hvcn1 voltage-gated hydrogen channel 1 [Ciona intestinalis (vase tunicate)] - Gene

Summary

Gene symbol: hvcn1
Gene description: voltage-gated hydrogen channel 1
See related: Ensembl:ENSCING00000014744
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Ciona intestinalis
Lineage: Eukaryota; Metazoa; Chordata; Tunicata; Ascidiacea; Phlebobranchia; Cionidae; Ciona
Also known as: VSOP; vsx1
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Genomic context

Location:: chromosome: Un

Exon count:: 6

Annotation release	Status	Assembly	Chr	Location
104	current	KH (GCF_000224145.3)	Unplaced Scaffold	NW_004190496.2 (43877..47027, complement)

NW_004190496.2 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Go to reference sequence details

Genomic Sequence:: NW_004190496 Unplaced Scaffold Reference KH Primary Assembly

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Gating charge displacement in a monomeric voltage-gated proton (Hv1) channel.
Title: Gating charge displacement in a monomeric voltage-gated proton (H(v)1) channel.

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General gene information

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Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables voltage-gated proton channel activity	IEA Inferred from Electronic Annotation more info	PubMed

Process	Evidence Code	Pubs
involved_in proton transmembrane transport	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in plasma membrane	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: voltage-gated hydrogen channel 1

Names: HV1; hydrogen voltage-gated channel 1; voltage sensor domain-only protein

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.