Mutagenetix > Incidental Mutation

Incidental Mutation 'R6495:Tas2r129'

520424

Institutional Source

Beutler Lab

Gene Symbol

Tas2r129

Ensembl Gene

ENSMUSG00000063762

Gene Name

taste receptor, type 2, member 129

Synonyms

Tas2r29, mt2r60, mGR29, T2R29

MMRRC Submission

044627-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.049) question?

Stock #

R6495 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

132928065-132929027 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 132928128 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 22 (I22V)

Ref Sequence

ENSEMBL: ENSMUSP00000067640 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000070991]

AlphaFold

Q7M709

Predicted Effect

probably benign
Transcript: ENSMUST00000070991
AA Change: I22V

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

SMART Domains

Protein: ENSMUSP00000067640
Gene: ENSMUSG00000063762
AA Change: I22V

Domain	Start	End	E-Value	Type
Pfam:TAS2R	1	302	2.3e-74	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 97.9%
20x: 93.8%

Validation Efficiency

100% (50/50)

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahnak2	T	A	12: 112,740,148 (GRCm39)	E502V	probably damaging	Het
Apbb1ip	T	A	2: 22,743,132 (GRCm39)	Y321*	probably null	Het
Apob	A	G	12: 8,040,394 (GRCm39)	K577R	probably null	Het
Arfgef3	A	G	10: 18,486,950 (GRCm39)		probably null	Het
Asap3	T	A	4: 135,955,790 (GRCm39)		probably null	Het
Atp13a5	C	T	16: 29,140,440 (GRCm39)		probably null	Het
Bcan	C	A	3: 87,903,904 (GRCm39)	A194S	possibly damaging	Het
Cacybp	T	C	1: 160,036,093 (GRCm39)	T32A	probably benign	Het
Cd82	A	G	2: 93,260,357 (GRCm39)	V90A	probably benign	Het
Chd5	C	T	4: 152,451,829 (GRCm39)	R714C	probably damaging	Het
Cpb2	T	C	14: 75,512,519 (GRCm39)	Y311H	probably damaging	Het
Cyp39a1	T	C	17: 44,002,585 (GRCm39)	Y267H	probably benign	Het
Dnajc6	C	T	4: 101,492,262 (GRCm39)	Q766*	probably null	Het
Dusp3	T	C	11: 101,872,653 (GRCm39)	I48V	probably benign	Het
Eif3c	A	T	7: 126,146,672 (GRCm39)	F809I	probably damaging	Het
Exosc10	C	T	4: 148,647,329 (GRCm39)	P213S	probably benign	Het
Galns	C	T	8: 123,327,349 (GRCm39)	G141D	probably damaging	Het
Gm3233	A	T	10: 77,594,886 (GRCm39)		probably benign	Het
Hadha	A	T	5: 30,325,048 (GRCm39)	L714H	probably benign	Het
Map3k20	T	C	2: 72,198,763 (GRCm39)	M123T	probably damaging	Het
Nt5dc1	A	G	10: 34,200,365 (GRCm39)	L217P	probably damaging	Het
Nubp2	A	T	17: 25,104,577 (GRCm39)	D54E	probably damaging	Het
Onecut1	C	T	9: 74,770,497 (GRCm39)	R307C	probably damaging	Het
Or5b116	T	A	19: 13,422,989 (GRCm39)	D204E	probably benign	Het
Pcdhb17	A	G	18: 37,618,720 (GRCm39)	Y170C	probably damaging	Het
Pkd2	T	A	5: 104,637,159 (GRCm39)	C591S	probably damaging	Het
Pramel15	T	C	4: 144,103,409 (GRCm39)	N239S	probably benign	Het
Pwp2	A	T	10: 78,012,961 (GRCm39)	V549E	probably damaging	Het
Rapsn	A	T	2: 90,866,973 (GRCm39)	S92C	probably damaging	Het
Rbm19	A	G	5: 120,257,745 (GRCm39)	S90G	probably damaging	Het
Rfc1	G	A	5: 65,431,158 (GRCm39)		probably null	Het
Rims2	T	A	15: 39,381,208 (GRCm39)	F1046L	probably benign	Het
S100a16	C	T	3: 90,449,735 (GRCm39)	R73C	probably benign	Het
Shroom3	T	C	5: 93,089,928 (GRCm39)	Y893H	possibly damaging	Het
Stt3b	T	A	9: 115,096,388 (GRCm39)	Y253F	possibly damaging	Het
Taar8b	A	G	10: 23,967,160 (GRCm39)	*345Q	probably null	Het
Tas2r119	G	A	15: 32,177,676 (GRCm39)	V81I	probably benign	Het
Tbc1d19	T	G	5: 54,046,555 (GRCm39)		probably null	Het
Tnip3	A	T	6: 65,582,846 (GRCm39)	I218F	probably benign	Het
Tnks	A	T	8: 35,307,120 (GRCm39)		probably null	Het
Ttc29	T	C	8: 79,008,963 (GRCm39)	Y278H	possibly damaging	Het
Tut7	T	C	13: 59,947,753 (GRCm39)	E454G	possibly damaging	Het
Uba7	T	A	9: 107,854,213 (GRCm39)	C214*	probably null	Het
Vmn2r115	A	T	17: 23,578,572 (GRCm39)	I682F	probably benign	Het
Vmn2r75	A	T	7: 85,813,287 (GRCm39)	M505K	probably benign	Het
Wdr19	A	T	5: 65,415,466 (GRCm39)	T1313S	probably benign	Het
Zbtb22	A	G	17: 34,136,224 (GRCm39)	D123G	probably damaging	Het
Zdhhc7	A	G	8: 120,813,395 (GRCm39)	I138T	probably benign	Het
Zfp706	T	C	15: 37,004,045 (GRCm39)	K7R	unknown	Het
Zkscan3	G	A	13: 21,572,075 (GRCm39)	P519L	probably damaging	Het

