Selected-GenAtlas references	SOURCE	GeneCards	NCBI Gene	Swiss-Prot	Orphanet	Ensembl
	HGNC	UniGene	Nucleotide	OMIM		UCSC

Home Page

FLASH GENE

Symbol

ALAS2

contributors: mct - updated : 09-07-2012

HGNC name	aminolevulinate, delta-, synthase 2
HGNC id	397

FLASH GENE DNA RNA EXPRESSION PROTEIN DISORDER ANIMAL & CELL MODELS

EXPRESSION

Type

expressed in	(based on citations)
organ(s)	System Organ level 1 Organ level 2 Organ level 3 Organ level 4 Level Pubmed Species Stage Rna symbol Digestive liver         Homo sapiens Fetal

tissue

System Tissue Tissue level 1 Tissue level 2 Level Pubmed Species Stage Rna symbol Blood / hematopoietic bone marrow       Homo sapiens Adult

cell lineage	erythroid cells
cell lines
fluid/secretion

at STAGE

PROTEIN

PHYSICAL PROPERTIES

STRUCTURE

motifs/domains

C-terminal ALAS2 AAs, identifying a region critical for the formation of an ALAS2·succinyl-CoA synthetase (SCS) enzyme complex that presumably is required for normal heme biosynthesis in mitochondria

HOMOLOGY

interspecies

homolog to murine Alas2

Homologene

FAMILY

class II of pyridoxal phosphate dependent aminotransferase family

CATEGORY

enzyme

SUBCELLULAR LOCALIZATION	intracellular
	intracellular,cytoplasm,organelle,mitochondria,inner
	intracellular,cytoplasm,organelle,mitochondria,matrix
	intracellular,nucleus
text	appears to be localized to the matrix side of the inner mitochondrial membrane in erythroid cells

basic FUNCTION	aminolevulinate, delta-,synthase 2, catalyzing the first step of porphyrin biosynthesis
	probable role of an ALAS2-succinyl-CoA synthetase complex in the regulation of erythroid heme biosynthesis
	rate-limiting enzyme for erythroid heme biosynthesis

CELLULAR PROCESS

PHYSIOLOGICAL PROCESS

PATHWAY

metabolism

porphyrin/heme

signaling

a component

INTERACTION

DNA

RNA

small molecule	cofactor,
	pyridoxal phosphate

protein

unique interaction of SUCLA2 with ALAS2 is involved in an important erythroid-specific function

cell & other

REGULATION

induced by	TGF-beta1, which may contribute to terminal differentiation of erythroid cells

ASSOCIATED DISORDERS

corresponding disease(s)

ASB , EPPX

related resource

MITOP database

Other morbid association(s)

Type Gene Modification Chromosome rearrangement Protein expression Protein Function constitutional germinal mutation     gain of function ALAS2 gain-of-function mutation contributes to the CEP (congenital erythropoietic porphyria) phenotype underscores the importance of modifier genes underlying CEP

Susceptibility

Variant & Polymorphism

Candidate gene

Marker

Therapy target

ANIMAL & CELL MODELS