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TMEM183BP transmembrane protein 183B, pseudogene [ Homo sapiens (human) ]

Gene ID: 653659, updated on 22-Sep-2022

Summary

Official Symbol
TMEM183BPprovided by HGNC
Official Full Name
transmembrane protein 183B, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:33205
See related
Ensembl:ENSG00000224831 MIM:611365; AllianceGenome:HGNC:33205
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TMEM183B; C1ORF37DUP; C1orf37-DUP
Summary
This locus was thought to represent a pseudogene of chromosome 1 open reading frame 37 because it is intronless and retains a polyA tail at the 3' end. It does however contain a complete open reading frame that subsequent research has demonstrated to be transcribed in a limited number of human tissues. The encoded protein may represent a transmembrane protein associated with cell membranes and be involved in cell-cell or cell-environment interactions. [provided by RefSeq, Jul 2010]
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Genomic context

See TMEM183BP in Genome Data Viewer
Location:
3q25.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (149982269..149983308, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (152733645..152734684, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (149700056..149701095, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene profilin 2 Neighboring gene uncharacterized LOC646903 Neighboring gene peptidylprolyl isomerase A pseudogene 73 Neighboring gene heterogeneous nuclear ribonucleoprotein A1 pseudogene 24

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • transmembrane protein 183B

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in regulation of protein stability IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Component Evidence Code Pubs
part_of SCF ubiquitin ligase complex IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
located_in membrane IEA
Inferred from Electronic Annotation
more info
 

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.

Genomic

  1. NG_070995.1 

    Range
    101..1140
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    149982269..149983308 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    152733645..152734684 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001079809.2: Suppressed sequence

    Description
    NM_001079809.2: This RefSeq was removed because it is now thought that this gene does not encode a protein.