Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02526:Tas2r135'

297089

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Tas2r135

Ensembl Gene

ENSMUSG00000056203

Gene Name

taste receptor, type 2, member 135

Synonyms

mt2r38, Tas2r35

Accession Numbers

Essential gene?

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

Stock #

IGL02526

Quality Score

Status

Chromosome

Chromosomal Location

42382463-42383428 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 42383214 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 251 (H251L)

Ref Sequence

ENSEMBL: ENSMUSP00000070247 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000070178
AA Change: H251L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000070247
Gene: ENSMUSG00000056203
AA Change: H251L

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

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acad10	A	G	5: 121,784,923 (GRCm39)	V231A	probably damaging	Het
Aff4	T	C	11: 53,297,509 (GRCm39)		probably benign	Het
Ano2	G	A	6: 125,849,714 (GRCm39)		probably null	Het
Aspm	A	G	1: 139,417,457 (GRCm39)	E2818G	probably benign	Het
Atp2a3	C	A	11: 72,866,165 (GRCm39)	H262N	probably benign	Het
Caprin1	T	C	2: 103,605,948 (GRCm39)		probably benign	Het
Clca3a2	T	C	3: 144,793,779 (GRCm39)	H292R	probably benign	Het
Dnah11	G	A	12: 118,143,353 (GRCm39)	T430M	possibly damaging	Het
Fgd6	A	G	10: 93,936,373 (GRCm39)	N902S	probably benign	Het
Grm3	A	G	5: 9,639,847 (GRCm39)	I66T	probably damaging	Het
H13	T	A	2: 152,530,602 (GRCm39)	F158L	probably damaging	Het
Kcnb2	A	G	1: 15,780,979 (GRCm39)	E617G	probably damaging	Het
Kcnh7	T	C	2: 62,680,781 (GRCm39)	S269G	possibly damaging	Het
Krit1	T	A	5: 3,872,103 (GRCm39)	I376N	probably damaging	Het
Lonrf2	T	A	1: 38,839,791 (GRCm39)	M435L	probably benign	Het
Map2	A	T	1: 66,419,876 (GRCm39)	D69V	possibly damaging	Het
Mon1b	G	T	8: 114,365,455 (GRCm39)	R261L	possibly damaging	Het
Myh3	C	T	11: 66,978,371 (GRCm39)	P453S	probably benign	Het
Or51d1	T	A	7: 102,348,291 (GRCm39)	V282D	possibly damaging	Het
Pi4k2b	T	C	5: 52,925,081 (GRCm39)	F442L	probably damaging	Het
Pla2g12b	T	A	10: 59,252,275 (GRCm39)	C49S	probably damaging	Het
Polr2a	C	T	11: 69,630,293 (GRCm39)	R1258Q	probably benign	Het
Prmt8	A	C	6: 127,688,786 (GRCm39)	S195A	probably damaging	Het
Pwp1	T	A	10: 85,717,967 (GRCm39)		probably null	Het
Rxfp1	C	A	3: 79,578,153 (GRCm39)		probably null	Het
Skor1	A	T	9: 63,053,159 (GRCm39)	M270K	probably damaging	Het
Slc12a4	T	C	8: 106,676,438 (GRCm39)	N495D	possibly damaging	Het
Slc26a3	T	C	12: 31,507,095 (GRCm39)	V350A	probably damaging	Het
Slc44a4	T	A	17: 35,147,463 (GRCm39)	V430D	probably damaging	Het
Slit2	C	A	5: 48,461,565 (GRCm39)	C1537*	probably null	Het
Tbr1	T	C	2: 61,642,042 (GRCm39)	F436L	probably benign	Het
Them6	A	T	15: 74,593,504 (GRCm39)	T121S	possibly damaging	Het
Tmem145	G	A	7: 25,007,657 (GRCm39)	M221I	probably benign	Het
Trrap	T	C	5: 144,761,360 (GRCm39)	V2300A	probably benign	Het
Usf3	C	A	16: 44,040,674 (GRCm39)	A1718D	possibly damaging	Het
Usp10	C	A	8: 120,675,514 (GRCm39)	S511Y	probably damaging	Het
Wdr38	A	T	2: 38,888,424 (GRCm39)	N7I	probably damaging	Het
Wnt9a	T	C	11: 59,219,331 (GRCm39)	F119S	probably damaging	Het
Zc3h7b	G	A	15: 81,677,338 (GRCm39)	G880S	probably benign	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
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
R1412:Tas2r135	UTSW	6	42,382,768 (GRCm39)	missense	probably benign	0.00
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

Posted On

2015-04-16