FAM155A

NALF1
Identifiers
Aliases	NALF1, family with sequence similarity 155 member A, NLF-1, NALCN channel auxiliary factor 1, FAM155A
External IDs	MGI: 2142765 HomoloGene: 83472 GeneCards: NALF1
Gene location (Human)
Chr.	Chromosome 13 (human)[1]
End	107,867,496 bp[1]
Gene location (Mouse)
Chr.	Chromosome 8 (mouse)[2]
End	9,821,161 bp[2]
RNA expression pattern
	Top expressed in
	endothelial cell; ; Brodmann area 23; ; middle temporal gyrus; ; amniotic fluid; ; postcentral gyrus; ; entorhinal cortex; ; superior frontal gyrus; ; Brodmann area 46; ; cerebellar vermis; ; frontal pole;
	Top expressed in
	subiculum; ; piriform cortex; ; dorsomedial hypothalamic nucleus; ; ventral tegmental area; ; mammillary body; ; ventromedial nucleus; ; medial dorsal nucleus; ; medial geniculate nucleus; ; suprachiasmatic nucleus; ; pineal gland;
	More reference expression data
	n/a
Gene ontology
Molecular function	stretch-activated, cation-selective, calcium channel activity;
Cellular component	membrane; integral component of membrane; plasma membrane;
Biological process	calcium ion import across plasma membrane;
	Sources:Amigo / QuickGO
Orthologs
	728215
	270028
	ENSG00000204442
	ENSMUSG00000079157
	B1AL88
	Q8CCS2
	NM_001080396
	NM_173446; NM_001347127
	NP_001073865
	NP_001334056; NP_775622
	Wikidata
View/Edit Human	View/Edit Mouse

Family with sequence similarity 155, member A is a protein that in humans is encoded by the FAM155A gene. [5]

References

GRCh38: Ensembl release 89: ENSG00000204442 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000079157 - 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.
"Entrez Gene: Family with sequence similarity 155, member A". Retrieved 2013-11-26.

Anney RJ, Lasky-Su J, O'Dúshláine C, Kenny E, Neale BM, Mulligan A, et al. (December 2008). "Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study". American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 147B (8): 1369–1378. doi:10.1002/ajmg.b.30871. PMID 18951430. S2CID 30325260.
Cross-Disorder Group of the Psychiatric Genomics Consortium (April 2013). "Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis". Lancet. 381 (9875): 1371–1379. doi:10.1016/S0140-6736(12)62129-1. PMC 3714010. PMID 23453885.
Wang K, Zhang H, Bloss CS, Duvvuri V, Kaye W, Schork NJ, et al. (September 2011). "A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa". Molecular Psychiatry. 16 (9): 949–959. doi:10.1038/mp.2010.107. PMC 3859494. PMID 21079607.
Li SH, McInnis MG, Margolis RL, Antonarakis SE, Ross CA (June 1993). "Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms". Genomics. 16 (3): 572–579. doi:10.1006/geno.1993.1232. PMID 8325628.
Terracciano A, Tanaka T, Sutin AR, Sanna S, Deiana B, Lai S, et al. (November 2010). "Genome-wide association scan of trait depression". Biological Psychiatry. 68 (9): 811–817. doi:10.1016/j.biopsych.2010.06.030. PMC 2955852. PMID 20800221.

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