Mutagenetix > Incidental Mutation

Incidental Mutation 'R5766:Taar7a'

446282

Institutional Source

Beutler Lab

Gene Symbol

Taar7a

Ensembl Gene

ENSMUSG00000095647

Gene Name

trace amine-associated receptor 7A

Synonyms

Taar7a, LOC215856

MMRRC Submission

044424-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.096) question?

Stock #

R5766 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

23992405-23993481 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 23993362 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Arginine at position 40 (S40R)

Ref Sequence

ENSEMBL: ENSMUSP00000077616 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078532]

AlphaFold

Q5QD12

Predicted Effect

probably benign
Transcript: ENSMUST00000078532
AA Change: S40R

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)

SMART Domains

Protein: ENSMUSP00000077616
Gene: ENSMUSG00000095647
AA Change: S40R

Domain	Start	End	E-Value	Type
Pfam:7tm_4	54	344	9.2e-10	PFAM
Pfam:7TM_GPCR_Srx	56	261	5.2e-9	PFAM
Pfam:7tm_1	64	326	3.2e-58	PFAM

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.3%
20x: 95.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9530053A07Rik	G	A	7: 28,137,329	W224*	probably null	Het
Aadacl3	A	G	4: 144,455,869	V343A	probably damaging	Het
AI429214	TCCCTGATGAAC	TC	8: 36,994,229		probably null	Het
Arid2	A	G	15: 96,372,205	T1400A	probably benign	Het
Arrdc1	G	A	2: 24,926,405	T184I	probably damaging	Het
Aspm	T	C	1: 139,479,002	F1876L	probably damaging	Het
Calhm1	C	T	19: 47,143,703	V158I	probably benign	Het
Caly	T	C	7: 140,070,397	K211E	probably benign	Het
Cenpe	T	C	3: 135,248,413	L1677P	probably damaging	Het
Cttnbp2	A	G	6: 18,381,033	V1388A	possibly damaging	Het
Dgkd	C	T	1: 87,880,449	R80*	probably null	Het
Dnah3	A	T	7: 119,978,222	I2072N	probably damaging	Het
Dnah8	A	G	17: 30,690,261	I1020M	probably benign	Het
Drc3	T	C	11: 60,393,821	V484A	probably benign	Het
Efcab8	A	G	2: 153,780,992	D27G	possibly damaging	Het
Fat4	G	A	3: 38,889,468	G837R	probably damaging	Het
Fgb	A	T	3: 83,046,176	C96S	probably damaging	Het
Flt4	G	C	11: 49,626,686	W278C	possibly damaging	Het
Fmnl2	T	C	2: 53,101,454	V327A	probably damaging	Het
Fras1	A	T	5: 96,731,689	Y2455F	possibly damaging	Het
Gm10549	C	A	18: 33,464,305		probably benign	Het
Gm13872	T	A	2: 102,737,909	I88N	probably damaging	Het
Hoxa6	A	G	6: 52,208,414	S71P	probably benign	Het
Hunk	T	A	16: 90,453,739	C148S	probably damaging	Het
Ighv1-18	A	C	12: 114,682,907	S26A	probably damaging	Het
Impg2	T	G	16: 56,259,820	D553E	possibly damaging	Het
Ints1	A	G	5: 139,772,145	I266T	probably benign	Het
Kpna3	G	T	14: 61,403,014	T33K	probably benign	Het
Lamb1	A	G	12: 31,299,931	D622G	probably damaging	Het
Lamp3	T	C	16: 19,701,317	T39A	probably damaging	Het
Mnt	C	T	11: 74,843,078		probably benign	Het
Msh4	A	G	3: 153,867,840	S726P	probably damaging	Het
Olfr539	T	A	7: 140,667,353	V22E	probably benign	Het
Pah	A	C	10: 87,567,347	K195Q	probably damaging	Het
Pdc	T	A	1: 150,333,500	*245K	probably null	Het
Pdzd8	A	T	19: 59,300,540	H809Q	possibly damaging	Het
Plekhd1	A	T	12: 80,722,366	I467L	probably benign	Het
Ppp2ca	A	G	11: 52,113,187	D57G	probably damaging	Het
Ralgapa1	A	T	12: 55,820,766	M1K	probably null	Het
Rfx2	T	A	17: 56,803,587	D133V	probably benign	Het
Scfd2	A	T	5: 74,462,651	L407Q	probably damaging	Het
Scp2d1	T	A	2: 144,824,037	S99T	possibly damaging	Het
Sec63	A	T	10: 42,801,681	N261I	probably damaging	Het
Slc8a1	T	C	17: 81,648,961	Y216C	probably damaging	Het
Son	T	A	16: 91,664,987		probably benign	Het
Syce1	T	C	7: 140,777,981	E285G	probably damaging	Het
Ube3a	A	T	7: 59,276,059	D216V	possibly damaging	Het
Vgll2	A	G	10: 52,027,563	D174G	probably damaging	Het
Vmn2r17	A	T	5: 109,427,273	T149S	possibly damaging	Het
Zbtb39	G	T	10: 127,742,688	C377F	probably damaging	Het
Zfp820	T	A	17: 21,820,002	N115I	probably damaging	Het
Zfp948	T	C	17: 21,584,816	S23P	probably benign	Het

Other mutations in Taar7a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00476:Taar7a	APN	10	23992396	unclassified	probably benign
IGL02408:Taar7a	APN	10	23992602	missense	probably benign
PIT4434001:Taar7a	UTSW	10	23993421	missense	probably benign
R0422:Taar7a	UTSW	10	23993274	missense	probably benign	0.02
R1029:Taar7a	UTSW	10	23992541	missense	possibly damaging	0.65
R1742:Taar7a	UTSW	10	23993219	missense	probably damaging	0.98
R2104:Taar7a	UTSW	10	23993061	missense	probably damaging	0.99
R2421:Taar7a	UTSW	10	23992517	missense	probably damaging	1.00
R3907:Taar7a	UTSW	10	23992559	missense	probably benign	0.25
R4021:Taar7a	UTSW	10	23993386	missense	probably benign	0.00
R5180:Taar7a	UTSW	10	23993148	missense	probably damaging	1.00
R5486:Taar7a	UTSW	10	23992458	missense	probably benign	0.00
R5507:Taar7a	UTSW	10	23992631	missense	probably damaging	0.98
R5587:Taar7a	UTSW	10	23992828	missense	probably benign	0.00
R5861:Taar7a	UTSW	10	23992439	missense	probably benign
R7201:Taar7a	UTSW	10	23992460	missense	probably benign	0.04
R7506:Taar7a	UTSW	10	23992994	missense	possibly damaging	0.50
R8810:Taar7a	UTSW	10	23993381	missense	probably benign	0.20
R9015:Taar7a	UTSW	10	23992835	missense	probably damaging	0.97
R9172:Taar7a	UTSW	10	23992779	missense	probably benign	0.16
R9686:Taar7a	UTSW	10	23993411	missense	probably benign	0.01
R9717:Taar7a	UTSW	10	23992901	missense	probably benign	0.01
R9720:Taar7a	UTSW	10	23992835	missense	probably benign	0.10
X0064:Taar7a	UTSW	10	23992617	missense	probably damaging	1.00
Z1177:Taar7a	UTSW	10	23992892	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- GAAGGGCATCACAGTCAGAC -3'
(R):5'- TGACGACTTAAGCCTTAGAGAG -3'

Sequencing Primer
(F):5'- GGCATCACAGTCAGACCCACTAAG -3'
(R):5'- GAATAACTAGATTCCTAAGCATGGC -3'

Posted On

2016-11-21