Mutagenetix > Incidental Mutation

Incidental Mutation 'R4765:Gpr37'

366056

Institutional Source

Beutler Lab

Gene Symbol

Gpr37

Ensembl Gene

ENSMUSG00000039904

Gene Name

G protein-coupled receptor 37

Synonyms

parkin-associated endothelin B-like receptor, Pael-R

MMRRC Submission

042406-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.141) question?

Stock #

R4765 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

25668522-25689979 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 25669107 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Alanine at position 579 (E579A)

Ref Sequence

ENSEMBL: ENSMUSP00000052185 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054867] [ENSMUST00000200812]

AlphaFold

Q9QY42

Predicted Effect

probably damaging
Transcript: ENSMUST00000054867
AA Change: E579A

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

SMART Domains

Protein: ENSMUSP00000052185
Gene: ENSMUSG00000039904
AA Change: E579A

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
low complexity region	101	116	N/A	INTRINSIC
Pfam:7tm_1	265	536	5.2e-33	PFAM
low complexity region	549	558	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000200812

SMART Domains

Protein: ENSMUSP00000144683
Gene: ENSMUSG00000039904

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
low complexity region	101	116	N/A	INTRINSIC
Pfam:7tm_1	265	421	3.4e-26	PFAM

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.1%
20x: 95.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the G protein-coupled receptor family. The encoded protein contains seven transmembrane domains and is found in cell and endoplasmic reticulum membranes. G protein-coupled receptors are involved in translating outside signals into G protein mediated intracellular effects. This gene product interacts with Parkin and is involved in juvenile Parkinson disease. [provided by RefSeq, Oct 2012]
PHENOTYPE: Mice homozygous for disruptions in this gene exhibit reduced striatal dopamine content, enhanced amphetamine sensitivity, reduced motor activity and coordination and increased percentage of body fat in females. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810021J22Rik	C	T	11: 58,771,987 (GRCm39)	R490C	probably benign	Het
Abcb11	A	T	2: 69,076,211 (GRCm39)	F1166I	probably damaging	Het
Acta2	T	C	19: 34,223,552 (GRCm39)	D181G	probably damaging	Het
Adgrv1	A	G	13: 81,255,038 (GRCm39)	I6195T	probably damaging	Het
Afg3l2	G	T	18: 67,554,329 (GRCm39)	L458M	probably damaging	Het
Ankfy1	T	G	11: 72,603,117 (GRCm39)	S49A	probably benign	Het
Azi2	A	T	9: 117,890,539 (GRCm39)		probably benign	Het
Bend3	A	T	10: 43,386,746 (GRCm39)	S380C	probably damaging	Het
Bicc1	T	C	10: 70,776,423 (GRCm39)	T759A	probably damaging	Het
Cdh10	G	T	15: 19,013,364 (GRCm39)	V655L	probably damaging	Het
Cdkn2aip	C	A	8: 48,166,582 (GRCm39)	W75L	probably damaging	Het
Cenpj	G	A	14: 56,787,002 (GRCm39)	R192*	probably null	Het
Cflar	T	C	1: 58,771,480 (GRCm39)	S203P	probably damaging	Het
Chd6	A	T	2: 160,808,164 (GRCm39)	C1683*	probably null	Het
Cpsf2	A	G	12: 101,963,699 (GRCm39)	Y476C	probably damaging	Het
Cyp4a12a	A	G	4: 115,183,388 (GRCm39)	D169G	possibly damaging	Het
D430041D05Rik	T	A	2: 104,044,441 (GRCm39)	R1536S	probably damaging	Het
Depdc5	A	C	5: 33,094,979 (GRCm39)	D752A	probably damaging	Het
Dnah9	C	T	11: 65,818,552 (GRCm39)	G78D	probably damaging	Het
