Species

Caenorhabditis elegans

Symbol

T06E4.7

Name

G protein-coupled receptor

Synonyms

CELE_T06E4.7

Biotype

protein coding gene

Automated Description

Predicted to be located in membrane.

WB Description

Predicted to be located in membrane.

Cross References

Additional Information

Literature

Orthology

Gene tree: PANTHER:PTHR22945

No data available

Links to orthology data in JBrowse by filter level: Stringent, Moderate, No filter, Best and Best Reverse

Paralogy

Gene symbol	Rank	Alignment Length (aa)	Similarity %	Identity %	Method Count	Method Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
srd-46	1	378	40	21	2 of 8	☐ ☐☐☑☐☑☐☐
srd-74	2	372	39	23	2 of 8	☐ ☐☐☑☐☑☐☐
srd-58	3	379	37	22	2 of 8	☐ ☐☐☑☐☑☐☐
srd-59	4	378	38	22	2 of 8	☐ ☐☐☑☐☑☐☐
srd-65	5	372	37	22	2 of 8	☐ ☐☐☑☐☑☐☐
srd-47	6	367	38	21	2 of 8	☐ ☐☐☑☐☑☐☐
srd-48	7	364	38	21	2 of 8	☐ ☐☐☑☐☑☐☐
srd-51	8	353	39	22	2 of 8	☐ ☐☐☑☐☑☐☐
srd-56	9	388	35	20	2 of 8	☐ ☐☐☑☐☑☐☐
srd-53	10	372	38	20	2 of 8	☐ ☐☐☑☐☑☐☐
srd-41	11	362	40	19	2 of 8	☐ ☐☐☑☐☑☐☐
srd-68	12	375	34	22	2 of 8	☐ ☐☐☑☐☑☐☐
srd-60	13	373	38	19	2 of 8	☐ ☐☐☑☐☑☐☐
srd-44	14	332	42	22	2 of 8	☐ ☐☐☑☐☑☐☐
srd-66	15	383	35	20	2 of 8	☐ ☐☐☑☐☑☐☐
srd-49	16	370	36	20	2 of 8	☐ ☐☐☑☐☑☐☐
srd-39	17	357	39	19	2 of 8	☐ ☐☐☑☐☑☐☐
srd-40	18	329	41	22	2 of 8	☐ ☐☐☑☐☑☐☐
srd-38	19	398	34	18	2 of 8	☐ ☐☐☑☐☑☐☐
srd-42	20	378	37	18	2 of 8	☐ ☐☐☑☐☑☐☐
srd-71	21	377	36	19	2 of 8	☐ ☐☐☑☐☑☐☐
srd-72	21	377	36	19	2 of 8	☐ ☐☐☑☐☑☐☐
srd-63	22	370	36	20	2 of 8	☐ ☐☐☑☐☑☐☐
srd-67	23	366	39	17	2 of 8	☐ ☐☐☑☐☑☐☐
srd-50	24	366	37	19	2 of 8	☐ ☐☐☑☐☑☐☐
srd-75	25	376	35	19	2 of 8	☐ ☐☐☑☐☑☐☐
srd-61	25	376	35	19	2 of 8	☐ ☐☐☑☐☑☐☐
srd-54	26	345	38	21	2 of 8	☐ ☐☐☑☐☑☐☐
srd-35	27	372	34	18	2 of 8	☐ ☐☐☑☐☑☐☐
srd-70	28	356	36	18	2 of 8	☐ ☐☐☑☐☑☐☐
srd-34	29	334	37	20	2 of 8	☐ ☐☐☑☐☑☐☐
srd-43	30	316	41	20	2 of 8	☐ ☐☐☑☐☑☐☐
srd-45	31	333	40	17	2 of 8	☐ ☐☐☑☐☑☐☐
srd-64	32	339	33	20	2 of 8	☐ ☐☐☑☐☑☐☐
srd-55	33	306	37	19	2 of 8	☐ ☐☐☑☐☑☐☐
srd-69	34	286	36	22	2 of 8	☐ ☐☐☑☐☑☐☐
srd-36	35	156	42	19	2 of 8	☐ ☐☐☑☐☑☐☐

Function - GO Annotations

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources: None
Other Sources: None

No data available

Disease Associations

	all annotations		all disease by infectious agent	bacterial infectious disease	fungal infectious disease	parasitic infectious disease	viral infectious disease		all disease of anatomical entity	cardiovascular system disease	central nervous system disease	endocrine system disease	gastrointestinal system disease	hematopoietic system disease	immune system disease	integumentary system disease	musculoskeletal system disease	peripheral nervous system disease	reproductive system disease	respiratory system disease	sensory system disease	thoracic disease	urinary system disease		all disease of cellular proliferation	benign neoplasm	cancer	pre-malignant neoplasm		all genetic disease	chromosomal disease	monogenic disease	polygenic disease		all other disease	disease of mental health	disease of metabolism	physical disorder	syndrome
T06E4.7 (Cel)

Cell color indicative of annotation volume

No data available

Alleles and Variants

Genome location

ChrV:9626396...9628345 + (1.95 kb)

Assembly version

WBcel235

Viewer Help

Variant Types and ConsequencesOnly variants associated to alleles are shown in the graphics above. See all variants in JBrowse.

Allele/Variant Symbol	Category	Variant
NC_003283.11:g.9627689T>C	variant	NC_003283.11:g.9627689T>C SNP synonymous variant
NC_003283.11:g.9628246G>A	variant	NC_003283.11:g.9628246G>A SNP 3 prime UTR variant
NC_003283.11:g.9628157G>T	variant	NC_003283.11:g.9628157G>T SNP 3 prime UTR variant
NC_003283.11:g.9627571C>T	variant	NC_003283.11:g.9627571C>T SNP missense variant
NC_003283.11:g.9627253G>A	variant	NC_003283.11:g.9627253G>A SNP intron variant
NC_003283.11:g.9626915A>T	variant	NC_003283.11:g.9626915A>T SNP intron variant
NC_003283.11:g.9627826C>T	variant	NC_003283.11:g.9627826C>T SNP missense variant
NC_003283.11:g.9627439C>T	variant	NC_003283.11:g.9627439C>T SNP intron variant
NC_003283.11:g.9626766C>T	variant	NC_003283.11:g.9626766C>T SNP intron variant
NC_003283.11:g.9627602G>A	variant	NC_003283.11:g.9627602G>A SNP synonymous variant

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View detailed Alleles/Variants information

Download all Alleles/Variants for all genes of the species

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location

ChrV:9626396...9628345 + (1.95 kb)

Assembly version

WBcel235

Viewer Help

Sequence Details

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Expression

Primary Sources

Other Sources

	all annotations		all anatomical structures	alimentary part of gastrointestinal system	chemosensory system	circulatory system	endocrine system	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mechanosensory system	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system	vestibulo-auditory system	visual system	endoderm	ectoderm	mesoderm	mesenchyme	adipose tissue	appendage	entire extraembryonic component	imaginal precursor	pharyngeal arch	other		all stages	embryo stage	post embryonic, pre-adult	post-juvenile adult stage		all cellular components	extracellular region	plasma membrane	synapse	cell junction	cell projection	cytoplasmic vesicle	endosome	vacuole	golgi apparatus	endoplasmic reticulum	cytosol	mitochondrion	nucleus	chromosome	cytoskeleton	protein-containing complex	other locations
T06E4.7 (Cel)

Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

No data available

Genetic Interactions

No data available