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npc2.1 NPC intracellular cholesterol transporter 2, tandem duplicate 1 [ Danio rerio (zebrafish) ]

Gene ID: 282673, updated on 2-Nov-2024

Summary

Official Symbol
npc2.1provided by ZNC
Official Full Name
NPC intracellular cholesterol transporter 2, tandem duplicate 1provided by ZNC
Primary source
ZFIN:ZDB-GENE-021206-13
See related
Ensembl:ENSDARG00000090912 AllianceGenome:ZFIN:ZDB-GENE-021206-13
Gene type
protein coding
RefSeq status
PROVISIONAL
Organism
Danio rerio
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Ostariophysi; Cypriniformes; Danionidae; Danioninae; Danio
Also known as
npc2; cb292; sb:cb292
Summary
Predicted to enable cholesterol binding activity. Acts upstream of or within several processes, including embryonic organ morphogenesis; nervous system development; and otic vesicle development. Predicted to be located in endoplasmic reticulum; extracellular region; and lysosome. Is expressed in several structures, including heart; liver; muscle; pleuroperitoneal region; and yolk syncytial layer. Human ortholog(s) of this gene implicated in Niemann-Pick disease and Niemann-Pick disease type C2. Orthologous to human NPC2 (NPC intracellular cholesterol transporter 2). [provided by Alliance of Genome Resources, Nov 2024]
Orthologs
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Genomic context

See npc2.1 in Genome Data Viewer
Location:
chromosome: 17
Exon count:
5
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCz11 (GCF_000002035.6) 17 NC_007128.7 (43030321..43031816, complement)
105 previous assembly GRCz10 (GCF_000002035.5) 17 NC_007128.6 (43039783..43041271, complement)

Chromosome 17 - NC_007128.7Genomic Context describing neighboring genes Neighboring gene gsk3b interacting protein Neighboring gene NPC intracellular cholesterol transporter 2, tandem duplicate 2 Neighboring gene iron-sulfur cluster assembly 2 Neighboring gene EMAP like 5 Neighboring gene uncharacterized LOC110438050

Genomic regions, transcripts, and products

Expression

  • Project title: Sequencing the Zebrafish transcriptome from a range of tissues and developmental stages Sequencing the Zebrafish transcriptome from a range of tissues and developmental stages
  • Description: Sequencing the Zebrafish transcriptome from a range of tissues and developmental stages
  • BioProject: PRJEB1986
  • Analysis date: Fri Dec 8 19:48:10 2017

General gene information

Markers

Gene Ontology Provided by ZFIN

Function Evidence Code Pubs
enables cholesterol binding IBA
Inferred from Biological aspect of Ancestor
more info
 
enables sterol binding IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
acts_upstream_of_or_within blood circulation IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within central nervous system development IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in cholesterol efflux IBA
Inferred from Biological aspect of Ancestor
more info
 
acts_upstream_of_or_within cholesterol metabolic process IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within inflammatory response IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in intracellular cholesterol transport IBA
Inferred from Biological aspect of Ancestor
more info
 
acts_upstream_of_or_within intracellular cholesterol transport IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within lipid metabolic process IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within lipid transport IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within motor behavior IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within myelination IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in nervous system development IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within notochord morphogenesis IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within otic vesicle development IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within otolith formation IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within steroid metabolic process IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within sterol transport IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in endoplasmic reticulum IEA
Inferred from Electronic Annotation
more info
 
located_in extracellular region IEA
Inferred from Electronic Annotation
more info
 
located_in lysosome IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
NPC intracellular cholesterol transporter 2
Names
16.5 kDa secretory protein
Niemann-Pick disease, type C2
epididymal secretory protein E1
niemann Pick type C2 protein homolog

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.

mRNA and Protein(s)

  1. NM_173224.1NP_775331.1  NPC intracellular cholesterol transporter 2 precursor

    See identical proteins and their annotated locations for NP_775331.1

    Status: PROVISIONAL

    Source sequence(s)
    AF291663
    UniProtKB/Swiss-Prot
    Q9DGJ3
    UniProtKB/TrEMBL
    A0A8M9PE29
    Related
    ENSDARP00000050398.6, ENSDART00000050399.9
    Conserved Domains (1) summary
    cd00916
    Location:24145
    Npc2_like; Niemann-Pick type C2 (Npc2) is a lysosomal protein in which a mutation in the gene causes a rare form of Niemann-Pick type C disease, an autosomal recessive lipid storage disorder characterized by accumulation of low-density lipoprotein-derived ...

RefSeqs of Annotated Genomes: GCF_000002035.6-RS_2024_08

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

Reference GRCz11 Primary Assembly

Genomic

  1. NC_007128.7 Reference GRCz11 Primary Assembly

    Range
    43030321..43031816 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_021467104.2XP_021322779.1  NPC intracellular cholesterol transporter 2 isoform X1

    UniProtKB/Swiss-Prot
    Q9DGJ3
    UniProtKB/TrEMBL
    A0A8M9PE29
    Related
    ENSDARP00000113663.1, ENSDART00000132754.2
    Conserved Domains (1) summary
    cd00916
    Location:24145
    Npc2_like; Niemann-Pick type C2 (Npc2) is a lysosomal protein in which a mutation in the gene causes a rare form of Niemann-Pick type C disease, an autosomal recessive lipid storage disorder characterized by accumulation of low-density lipoprotein-derived ...