SLC71A2

SLC71A2
Identifiers
Aliases	SLC71A2, hippocampus abundant transcript-like protein 1, hippocampus abundant transcript-like 1, Major facilitator superfamily domain containing 14B, HIATL1
External IDs	MGI: 1913881; GeneCards: SLC71A2
Gene location (Human)
Chr.	Chromosome 9 (human)
End	94,461,042 bp
Gene location (Mouse)
Chr.	Chromosome 13 (mouse)
End	65,260,789 bp
RNA expression pattern
	Top expressed in
	skin of arm; ; gingival epithelium; ; secondary oocyte; ; mucosa of ileum; ; pancreatic epithelial cell; ; palpebral conjunctiva; ; monocyte; ; epithelium of nasopharynx; ; tibia; ; skin of thigh;
	Top expressed in
	granulocyte; ; skin of external ear; ; pineal gland; ; skin of back; ; molar; ; stroma of bone marrow; ; olfactory epithelium; ; atrium; ; left colon; ; fetal liver hematopoietic progenitor cell;
	More reference expression data
	n/a
Gene ontology
Molecular function	transporter activity;
Cellular component	membrane; integral component of membrane;
Biological process	transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
Databases	NCBI: entry; OMA: entry
	84641
	66631
	ENSG00000148110
	ENSMUSG00000038212
	Q5SR56
	Q8CIA9
	NM_032558
	NM_001083901; NM_133680
	NP_115947
	NP_001077370; NP_598441
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 71 member 2 is a protein that in humans is encoded by the gene SLC71A2 (previously MFSD14B and HIATL1). It has previously been described as an atypical solute carrier of MFS type. It is predicted to be located in intracellular membranes.

MFSD14B forms a cluster with AMTF1, together with MFSD9, MFSD10 and MFSD14A.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000148110 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000038212 – 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.
↑ Perland E, Fredriksson R (March 2017). "Classification Systems of Secondary Active Transporters". Trends in Pharmacological Sciences. 38 (3): 305–315. doi:10.1016/j.tips.2016.11.008. PMID 27939446.
↑ Lekholm E, Perland E, Eriksson MM, Hellsten SV, Lindberg FA, Rostami J, et al. (2017). "Putative Membrane-Bound Transporters MFSD14A and MFSD14B Are Neuronal and Affected by Nutrient Availability". Frontiers in Molecular Neuroscience. 10 11. doi:10.3389/fnmol.2017.00011. PMC 5263138. PMID 28179877.
↑ Perland E, Bagchi S, Klaesson A, Fredriksson R (September 2017). "Characteristics of 29 novel atypical solute carriers of major facilitator superfamily type: evolutionary conservation, predicted structure and neuronal co-expression". Open Biology. 7 (9) 170142. doi:10.1098/rsob.170142. PMC 5627054. PMID 28878041.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000148110 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000038212 – 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.

[5] Perland E, Fredriksson R (March 2017). "Classification Systems of Secondary Active Transporters". Trends in Pharmacological Sciences. 38 (3): 305–315. doi:10.1016/j.tips.2016.11.008. PMID 27939446.

[6] Lekholm E, Perland E, Eriksson MM, Hellsten SV, Lindberg FA, Rostami J, et al. (2017). "Putative Membrane-Bound Transporters MFSD14A and MFSD14B Are Neuronal and Affected by Nutrient Availability". Frontiers in Molecular Neuroscience. 10 11. doi:10.3389/fnmol.2017.00011. PMC 5263138. PMID 28179877.

[7] Perland E, Bagchi S, Klaesson A, Fredriksson R (September 2017). "Characteristics of 29 novel atypical solute carriers of major facilitator superfamily type: evolutionary conservation, predicted structure and neuronal co-expression". Open Biology. 7 (9) 170142. doi:10.1098/rsob.170142. PMC 5627054. PMID 28878041.