Mutagenetix > Incidental Mutation

Incidental Mutation 'R6809:Taar7b'

533713

Institutional Source

Beutler Lab

Gene Symbol

Taar7b

Ensembl Gene

ENSMUSG00000095171

Gene Name

trace amine-associated receptor 7B

Synonyms

LOC209517

MMRRC Submission

044922-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.114) question?

Stock #

R6809 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

23875837-23876913 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 23876756 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 307 (V307A)

Ref Sequence

ENSEMBL: ENSMUSP00000090328 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000092658]

AlphaFold

Q5QD11

Predicted Effect

probably benign
Transcript: ENSMUST00000092658
AA Change: V307A

PolyPhen 2 Score 0.031 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000090328
Gene: ENSMUSG00000095171
AA Change: V307A

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srx	56	261	1.9e-7	PFAM
Pfam:7tm_1	64	326	7.3e-59	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 95.1%

Validation Efficiency

96% (51/53)

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A130010J15Rik	T	A	1: 192,857,089 (GRCm39)	V147E	possibly damaging	Het
Abtb3	A	G	10: 85,467,240 (GRCm39)	T732A	probably benign	Het
Adgrv1	A	T	13: 81,621,072 (GRCm39)	M3893K	probably benign	Het
Aox3	T	C	1: 58,157,840 (GRCm39)	S66P	probably damaging	Het
Apeh	G	A	9: 107,969,878 (GRCm39)	H186Y	probably damaging	Het
Bloc1s5	A	G	13: 38,787,961 (GRCm39)	V141A	probably benign	Het
Bltp1	A	G	3: 36,928,431 (GRCm39)	N61S	probably damaging	Het
Col28a1	T	C	6: 7,999,468 (GRCm39)	Y1083C	probably damaging	Het
Crb1	A	G	1: 139,170,864 (GRCm39)	V842A	probably benign	Het
Dapk1	A	G	13: 60,899,103 (GRCm39)	S858G	probably benign	Het
Dlgap2	G	T	8: 14,229,619 (GRCm39)		probably benign	Het
Dpysl4	A	G	7: 138,673,576 (GRCm39)	D199G	probably benign	Het
Eml6	C	T	11: 29,753,161 (GRCm39)	V917I	probably benign	Het
Fut9	T	A	4: 25,620,647 (GRCm39)	T56S	probably benign	Het
Gtdc1	G	C	2: 44,465,563 (GRCm39)	S214*	probably null	Het
Gtdc1	A	G	2: 44,715,396 (GRCm39)	F49S	probably damaging	Het
Hoxd9	A	G	2: 74,529,590 (GRCm39)	Y282C	probably damaging	Het
Hrc	A	G	7: 44,985,803 (GRCm39)	E318G	probably benign	Het
Ikzf2	T	C	1: 69,609,661 (GRCm39)	T195A	probably damaging	Het
Krt36	A	T	11: 99,996,335 (GRCm39)	S30T	probably benign	Het
Lrp1	A	G	10: 127,390,925 (GRCm39)	F2991L	probably benign	Het
Lrrc34	T	A	3: 30,688,749 (GRCm39)	Q184L	possibly damaging	Het
Mapk1	A	T	16: 16,853,326 (GRCm39)	M49L	probably benign	Het
Mroh2a	G	T	1: 88,162,938 (GRCm39)	Q360H	probably benign	Het
Mrpl48	A	G	7: 100,195,574 (GRCm39)		probably benign	Het
Ncln	A	G	10: 81,323,512 (GRCm39)		probably null	Het
Nol4	T	A	18: 23,053,882 (GRCm39)	Q96L	probably damaging	Het
Or2y1e	G	T	11: 49,218,687 (GRCm39)	V150L	probably benign	Het
Or5g25	G	A	2: 85,478,317 (GRCm39)	A116V	probably damaging	Het
Padi2	A	G	4: 140,674,077 (GRCm39)		probably null	Het
Pak5	T	G	2: 135,939,501 (GRCm39)	I545L	possibly damaging	Het
Paqr5	T	A	9: 61,876,064 (GRCm39)	R157W	probably null	Het
Pard3b	G	A	1: 62,200,340 (GRCm39)	R293H	probably damaging	Het
Phf11d	C	A	14: 59,593,844 (GRCm39)	C110F	probably damaging	Het
Pkn2	G	A	3: 142,504,765 (GRCm39)	P804S	probably damaging	Het
Pnpla6	G	A	8: 3,584,611 (GRCm39)	C743Y	possibly damaging	Het
Pramel14	A	G	4: 143,719,651 (GRCm39)	V238A	probably benign	Het
Pramel58	C	A	5: 94,831,277 (GRCm39)	Q95K	probably benign	Het
Psip1	A	G	4: 83,386,879 (GRCm39)	M164T	probably benign	Het
Rgs22	C	G	15: 36,048,910 (GRCm39)	S914T	probably damaging	Het
Rufy4	G	A	1: 74,172,206 (GRCm39)	V310I	probably benign	Het
Ryr2	G	A	13: 11,741,816 (GRCm39)	L2122F	probably damaging	Het
Sgcb	T	G	5: 73,798,036 (GRCm39)	N142T	probably benign	Het
Slc27a6	A	G	18: 58,738,126 (GRCm39)	E394G	probably benign	Het
Slc29a2	T	C	19: 5,079,271 (GRCm39)	V298A	probably damaging	Het
Slf2	C	A	19: 44,931,907 (GRCm39)	T654N	probably damaging	Het
Spata4	A	C	8: 55,055,368 (GRCm39)	K123Q	possibly damaging	Het
Tenm4	G	A	7: 96,202,703 (GRCm39)	R106H	probably benign	Het
Ttn	T	C	2: 76,693,983 (GRCm39)	E295G	possibly damaging	Het
Ubqln4	A	T	3: 88,462,679 (GRCm39)	Q48L	possibly damaging	Het
Ugt1a10	T	A	1: 87,983,647 (GRCm39)	D148E	probably damaging	Het
Vmn2r85	T	A	10: 130,261,795 (GRCm39)	N181Y	probably benign	Het
Wdfy3	C	T	5: 102,071,813 (GRCm39)	V1026I	possibly damaging	Het

