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OCA2 OCA2 melanosomal transmembrane protein [ Gallus gallus (chicken) ]

Gene ID: 428009, updated on 3-Apr-2024

Summary

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Official Symbol
OCA2provided by CGNC
Official Full Name
OCA2 melanosomal transmembrane proteinprovided by CGNC
Primary source
CGNC:12554
See related
Ensembl:ENSGALG00010002896
Gene type
protein coding
RefSeq status
MODEL
Organism
Gallus gallus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Galloanserae; Galliformes; Phasianidae; Phasianinae; Gallus
Orthologs
human mouse all
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Genomic context

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Location:
chromosome: 1
Exon count:
27
Annotation release Status Assembly Chr Location
106 current bGalGal1.mat.broiler.GRCg7b (GCF_016699485.2) 1 NC_052532.1 (130732056..130937048)
106 current bGalGal1.pat.whiteleghornlayer.GRCg7w (GCF_016700215.2) 1 NC_052573.1 (130687805..130892262)

Chromosome 1 - NC_052532.1Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107051964 Neighboring gene HECT and RLD domain containing E3 ubiquitin protein ligase 2 Neighboring gene uncharacterized LOC100858753 Neighboring gene uncharacterized LOC121107738 Neighboring gene uncharacterized LOC121107754

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

General gene information

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Homology

Gene Ontology Provided by RefSeq

Process Evidence Code Pubs
involved_in melanin biosynthetic process IEA
Inferred from Electronic Annotation
more info
 PubMed 
involved_in melanocyte differentiation IEA
Inferred from Electronic Annotation
more info
 PubMed 
involved_in transmembrane transport IEA
Inferred from Electronic Annotation
more info
 PubMed 
Component Evidence Code Pubs
located_in melanosome membrane IEA
Inferred from Electronic Annotation
more info
 PubMed 

General protein information

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Preferred Names
P protein
Names
oculocutaneous albinism II (pink-eye dilution homolog, mouse)

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Gallus gallus Annotation Release 106 details...Open this link in a new tab

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

Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly

Genomic

  1. NC_052532.1 Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly

    Range
    130732056..130937048
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_040662061.2 → XP_040517995.1  P protein isoform X3

    UniProtKB/TrEMBL
    A0A8V0XHD9
    Conserved Domains (1) summary
    cd01116
    Location:358 → 839
    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 ...

  2. XM_004938466.5 → XP_004938523.1  P protein isoform X1

    UniProtKB/TrEMBL
    A0A8V0XEN3, A0A8V0XHD9
    Related
    ENSGALP00010004099.1, ENSGALT00010006708.1
    Conserved Domains (2) summary
    COG1055
    Location:351 → 849
    ArsB; Na+/H+ antiporter NhaD or related arsenite permease [Inorganic ion transport and metabolism]
    cd01116
    Location:358 → 849
    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 ...

  3. XM_025146634.3 → XP_025002402.1  P protein isoform X2

    UniProtKB/TrEMBL
    A0A8V0XHD9
    Related
    ENSGALP00010004100.1, ENSGALT00010006709.1
    Conserved Domains (1) summary
    cd01116
    Location:350 → 841
    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 ...

  4. XM_025146636.3 → XP_025002404.1  P protein isoform X4

    UniProtKB/TrEMBL
    F1NES9, I0J1E3, I0J1E4
    Conserved Domains (1) summary
    cd01116
    Location:225 → 716
    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 ...

  5. XM_046906233.1 → XP_046762189.1  P protein isoform X2

Alternate bGalGal1.pat.whiteleghornlayer.GRCg7w

Genomic

  1. NC_052573.1 Alternate bGalGal1.pat.whiteleghornlayer.GRCg7w

    Range
    130687805..130892262
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_040661170.2 → XP_040517104.1  P protein isoform X5

    UniProtKB/TrEMBL
    A0A8V0XHD9
    Conserved Domains (1) summary
    cd01116
    Location:358 → 839
    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 ...

  2. XM_040661171.2 → XP_040517105.1  P protein isoform X6

    UniProtKB/TrEMBL
    A0A8V0XHD9
    Conserved Domains (1) summary
    cd01116
    Location:350 → 831
    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 ...

  3. XM_040661174.2 → XP_040517108.1  P protein isoform X7

    UniProtKB/TrEMBL
    I0J1E3
    Conserved Domains (1) summary
    cd01116
    Location:225 → 706
    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 ...

  4. XM_040661172.2 → XP_040517106.1  P protein isoform X1

    UniProtKB/TrEMBL
    A0A8V0XHD9
    Conserved Domains (1) summary
    cd01116
    Location:358 → 849
    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 ...

  5. XM_040661173.2 → XP_040517107.1  P protein isoform X2

    UniProtKB/TrEMBL
    A0A8V0XHD9
    Conserved Domains (1) summary
    cd01116
    Location:350 → 841
    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 ...
Nucleotide Protein Strain
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