Mutagenetix > Incidental Mutation

Incidental Mutation 'R1412:Tas2r135'

159630

Institutional Source

Beutler Lab

Gene Symbol

Tas2r135

Ensembl Gene

ENSMUSG00000056203

Gene Name

taste receptor, type 2, member 135

Synonyms

mt2r38, Tas2r35

MMRRC Submission

039468-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.051) question?

Stock #

R1412 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

42382463-42383428 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 42382768 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Methionine at position 102 (I102M)

Ref Sequence

ENSEMBL: ENSMUSP00000070247 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057398] [ENSMUST00000070178]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000057398

SMART Domains

Protein: ENSMUSP00000057910
Gene: ENSMUSG00000046652

Domain	Start	End	E-Value	Type
Pfam:TAS2R	1	293	6.7e-68	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000070178
AA Change: I102M

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000070247
Gene: ENSMUSG00000056203
AA Change: I102M

Domain	Start	End	E-Value	Type
Pfam:TAS2R	22	320	1.3e-63	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 98.8%
3x: 97.8%
10x: 94.4%
20x: 86.5%

Validation Efficiency

98% (48/49)

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810009A15Rik	T	C	19: 8,867,359 (GRCm39)		probably benign	Het
Abca15	C	T	7: 119,944,546 (GRCm39)	R394C	possibly damaging	Het
Adamts9	T	C	6: 92,773,414 (GRCm39)	Q1152R	probably benign	Het
Adgrv1	C	T	13: 81,243,569 (GRCm39)	G6277E	probably damaging	Het
Agbl2	A	G	2: 90,619,298 (GRCm39)	N41S	probably benign	Het
Akap7	A	T	10: 25,165,495 (GRCm39)		probably null	Het
Arl6ip1	A	G	7: 117,719,591 (GRCm39)	I179T	possibly damaging	Het
Atp1a4	C	T	1: 172,059,576 (GRCm39)	D839N	probably damaging	Het
B3galt4	G	A	17: 34,169,813 (GRCm39)	R142C	probably damaging	Het
C1qtnf12	T	C	4: 156,047,190 (GRCm39)	V52A	probably benign	Het
C1qtnf2	A	G	11: 43,381,959 (GRCm39)	Y257C	probably damaging	Het
Cdc123	A	T	2: 5,808,776 (GRCm39)	D233E	possibly damaging	Het
Chdh	G	A	14: 29,756,680 (GRCm39)	E369K	probably benign	Het
D630045J12Rik	A	G	6: 38,172,695 (GRCm39)	V491A	probably benign	Het
Focad	T	C	4: 88,196,498 (GRCm39)		probably null	Het
Gabbr1	T	C	17: 37,365,805 (GRCm39)		probably null	Het
Hat1	G	T	2: 71,250,961 (GRCm39)	E170*	probably null	Het
Hs3st5	A	T	10: 36,708,672 (GRCm39)	H69L	probably benign	Het
Igsf10	T	C	3: 59,235,196 (GRCm39)		probably benign	Het
Itga2b	A	T	11: 102,347,831 (GRCm39)	L890Q	probably benign	Het
Or52e8b	A	G	7: 104,673,402 (GRCm39)	F262L	probably damaging	Het
Or7d11	C	G	9: 19,966,711 (GRCm39)	G16A	possibly damaging	Het
Parp10	A	G	15: 76,127,284 (GRCm39)	L51P	probably damaging	Het
Pbld2	A	G	10: 62,883,301 (GRCm39)	T108A	probably damaging	Het
Pdlim2	A	T	14: 70,411,773 (GRCm39)		probably benign	Het
Pikfyve	T	C	1: 65,241,989 (GRCm39)	V243A	possibly damaging	Het
Pla2g12b	G	A	10: 59,239,804 (GRCm39)		probably null	Het
Raly	A	G	2: 154,699,315 (GRCm39)	T40A	possibly damaging	Het
Rasgrp3	G	T	17: 75,816,822 (GRCm39)		probably null	Het
Rbpms2	ACTGCTGCTGCTGCTGC	ACTGCTGCTGCTGCTGCTGC	9: 65,558,948 (GRCm39)		probably benign	Het
Smim22	G	C	16: 4,825,649 (GRCm39)	E11D	possibly damaging	Het
Socs2	T	C	10: 95,250,780 (GRCm39)	S18G	probably benign	Het
Srgap2	T	C	1: 131,228,151 (GRCm39)	E720G	possibly damaging	Het
Tex19.2	A	G	11: 121,007,761 (GRCm39)	V229A	possibly damaging	Het
Vmn1r234	T	A	17: 21,449,512 (GRCm39)	I142N	probably benign	Het
Vps35l	A	T	7: 118,409,194 (GRCm39)	I612F	probably damaging	Het
Vwa3a	C	T	7: 120,379,377 (GRCm39)	T494I	probably damaging	Het
Vwa8	C	T	14: 79,145,670 (GRCm39)	R116C	probably damaging	Het
Zfhx3	A	G	8: 109,641,199 (GRCm39)	D1166G	possibly damaging	Het

Other mutations in Tas2r135

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01357:Tas2r135	APN	6	42,383,078 (GRCm39)	missense	probably benign	0.00
IGL01395:Tas2r135	APN	6	42,382,846 (GRCm39)	nonsense	probably null
IGL02479:Tas2r135	APN	6	42,382,685 (GRCm39)	nonsense	probably null
IGL02526:Tas2r135	APN	6	42,383,214 (GRCm39)	missense	probably damaging	1.00
IGL02806:Tas2r135	APN	6	42,383,382 (GRCm39)	missense	probably benign	0.00
IGL02982:Tas2r135	APN	6	42,383,187 (GRCm39)	missense	probably benign
IGL03057:Tas2r135	APN	6	42,378,061 (GRCm39)	unclassified	probably benign
R0057:Tas2r135	UTSW	6	42,383,354 (GRCm39)	missense	probably benign	0.07
R0104:Tas2r135	UTSW	6	42,383,258 (GRCm39)	missense	possibly damaging	0.79
R4517:Tas2r135	UTSW	6	42,383,013 (GRCm39)	missense	probably benign
R4629:Tas2r135	UTSW	6	42,383,160 (GRCm39)	missense	probably benign	0.03
R5788:Tas2r135	UTSW	6	42,382,531 (GRCm39)	missense	probably damaging	1.00
R6021:Tas2r135	UTSW	6	42,383,321 (GRCm39)	missense	probably damaging	1.00
R6586:Tas2r135	UTSW	6	42,382,952 (GRCm39)	missense	probably benign	0.18
R7180:Tas2r135	UTSW	6	42,382,685 (GRCm39)	nonsense	probably null
R7458:Tas2r135	UTSW	6	42,382,881 (GRCm39)	missense	possibly damaging	0.95
R7850:Tas2r135	UTSW	6	42,383,072 (GRCm39)	missense	probably benign
R9113:Tas2r135	UTSW	6	42,383,315 (GRCm39)	missense	probably benign	0.00
Z1176:Tas2r135	UTSW	6	42,383,168 (GRCm39)	missense	probably benign	0.03

Predicted Primers

PCR Primer
(F):5'- TCATGTCCACAGGAGAAATGAGCAC -3'
(R):5'- CCAGTGACATTCCAAGGTTGATGGC -3'

Sequencing Primer
(F):5'- ACAGGCCATACAGTTCTTGG -3'
(R):5'- GGATACTAGTTAAGCTCGACATCCC -3'

Posted On

2014-03-14