Mutagenetix > Incidental Mutation

Incidental Mutation 'R0426:Galr2'

38670

Institutional Source

Beutler Lab

Gene Symbol

Galr2

Ensembl Gene

ENSMUSG00000020793

Gene Name

galanin receptor 2

Synonyms

mGalR, GalR2

MMRRC Submission

038628-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.077) question?

Stock #

R0426 (G1)

Quality Score

168

Status

Validated

Chromosome

Chromosomal Location

116280939-116283938 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 116281691 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Aspartic acid at position 69 (A69D)

Ref Sequence

ENSEMBL: ENSMUSP00000054062 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000055872]

AlphaFold

O88854

Predicted Effect

probably damaging
Transcript: ENSMUST00000055872
AA Change: A69D

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

SMART Domains

Protein: ENSMUSP00000054062
Gene: ENSMUSG00000020793
AA Change: A69D

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srsx	35	306	4.1e-12	PFAM
Pfam:7tm_1	41	291	6.4e-52	PFAM
Pfam:7TM_GPCR_Srv	62	307	1.2e-7	PFAM
Pfam:7TM_GPCR_Srw	184	308	4.7e-8	PFAM
low complexity region	347	358	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154277

Meta Mutation Damage Score

0.7092

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.7%
20x: 93.9%

Validation Efficiency

96% (86/90)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Galanin is an important neuromodulator present in the brain, gastrointestinal system, and hypothalamopituitary axis. It is a 30-amino acid non-C-terminally amidated peptide that potently stimulates growth hormone secretion, inhibits cardiac vagal slowing of heart rate, abolishes sinus arrhythmia, and inhibits postprandial gastrointestinal motility. The actions of galanin are mediated through interaction with specific membrane receptors that are members of the 7-transmembrane family of G protein-coupled receptors. GALR2 interacts with the N-terminal residues of the galanin peptide. The primary signaling mechanism for GALR2 is through the phospholipase C/protein kinase C pathway (via Gq), in contrast to GALR1, which communicates its intracellular signal by inhibition of adenylyl cyclase through Gi. However, it has been demonstrated that GALR2 couples efficiently to both the Gq and Gi proteins to simultaneously activate 2 independent signal transduction pathways. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for disruptions in this gene display a reduction in exploratory activity. There is also a modest shift in the distribution of different lymphocyte cell types. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A830010M20Rik	C	T	5: 107,510,373 (GRCm38)	T1603I	probably damaging	Het
Abca8b	G	T	11: 109,955,027 (GRCm38)		probably benign	Het
Acadl	A	T	1: 66,841,646 (GRCm38)	F320L	probably damaging	Het
Acsbg1	T	C	9: 54,622,746 (GRCm38)	D222G	probably benign	Het
Anapc15	A	G	7: 101,898,033 (GRCm38)	T39A	probably benign	Het
Ano3	A	T	2: 110,661,174 (GRCm38)	V919E	probably damaging	Het
Arhgef12	T	C	9: 42,970,990 (GRCm38)		probably null	Het
Atad5	T	A	11: 80,112,832 (GRCm38)	I1091N	probably benign	Het
Atf1	A	T	15: 100,232,827 (GRCm38)	H26L	possibly damaging	Het
Atp10a	T	C	7: 58,784,734 (GRCm38)	M252T	probably benign	Het
Cd55	C	T	1: 130,448,372 (GRCm38)	R347H	probably benign	Het
Cdc27	A	C	11: 104,513,027 (GRCm38)		probably null	Het
Cdh9	G	A	15: 16,823,454 (GRCm38)		probably null	Het
Cdk11b	T	C	4: 155,642,512 (GRCm38)		probably benign	Het
Cep70	A	G	9: 99,297,684 (GRCm38)	D567G	probably benign	Het
Cep78	A	T	19: 15,970,970 (GRCm38)	Y382*	probably null	Het
Col9a2	T	C	4: 121,044,660 (GRCm38)		probably benign	Het
Cyp2d12	G	A	15: 82,558,963 (GRCm38)	D409N	probably benign	Het
Ddx39	A	G	8: 83,721,769 (GRCm38)	T217A	probably benign	Het
Dennd1b	T	A	1: 139,170,196 (GRCm38)	D733E	probably benign	Het
Dicer1	A	G	12: 104,702,542 (GRCm38)	S1294P	probably damaging	Het
