U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

C1orf226 chromosome 1 open reading frame 226 [ Homo sapiens (human) ]

Gene ID: 400793, updated on 5-Aug-2022

Summary

Official Symbol
C1orf226provided by HGNC
Official Full Name
chromosome 1 open reading frame 226provided by HGNC
Primary source
HGNC:HGNC:34351
See related
Ensembl:ENSG00000239887 AllianceGenome:HGNC:34351
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
Expression
Ubiquitous expression in colon (RPKM 4.5), adrenal (RPKM 4.4) and 23 other tissues See more
Orthologs
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See C1orf226 in Genome Data Viewer
Location:
1q23.3
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (162378841..162386812)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (161722817..161730827)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (162348631..162356602)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene nitric oxide synthase 1 adaptor protein Neighboring gene microRNA 556 Neighboring gene Sharpr-MPRA regulatory region 12682 Neighboring gene Sharpr-MPRA regulatory region 4437 Neighboring gene spermatogenesis associated 46 Neighboring gene SH2 domain containing 1B

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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Potential readthrough

Included gene: NOS1AP

Homology

Clone Names

  • FLJ13137, FLJ43132, FLJ55152

General protein information

Preferred Names
uncharacterized protein C1orf226

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_001085375.2NP_001078844.1  uncharacterized protein C1orf226 isoform 2

    See identical proteins and their annotated locations for NP_001078844.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) has multiple differences, compared to variant 1. The resulting protein (isoform 2) has a shorter N-terminus when it is compared to variant 1.
    Source sequence(s)
    AI480219, AK125122, AL512785
    Consensus CDS
    CCDS53422.1
    UniProtKB/Swiss-Prot
    A1L170, B4DF31
    Related
    ENSP00000437071.1, ENST00000458626.4
    Conserved Domains (1) summary
    pfam15429
    Location:1272
    DUF4628; Domain of unknown function (DUF4628)
  2. NM_001135240.3NP_001128712.1  uncharacterized protein C1orf226 isoform 1

    See identical proteins and their annotated locations for NP_001128712.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) encodes the longer protein (isoform 1).
    Source sequence(s)
    AI480219, AK293907, AL512785, DR000934
    Consensus CDS
    CCDS44268.1
    UniProtKB/Swiss-Prot
    A1L170
    Related
    ENSP00000413150.2, ENST00000426197.2
    Conserved Domains (1) summary
    pfam15429
    Location:44315
    DUF4628; Domain of unknown function (DUF4628)

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    162378841..162386812
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    161722817..161730827
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)