GMNC
Geminin coiled-coil domain-containing protein 1
Also known as: GEMC1, GEMC1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NCL1
- Gene
- GMNC
- Ensembl
- ENSG00000205835
- Chromosome
- 3
- Canonical length
- 334 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable chromatin binding activity. Predicted to be involved in negative regulation of cell cycle and regulation of DNA-templated DNA replication initiation. Predicted to act upstream of or within several processes, including cerebrospinal fluid circulation; multi-ciliated epithelial cell differentiation; and seminiferous tubule development. Predicted to be located in extracellular region. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
334 residues, UniProt reviewed canonical sequence.
>A6NCL1|GMNC
1 MNTILPCQDQ YFVGGQSYNC PYSTTTSESS VDVSTETWVS FWAAGLLDNR ELQQAPQAQE
61 SFSDSNFPLP DLCSWEEAQL SSQLYRNKQL QDTLVQKEEE LARLHEENNH LRQYLNSALV
121 KCLEEKAKKL LSSDEFSKAY GKFRKGKRKS KEQRYSPAEI PHPKNAKRNL SSEFANCEEQ
181 AGPPVDPWVL QTLGLKDLDT IDDTSSANYS ALASHPRRVA STFSQFPDDA VDYKNIPRED
241 MPIDYRGDRT TPLHSTATHG EDFHILSQLS NPPVGLKTLP YYTAHVSPNK TEMAFSTSLS
301 PHCNVKTHSF HQGQAFVRRD EEGGWKFTWV PKQSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GMNC can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.63
- Highest tissue expression
- 7.6 nTPM
Expression across tissuesHPA
Tissue
- fallopian tube: 7.6 nTPM
- liver: 3.9 nTPM
- choroid plexus: 2.8 nTPM
- kidney: 1.8 nTPM
- testis: 0.9 nTPM
- endometrium: 0.8 nTPM
Single-cell type
- cardiomyocytes: 78 nCPM
- late spermatids: 64 nCPM
- choroid plexus epithelial cells: 57 nCPM
- early spermatids: 56 nCPM
- late primary spermatocytes: 43 nCPM
- early primary spermatocytes: 40 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 5.8 nTPM
- white matter: 4.8 nTPM
- hypothalamus: 3.8 nTPM
- midbrain: 1.6 nTPM
- spinal cord: 1.5 nTPM
- basal ganglia: 1.4 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.55
- gnomAD pLI
- 0.45
- gnomAD missense Z
- 0.53
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cerebrospinal fluid circulation
- cilium assembly
- DNA replication
- multi-ciliated epithelial cell differentiation
- multicellular organism growth
- negative regulation of cell cycle
- positive regulation of transcription by RNA polymerase II
- regulation of DNA-templated DNA replication initiation
- seminiferous tubule development
- single fertilization
- spermatogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Geminin coiled-coil domain-containing protein 1, central coiled-coil domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GMNC as an antibody target. Whether an autoantibody or antibody against GMNC could matter depends on whether native GMNC is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GMNC is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label GMNC as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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