FMC1 - formation of mitochondrial complex V assembly factor 1 homolog Gene

Also Known as C7orf55; HSPC268

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 154791

About FMC1

This gene has 5 transcripts (splice variants) and 163 orthologues. Broad expression in testis (RPKM 11.0), kidney (RPKM 8.7) and 25 other tissues.

Summary

Involved in mitochondrial proton-transporting ATP Synthase complex assembly. Located in mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

FMC1 Products (1)

mRNA Protein Name
NM_197964.5 NP_932068.2 protein FMC1 homolog

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
28719601 GOA
Biological Process GO Annotation Evidence References Source
involved in mitochondrial proton-transporting ATP synthase complex assembly IMP
IMP: Inferred from mutant phenotype
28719601 GOA
Cellular Component GO Annotation Evidence References Source
located in mitochondrion IDA
IDA: Inferred from direct assay
28719601 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

protein FMC1 homolog

  • ATP synthase assembly factor FMC1, mitochondrial

Related Diseases

Diseases Alias
Syringomyelia

  • Hydromyelia
Neuropathy, Ataxia, And Retinitis Pigmentosa

  • Narp Syndrome

  • NARP

  • Neurogenic Muscle Weakness, Ataxia, And Retinitis Pigmentosa

  • Neurogenic Muscle Weakness-Ataxia-Retinitis Pigmentosa Syndrome

  • Neuropathy-Ataxia-Retinitis Pigmentosa Syndrome

  • Neuropathy, Ataxia And Retinitis Pigmentosa

  • Neuropathy Ataxia Retinitis Pigmentosa Syndrome

  • Neuropathy, Ataxia, And Retinitis Pigmentos

  • Neuropathy Ataxia And Retinitis Pigmentosa

  • Neuropathy, Ataxia, Retinitis Pigmentosa

  • Neuropathy Ataxia And Retinis Pigmentosa

  • Narp - [Neuropathy, Ataxia And Retinitis Pigmentosa] Syndrome
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS04999 FMC1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus FMC1 RGD RGD:1559476
Mus musculus FMC1 MGD MGI:1913367
Bos taurus FMC1 VGNC VGNC:107224
Others FMC1 NCBI