Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01618:Taar7f'

92457

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Taar7f

Ensembl Gene

ENSMUSG00000100950

Gene Name

trace amine-associated receptor 7F

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.085) question?

Stock #

IGL01618

Quality Score

Status

Chromosome

Chromosomal Location

23925408-23926484 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 23926239 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Serine at position 278 (A278S)

Ref Sequence

ENSEMBL: ENSMUSP00000071611 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000071691]

AlphaFold

Q5QD08

Predicted Effect

possibly damaging
Transcript: ENSMUST00000071691
AA Change: A278S

PolyPhen 2 Score 0.559 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000071611
Gene: ENSMUSG00000100950
AA Change: A278S

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srx	56	261	1.6e-7	PFAM
Pfam:7TM_GPCR_Srsx	58	341	2e-10	PFAM
Pfam:7tm_1	64	326	6.6e-58	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000119318

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 47 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acsl5	C	T	19: 55,261,265 (GRCm39)	A74V	probably benign	Het
Adh4	C	T	3: 138,134,788 (GRCm39)		probably benign	Het
Aldh1a3	G	A	7: 66,058,978 (GRCm39)	T239I	probably damaging	Het
Anxa9	A	G	3: 95,207,847 (GRCm39)		probably null	Het
Atp5me	C	A	5: 108,581,899 (GRCm39)	K28N	probably damaging	Het
C9	T	G	15: 6,489,149 (GRCm39)	Y169D	probably benign	Het
Chat	T	A	14: 32,168,849 (GRCm39)		probably null	Het
Csmd3	C	T	15: 47,874,479 (GRCm39)	E706K	probably benign	Het
Ctbs	A	G	3: 146,160,867 (GRCm39)	K145E	probably benign	Het
Dennd5a	A	G	7: 109,533,302 (GRCm39)	M156T	probably damaging	Het
Dhx29	A	G	13: 113,101,756 (GRCm39)	Y1275C	probably damaging	Het
Dpp10	A	T	1: 123,295,596 (GRCm39)	F517Y	probably benign	Het
Dst	G	A	1: 34,227,990 (GRCm39)	W1536*	probably null	Het
Galc	T	C	12: 98,218,340 (GRCm39)	T171A	possibly damaging	Het
Gsap	T	C	5: 21,431,246 (GRCm39)	I190T	probably damaging	Het
Hars2	A	T	18: 36,922,630 (GRCm39)	R388*	probably null	Het
Igsf21	C	T	4: 139,834,675 (GRCm39)	G66S	possibly damaging	Het
Itgbl1	T	A	14: 124,065,211 (GRCm39)	S122T	possibly damaging	Het
Jhy	G	T	9: 40,872,260 (GRCm39)	T83K	possibly damaging	Het
Kcne4	A	T	1: 78,795,525 (GRCm39)	M58L	possibly damaging	Het
Lamc3	T	A	2: 31,802,119 (GRCm39)	I509N	probably damaging	Het
Lpar6	T	C	14: 73,476,506 (GRCm39)	S156P	probably damaging	Het
Man2c1	T	C	9: 57,048,840 (GRCm39)		probably benign	Het
Marchf11	T	C	15: 26,409,285 (GRCm39)	I328T	possibly damaging	Het
Mc3r	T	A	2: 172,091,290 (GRCm39)	C171S	probably benign	Het
Muc4	A	T	16: 32,577,001 (GRCm39)	Q2167L	unknown	Het
Myom1	T	C	17: 71,406,988 (GRCm39)	V1135A	possibly damaging	Het
Nectin1	C	T	9: 43,702,555 (GRCm39)	R101*	probably null	Het
Nxpe4	T	C	9: 48,305,440 (GRCm39)	S277P	possibly damaging	Het
Or1e35	T	C	11: 73,798,303 (GRCm39)	N5S	probably damaging	Het
Or2a52	T	A	6: 43,144,637 (GRCm39)	V215E	probably damaging	Het
Or52r1c	G	A	7: 102,735,582 (GRCm39)	V281I	probably benign	Het
Or5b106	T	A	19: 13,123,614 (GRCm39)	K136N	probably benign	Het
Or5w19	A	C	2: 87,698,488 (GRCm39)	D51A	probably damaging	Het
Pappa2	G	T	1: 158,684,948 (GRCm39)	N730K	probably damaging	Het
Prepl	A	G	17: 85,373,709 (GRCm39)	V586A	probably damaging	Het
Prrc2a	T	C	17: 35,368,529 (GRCm39)	Y2098C	probably damaging	Het
Rdh16	G	A	10: 127,637,176 (GRCm39)	C37Y	probably damaging	Het
Rnd1	A	T	15: 98,571,746 (GRCm39)	M100K	probably benign	Het
Sema3c	A	G	5: 17,877,504 (GRCm39)	N204D	probably damaging	Het
Susd4	A	G	1: 182,686,026 (GRCm39)		probably null	Het
Tle4	T	A	19: 14,522,178 (GRCm39)	M122L	probably benign	Het
Trim9	C	T	12: 70,295,125 (GRCm39)	V662I	probably benign	Het
Vmn2r10	C	A	5: 109,150,345 (GRCm39)	C233F	probably damaging	Het
Vmn2r98	A	C	17: 19,285,521 (GRCm39)	T114P	possibly damaging	Het
Zfyve21	C	T	12: 111,794,247 (GRCm39)		probably benign	Het
Zng1	T	C	19: 24,918,140 (GRCm39)	E210G	possibly damaging	Het

