Mutagenetix > Incidental Mutation

Incidental Mutation 'R4088:Gpr26'

371058

Institutional Source

Beutler Lab

Gene Symbol

Gpr26

Ensembl Gene

ENSMUSG00000040125

Gene Name

G protein-coupled receptor 26

Synonyms

9630036A11Rik

MMRRC Submission

040981-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.062) question?

Stock #

R4088 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

131567891-131587362 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 131568805 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Phenylalanine at position 50 (C50F)

Ref Sequence

ENSEMBL: ENSMUSP00000041664 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000045840] [ENSMUST00000124096]

AlphaFold

Q8BZA7

Predicted Effect

probably benign
Transcript: ENSMUST00000045840
AA Change: C50F

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

SMART Domains

Protein: ENSMUSP00000041664
Gene: ENSMUSG00000040125
AA Change: C50F

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srsx	15	309	1.9e-7	PFAM
Pfam:7tm_1	22	294	1.4e-33	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000124096

SMART Domains

Protein: ENSMUSP00000130971
Gene: ENSMUSG00000030849

Domain	Start	End	E-Value	Type
Pfam:Pkinase	1	118	4.8e-19	PFAM
Pfam:Pkinase_Tyr	1	118	1.7e-50	PFAM
low complexity region	146	160	N/A	INTRINSIC

Meta Mutation Damage Score

0.0615

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.5%

Validation Efficiency

96% (55/57)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a G protein-couple receptor protein. G-protein-coupled receptors are a large family of membrane proteins that are involved in cellular responses to environmental stimuli, neurotransmitters, and hormones. The encoded protein may play a role in neurodegenerative diseases. Epigenetic silencing of this gene has been observed in gliomas. [provided by RefSeq, Sep 2016]
PHENOTYPE: Mice homozygous for one null allele exhibit increased anxiety- and depression-related behaviors and alcohol preference. Female mice homozygous for another allele display increased susceptibility to diet-induced obesity with increased food intake. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A430110L20Rik	T	C	1: 181,055,274 (GRCm39)		noncoding transcript	Het
Alox12b	G	T	11: 69,049,211 (GRCm39)	V87L	probably benign	Het
Arsk	T	G	13: 76,246,533 (GRCm39)	N32T	probably benign	Het
Baz1b	T	A	5: 135,245,794 (GRCm39)	N414K	probably damaging	Het
Cacna1e	A	T	1: 154,287,929 (GRCm39)		probably null	Het
Cdc73	A	G	1: 143,484,252 (GRCm39)		probably benign	Het
Cdhr2	A	G	13: 54,865,701 (GRCm39)	D233G	probably null	Het
Cep250	G	A	2: 155,834,552 (GRCm39)	R2159K	probably damaging	Het
Col4a4	T	A	1: 82,501,643 (GRCm39)	Y370F	unknown	Het
Cyp2b9	T	C	7: 25,872,881 (GRCm39)	L8P	probably damaging	Het
Ddx4	A	G	13: 112,750,295 (GRCm39)	V386A	probably benign	Het
Dnajc28	G	A	16: 91,413,755 (GRCm39)	T187M	probably damaging	Het
Dnajc6	T	A	4: 101,496,593 (GRCm39)	V920E	probably damaging	Het
Eef2kmt	A	T	16: 5,070,899 (GRCm39)	I50N	probably damaging	Het
Esyt3	T	C	9: 99,206,290 (GRCm39)	M40V	probably benign	Het
Gkn3	C	T	6: 87,360,507 (GRCm39)	A163T	probably damaging	Het
Hmcn1	A	G	1: 150,578,967 (GRCm39)	I1993T	possibly damaging	Het
Hsdl2	T	A	4: 59,610,636 (GRCm39)	L211Q	unknown	Het
Khdrbs2	A	G	1: 32,372,605 (GRCm39)	E93G	probably damaging	Het
Kif13b	T	C	14: 65,004,904 (GRCm39)		probably null	Het
Kif15	T	A	9: 122,815,254 (GRCm39)	L423I	probably benign	Het
Kmt2c	A	G	5: 25,492,711 (GRCm39)	V834A	probably benign	Het
Lama3	T	A	18: 12,637,365 (GRCm39)	Y28*	probably null	Het
Map4k2	A	T	19: 6,403,186 (GRCm39)	H763L	probably damaging	Het
Mrtfb	T	C	16: 13,202,064 (GRCm39)	F120S	probably damaging	Het
Ndufs3	C	T	2: 90,728,689 (GRCm39)		probably benign	Het
Nfasc	A	T	1: 132,523,329 (GRCm39)	V887E	probably damaging	Het
Npsr1	G	A	9: 24,225,065 (GRCm39)	E358K	possibly damaging	Het
Nrcam	T	C	12: 44,618,985 (GRCm39)	L828P	possibly damaging	Het
Oprm1	T	C	10: 6,780,234 (GRCm39)	Y299H	probably damaging	Het
Or1j15	T	A	2: 36,459,030 (GRCm39)	L140H	probably damaging	Het
Osbpl8	T	C	10: 111,125,651 (GRCm39)	V777A	possibly damaging	Het
Pcnt	T	C	10: 76,263,848 (GRCm39)	E372G	probably damaging	Het
Plekhh2	T	C	17: 84,925,427 (GRCm39)	V1408A	probably benign	Het
Sbk2	T	C	7: 4,960,627 (GRCm39)	Y181C	probably damaging	Het
Sf1	G	A	19: 6,418,470 (GRCm39)		probably null	Het
Slc26a9	A	G	1: 131,695,587 (GRCm39)	E765G	possibly damaging	Het
Stab2	A	G	10: 86,758,049 (GRCm39)	L1073P	probably damaging	Het
Sypl2	A	G	3: 108,124,992 (GRCm39)	I123T	possibly damaging	Het
Taar3	A	G	10: 23,825,757 (GRCm39)	D101G	possibly damaging	Het
Thsd4	T	C	9: 59,904,505 (GRCm39)	R204G	probably benign	Het
Traf3ip3	A	G	1: 192,863,628 (GRCm39)	V414A	probably damaging	Het
Trim14	T	A	4: 46,523,709 (GRCm39)	T110S	probably benign	Het
Trim65	G	A	11: 116,017,305 (GRCm39)	Q386*	probably null	Het
Ttn	G	A	2: 76,748,114 (GRCm39)	Q4312*	probably null	Het
Ubtfl1	T	C	9: 18,321,264 (GRCm39)	V264A	probably damaging	Het
Vmn1r58	C	A	7: 5,413,654 (GRCm39)	W192L	probably damaging	Het
Washc5	C	A	15: 59,211,711 (GRCm39)	C969F	probably damaging	Het
Zdhhc14	A	G	17: 5,777,131 (GRCm39)	K296R	probably benign	Het
Zfp281	T	A	1: 136,553,859 (GRCm39)	I279N	probably damaging	Het
Zfp9	G	T	6: 118,441,730 (GRCm39)	P311T	probably damaging	Het

