FAM155A

Protein-coding gene in the species Homo sapiens
NALF1
Identifiers
AliasesNALF1, family with sequence similarity 155 member A, NLF-1, NALCN channel auxiliary factor 1, FAM155A
External IDsMGI: 2142765; HomoloGene: 83472; GeneCards: NALF1; OMA:NALF1 - orthologs
Gene location (Human)
Chromosome 13 (human)
Chr.Chromosome 13 (human)[1]
Chromosome 13 (human)
Genomic location for NALF1
Genomic location for NALF1
Band13q33.3Start107,163,510 bp[1]
End107,867,496 bp[1]
Gene location (Mouse)
Chromosome 8 (mouse)
Chr.Chromosome 8 (mouse)[2]
Chromosome 8 (mouse)
Genomic location for NALF1
Genomic location for NALF1
Band8|8 A1.1Start9,255,902 bp[2]
End9,821,161 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • endothelial cell

  • Brodmann area 23

  • buccal mucosa cell

  • middle temporal gyrus

  • amniotic fluid

  • lateral nuclear group of thalamus

  • primary visual cortex

  • postcentral gyrus

  • entorhinal cortex

  • superior frontal gyrus
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
BioGPS
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
SpeciesHumanMouse
Entrez

728215

270028

Ensembl

ENSG00000204442

ENSMUSG00000079157

UniProt

B1AL88

Q8CCS2

RefSeq (mRNA)

NM_001080396

NM_173446
NM_001347127

RefSeq (protein)

NP_001073865

NP_001334056
NP_775622

Location (UCSC)Chr 13: 107.16 – 107.87 MbChr 8: 9.26 – 9.82 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000204442 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000079157 – 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. ^ "Entrez Gene: Family with sequence similarity 155, member A". Retrieved 2013-11-26.

Further reading

  • 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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