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HCM1 Hcm1p [ Saccharomyces cerevisiae S288C ]

Gene ID: 850429, updated on 4-Feb-2026
Official Symbol
HCM1
Official Full Name
Hcm1p
Primary source
SGD:S000000661
Locus tag
YCR065W
See related
AllianceGenome:SGD:S000000661; FungiDB:YCR065W; VEuPathDB:YCR065W
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Saccharomyces cerevisiae S288C (strain: S288C)
Lineage
Eukaryota; Fungi; Dikarya; Ascomycota; Saccharomycotina; Saccharomycetes; Saccharomycetales; Saccharomycetaceae; Saccharomyces
Summary
Enables DNA-binding transcription factor activity and mitochondrial transcription factor activity. Involved in several processes, including cellular response to oxidative stress; regulation of DNA-templated transcription; and spindle pole body organization. Located in chromatin; cytoplasm; and nucleus. Is active in mitochondrion. Human ortholog(s) of this gene implicated in blepharophimosis, ptosis, and epicanthus inversus syndrome; lung non-small cell carcinoma; primary ciliary dyskinesia 43; primary ovarian insufficiency 3; and type 2 diabetes mellitus. Orthologous to several human genes including FOXA2 (forkhead box A2); FOXD2 (forkhead box D2); and FOXJ1 (forkhead box J1). [provided by Alliance of Genome Resources, Jul 2025]
Orthologs
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See HCM1 in Genome Data Viewer
Location:
chromosome: III
Exon count:
1
Sequence:
Chromosome: III; NC_001135.5 (229310..231004)

Chromosome III - NC_001135.5Genomic Context describing neighboring genes Neighboring gene tRNA-Ser Neighboring gene U2 snRNP complex subunit BUD31 Neighboring gene E3 ubiquitin-protein ligase RAD18 Neighboring gene GTPase-activating protein SED4

Genomic Sequence:
NC_001135.5

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
Products Interactant Other Gene Complex Source Pubs Description

Gene Ontology Provided by SGD

Component Evidence Code Pubs
located_in chromatin IDA
Inferred from Direct Assay
more info
PubMed 
located_in cytoplasm IDA
Inferred from Direct Assay
more info
PubMed 
located_in cytoplasm IEA
Inferred from Electronic Annotation
more info
 
is_active_in mitochondrion IDA
Inferred from Direct Assay
more info
PubMed 
is_active_in nucleus IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in nucleus IDA
Inferred from Direct Assay
more info
PubMed 
located_in nucleus IEA
Inferred from Electronic Annotation
more info
 
Preferred Names
Hcm1p
NP_009991.2
  • Forkhead transcription factor; drives S-phase activation of genes involved in chromosome segregation, spindle dynamics, budding; also activates genes involved in respiration, use of alternative energy sources, NAD synthesis, oxidative stress resistance; regulated by cell wall integrity checkpoint; key factor in early adaptation to nutrient deficiency and diauxic shift; suppressor of calmodulin mutants with specific SPB assembly defects; ortholog of C. elegans lifespan regulator PHA-4

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Genome Annotation

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

Reference assembly

Genomic

  1. NC_001135.5 Reference assembly

    Range
    229310..231004
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001178776.1NP_009991.2  Hcm1p

    See identical proteins and their annotated locations for NP_009991.2

    Status: REVIEWED

    UniProtKB/Swiss-Prot
    D6VR68, P25364
    UniProtKB/TrEMBL
    A6ZTN9, B5VEZ6, C7GUY0
    Conserved Domains (1) summary
    COG5025
    Location:20564
    COG5025; Transcription factor of the Forkhead/HNF3 family [Transcription]