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TIMP4 TIMP metallopeptidase inhibitor 4 [ Piliocolobus tephrosceles (Ugandan red Colobus) ]

Gene ID: 111546913, updated on 15-Mar-2024

Summary

Gene symbol
TIMP4
Gene description
TIMP metallopeptidase inhibitor 4
See related
Ensembl:ENSPTEG00000037942
Gene type
protein coding
RefSeq status
MODEL
Organism
Piliocolobus tephrosceles
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Colobinae; Piliocolobus
Orthologs
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Genomic context

Location:
chromosome: 2
Exon count:
5
Annotation release Status Assembly Chr Location
102 current ASM277652v3 (GCF_002776525.3) 2 NC_045435.1 (48938006..48944223)
100 previous assembly ASM277652v1 (GCF_002776525.1) Unplaced Scaffold NW_019317444.1 (561872..568089)

Chromosome 2 - NC_045435.1Genomic Context describing neighboring genes Neighboring gene peroxisome proliferator activated receptor gamma Neighboring gene glutathione S-transferase Mu 1 pseudogene Neighboring gene synapsin II Neighboring gene actin-related protein 2/3 complex subunit 3-like Neighboring gene actin, cytoplasmic 2-like

Genomic regions, transcripts, and products

General protein information

Preferred Names
metalloproteinase inhibitor 4

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Piliocolobus tephrosceles Annotation Release 102 details...Open this link in a new tab

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

Reference ASM277652v3

Genomic

  1. NC_045435.1 Reference ASM277652v3

    Range
    48938006..48944223
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_023218415.1XP_023074183.1  metalloproteinase inhibitor 4

    UniProtKB/TrEMBL
    A0A8C9ISP7
    Related
    ENSPTEP00000041415.1, ENSPTET00000055328.1
    Conserved Domains (1) summary
    cd03585
    Location:30213
    NTR_TIMP; NTR domain, TIMP subfamily; TIMPs, or tissue inibitors of metalloproteases, are essential regulators of extracellular matrix turnover and remodeling. They form complexes with matrix metalloproteases (MMPs) and inactivate them irreversibly by ...