Other mutations in Taar7f

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00936:Taar7f	APN	10	23,926,066 (GRCm39)	missense	probably benign
IGL02567:Taar7f	APN	10	23,926,323 (GRCm39)	missense	probably damaging	0.97
R0096:Taar7f	UTSW	10	23,926,152 (GRCm39)	missense	probably benign	0.00
R0139:Taar7f	UTSW	10	23,926,312 (GRCm39)	missense	probably benign	0.04
R0363:Taar7f	UTSW	10	23,925,839 (GRCm39)	missense	probably damaging	1.00
R1776:Taar7f	UTSW	10	23,925,546 (GRCm39)	missense	probably benign	0.14
R1952:Taar7f	UTSW	10	23,925,747 (GRCm39)	missense	probably damaging	1.00
R2049:Taar7f	UTSW	10	23,926,323 (GRCm39)	missense	possibly damaging	0.65
R2280:Taar7f	UTSW	10	23,925,417 (GRCm39)	missense	probably benign
R3120:Taar7f	UTSW	10	23,925,478 (GRCm39)	missense	probably benign
R4210:Taar7f	UTSW	10	23,925,921 (GRCm39)	missense	probably damaging	1.00
R4211:Taar7f	UTSW	10	23,925,921 (GRCm39)	missense	probably damaging	1.00
R4587:Taar7f	UTSW	10	23,926,473 (GRCm39)	missense	probably damaging	0.97
R5092:Taar7f	UTSW	10	23,925,451 (GRCm39)	missense	probably benign
R5512:Taar7f	UTSW	10	23,926,321 (GRCm39)	missense	possibly damaging	0.89
R7439:Taar7f	UTSW	10	23,925,885 (GRCm39)	missense	possibly damaging	0.88
R7441:Taar7f	UTSW	10	23,925,885 (GRCm39)	missense	possibly damaging	0.88
R7839:Taar7f	UTSW	10	23,925,967 (GRCm39)	missense	possibly damaging	0.90
R8326:Taar7f	UTSW	10	23,925,811 (GRCm39)	missense	possibly damaging	0.81
R9443:Taar7f	UTSW	10	23,926,311 (GRCm39)	missense	probably benign	0.00
R9687:Taar7f	UTSW	10	23,925,727 (GRCm39)	missense	probably benign	0.19
RF021:Taar7f	UTSW	10	23,926,321 (GRCm39)	missense	possibly damaging	0.89

Posted On

2013-12-09