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OCA2 OCA2 melanosomal transmembrane protein [ Rhinopithecus roxellana (golden snub-nosed monkey) ]

Gene ID: 104655701, updated on 12-Mar-2024

Summary

Gene symbol
OCA2
Gene description
OCA2 melanosomal transmembrane protein
See related
Ensembl:ENSRROG00000031791
Gene type
protein coding
RefSeq status
MODEL
Organism
Rhinopithecus roxellana
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Colobinae; Rhinopithecus
Orthologs
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Genomic context

Location:
chromosome: 5
Exon count:
24
Annotation release Status Assembly Chr Location
101 current ASM756505v1 (GCF_007565055.1) 5 NC_044553.1 (126473145..126822241)
100 previous assembly Rrox_v1 (GCF_000769185.1) Unplaced Scaffold NW_010829834.1 (14419..361288)

Chromosome 5 - NC_044553.1Genomic Context describing neighboring genes Neighboring gene E3 ubiquitin-protein ligase HERC2-like Neighboring gene NIPA magnesium transporter 1 Neighboring gene 60S ribosomal protein L5 pseudogene Neighboring gene U6 spliceosomal RNA Neighboring gene gamma-aminobutyric acid type A receptor subunit gamma3 Neighboring gene uncharacterized LOC104655702

Genomic regions, transcripts, and products

General protein information

Preferred Names
LOW QUALITY PROTEIN: P protein

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Rhinopithecus roxellana Annotation Release 101 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference ASM756505v1 Primary Assembly

Genomic

  1. NC_044553.1 Reference ASM756505v1 Primary Assembly

    Range
    126473145..126822241
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_010355208.2XP_010353510.2  LOW QUALITY PROTEIN: P protein

    UniProtKB/TrEMBL
    A0A2K6PF79
    Conserved Domains (1) summary
    cd01116
    Location:338829
    P_permease; Permease P (pink-eyed dilution). Mutations in the human melanosomal P gene were responsible for classic phenotype of oculocutaneous albinism type 2 (OCA2). Although the precise function of the P protein is unknown, it was predicted to regulate the ...