Mutagenetix > Incidental Mutation

Incidental Mutation 'R6541:Taar7d'

520772

Institutional Source

Beutler Lab

Gene Symbol

Taar7d

Ensembl Gene

ENSMUSG00000095569

Gene Name

trace amine-associated receptor 7D

Synonyms

MMRRC Submission

044667-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.178) question?

Stock #

R6541 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

23903120-23904196 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 23904129 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 337 (I337T)

Ref Sequence

ENSEMBL: ENSMUSP00000090327 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000092657]

AlphaFold

Q5QD10

Predicted Effect

probably benign
Transcript: ENSMUST00000092657
AA Change: I337T

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)

SMART Domains

Protein: ENSMUSP00000090327
Gene: ENSMUSG00000095569
AA Change: I337T

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srx	56	261	6.5e-9	PFAM
Pfam:7TM_GPCR_Srsx	58	341	2e-10	PFAM
Pfam:7tm_1	64	326	1.5e-57	PFAM

Meta Mutation Damage Score

0.0703

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 97.8%

Validation Efficiency

97% (36/37)

Allele List at MGI

Other mutations in this stock

Total: 36 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ass1	T	C	2: 31,400,245 (GRCm39)	V321A	probably damaging	Het
BC028528	T	A	3: 95,795,530 (GRCm39)	M91L	probably benign	Het
Bicra	T	C	7: 15,713,054 (GRCm39)	T998A	probably benign	Het
Cdkl3	T	G	11: 51,913,571 (GRCm39)	L220R	probably damaging	Het
Cluh	A	G	11: 74,548,040 (GRCm39)	D117G	probably damaging	Het
Cplane1	T	C	15: 8,248,779 (GRCm39)	V1776A	possibly damaging	Het
Crygf	T	C	1: 65,967,224 (GRCm39)	F116S	probably damaging	Het
Ergic2	T	A	6: 148,084,648 (GRCm39)	Y20F	probably damaging	Het
Esf1	A	G	2: 140,009,799 (GRCm39)	V179A	probably benign	Het
Gm28360	T	C	1: 117,758,047 (GRCm39)		probably benign	Het
Hhatl	C	T	9: 121,614,210 (GRCm39)	V385I	probably damaging	Het
Iba57	A	T	11: 59,049,689 (GRCm39)	D219E	possibly damaging	Het
Il36b	T	A	2: 24,049,827 (GRCm39)	V146D	probably damaging	Het
Itgal	T	A	7: 126,910,734 (GRCm39)	V176E	probably damaging	Het
Kdm3a	T	C	6: 71,571,517 (GRCm39)	M1060V	possibly damaging	Het
Kif18b	T	C	11: 102,805,092 (GRCm39)	K351R	probably damaging	Het
Mroh9	A	G	1: 162,885,607 (GRCm39)	F342L	possibly damaging	Het
Ndufa11	T	A	17: 57,024,867 (GRCm39)	S10T	probably benign	Het
Or2bd2	A	T	7: 6,443,492 (GRCm39)	N198Y	probably benign	Het
Or5w19	T	C	2: 87,698,638 (GRCm39)	F101S	probably benign	Het
Or6b6	A	T	7: 106,571,410 (GRCm39)	F47Y	probably benign	Het
Or7h8	T	A	9: 20,123,695 (GRCm39)	F17I	probably benign	Het
Pacsin3	A	G	2: 91,093,129 (GRCm39)	E207G	probably damaging	Het
Pcsk1	T	A	13: 75,274,103 (GRCm39)	L136Q	probably damaging	Het
Prr18	G	T	17: 8,560,168 (GRCm39)	R108L	possibly damaging	Het
Rdh5	A	G	10: 128,753,977 (GRCm39)	V44A	possibly damaging	Het
Rnd2	C	T	11: 101,359,825 (GRCm39)	L57F	probably damaging	Het
Sh2d4b	T	C	14: 40,542,748 (GRCm39)	T343A	probably benign	Het
Slc16a10	T	C	10: 39,913,268 (GRCm39)	N480S	probably benign	Het
Spaca7b	T	A	8: 11,712,613 (GRCm39)	Q79L	probably benign	Het
Sval3	A	T	6: 41,949,380 (GRCm39)	N73Y	probably damaging	Het
Ttn	T	A	2: 76,577,039 (GRCm39)	Q24618L	possibly damaging	Het
Ugt1a9	T	A	1: 87,999,318 (GRCm39)	V256E	probably damaging	Het
Vmn2r108	T	A	17: 20,701,480 (GRCm39)	I7F	probably benign	Het
Vmn2r55	A	G	7: 12,404,939 (GRCm39)	S155P	probably damaging	Het
Vwa3b	T	A	1: 37,090,842 (GRCm39)	V169E	probably damaging	Het

Other mutations in Taar7d

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01719:Taar7d	APN	10	23,903,865 (GRCm39)	missense	probably benign	0.00
IGL02070:Taar7d	APN	10	23,904,152 (GRCm39)	missense	probably benign	0.00
IGL02280:Taar7d	APN	10	23,904,006 (GRCm39)	missense	probably damaging	1.00
IGL02525:Taar7d	APN	10	23,903,994 (GRCm39)	missense	possibly damaging	0.80
IGL03115:Taar7d	APN	10	23,903,539 (GRCm39)	missense	probably benign	0.10
IGL03339:Taar7d	APN	10	23,903,204 (GRCm39)	missense	possibly damaging	0.92
R1509:Taar7d	UTSW	10	23,904,102 (GRCm39)	missense	probably damaging	0.99
R1826:Taar7d	UTSW	10	23,903,474 (GRCm39)	missense	probably damaging	0.99
R2016:Taar7d	UTSW	10	23,903,642 (GRCm39)	missense	probably benign	0.11
R2051:Taar7d	UTSW	10	23,903,904 (GRCm39)	missense	probably benign	0.00
R6075:Taar7d	UTSW	10	23,903,558 (GRCm39)	missense	probably benign	0.21
R8165:Taar7d	UTSW	10	23,903,495 (GRCm39)	missense	probably benign	0.07
R9222:Taar7d	UTSW	10	23,904,124 (GRCm39)	missense	probably benign	0.08
R9456:Taar7d	UTSW	10	23,903,287 (GRCm39)	missense	probably benign
R9481:Taar7d	UTSW	10	23,903,739 (GRCm39)	missense	probably benign	0.00
X0067:Taar7d	UTSW	10	23,903,906 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGCCAGAGCATCAGAAAGCTAC -3'
(R):5'- ATGTGTTCAGGTCCCAGCTG -3'

Sequencing Primer
(F):5'- AAACCCTGGGCATCGCAG -3'
(R):5'- GGTCCCAGCTGAAGCATAATTC -3'

Posted On

2018-06-06