Dnah3	T	C	7: 119,943,572 (GRCm38)	E3539G	probably benign	Het
Dnmbp	A	G	19: 43,852,436 (GRCm38)		probably benign	Het
Dysf	T	C	6: 84,149,757 (GRCm38)	L1332P	probably damaging	Het
F5	A	G	1: 164,182,840 (GRCm38)	D380G	probably damaging	Het
Fam160a2	A	C	7: 105,389,473 (GRCm38)	C186W	probably damaging	Het
Fam171a1	T	C	2: 3,225,396 (GRCm38)	V522A	probably benign	Het
Grk2	T	C	19: 4,290,600 (GRCm38)		probably null	Het
Gtf3c1	A	T	7: 125,663,016 (GRCm38)	Y1119*	probably null	Het
Hgd	A	T	16: 37,588,685 (GRCm38)		probably benign	Het
Ildr2	G	T	1: 166,308,899 (GRCm38)	V436L	probably benign	Het
Intu	G	A	3: 40,675,305 (GRCm38)	C355Y	probably damaging	Het
Irf2bpl	G	T	12: 86,883,096 (GRCm38)	P268T	probably benign	Het
Jarid2	T	C	13: 44,840,882 (GRCm38)		probably null	Het
Jup	A	T	11: 100,372,401 (GRCm38)	M716K	probably benign	Het
Kank1	G	A	19: 25,411,473 (GRCm38)	V809I	probably damaging	Het
Kdm1b	T	A	13: 47,064,244 (GRCm38)		probably benign	Het
Kdm3a	C	T	6: 71,600,755 (GRCm38)	C687Y	probably damaging	Het
Kdm5d	T	A	Y: 942,437 (GRCm38)		probably benign	Het
Kifap3	T	A	1: 163,865,552 (GRCm38)		probably benign	Het
Macf1	T	A	4: 123,483,660 (GRCm38)	K1400*	probably null	Het
Majin	A	G	19: 6,212,117 (GRCm38)		probably benign	Het
Mb21d1	G	A	9: 78,435,738 (GRCm38)		probably benign	Het
Mctp1	A	G	13: 77,020,821 (GRCm38)	I846V	probably benign	Het
Mrgpra2b	T	A	7: 47,464,127 (GRCm38)	I286F	possibly damaging	Het
Neil3	T	G	8: 53,609,396 (GRCm38)		probably benign	Het
Nox3	G	T	17: 3,695,563 (GRCm38)	N23K	probably damaging	Het
Nt5c3	T	C	6: 56,883,812 (GRCm38)	K219E	probably benign	Het
Olfr1458	G	A	19: 13,103,278 (GRCm38)	R3C	possibly damaging	Het
Olfr213	A	T	6: 116,540,485 (GRCm38)	N11Y	probably damaging	Het
Olfr389	T	A	11: 73,776,437 (GRCm38)	M297L	probably benign	Het
Olfr524	A	C	7: 140,202,116 (GRCm38)	F218C	possibly damaging	Het
Olfr548-ps1	T	A	7: 102,542,686 (GRCm38)	I250N	probably damaging	Het
Olfr954	T	C	9: 39,461,593 (GRCm38)	L54P	probably damaging	Het
Pacsin2	A	G	15: 83,379,795 (GRCm38)	V347A	possibly damaging	Het
Pcdhb7	A	T	18: 37,342,804 (GRCm38)	E331V	probably damaging	Het
Pcid2	A	C	8: 13,081,262 (GRCm38)		probably null	Het
Pcsk9	T	C	4: 106,450,077 (GRCm38)	D323G	possibly damaging	Het
Pdhb	T	C	14: 8,169,801 (GRCm38)	E203G	probably damaging	Het
Phlpp2	A	G	8: 109,928,463 (GRCm38)	Y630C	probably benign	Het
Pidd1	C	T	7: 141,439,133 (GRCm38)	A812T	probably damaging	Het
Plau	G	A	14: 20,842,314 (GRCm38)	R389H	probably benign	Het
Plekhg6	G	A	6: 125,364,629 (GRCm38)		probably null	Het
Ppox	T	C	1: 171,277,749 (GRCm38)	Y321C	probably damaging	Het
Pxdn	A	G	12: 29,987,066 (GRCm38)	N281S	possibly damaging	Het
Pycrl	A	T	15: 75,918,388 (GRCm38)	M138K	probably benign	Het
Radil	T	C	5: 142,497,873 (GRCm38)	Y526C	probably damaging	Het
Ranbp3	C	A	17: 56,707,169 (GRCm38)	D233E	probably benign	Het
Rhpn1	A	G	15: 75,711,872 (GRCm38)	Q402R	possibly damaging	Het
Sec23b	T	A	2: 144,568,612 (GRCm38)		probably benign	Het
Sel1l2	A	T	2: 140,240,912 (GRCm38)	L602*	probably null	Het
Sema5b	G	A	16: 35,646,355 (GRCm38)	G209D	probably damaging	Het
Svep1	T	C	4: 58,073,333 (GRCm38)	Y1992C	possibly damaging	Het
Syncrip	T	A	9: 88,456,259 (GRCm38)		probably benign	Het
Synj1	G	T	16: 90,967,354 (GRCm38)	A65E	probably damaging	Het
Taar2	G	A	10: 23,941,495 (GRCm38)	R311H	probably benign	Het
Tecrl	T	C	5: 83,354,763 (GRCm38)		probably benign	Het
Tenm4	G	T	7: 96,777,851 (GRCm38)	G698C	probably damaging	Het
Tmem209	G	A	6: 30,491,182 (GRCm38)	L259F	probably damaging	Het
Tmem247	G	A	17: 86,918,503 (GRCm38)	E124K	possibly damaging	Het
Tnks2	C	A	19: 36,852,821 (GRCm38)	A218E	probably damaging	Het
Tppp	T	A	13: 74,021,311 (GRCm38)	F57I	probably damaging	Het
Trim36	A	G	18: 46,172,525 (GRCm38)	W452R	probably damaging	Het
Vars2	A	T	17: 35,664,584 (GRCm38)	V262E	probably damaging	Het
Vmn2r92	C	T	17: 18,167,957 (GRCm38)	A408V	probably damaging	Het
Zfp516	G	T	18: 82,955,772 (GRCm38)	A32S	probably benign	Het
Zfy2	G	T	Y: 2,107,348 (GRCm38)	L429I	possibly damaging	Het

