Solute Carrier Family 35 Member F4

Alternative Names

SLC35F4
C14orf36
FLJ37712

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NCBI Gene ID

341880

Uniprot ID

A4IF30

Length

418,408 bases

No. of Exons

No. of isoforms

Protein Name

Solute carrier family 35 member F4

Molecular Mass

57809 Da

Amino Acid Count

521

Genomic Location

chr14:57,563,920-57,982,327

Gene Map Locus

14q22.3-q23.1

Description

SLC35F4 (Solute Carrier Family 35 Member F4) is a Protein Coding gene. Diseases associated with SLC35F4 include Spinocerebellar Ataxia, Autosomal Recessive 12. [From Genecards]

Epidemiology in the Arab World

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United Arab Emirates

Variant Name	Country	Genomic Location	Clinvar Clinical Significance	CTGA Clinical Significance	Condition(s)	HGVS Expressions	dbSNP	Clinvar
NM_001306087.2:c.588-1934_588-1931dup	United Arab Emirates	NC_000014.9:g.57583366_57583369dup				NM_001306087.2:c.588-1934_588-1931dup; NP_001293016.1:p.?	2308163

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External Links

https://www.genecards.org/cgi-bin/carddisp.pl?gene=slc35f4

Contributors

Pratibha Nair: 15.03.2022

Edit History

Pratibha Nair: 15.03.2022