XB-FEAT-992966: Difference between revisions
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= | = iba57 = | ||
This is the community wiki page for the gene '' | This is the community wiki page for the gene ''iba57'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
08/03/2015 Human name has changed for Entrez Gene: 200205. From IBA57, iron-sulfur cluster assembly homolog (S. cerevisiae) to IBA57 homolog, iron-sulfur cluster assembly | |||
= nomenclature changes= | |||
12/18/2017 | |||
Human name has changed for Entrez Gene: 200205. From IBA57 homolog, iron-sulfur cluster assembly to IBA57, iron-sulfur cluster assembly | |||
=NCBI Summary= | |||
The protein encoded by this gene localizes to the mitochondrion and is part of the iron-sulfur cluster assembly pathway. The encoded protein functions late in the biosynthesis of mitochondrial 4Fe-4S proteins. Defects in this gene have been associated with autosomal recessive spastic paraplegia-74 and with multiple mitochondrial dysfunctions syndrome-3. Two transcript variants encoding different isoforms have been found for this gene. The smaller isoform is not likely to be localized to the mitochondrion since it lacks the amino-terminal transit peptide. [provided by RefSeq, Jul 2015] | |||
Latest revision as of 08:29, 3 January 2018
iba57
This is the community wiki page for the gene iba57 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
08/03/2015 Human name has changed for Entrez Gene: 200205. From IBA57, iron-sulfur cluster assembly homolog (S. cerevisiae) to IBA57 homolog, iron-sulfur cluster assembly
nomenclature changes
12/18/2017
Human name has changed for Entrez Gene: 200205. From IBA57 homolog, iron-sulfur cluster assembly to IBA57, iron-sulfur cluster assembly
NCBI Summary
The protein encoded by this gene localizes to the mitochondrion and is part of the iron-sulfur cluster assembly pathway. The encoded protein functions late in the biosynthesis of mitochondrial 4Fe-4S proteins. Defects in this gene have been associated with autosomal recessive spastic paraplegia-74 and with multiple mitochondrial dysfunctions syndrome-3. Two transcript variants encoding different isoforms have been found for this gene. The smaller isoform is not likely to be localized to the mitochondrion since it lacks the amino-terminal transit peptide. [provided by RefSeq, Jul 2015]