Other mutations in Galr2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01012:Galr2	APN	11	116,283,170 (GRCm38)	missense	probably damaging	1.00
PIT4418001:Galr2	UTSW	11	116,283,258 (GRCm38)	missense	probably benign	0.35
PIT4445001:Galr2	UTSW	11	116,281,648 (GRCm38)	missense	probably benign	0.13
R1869:Galr2	UTSW	11	116,283,243 (GRCm38)	missense	possibly damaging	0.87
R2059:Galr2	UTSW	11	116,282,939 (GRCm38)	missense	probably damaging	1.00
R4579:Galr2	UTSW	11	116,281,499 (GRCm38)	missense	probably benign
R4666:Galr2	UTSW	11	116,283,629 (GRCm38)	missense	probably benign
R5832:Galr2	UTSW	11	116,281,631 (GRCm38)	missense	probably damaging	1.00
R5974:Galr2	UTSW	11	116,283,026 (GRCm38)	missense	possibly damaging	0.62
R7081:Galr2	UTSW	11	116,283,048 (GRCm38)	missense	probably damaging	0.99
R7155:Galr2	UTSW	11	116,283,582 (GRCm38)	missense	possibly damaging	0.94
R7696:Galr2	UTSW	11	116,283,167 (GRCm38)	missense	probably damaging	1.00
R7810:Galr2	UTSW	11	116,283,120 (GRCm38)	missense	probably benign	0.23
R8921:Galr2	UTSW	11	116,283,147 (GRCm38)	missense	probably damaging	1.00
R9231:Galr2	UTSW	11	116,283,509 (GRCm38)	missense	probably benign
R9514:Galr2	UTSW	11	116,283,626 (GRCm38)	missense	probably benign
X0009:Galr2	UTSW	11	116,283,323 (GRCm38)	missense	probably benign	0.14
X0026:Galr2	UTSW	11	116,281,751 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- GTGATACCATGAATGGCTCGGACAG -3'
(R):5'- AGTCACGGAGTCTTAGTCCCCTTTC -3'

Sequencing Primer
(F):5'- ACTCGAGCCAGGAAGGTG -3'
(R):5'- CAGTGCAAGCTCCTACCTG -3'

Posted On

2013-05-23