 4,973,501 (GRCm39)	A41D	probably damaging	Het
Slc24a3	T	A	2: 145,455,636 (GRCm39)		probably benign	Het
Slc28a3	T	C	13: 58,707,104 (GRCm39)	I565V	probably benign	Het
Slc35a3	T	C	3: 116,468,887 (GRCm39)	T275A	probably benign	Het
Spink12	A	G	18: 44,237,731 (GRCm39)	N3S	possibly damaging	Het
Srp72	C	A	5: 77,146,098 (GRCm39)	T633K	probably benign	Het
Tab3	G	T	X: 84,658,063 (GRCm39)	V197F	probably damaging	Het
Taf2	A	G	15: 54,915,633 (GRCm39)	L431P	probably damaging	Het
Tmprss11e	T	C	5: 86,863,502 (GRCm39)	T188A	possibly damaging	Het
Trpv1	T	C	11: 73,141,606 (GRCm39)	V175A	probably damaging	Het
Usp21	T	C	1: 171,109,746 (GRCm39)		probably benign	Het
Vmn1r25	A	G	6: 57,955,572 (GRCm39)	V239A	possibly damaging	Het
Zbbx	C	T	3: 75,012,978 (GRCm39)	G151E	probably damaging	Het
Zfhx4	G	T	3: 5,464,384 (GRCm39)	C1514F	probably damaging	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
R1069:Tas2r131	UTSW	6	132,934,788 (GRCm39)	missense	probably benign	0.01
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'- GAAATGAGGCGCTAGTTCTTG -3'
(R):5'- GGGCATAGAGACTGTCTGTACTAG -3'

Sequencing Primer
(F):5'- AAATGAGGCGCTAGTTCTTGTATGG -3'
(R):5'- AGTATGTGTGAATATCAACCTAATGG -3'

Posted On

2015-05-15