Other mutations in Taar7b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00330:Taar7b	APN	10	23,876,740 (GRCm39)	missense	probably benign	0.01
IGL00771:Taar7b	APN	10	23,876,096 (GRCm39)	missense	probably benign	0.01
IGL01662:Taar7b	APN	10	23,875,874 (GRCm39)	missense	probably benign	0.02
IGL02186:Taar7b	APN	10	23,875,879 (GRCm39)	missense	probably benign	0.00
IGL02399:Taar7b	APN	10	23,876,050 (GRCm39)	missense	probably damaging	0.99
IGL02514:Taar7b	APN	10	23,876,882 (GRCm39)	missense	probably benign	0.00
IGL02601:Taar7b	APN	10	23,876,204 (GRCm39)	missense	probably damaging	1.00
IGL02717:Taar7b	APN	10	23,876,258 (GRCm39)	missense	probably damaging	1.00
IGL02724:Taar7b	APN	10	23,876,581 (GRCm39)	missense	probably benign
IGL02725:Taar7b	APN	10	23,875,961 (GRCm39)	missense	probably benign	0.03
R0103:Taar7b	UTSW	10	23,876,192 (GRCm39)	missense	probably benign	0.00
R2060:Taar7b	UTSW	10	23,876,573 (GRCm39)	missense	possibly damaging	0.95
R4973:Taar7b	UTSW	10	23,876,243 (GRCm39)	missense	probably benign	0.08
R5055:Taar7b	UTSW	10	23,876,845 (GRCm39)	missense	possibly damaging	0.75
R5068:Taar7b	UTSW	10	23,876,359 (GRCm39)	missense	probably benign	0.00
R5069:Taar7b	UTSW	10	23,876,359 (GRCm39)	missense	probably benign	0.00
R5070:Taar7b	UTSW	10	23,876,359 (GRCm39)	missense	probably benign	0.00
R5205:Taar7b	UTSW	10	23,875,916 (GRCm39)	missense	probably benign	0.05
R5994:Taar7b	UTSW	10	23,876,246 (GRCm39)	missense	probably damaging	1.00
R6131:Taar7b	UTSW	10	23,876,615 (GRCm39)	missense	probably benign	0.20
R6302:Taar7b	UTSW	10	23,876,158 (GRCm39)	missense	possibly damaging	0.57
R6332:Taar7b	UTSW	10	23,875,849 (GRCm39)	missense	probably benign	0.05
R7126:Taar7b	UTSW	10	23,875,960 (GRCm39)	missense	possibly damaging	0.93
R7520:Taar7b	UTSW	10	23,876,381 (GRCm39)	missense	probably damaging	0.99
R8962:Taar7b	UTSW	10	23,876,359 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- ATGAGCAAGCAGACTGCCAG -3'
(R):5'- TGTCTTTGGGTCACAAGCG -3'

Sequencing Primer
(F):5'- CAGGGCATCAGACAGCTAC -3'
(R):5'- GAACAGACCTGGGCACTCAGTC -3'

Posted On

2018-09-12