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GREP1 glycine rich extracellular protein 1 [ Homo sapiens (human) ]

Gene ID: 283875, updated on 15-Dec-2021

Summary

Official Symbol
GREP1provided by HGNC
Official Full Name
glycine rich extracellular protein 1provided by HGNC
Primary source
HGNC:HGNC:27549
See related
Ensembl:ENSG00000262152
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
LINC00514; LA16c-380H5.1; LA16c-380H5.3
Expression
Low expression observed in reference dataset See more
Orthologs
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Genomic context

See GREP1 in Genome Data Viewer
Location:
16p13.3
Exon count:
35
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 16 NC_000016.10 (2988262..3002011)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (3039055..3044510)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene kringle containing transmembrane protein 2 Neighboring gene progestin and adipoQ receptor family member 4 Neighboring gene protein kinase, membrane associated tyrosine/threonine 1 Neighboring gene Sharpr-MPRA regulatory region 11969 Neighboring gene uncharacterized LOC107984895 Neighboring gene Sharpr-MPRA regulatory region 8596

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

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

General gene information

Markers

Homology

Clone Names

  • FLJ46402

General protein information

Preferred Names
glycine rich extracellular protein 1
Names
long intergenic non-protein coding RNA 514

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_001396456.1NP_001383385.1  glycine rich extracellular protein 1 isoform 1 precursor

    Status: VALIDATED

    Source sequence(s)
    AC004233
  2. NM_001396457.1NP_001383386.1  glycine rich extracellular protein 1 isoform 2 precursor

    Status: VALIDATED

    Source sequence(s)
    AC004233
  3. NM_001396458.1NP_001383387.1  glycine rich extracellular protein 1 isoform 3 precursor

    Status: VALIDATED

    Source sequence(s)
    AC004233
    Related
    ENSP00000488558.1, ENST00000573315.2
  4. NM_001396459.1NP_001383388.1  glycine rich extracellular protein 1 isoform 4

    Status: VALIDATED

    Source sequence(s)
    AC004233
  5. NM_001396460.1NP_001383389.1  glycine rich extracellular protein 1 isoform 5

    Status: VALIDATED

    Source sequence(s)
    AC004233
  6. NM_001396461.1NP_001383390.1  glycine rich extracellular protein 1 isoform 6

    Status: VALIDATED

    Source sequence(s)
    AC004233

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p13 Primary Assembly

    Range
    2988262..3002011
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_033861.1: Suppressed sequence

    Description
    NR_033861.1: This RefSeq was removed because currently there is insufficient support for the transcript.
  2. NR_110947.1: Suppressed sequence

    Description
    NR_110947.1: This RefSeq was removed because currently there is insufficient support for the transcript.
  3. NR_110948.1: Suppressed sequence

    Description
    NR_110948.1: This RefSeq was removed because currently there is insufficient support for the transcript.
  4. NR_110949.1: Suppressed sequence

    Description
    NR_110949.1: This RefSeq was removed because currently there is insufficient support for the transcript.
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