Other mutations in Tas2r129

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02227:Tas2r129	APN	6	132,928,357 (GRCm39)	nonsense	probably null
R0389:Tas2r129	UTSW	6	132,928,159 (GRCm39)	missense	probably benign	0.26
R0443:Tas2r129	UTSW	6	132,928,159 (GRCm39)	missense	probably benign	0.26
R0487:Tas2r129	UTSW	6	132,928,907 (GRCm39)	missense	probably benign	0.31
R0487:Tas2r129	UTSW	6	132,928,906 (GRCm39)	missense	probably benign	0.26
R0576:Tas2r129	UTSW	6	132,928,497 (GRCm39)	missense	probably benign	0.38
R1253:Tas2r129	UTSW	6	132,928,999 (GRCm39)	missense	probably benign	0.11
R3124:Tas2r129	UTSW	6	132,928,411 (GRCm39)	missense	probably damaging	1.00
R4493:Tas2r129	UTSW	6	132,928,317 (GRCm39)	missense	probably benign	0.31
R4494:Tas2r129	UTSW	6	132,928,317 (GRCm39)	missense	probably benign	0.31
R4591:Tas2r129	UTSW	6	132,928,574 (GRCm39)	missense	probably benign	0.10
R6156:Tas2r129	UTSW	6	132,928,455 (GRCm39)	missense	probably benign	0.31
R7600:Tas2r129	UTSW	6	132,928,137 (GRCm39)	nonsense	probably null
R7608:Tas2r129	UTSW	6	132,928,156 (GRCm39)	missense	probably damaging	0.98
R8498:Tas2r129	UTSW	6	132,928,815 (GRCm39)	missense	probably benign	0.01
R8870:Tas2r129	UTSW	6	132,928,522 (GRCm39)	missense	probably damaging	0.98
R9276:Tas2r129	UTSW	6	132,928,576 (GRCm39)	missense	probably benign	0.12

Predicted Primers

PCR Primer
(F):5'- CTCAAATATTCTCCACACCACTTGG -3'
(R):5'- CTTCTAGTTACCAACACGTGTG -3'

Sequencing Primer
(F):5'- TCGCTCTCACAGAAAAAGAGATATG -3'
(R):5'- GTGTATAGCGTAGACACTGCTATAAC -3'

Posted On

2018-06-06