RFT1

Protein RFT1 homolog is a protein that in humans is encoded by the RFT1 gene.^[5][6]

AliasesRFT1, CDG1N, RFT1 homolog

External IDsOMIM: 611908; MGI: 3607791; HomoloGene: 5343; GeneCards: RFT1; OMA:RFT1 - orthologs

Chr.Chromosome 3 (human)^[1]

End53,130,453 bp^[1]

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RFT1
Identifiers
Aliases	RFT1, CDG1N, RFT1 homolog
External IDs	OMIM: 611908; MGI: 3607791; HomoloGene: 5343; GeneCards: RFT1; OMA:RFT1 - orthologs
Gene location (Human) Chr. Chromosome 3 (human)[1] Band 3p21.1 Start 53,088,483 bp[1] End 53,130,453 bp[1]
Gene location (Mouse) Chr. Chromosome 14 (mouse)[2] Band 14|14 B Start 30,376,317 bp[2] End 30,413,274 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in gonad body of pancreas islet of Langerhans stromal cell of endometrium appendix right adrenal gland rectum left adrenal gland white blood cell monocyte Top expressed in proximal tubule spermatocyte white adipose tissue adrenal gland hepatobiliary system liver right kidney lens placenta ovary More reference expression data BioGPS n/a
Gene ontology Molecular function lipid transporter activity Cellular component endoplasmic reticulum membrane integral component of membrane membrane Biological process carbohydrate transport glycolipid translocation lipid transport Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 91869 328370 Ensembl ENSG00000163933 ENSMUSG00000052395 UniProt Q96AA3 Q8C3B8 RefSeq (mRNA) NM_052859 NM_177815 RefSeq (protein) NP_443091 NP_808483 Location (UCSC) Chr 3: 53.09 – 53.13 Mb Chr 14: 30.38 – 30.41 Mb PubMed search [3] [4]
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Defects are associated with congenital disorder of glycosylation type 1N.^[6]