Mutagenetix > Incidental Mutation

Incidental Mutation 'R0656:Gpr82'

62561

Institutional Source

Beutler Lab

Gene Symbol

Gpr82

Ensembl Gene

ENSMUSG00000047678

Gene Name

G protein-coupled receptor 82

Synonyms

MMRRC Submission

038841-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0656 (G1)

Quality Score

137

Status

Validated

Chromosome

Chromosomal Location

13527602-13533672 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 13531829 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 126 (S126P)

Ref Sequence

ENSEMBL: ENSMUSP00000062535 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000033321] [ENSMUST00000053659] [ENSMUST00000115436] [ENSMUST00000115438] [ENSMUST00000124710] [ENSMUST00000156096]

AlphaFold

Q8BZR0

Predicted Effect

probably benign
Transcript: ENSMUST00000033321

SMART Domains

Protein: ENSMUSP00000033321
Gene: ENSMUSG00000031012

Domain	Start	End	E-Value	Type
S_TKc	12	276	1.22e-100	SMART
L27	340	395	8.68e-14	SMART
L27	399	452	1.67e-15	SMART
PDZ	493	565	4.01e-14	SMART
SH3	597	663	1.75e-12	SMART
low complexity region	685	697	N/A	INTRINSIC
GuKc	720	896	7.41e-78	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000053659
AA Change: S126P

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000062535
Gene: ENSMUSG00000047678
AA Change: S126P

Domain	Start	End	E-Value	Type
Pfam:7tm_1	32	310	5.8e-23	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000115436

SMART Domains

Protein: ENSMUSP00000111096
Gene: ENSMUSG00000031012

Domain	Start	End	E-Value	Type
S_TKc	12	276	1.22e-100	SMART
L27	340	395	8.68e-14	SMART
L27	399	452	1.67e-15	SMART
PDZ	493	565	4.01e-14	SMART
SH3	586	652	1.75e-12	SMART
low complexity region	674	686	N/A	INTRINSIC
GuKc	709	885	7.41e-78	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000115438

SMART Domains

Protein: ENSMUSP00000111098
Gene: ENSMUSG00000031012

Domain	Start	End	E-Value	Type
S_TKc	12	276	1.22e-100	SMART
L27	340	395	8.68e-14	SMART
L27	399	452	1.67e-15	SMART
PDZ	493	565	4.01e-14	SMART
SH3	609	675	1.75e-12	SMART
low complexity region	697	709	N/A	INTRINSIC
GuKc	732	908	7.41e-78	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000124710

SMART Domains

Protein: ENSMUSP00000119584
Gene: ENSMUSG00000031012

Domain	Start	End	E-Value	Type
Pfam:Pkinase	12	155	9.7e-33	PFAM
Pfam:Pkinase_Tyr	12	155	6.4e-16	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000128012

SMART Domains

Protein: ENSMUSP00000114187
Gene: ENSMUSG00000031012

Domain	Start	End	E-Value	Type
Pfam:Pkinase	1	137	1.1e-32	PFAM
Pfam:Pkinase_Tyr	2	134	2.3e-10	PFAM
L27	207	249	1.81e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152358

Predicted Effect

probably benign
Transcript: ENSMUST00000156096

SMART Domains

Protein: ENSMUSP00000120299
Gene: ENSMUSG00000031012

Domain	Start	End	E-Value	Type
S_TKc	1	250	2.71e-84	SMART
L27	314	369	8.68e-14	SMART
L27	373	426	1.67e-15	SMART
PDZ	467	539	4.01e-14	SMART
SH3	560	626	1.75e-12	SMART
low complexity region	648	660	N/A	INTRINSIC
GuKc	683	859	7.41e-78	SMART

