Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
80255
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 35 member F5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC35F5
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q14.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021638 hsa-miR-142-3p Microarray 17612493
MIRT029701 hsa-miR-26b-5p Microarray 19088304
MIRT699338 hsa-miR-106a-5p HITS-CLIP 22927820
MIRT439608 hsa-miR-106b-5p HITS-CLIP 22927820
MIRT699337 hsa-miR-17-5p HITS-CLIP 22927820
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619997 23617 ENSG00000115084
Protein
UniProt ID Q8WV83
Protein name Solute carrier family 35 member F5 (Hepatitis C virus NS5A-transactivated protein 3) (HCV NS5A-transactivated protein 3)
Protein function Putative solute transporter.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00892 EamA 225 316 EamA-like transporter family Family
Tissue specificity TISSUE SPECIFICITY: Expressed in colorectal cancer cells. {ECO:0000269|PubMed:16477629}.
Sequence
MVPPRRHRGAGRPGVLSSSPPFRLRSAKFSGIALEDLRRALKTRLQMVCVFVMNRMNSQN
SGFTQRRRMALGIVILLLVDVIWVASSELTSYVFTQYNKPFFSTFAKTSMFVLYLLGFII
WKPWRQQCTRGLRGKHAAFFADAEGYFAACTTDTTMNSSLSEPLYVPVKFHDLPSEKPES
TNIDTEKTPKKSRVRFSNIMEIRQLPSSHALEAKLSRMSYPVKEQESILKTVGKLTATQV
AKISFFFCFVWFLANLSYQEALSDTQVAIVNILSSTSGLFTLILAAVFPSNSGDRFTLSK
LLAVILSIGGVVLVNL
AGSEKPAGRDTVGSIWSLAGAMLYAVYIVMIKRKVDREDKLDIP
MFFGFVGLFNLLLLWPGFFLLHYTGFEDFEFPNKVVLMCIIINGLIGTVLSEFLWLWGCF
LTSSLIGTLALSLTIPLSIIADMCMQKVQFSWLFFAGAIPVFFSFFIVTLLCHYNNWDPV
MVGIRRIFAFICRKHRIQRVPEDSEQCESLISMHSVSQEDGAS
Sequence length 523
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Multiple Congenital Anomalies multiple congenital anomalies/dysmorphic syndrome GenCC