Drc1	G	T	5: 30,506,075 (GRCm39)	Q249H	probably benign	Het
Drg1	T	C	11: 3,200,280 (GRCm39)	I364V	probably benign	Het
Dtymk	T	C	1: 93,720,631 (GRCm39)	H130R	probably damaging	Het
Elac2	T	G	11: 64,883,048 (GRCm39)	F140V	probably damaging	Het
Enpp2	A	G	15: 54,739,068 (GRCm39)	V353A	possibly damaging	Het
Fat2	T	C	11: 55,172,013 (GRCm39)	D2900G	probably damaging	Het
Fermt2	G	T	14: 45,699,693 (GRCm39)	T536K	probably benign	Het
Foxj2	G	T	6: 122,810,230 (GRCm39)	Q196H	probably benign	Het
Gadl1	A	G	9: 115,795,381 (GRCm39)	K328R	probably null	Het
Gata6	A	G	18: 11,054,394 (GRCm39)	T108A	probably benign	Het
Gm16503	G	T	4: 147,625,554 (GRCm39)	G16V	unknown	Het
Gps2	T	C	11: 69,807,187 (GRCm39)		probably benign	Het
Hcn4	A	T	9: 58,765,260 (GRCm39)	I581F	unknown	Het
Hfm1	T	A	5: 106,990,405 (GRCm39)	Y1335F	probably benign	Het
Igsf10	A	T	3: 59,237,126 (GRCm39)	S1018R	probably benign	Het
Katnal2	C	T	18: 77,065,239 (GRCm39)		probably null	Het
Kctd8	T	C	5: 69,498,191 (GRCm39)	K152E	possibly damaging	Het
Lrp8	T	C	4: 107,711,592 (GRCm39)	C459R	probably damaging	Het
Ly6l	A	T	15: 75,321,543 (GRCm39)	I48L	probably benign	Het
Megf10	A	T	18: 57,420,866 (GRCm39)	I835F	possibly damaging	Het
Mei1	A	T	15: 81,996,686 (GRCm39)	I946F	possibly damaging	Het
Mrtfb	C	A	16: 13,230,458 (GRCm39)	P1048T	probably damaging	Het
Myo7b	G	C	18: 32,094,953 (GRCm39)	L1881V	probably benign	Het
Nfkbiz	T	C	16: 55,639,387 (GRCm39)		probably null	Het
Or4b13	T	A	2: 90,082,807 (GRCm39)	Y175F	probably damaging	Het
Or5b24	T	C	19: 12,912,440 (GRCm39)	C113R	possibly damaging	Het
Pcdhgc5	T	C	18: 37,955,122 (GRCm39)	S799P	probably benign	Het
Plk4	A	G	3: 40,756,457 (GRCm39)	E97G	probably damaging	Het
Pole2	A	T	12: 69,268,826 (GRCm39)	H114Q	possibly damaging	Het
Rad9a	C	A	19: 4,250,488 (GRCm39)	V109L	probably benign	Het
Scn8a	A	G	15: 100,938,352 (GRCm39)	H1917R	probably benign	Het
Scyl2	C	T	10: 89,495,160 (GRCm39)	V304I	probably damaging	Het
Serpina3f	G	C	12: 104,185,690 (GRCm39)	E298D	probably benign	Het
Shoc2	A	G	19: 53,976,734 (GRCm39)	E208G	probably benign	Het
Sin3a	G	A	9: 57,004,087 (GRCm39)	V280I	probably benign	Het
Slc26a2	A	T	18: 61,332,558 (GRCm39)	I291N	probably damaging	Het
Slc4a7	T	G	14: 14,762,414 (GRCm38)	D600E	probably damaging	Het
Slc5a6	A	T	5: 31,195,427 (GRCm39)	F430L	possibly damaging	Het
Snx19	A	C	9: 30,351,453 (GRCm39)	Q840H	probably damaging	Het
Spast	C	A	17: 74,676,211 (GRCm39)	D340E	probably damaging	Het
Sprr4	G	A	3: 92,407,716 (GRCm39)	P29S	unknown	Het
Stk11ip	T	G	1: 75,503,799 (GRCm39)	L239R	probably damaging	Het
Thoc6	A	G	17: 23,889,862 (GRCm39)	L20P	probably damaging	Het
Tnfrsf8	A	T	4: 145,023,447 (GRCm39)	S129T	probably benign	Het
Tnrc6c	A	G	11: 117,633,753 (GRCm39)	I1284V	probably benign	Het
Ttn	T	C	2: 76,602,851 (GRCm39)	Y16711C	probably damaging	Het
Ttn	A	G	2: 76,541,331 (GRCm39)	L33885P	probably damaging	Het
Ubn2	T	A	6: 38,456,075 (GRCm39)	C501S	probably damaging	Het
Ubr1	A	T	2: 120,793,923 (GRCm39)	L87*	probably null	Het
Uhmk1	T	C	1: 170,027,470 (GRCm39)	Y320C	probably damaging	Het
Vldlr	T	C	19: 27,217,947 (GRCm39)	V465A	probably damaging	Het
Vmn1r1	C	T	1: 181,985,471 (GRCm39)	A65T	probably benign	Het
Vmn2r25	C	T	6: 123,800,182 (GRCm39)	C720Y	probably damaging	Het
Xrra1	T	C	7: 99,555,775 (GRCm39)	Y381H	probably benign	Het
Zfhx4	T	C	3: 5,465,212 (GRCm39)	L1790P	probably benign	Het
Zscan4d	T	A	7: 10,896,594 (GRCm39)	M259L	probably benign	Het

