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OIT3 oncoprotein induced transcript 3 [ Homo sapiens (human) ]

Gene ID: 170392, updated on 9-Jun-2025
Official Symbol
OIT3provided by HGNC
Official Full Name
oncoprotein induced transcript 3provided by HGNC
Primary source
HGNC:HGNC:29953
See related
Ensembl:ENSG00000138315 MIM:609330; AllianceGenome:HGNC:29953
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
LZP
Summary
This gene was identified due to its downregulation in hepatocarcinomas. The encoded protein may be involved in liver development and function. [provided by RefSeq, Sep 2016]
Expression
Biased expression in liver (RPKM 29.6), small intestine (RPKM 2.8) and 3 other tissues See more
Orthologs
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See OIT3 in Genome Data Viewer
Location:
10q22.1
Exon count:
9
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (72893739..72933036)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (73765121..73804414)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (74653497..74692794)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene mitochondrial calcium uniporter Neighboring gene microRNA 4676 Neighboring gene uncharacterized LOC124902450 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr10:74516687-74517186 Neighboring gene Sharpr-MPRA regulatory region 7737 Neighboring gene Sharpr-MPRA regulatory region 6662 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:74658515-74658725 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3553 Neighboring gene Sharpr-MPRA regulatory region 12879 Neighboring gene nucleophosmin 1 pseudogene 24 Neighboring gene uncharacterized LOC124902451 Neighboring gene phospholipase A2 group XIIB Neighboring gene H3K27ac hESC enhancer GRCh37_chr10:74741016-74741516 Neighboring gene ribosomal protein L17 pseudogene 50

  • Project title: Tissue-specific circular RNA induction during human fetal development
  • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
  • BioProject: PRJNA270632
  • Publication: PMID 26076956
  • Analysis date: Mon Apr 2 22:54:59 2018

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
Products Interactant Other Gene Complex Source Pubs Description

Markers

Clone Names

  • FLJ39116

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables calcium ion binding IEA
Inferred from Electronic Annotation
more info
 
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
Process Evidence Code Pubs
acts_upstream_of_or_within renal system process IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
is_active_in cell surface IBA
Inferred from Biological aspect of Ancestor
more info
 
is_active_in extracellular space IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in nuclear envelope IEA
Inferred from Electronic Annotation
more info
 
located_in nucleus IEA
Inferred from Electronic Annotation
more info
 
Preferred Names
oncoprotein-induced transcript 3 protein
Names
liver-specific ZP domain-containing protein
liver-specific zona pellucida domain-containing protein

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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.

Genomic

  1. NG_051614.1 RefSeqGene

    Range
    5184..44481
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_152635.3NP_689848.1  oncoprotein-induced transcript 3 protein precursor

    See identical proteins and their annotated locations for NP_689848.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) represents the longer transcript and encodes the protein.
    Source sequence(s)
    AC069548, AY358339
    Consensus CDS
    CCDS7318.1
    UniProtKB/Swiss-Prot
    A0AVP3, Q8N1M8, Q8WWZ8
    Related
    ENSP00000333900.5, ENST00000334011.10
    Conserved Domains (3) summary
    smart00241
    Location:268513
    ZP; Zona pellucida (ZP) domain
    pfam00100
    Location:394513
    Zona_pellucida; Zona pellucida-like domain
    pfam14670
    Location:227262
    FXa_inhibition; Coagulation Factor Xa inhibitory site

RNA

  1. NR_130125.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) lacks an internal exon compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AC069548, AY358339, BC126440

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    72893739..72933036
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    73765121..73804414
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)