HEXB

GENE INFORMATION

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Gene name

HEXB

Synonyms

Description

Hexosaminidase B (beta polypeptide) (HGNC Symbol)

Entrez gene summary

Hexosaminidase B is the beta subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Beta subunit gene mutations lead to Sandhoff disease (GM2-gangliosidosis type II). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]

Chromosome

5

Cytoband

q13.3

Chromosome location (bp)

74640023 - 74722647

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000049860 (version 78.38)

Entrez gene

3074

UniProt

P07686 (UniProt - Evidence at protein level)

neXtProt

NX_P07686

Antibodypedia

HEXB antibodies
 

PROTEIN VIEW

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HEXB-001
 
HEXB-002
 
HEXB-007
 
HEXB-009
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

HEXB-001 ENSP00000261416
ENST00000261416
P07686
Show all »
Show » Show » 556 63.1 Yes 0
HEXB-002 ENSP00000426285
ENST00000511181
Q5URX0
Show all »
Show » Show » 331 38.3 No 0
HEXB-007 ENSP00000423713
ENST00000513336
D6REQ8
Show all »
Show » Show » 202 23.1 No 0
HEXB-009 ENSP00000424939
ENST00000509579
D6REQ8
Show all »
Show » 35 4.2 No 0