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

Homo sapiens

Also known as C7orf55; HSPC268

Gene ID: 154791 | Gene type: protein coding

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	Reference	Source
enables protein binding	IPI IPI: Inferred from physical interaction	28719601	GOA

Biological Process GO Annotation	Evidence	Reference	Source
involved in mitochondrial proton-transporting ATP synthase complex assembly	IMP IMP: Inferred from mutant phenotype	28719601	GOA

Cellular Component GO Annotation	Evidence	Reference	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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS04999	FMC1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	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

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