Mutagenetix > Incidental Mutation

Incidental Mutation 'R0731:Gpr83'

67563

Institutional Source

Beutler Lab

Gene Symbol

Gpr83

Ensembl Gene

ENSMUSG00000031932

Gene Name

G protein-coupled receptor 83

Synonyms

RP82, GIR, Gir, glucocorticoid-induced receptor, RP39, Gpr72, RP105

MMRRC Submission

038912-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.080) question?

Stock #

R0731 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

14860210-14870789 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 14868644 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 331 (R331G)

Ref Sequence

ENSEMBL: ENSMUSP00000111287 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000034408] [ENSMUST00000115624]

AlphaFold

P30731

Predicted Effect

probably benign
Transcript: ENSMUST00000034408
AA Change: R373G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000034408
Gene: ENSMUSG00000031932
AA Change: R373G

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
Pfam:7tm_4	78	271	2.4e-8	PFAM
Pfam:7TM_GPCR_Srsx	82	360	6.6e-16	PFAM
Pfam:7tm_1	88	345	9e-52	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000115624
AA Change: R331G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000111287
Gene: ENSMUSG00000031932
AA Change: R331G

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
Pfam:7tm_1	88	133	1.1e-10	PFAM
Pfam:7TM_GPCR_Srsx	128	318	1.8e-6	PFAM
Pfam:7tm_1	129	303	1.4e-28	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133278

Meta Mutation Damage Score

0.0766

Coding Region Coverage

1x: 99.4%
3x: 98.9%
10x: 97.6%
20x: 95.5%

Validation Efficiency

97% (73/75)

MGI Phenotype

PHENOTYPE: Mice homozygous for a null allele exhibit normal regulatory T cell development. Mice homozygous for a different targeted allele exhibit attenuated stress-evoked anxiety, increased sucrose preference and delayed spatial learning. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930430F08Rik	T	C	10: 100,586,203	T66A	probably damaging	Het
4933406M09Rik	A	C	1: 134,389,975	M162L	probably benign	Het
Acsm3	A	T	7: 119,768,024	R27*	probably null	Het
Actg1	A	G	11: 120,346,949	F255S	probably damaging	Het
Ahdc1	T	A	4: 133,062,951	V501E	possibly damaging	Het
Alpk2	A	T	18: 65,305,390	D1444E	probably damaging	Het
Btaf1	T	G	19: 36,997,495		probably null	Het
Cacnb2	A	G	2: 14,985,706	H489R	possibly damaging	Het
Ccdc162	C	A	10: 41,579,143	K398N	probably damaging	Het
Cd79b	G	T	11: 106,312,433	S145R	probably damaging	Het
Cdh11	T	A	8: 102,668,019	N264Y	probably damaging	Het
Celsr1	T	C	15: 85,901,597	D2892G	probably benign	Het
Chuk	A	G	19: 44,103,766		probably benign	Het
Clk3	T	C	9: 57,751,126		probably benign	Het
Dcaf8	A	T	1: 172,172,509	D78V	possibly damaging	Het
Dctn1	A	G	6: 83,183,089	T87A	probably damaging	Het
Ddx50	T	C	10: 62,616,249	N732D	unknown	Het
Dnah5	A	T	15: 28,311,143	Y1756F	possibly damaging	Het
Dock3	A	T	9: 106,969,856	V858E	probably damaging	Het
Fer1l4	A	G	2: 156,024,070	F1566S	probably benign	Het
Fpr-rs7	T	C	17: 20,113,854	I125V	probably benign	Het
Fuca2	C	T	10: 13,506,027	P228L	probably benign	Het
Galntl6	A	G	8: 58,535,984	F57L	probably benign	Het
Gigyf2	T	A	1: 87,407,727		probably benign	Het
Gm16505	A	T	13: 3,361,329		noncoding transcript	Het
Gm4781	T	C	10: 100,396,777		noncoding transcript	Het
Gm9956	T	A	10: 56,745,543	Y100*	probably null	Het
Gpr137c	T	A	14: 45,246,349	C178S	probably damaging	Het
Hlcs	T	A	16: 94,131,852	H851L	probably damaging	Het
Kbtbd6	C	A	14: 79,451,884	Y6*	probably null	Het
Kif23	T	C	9: 61,925,032	R610G	possibly damaging	Het
Kifc3	G	A	8: 95,105,733	T487I	probably damaging	Het
Klra5	A	C	6: 129,908,796	D133E	possibly damaging	Het
Klra6	T	C	6: 130,022,705	E100G	probably damaging	Het
Klre1	T	A	6: 129,585,568		probably benign	Het
Lancl1	C	T	1: 67,009,910		probably null	Het
Lgr6	C	T	1: 134,994,010	A199T	probably damaging	Het
Man1b1	A	G	2: 25,338,155	I146V	possibly damaging	Het
Map4k5	T	A	12: 69,874,264		probably benign	Het
Mast3	A	G	8: 70,781,321	S178P	probably damaging	Het
Mau2	A	G	8: 70,023,612		probably null	Het
Mkrn2	A	T	6: 115,614,651	N312Y	probably damaging	Het
Mrvi1	T	C	7: 110,876,900	S615G	probably benign	Het
Myh1	A	G	11: 67,202,533	E150G	probably damaging	Het
Myo7b	T	A	18: 31,961,825		probably null	Het
Nyap1	A	G	5: 137,735,298	V491A	probably damaging	Het
Olfr1284	A	G	2: 111,379,293	M98V	probably damaging	Het
Olfr484	T	C	7: 108,124,734	I176M	probably benign	Het
Olfr518	A	T	7: 108,881,533	N24K	probably damaging	Het
Olfr954	T	C	9: 39,461,532	F34L	probably damaging	Het
Oxsm	A	T	14: 16,240,893	H385Q	probably damaging	Het
Pbld2	T	C	10: 63,056,811	S242P	probably damaging	Het
Pdzd7	T	C	19: 45,029,305	Y675C	probably damaging	Het
Pnkd	T	A	1: 74,351,541	H266Q	probably damaging	Het
Rbfox2	A	G	15: 77,099,279	S141P	probably benign	Het
Rdx	A	G	9: 52,068,218	T214A	probably benign	Het
Ripor2	A	T	13: 24,680,644	E219V	probably damaging	Het
Rufy2	G	A	10: 63,011,844		probably benign	Het
Slf2	T	A	19: 44,975,726		probably benign	Het
Snrnp200	G	T	2: 127,226,145		probably benign	Het
Snx7	T	A	3: 117,829,671		probably benign	Het
Stt3a	T	C	9: 36,735,512	I602V	probably damaging	Het
Tacr3	G	A	3: 134,855,000		probably null	Het
Tcerg1	C	T	18: 42,571,840	T978M	probably damaging	Het
Tcf7l1	G	T	6: 72,788,269	P126Q	possibly damaging	Het
Trank1	A	G	9: 111,365,488	D860G	probably damaging	Het
Try4	T	C	6: 41,304,367	L81P	probably benign	Het
Ucp1	T	C	8: 83,297,847		probably benign	Het
Ugt2b38	G	A	5: 87,420,452	A328V	probably damaging	Het
Wfikkn1	T	A	17: 25,878,017	R444S	probably damaging	Het
Zfc3h1	A	G	10: 115,410,632	T875A	probably benign	Het
Zfp11	A	G	5: 129,657,264	S378P	probably damaging	Het
Zfp984	T	A	4: 147,756,232	N54I	probably damaging	Het

