SLC35F1

SLC35F1
Identifiers
Aliases	SLC35F1, C6orf169, dJ230I3.1, solute carrier family 35 member F1
External IDs	MGI: 2139810; GeneCards: SLC35F1
Gene location (Human)
Chr.	Chromosome 6 (human)
End	118,317,676 bp
Gene location (Mouse)
Chr.	Chromosome 10 (mouse)
End	52,987,718 bp
RNA expression pattern
	Top expressed in
	ventricular zone; ; endothelial cell; ; Brodmann area 46; ; buccal mucosa cell; ; spinal ganglia; ; parietal lobe; ; middle temporal gyrus; ; postcentral gyrus; ; superior frontal gyrus; ; Brodmann area 23;
	Top expressed in
	olfactory tubercle; ; lateral septal nucleus; ; nucleus accumbens; ; ventricular zone; ; nucleus of stria terminalis; ; piriform cortex; ; ventral tegmental area; ; amygdala; ; supraoptic nucleus; ; globus pallidus;
	More reference expression data
	n/a
Gene ontology
Molecular function	transmembrane transporter activity;
Cellular component	membrane; integral component of membrane;
Biological process	transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
Databases	NCBI: entry; OMA: entry
	222553
	215085
	ENSG00000196376
	ENSMUSG00000038602
	Q5T1Q4
	Q8BGK5
	NM_001029858
	NM_178675
	NP_001025029
	NP_848790
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 35, member F1 is a protein that in humans is encoded by the SLC35F1 gene. The gene is also known as C6orf169 or dJ230I3.1.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000196376 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000038602 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
1 2 "Solute carrier family 35, member F1". Retrieved 2011-12-04.

Sotoodehnia N, Isaacs A, de Bakker PI, Dörr M, Newton-Cheh C, Nolte IM, et al. (December 2010). "Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction". Nature Genetics. 42 (12): 1068–1076. doi:10.1038/ng.716. PMC 3338195. PMID 21076409.
Eijgelsheim M, Newton-Cheh C, Sotoodehnia N, de Bakker PI, Müller M, Morrison AC, et al. (October 2010). "Genome-wide association analysis identifies multiple loci related to resting heart rate". Human Molecular Genetics. 19 (19): 3885–3894. doi:10.1093/hmg/ddq303. PMC 3657480. PMID 20639392.

This article on a gene on human chromosome 6 is a stub. You can help Wikipedia by adding missing information.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000196376 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000038602 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] 1 2 "Solute carrier family 35, member F1". Retrieved 2011-12-04.

SLC35F1

References

Further reading