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TREML3P triggering receptor expressed on myeloid cells like 3, pseudogene [ Homo sapiens (human) ]

Gene ID: 340206, updated on 25-Oct-2022

Summary

Official Symbol
TREML3Pprovided by HGNC
Official Full Name
triggering receptor expressed on myeloid cells like 3, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:30806
See related
Ensembl:ENSG00000290563 MIM:609716; AllianceGenome:HGNC:30806
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TLT3; TREML3
Summary
TREML3 is located in a gene cluster on chromosome 6 with the single Ig variable (IgV) domain activating receptors TREM1 (MIM 605085) and TREM2 (MIM 605086), but it has distinct structural and functional properties (Allcock et al., 2003 [PubMed 12645956]).[supplied by OMIM, Mar 2008]
Expression
Low expression observed in reference dataset See more
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Genomic context

See TREML3P in Genome Data Viewer
Location:
6p21.1
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (41208554..41217947, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (41037099..41046492, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (41176292..41185685, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986595 Neighboring gene triggering receptor expressed on myeloid cells like 2 Neighboring gene uncharacterized LOC105375055 Neighboring gene triggering receptor expressed on myeloid cells like 4

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

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.

RNA

  1. NR_027256.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL391903
    Related
    ENST00000564680.5

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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    41208554..41217947 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    41037099..41046492 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)