AFG3L2

GENE INFORMATION

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Gene name

AFG3L2 (HGNC Symbol)

Synonyms

SCA28

Description

AFG3 ATPase family member 3-like 2 (S. cerevisiae) (HGNC Symbol)

Entrez gene summary

This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008]

Chromosome

18 (Chromosome progress)

Cytoband

p11.21

Chromosome location (bp)

12328943 - 12377313

Ensembl

ENSG00000141385 (version 73.37)

Entrez gene

10939

UniProt

Q9Y4W6 (UniProt - Evidence at protein level)

neXtProt

NX_Q9Y4W6

Antibodypedia

AFG3L2 antibodies
 

PROTEIN VIEW

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AFG3L2-001
 
AFG3L2-002
 
 
 
 
 

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)

AFG3L2-001 ENSP00000269143
ENST00000269143
Q9Y4W6
Show all »
Show » Show » 797 88.6 No 2
AFG3L2-002 ENSP00000467236
ENST00000590811
Show » Show » 209 23.5 No 2