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COLQ collagen like tail subunit of asymmetric acetylcholinesterase [ Felis catus (domestic cat) ]

Gene ID: 101093134, updated on 14-May-2025
Official Symbol
COLQ
Official Full Name
collagen like tail subunit of asymmetric acetylcholinesterase
Primary source
VGNC:VGNC:61073
See related
Ensembl:ENSFCTG00005025219
Gene type
protein coding
RefSeq status
MODEL
Organism
Felis catus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Carnivora; Feliformia; Felidae; Felinae; Felis
Orthologs
human mouse all
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See COLQ in Genome Data Viewer
Location:
chromosome: C2
Exon count:
18
Annotation release Status Assembly Chr Location
105 current F.catus_Fca126_mat1.0 (GCF_018350175.1) C2 NC_058376.1 (132505730..132565923, complement)
104 previous assembly Felis_catus_9.0 (GCF_000181335.3) C2 NC_018731.3 (135045497..135141645, complement)

Chromosome C2 - NC_058376.1Genomic Context describing neighboring genes Neighboring gene SH3 domain binding protein 5 Neighboring gene uncharacterized LOC123380137 Neighboring gene methyltransferase 6, tRNA N3-cytidine Neighboring gene uncharacterized LOC123380138 Neighboring gene ELL associated factor 1 Neighboring gene 2-hydroxyacyl-CoA lyase 1 Neighboring gene biotinidase Neighboring gene ankyrin repeat domain 28 Neighboring gene WW domain-binding protein 11-like

Go to nucleotide: Graphics FASTA GenBank

Related articles in PubMed

  1. COLQ variant associated with Devon Rex and Sphynx feline hereditary myopathy. Gandolfi B, et al. Anim Genet, 2015 Dec. PMID 26374066, Free PMC Article
  2. A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome. Abitbol M, et al. PLoS One, 2015. PMID 26327126, Free PMC Article
  3. TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations. Tang H, et al. Bioinformatics, 2019 Feb 1. PMID 30032202, Free PMC Article

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. reported in Sphynx and Devon Rex breeds is a CMS caused by a unique c.1190G>A missense mutation in COLQ, presumably transmitted through a founder effect
    Title: A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome.
  2. association between the COLQ variant and congenital myasthenic syndrome
    Title: COLQ variant associated with Devon Rex and Sphynx feline hereditary myopathy.
Submit: New GeneRIF Correction

Homology

Gene Ontology Provided by RefSeq

Function Evidence Code Pubs
enables heparin binding IEA
Inferred from Electronic Annotation
more info
 PubMed 
Preferred Names
acetylcholinesterase collagenic tail peptide

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RefSeqs of Annotated Genomes: Felis catus Annotation Release 105 details...Open this link in a new tab

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

Reference F.catus_Fca126_mat1.0 Primary Assembly

Genomic

  1. NC_058376.1 Reference F.catus_Fca126_mat1.0 Primary Assembly

    Range
    132505730..132565923 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_003992132.4 → XP_003992181.2  acetylcholinesterase collagenic tail peptide isoform X1

    UniProtKB/TrEMBL
    A0A2I2U9H1
    Related
    ENSFCTP00005050763.1, ENSFCTT00005071551.1
    Conserved Domains (1) summary
    pfam13948
    Location:375 → 400
    DUF4215; Domain of unknown function (DUF4215)

  2. XM_003992134.5 → XP_003992183.2  acetylcholinesterase collagenic tail peptide isoform X2

    UniProtKB/TrEMBL
    M3WEV2
    Related
    ENSFCTP00005050921.1, ENSFCTT00005071805.1
    Conserved Domains (1) summary
    TIGR02232
    Location:362 → 387
    myxo_disulf_rpt; Myxococcus cysteine-rich repeat
Nucleotide Protein
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