Other mutations in Gpr26

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01065:Gpr26	APN	7	131,569,230 (GRCm39)	missense	probably damaging	1.00
IGL01345:Gpr26	APN	7	131,569,161 (GRCm39)	missense	possibly damaging	0.90
IGL01658:Gpr26	APN	7	131,585,834 (GRCm39)	missense	probably benign
IGL02724:Gpr26	APN	7	131,576,121 (GRCm39)	critical splice donor site	probably null
R0408:Gpr26	UTSW	7	131,576,001 (GRCm39)	splice site	probably null
R0408:Gpr26	UTSW	7	131,569,249 (GRCm39)	missense	possibly damaging	0.81
R0547:Gpr26	UTSW	7	131,586,026 (GRCm39)	missense	probably benign	0.01
R2508:Gpr26	UTSW	7	131,568,823 (GRCm39)	missense	probably damaging	0.98
R4630:Gpr26	UTSW	7	131,568,709 (GRCm39)	missense	probably damaging	1.00
R4680:Gpr26	UTSW	7	131,576,082 (GRCm39)	missense	probably benign	0.34
R4756:Gpr26	UTSW	7	131,569,230 (GRCm39)	missense	probably damaging	1.00
R5229:Gpr26	UTSW	7	131,585,976 (GRCm39)	missense	probably damaging	1.00
R5610:Gpr26	UTSW	7	131,568,694 (GRCm39)	missense	possibly damaging	0.94
R6605:Gpr26	UTSW	7	131,585,893 (GRCm39)	missense	possibly damaging	0.91
R6653:Gpr26	UTSW	7	131,585,830 (GRCm39)	missense	probably benign	0.00
R7213:Gpr26	UTSW	7	131,569,219 (GRCm39)	missense	probably damaging	1.00
R7351:Gpr26	UTSW	7	131,576,094 (GRCm39)	missense	probably damaging	1.00
R7768:Gpr26	UTSW	7	131,576,077 (GRCm39)	missense	probably damaging	0.99
R7887:Gpr26	UTSW	7	131,568,702 (GRCm39)	missense	probably benign
R8822:Gpr26	UTSW	7	131,568,997 (GRCm39)	missense	probably damaging	0.98
R9382:Gpr26	UTSW	7	131,568,963 (GRCm39)	missense	probably damaging	1.00
R9508:Gpr26	UTSW	7	131,585,830 (GRCm39)	missense	probably benign	0.00
Z1088:Gpr26	UTSW	7	131,585,823 (GRCm39)	frame shift	probably null
Z1176:Gpr26	UTSW	7	131,568,954 (GRCm39)	missense	probably damaging	1.00
Z1176:Gpr26	UTSW	7	131,568,777 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGTGAACACTCGCCTAGGTG -3'
(R):5'- TAGCTCAGCGGAAAGACCAC -3'

Sequencing Primer
(F):5'- AACACTCGCCTAGGTGATCGC -3'
(R):5'- ACAGCCACCCAGCGGTC -3'

Posted On

2016-02-10