Meta Mutation Damage Score

0.0759

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.3%
20x: 94.2%

Validation Efficiency

98% (92/94)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is an orphan G protein-coupled receptor of unknown function. The encoded protein is a member of a family of proteins that contain seven transmembrane domains and transduce extracellular signals through heterotrimeric G proteins. [provided by RefSeq, Sep 2011]
PHENOTYPE: Mice homozygous for disruptions of this gene display a normal phenotype. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930533K18Rik	T	A	10: 70,704,630 (GRCm39)		noncoding transcript	Het
Alox5	A	G	6: 116,400,291 (GRCm39)		probably benign	Het
Anxa11	T	A	14: 25,874,421 (GRCm39)	D203E	probably damaging	Het
Atp12a	A	T	14: 56,611,938 (GRCm39)	N371Y	probably damaging	Het
Bloc1s6	A	G	2: 122,584,543 (GRCm39)	I39M	probably benign	Het
Celsr3	A	C	9: 108,711,854 (GRCm39)	I1688L	possibly damaging	Het
Cgn	T	C	3: 94,682,204 (GRCm39)		probably benign	Het
Chd4	A	T	6: 125,079,930 (GRCm39)	I453F	probably damaging	Het
Dbnl	A	G	11: 5,747,321 (GRCm39)	T247A	probably benign	Het
Dpysl3	T	C	18: 43,571,136 (GRCm39)	E46G	possibly damaging	Het
Dsg1a	T	C	18: 20,468,949 (GRCm39)		probably benign	Het
Fbp1	C	T	13: 63,019,099 (GRCm39)	E150K	probably benign	Het
Flnb	T	A	14: 7,927,352 (GRCm38)	L1854Q	probably damaging	Het
Gcn1	C	T	5: 115,727,362 (GRCm39)	T714M	probably benign	Het
Gm12216	A	T	11: 53,704,162 (GRCm39)		probably benign	Het
Hmbs	T	A	9: 44,248,657 (GRCm39)	H256L	probably benign	Het
Ibsp	A	T	5: 104,457,886 (GRCm39)		probably null	Het
Ints13	A	G	6: 146,453,959 (GRCm39)	V240A	probably benign	Het
Iqca1l	C	T	5: 24,754,760 (GRCm39)	V337M	possibly damaging	Het
Kalrn	T	C	16: 33,852,837 (GRCm39)	D343G	probably damaging	Het
Kin	T	C	2: 10,090,531 (GRCm39)		probably benign	Het
Klhdc1	T	C	12: 69,304,804 (GRCm39)	V192A	probably benign	Het
Lpar3	T	A	3: 145,946,426 (GRCm39)	C35S	possibly damaging	Het
Lrrtm4	A	G	6: 79,998,953 (GRCm39)	I122V	possibly damaging	Het
Mfsd13a	C	T	19: 46,354,943 (GRCm39)	T40I	probably benign	Het
Mgat4c	T	C	10: 102,224,452 (GRCm39)	M222T	probably damaging	Het
Muc4	C	A	16: 32,570,488 (GRCm39)	S516Y	possibly damaging	Het
Myo1e	A	T	9: 70,274,956 (GRCm39)	Q703L	probably damaging	Het
Neb	A	G	2: 52,115,570 (GRCm39)		probably benign	Het
Necab3	T	G	2: 154,388,223 (GRCm39)	E239A	probably null	Het
Npr1	G	T	3: 90,368,676 (GRCm39)	N461K	probably benign	Het
Or4k44	T	C	2: 111,367,972 (GRCm39)	I221V	probably damaging	Het
Pcdhb2	A	G	18: 37,428,543 (GRCm39)	Y172C	probably damaging	Het
Pcdhb7	A	G	18: 37,474,954 (GRCm39)	D30G	probably benign	Het
Phf12	A	C	11: 77,920,158 (GRCm39)	Q898P	probably benign	Het
Plekhn1	T	C	4: 156,309,821 (GRCm39)	E132G	possibly damaging	Het
Ptpn3	A	G	4: 57,270,075 (GRCm39)	V29A	probably benign	Het
Rundc3b	T	A	5: 8,619,529 (GRCm39)	I143F	probably damaging	Het
Ryr3	T	G	2: 112,478,651 (GRCm39)		probably benign	Het
Sash1	A	G	10: 8,626,901 (GRCm39)		probably null	Het
Slc4a2	A	G	5: 24,636,257 (GRCm39)	D201G	probably benign	Het
Tecpr1	T	A	5: 144,150,871 (GRCm39)		probably null	Het
Timm21	T	C	18: 84,967,326 (GRCm39)	H150R	probably damaging	Het
Tmem79	T	C	3: 88,240,241 (GRCm39)	T236A	probably damaging	Het
Usp34	G	T	11: 23,422,967 (GRCm39)	V3095F	probably damaging	Het
Vmn1r8	A	T	6: 57,013,573 (GRCm39)	Q208L	probably benign	Het

Other mutations in Gpr82

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0654:Gpr82	UTSW	X	13,531,829 (GRCm39)	missense	probably benign	0.02
R2102:Gpr82	UTSW	X	13,532,274 (GRCm39)	missense	probably benign	0.02
R3854:Gpr82	UTSW	X	13,531,577 (GRCm39)	missense	probably benign	0.21
R3856:Gpr82	UTSW	X	13,531,577 (GRCm39)	missense	probably benign	0.21
R4052:Gpr82	UTSW	X	13,531,898 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- ACCATCCGTGATTTCTACCACAGC -3'
(R):5'- GATTGTAGCACTGGCTCTGTCCTTC -3'

Sequencing Primer
(F):5'- GGCAAATCTTGTGACTGCAAAC -3'
(R):5'- CTTCTGTAGCCTCGACTACTG -3'

Posted On

2013-07-30