Other mutations in Gpr37

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00786:Gpr37	APN	6	25,669,317 (GRCm39)	missense	possibly damaging	0.65
IGL01595:Gpr37	APN	6	25,669,572 (GRCm39)	missense	probably damaging	1.00
IGL01670:Gpr37	APN	6	25,669,833 (GRCm39)	missense	probably damaging	1.00
IGL02552:Gpr37	APN	6	25,688,686 (GRCm39)	missense	probably benign	0.05
IGL03331:Gpr37	APN	6	25,669,728 (GRCm39)	missense	probably benign	0.26
R0375:Gpr37	UTSW	6	25,669,290 (GRCm39)	missense	probably benign	0.08
R0534:Gpr37	UTSW	6	25,669,823 (GRCm39)	nonsense	probably null
R0892:Gpr37	UTSW	6	25,688,206 (GRCm39)	missense	probably damaging	1.00
R1481:Gpr37	UTSW	6	25,669,137 (GRCm39)	missense	probably damaging	0.99
R1700:Gpr37	UTSW	6	25,669,623 (GRCm39)	missense	probably benign	0.09
R2083:Gpr37	UTSW	6	25,688,416 (GRCm39)	missense	possibly damaging	0.62
R2089:Gpr37	UTSW	6	25,689,062 (GRCm39)	missense	possibly damaging	0.73
R2091:Gpr37	UTSW	6	25,689,062 (GRCm39)	missense	possibly damaging	0.73
R2091:Gpr37	UTSW	6	25,689,062 (GRCm39)	missense	possibly damaging	0.73
R2112:Gpr37	UTSW	6	25,669,380 (GRCm39)	missense	possibly damaging	0.91
R2847:Gpr37	UTSW	6	25,666,945 (GRCm39)	unclassified	probably benign
R2848:Gpr37	UTSW	6	25,666,945 (GRCm39)	unclassified	probably benign
R4119:Gpr37	UTSW	6	25,688,425 (GRCm39)	missense	possibly damaging	0.90
R4611:Gpr37	UTSW	6	25,669,623 (GRCm39)	missense	probably benign	0.09
R4734:Gpr37	UTSW	6	25,689,085 (GRCm39)	missense	possibly damaging	0.53
R5163:Gpr37	UTSW	6	25,669,614 (GRCm39)	missense	possibly damaging	0.87
R5669:Gpr37	UTSW	6	25,669,351 (GRCm39)	missense	probably benign	0.05
R6548:Gpr37	UTSW	6	25,688,812 (GRCm39)	missense	probably benign	0.32
R6760:Gpr37	UTSW	6	25,669,168 (GRCm39)	missense	probably benign	0.00
R7030:Gpr37	UTSW	6	25,689,004 (GRCm39)	missense	possibly damaging	0.92
R7278:Gpr37	UTSW	6	25,669,341 (GRCm39)	missense	possibly damaging	0.68
R7392:Gpr37	UTSW	6	25,688,786 (GRCm39)	missense	probably benign	0.34
R7726:Gpr37	UTSW	6	25,669,116 (GRCm39)	missense	possibly damaging	0.94
R7754:Gpr37	UTSW	6	25,689,049 (GRCm39)	missense	probably damaging	0.99
R7757:Gpr37	UTSW	6	25,688,207 (GRCm39)	missense	probably benign	0.26
R8344:Gpr37	UTSW	6	25,669,530 (GRCm39)	missense	probably damaging	1.00
R8734:Gpr37	UTSW	6	25,688,201 (GRCm39)	missense	probably benign	0.17
R8839:Gpr37	UTSW	6	25,669,369 (GRCm39)	missense	probably benign	0.15
V7732:Gpr37	UTSW	6	25,669,122 (GRCm39)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- TGAGACTGTTGGCCTCCTTC -3'
(R):5'- GCTCAACATCATCAGCCAGTTC -3'

Sequencing Primer
(F):5'- TCCTCTACTTGCTTTTCAAAATGTG -3'
(R):5'- AACATCATCAGCCAGTTCCTTTTG -3'

Posted On

2015-12-21