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HPA
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  • SUMMARY

  • TISSUE

  • BRAIN

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PROTEIN SUMMARY GENE INFORMATION RNA DATA ANTIBODY DATA
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

FECH
Synonyms
Gene descriptioni

Full gene name according to HGNC.

Ferrochelatase
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Disease related genes
Enzymes
Human disease related genes
Metabolic proteins
Potential drug targets
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 18
Cytoband q21.31
Chromosome location (bp) 57544377 - 57586732
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

5
Ensembl ENSG00000066926 (version 109)
Entrez gene 2235
HGNC HGNC:3647
UniProt P22830 (UniProt - Evidence at protein level)
neXtProt NX_P22830
GeneCards FECH
Antibodypedia FECH antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

Catalyzes the ferrous insertion into protoporphyrin IX.... show less
Molecular function (UniProt)i

Keywords assigned by UniProt to proteins due to their particular molecular function.

Lyase
Biological process (UniProt)i

Keywords assigned by UniProt to proteins because they are involved in a particular biological process.

Heme biosynthesis, Porphyrin biosynthesis
Ligand (UniProt)i

Keywords assigned by UniProt to proteins because they bind, are associated with, or whose activity is dependent of some molecule.

2Fe-2S, Iron, Iron-sulfur, Metal-binding
Gene summary (Entrez)i

Useful information about the gene from Entrez

The protein encoded by this gene is localized to the mitochondrion, where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Mutations in this gene are associated with erythropoietic protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. A pseudogene of this gene is found on chromosome 3.[provided by RefSeq, May 2010]... show less
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Splice variant SwissProt TrEMBL Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
FECH-201
ENSP00000262093
ENST00000262093
P22830
[Direct mapping] Ferrochelatase, mitochondrial
Show all
Enzymes
   ENZYME proteins
   Lyases
Metabolic proteins
   Phobius predicted secreted proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Potential drug targets
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of cofactor/vitamin metabolism
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0004325 [ferrochelatase activity]
GO:0005506 [iron ion binding]
GO:0005515 [protein binding]
GO:0005739 [mitochondrion]
GO:0005743 [mitochondrial inner membrane]
GO:0005759 [mitochondrial matrix]
GO:0006091 [generation of precursor metabolites and energy]
GO:0006779 [porphyrin-containing compound biosynthetic process]
GO:0006783 [heme biosynthetic process]
GO:0008198 [ferrous iron binding]
GO:0008203 [cholesterol metabolic process]
GO:0009416 [response to light stimulus]
GO:0009589 [detection of UV]
GO:0010468 [regulation of gene expression]
GO:0010999 [regulation of eIF2 alpha phosphorylation by heme]
GO:0016020 [membrane]
GO:0016829 [lyase activity]
GO:0020037 [heme binding]
GO:0030218 [erythrocyte differentiation]
GO:0030350 [iron-responsive element binding]
GO:0034379 [very-low-density lipoprotein particle assembly]
GO:0042803 [protein homodimerization activity]
GO:0046501 [protoporphyrinogen IX metabolic process]
GO:0046872 [metal ion binding]
GO:0046906 [tetrapyrrole binding]
GO:0046984 [regulation of hemoglobin biosynthetic process]
GO:0051536 [iron-sulfur cluster binding]
GO:0051537 [2 iron, 2 sulfur cluster binding]
GO:0055072 [iron ion homeostasis]
Show all
423 aa
47.9 kDa
No 0
FECH-202
ENSP00000372326
ENST00000382873
A0A499FJN5
[Direct mapping] Ferrochelatase
Show all
Metabolic proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of cofactor/vitamin metabolism
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0004325 [ferrochelatase activity]
GO:0005743 [mitochondrial inner membrane]
GO:0006779 [porphyrin-containing compound biosynthetic process]
GO:0006783 [heme biosynthetic process]
GO:0016829 [lyase activity]
Show all
351 aa
40.2 kDa
No 0
FECH-207
ENSP00000465363
ENST00000591977
K7EJX5
[Direct mapping] Ferrochelatase
Show all
Metabolic proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of cofactor/vitamin metabolism
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0004325 [ferrochelatase activity]
GO:0005743 [mitochondrial inner membrane]
GO:0006779 [porphyrin-containing compound biosynthetic process]
GO:0006783 [heme biosynthetic process]
GO:0016829 [lyase activity]
Show all
143 aa
16.2 kDa
No 0
FECH-209
ENSP00000466263
ENST00000592699
K7ELX4
[Direct mapping] Ferrochelatase, mitochondrial
Show all
Metabolic proteins
   Phobius predicted secreted proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of cofactor/vitamin metabolism
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0004325 [ferrochelatase activity]
GO:0006779 [porphyrin-containing compound biosynthetic process]
GO:0006783 [heme biosynthetic process]
GO:0016829 [lyase activity]
Show all
326 aa
37 kDa
No 0
FECH-212
ENSP00000498358
ENST00000652755
P22830
[Direct mapping] Ferrochelatase, mitochondrial
Show all
Enzymes
   ENZYME proteins
   Lyases
Metabolic proteins
   Phobius predicted secreted proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Potential drug targets
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of cofactor/vitamin metabolism
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0004325 [ferrochelatase activity]
GO:0005515 [protein binding]
GO:0005739 [mitochondrion]
GO:0005743 [mitochondrial inner membrane]
GO:0005759 [mitochondrial matrix]
GO:0006091 [generation of precursor metabolites and energy]
GO:0006779 [porphyrin-containing compound biosynthetic process]
GO:0006783 [heme biosynthetic process]
GO:0008198 [ferrous iron binding]
GO:0009416 [response to light stimulus]
GO:0016020 [membrane]
GO:0016829 [lyase activity]
GO:0042803 [protein homodimerization activity]
GO:0046501 [protoporphyrinogen IX metabolic process]
GO:0046872 [metal ion binding]
GO:0051536 [iron-sulfur cluster binding]
GO:0051537 [2 iron, 2 sulfur cluster binding]
Show all
429 aa
48.6 kDa
No 0

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