Other mutations in Gpr83

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00579:Gpr83	APN	9	14860601	missense	probably benign	0.00
bland	UTSW	9	14866983	critical splice donor site	probably null
R0243:Gpr83	UTSW	9	14864842	missense	possibly damaging	0.96
R0349:Gpr83	UTSW	9	14868267	missense	probably damaging	1.00
R1519:Gpr83	UTSW	9	14868197	missense	probably null	1.00
R1678:Gpr83	UTSW	9	14866849	missense	probably damaging	1.00
R1826:Gpr83	UTSW	9	14868333	missense	possibly damaging	0.53
R1827:Gpr83	UTSW	9	14868333	missense	possibly damaging	0.53
R1828:Gpr83	UTSW	9	14868333	missense	possibly damaging	0.53
R2938:Gpr83	UTSW	9	14864871	missense	probably benign	0.23
R3760:Gpr83	UTSW	9	14860738	missense	probably benign	0.03
R4038:Gpr83	UTSW	9	14860777	missense	possibly damaging	0.77
R4438:Gpr83	UTSW	9	14864838	missense	probably damaging	0.99
R4657:Gpr83	UTSW	9	14866983	critical splice donor site	probably null
R4731:Gpr83	UTSW	9	14866174	intron	probably benign
R5150:Gpr83	UTSW	9	14860805	missense	probably damaging	1.00
R7770:Gpr83	UTSW	9	14866874	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACCGTGAAGATGCTGGTGCTTG -3'
(R):5'- TGCAAATCAGATGGGGCTGGAC -3'

Sequencing Primer
(F):5'- GGTTCCCTCTCAACTGCTATG -3'
(R):5'- TTGTGAGAGGAAAGAACCCTCC -3'

Posted On

2013-09-03