Mutagenetix > Incidental Mutation

Incidental Mutation 'R9382:Gpr26'

710106

Institutional Source

Beutler Lab

Gene Symbol

Gpr26

Ensembl Gene

ENSMUSG00000040125

Gene Name

G protein-coupled receptor 26

Synonyms

9630036A11Rik

MMRRC Submission

Accession Numbers

Essential gene?

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

Stock #

R9382 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

131567891-131587362 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 131568963 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Asparagine at position 103 (D103N)

Ref Sequence

ENSEMBL: ENSMUSP00000041664 (fasta)

Gene Model

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

AlphaFold

Q8BZA7

Predicted Effect

probably damaging
Transcript: ENSMUST00000045840
AA Change: D103N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000041664
Gene: ENSMUSG00000040125
AA Change: D103N

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

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

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: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca8b	G	A	11: 109,870,711 (GRCm39)	S147L	probably benign	Het
Abraxas1	A	G	5: 100,957,649 (GRCm39)	V190A	probably benign	Het
Aoc1l2	A	T	6: 48,907,298 (GRCm39)	K99N	probably benign	Het
Aox1	T	A	1: 58,104,501 (GRCm39)	H559Q	possibly damaging	Het
Arhgap31	C	T	16: 38,422,988 (GRCm39)	G1026D	probably benign	Het
C1ra	T	C	6: 124,490,819 (GRCm39)	F71L	probably benign	Het
C530025M09Rik	T	C	2: 149,672,640 (GRCm39)	H165R	unknown	Het
Celf2	A	T	2: 6,726,404 (GRCm39)	M43K	probably damaging	Het
Celsr3	T	C	9: 108,706,961 (GRCm39)	V1148A	possibly damaging	Het
Cmya5	T	G	13: 93,229,884 (GRCm39)	K1735Q	probably benign	Het
Cntln	A	C	4: 84,968,318 (GRCm39)	M846L	probably benign	Het
Cntn5	T	C	9: 9,673,817 (GRCm39)	T762A	probably benign	Het
Col11a1	T	A	3: 113,899,046 (GRCm39)	L525Q	unknown	Het
Col12a1	T	C	9: 79,589,364 (GRCm39)	T1064A	probably benign	Het
Cyc1	T	C	15: 76,229,273 (GRCm39)	V211A	possibly damaging	Het
Ddx56	A	G	11: 6,215,516 (GRCm39)	S296P	probably damaging	Het
Deptor	A	T	15: 54,975,798 (GRCm39)		probably benign	Het
Ezh1	C	T	11: 101,094,265 (GRCm39)	R409H	possibly damaging	Het
Fam228b	T	A	12: 4,798,147 (GRCm39)	E190V	probably damaging	Het
Fkbp15	A	T	4: 62,237,210 (GRCm39)	L635H	probably damaging	Het
Frem1	G	A	4: 82,901,622 (GRCm39)	L969F	possibly damaging	Het
Gabrg2	T	C	11: 41,858,433 (GRCm39)	R232G	probably benign	Het
Grid2ip	T	G	5: 143,361,103 (GRCm39)		probably null	Het
Ints7	T	C	1: 191,351,793 (GRCm39)	V834A	probably damaging	Het
Kcnh7	T	A	2: 62,667,612 (GRCm39)	H309L	probably benign	Het
Mael	T	C	1: 166,053,282 (GRCm39)	E241G	probably damaging	Het
Neb	T	A	2: 52,122,277 (GRCm39)	E584V		Het
Nexn	C	T	3: 151,959,401 (GRCm39)	V23M	probably damaging	Het
Npas1	T	C	7: 16,190,231 (GRCm39)		probably null	Het
Or51f1	T	C	7: 102,506,014 (GRCm39)	I158M	probably benign	Het
Pcdh17	T	G	14: 84,685,522 (GRCm39)	V663G	probably damaging	Het
Pga5	C	T	19: 10,646,897 (GRCm39)	G303S	probably damaging	Het
Poln	T	A	5: 34,164,842 (GRCm39)	K844N	probably damaging	Het
Prkar1b	C	T	5: 139,036,442 (GRCm39)	D227N	probably damaging	Het
Proc	T	A	18: 32,256,336 (GRCm39)	I444F	probably damaging	Het
Ptprn	G	T	1: 75,229,135 (GRCm39)	H791N	probably benign	Het
Ror1	T	C	4: 100,191,709 (GRCm39)	S160P	probably benign	Het
Satb2	T	A	1: 56,870,797 (GRCm39)		probably null	Het
Slc43a3	C	T	2: 84,780,771 (GRCm39)	A332V	probably benign	Het
Sp100	G	A	1: 85,627,336 (GRCm39)	V410M	probably damaging	Het
Srgap2	T	C	1: 131,217,346 (GRCm39)	T989A	probably benign	Het
Ssc5d	T	C	7: 4,930,283 (GRCm39)		probably null	Het
Tll2	A	G	19: 41,116,997 (GRCm39)	Y273H	probably benign	Het
Tub	T	C	7: 108,626,211 (GRCm39)	V295A	possibly damaging	Het
Unc13b	T	A	4: 43,172,512 (GRCm39)	D1113E	unknown	Het
Usp9y	C	A	Y: 1,364,776 (GRCm39)	M1012I	probably benign	Het
Vmn1r238	A	G	18: 3,122,676 (GRCm39)	V246A	probably damaging	Het
Vmn2r88	T	G	14: 51,656,197 (GRCm39)	V802G		Het
Wnt7b	T	C	15: 85,443,175 (GRCm39)	Q76R	probably damaging	Het
Zan	T	C	5: 137,389,917 (GRCm39)	R4852G	unknown	Het
Zfp618	A	T	4: 63,051,258 (GRCm39)	T680S	probably damaging	Het
Zfp784	T	A	7: 5,041,338 (GRCm39)	D25V	unknown	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
R4088:Gpr26	UTSW	7	131,568,805 (GRCm39)	missense	probably benign	0.00
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
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'- ACTCTCAACCTCACGTGTGG -3'
(R):5'- CTTGAGGTACGTGAAGCAGAGC -3'

Sequencing Primer
(F):5'- TGGCAACCTGCTGTGTAC -3'
(R):5'- GCGCTGGTGAAGACAGC -3'

Posted On

2022-04-18