ZFIN ID: ZDB-GENE-080716-17
Gene Name: solute carrier family 35 member A1
Gene Symbol: slc35a1    Nomenclature History

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Previous Names: wu:fl06g06, zgc:194176, zgc:194179

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(Including Attributions)
Gene Type: protein_coding_gene
Location: Chr: 20 Mapping Details/Browsers
Description: Predicted to have sialic acid transmembrane transporter activity. Predicted to be involved in pyrimidine nucleotide-sugar transmembrane transport. Predicted to localize to the integral component of Golgi membrane. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIf. Orthologous to human SLC35A1 (solute carrier family 35 member A1).
Genome Resources: Alliance (1),  Gene:100004536 (1),  Ensembl(GRCz11):ENSDARG00000040180 (2)
GENE EXPRESSION No data available
MUTATIONS AND SEQUENCE TARGETING REAGENTS No data available
PHENOTYPE No data available
DISEASE ASSOCIATED WITH slc35a1 HUMAN ORTHOLOG
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
congenital disorder of glycosylation type IIf Alliance Congenital disorder of glycosylation, type IIf 603585
DISEASE ASSOCIATED WITH slc35a1 VIA EXPERIMENTAL MODELS No data available
PROTEIN FAMILIES, DOMAINS AND SITES
Type InterPro ID Name
Family IPR007271 Nucleotide-sugar transporter
TRANSCRIPTS
Type Name Length (nt) Analysis
mRNA slc35a1-202 (1)    Ensembl 670
Browsers: UCSCNCBIEnsemblZFIN
INTERACTIONS AND PATHWAYS
ANTIBODIES No data available
PLASMIDS No data available
CONSTRUCTS WITH SEQUENCES FROM slc35a1 No data available
MARKER RELATIONSHIPS
slc35a1 Contained in: [Fosmid] CH1073-493K20 (1)
slc35a1 Encodes: [EST] fl06g06
[cDNA] MGC:194176 (1), MGC:194179 (1)
SEQUENCE INFORMATION
Type Accession # Length (bp/aa) Analysis
RNA RefSeq:NM_001128811 (1)
Genomic GenBank:CABZ01077208 (1) 65054 bp
Select Tool
Polypeptide UniProtKB:B3DIQ6 (1) 337 aa
Sequence Information (all 17)
ORTHOLOGY for slc35a1 ( Chr: 20 )
CITATIONS (15)