FAM155A

FAM155A
Identifikatori
Aliasi	NALF1
Vanjski ID-jevi	MGI: 2142765 HomoloGene: 83472 GeneCards: NALF1
Lokacija gena (čovjek) Hrom. Hromosom 13 (čovjek) Bend 13q33.3 Početak 107,163,510 bp Kraj 107,867,496 bp
Lokacija gena (miš) Hrom. Hromosom 8 (miš) Bend 8|8 A1.1 Početak 9,255,902 bp Kraj 9,821,161 bp
Ontologija gena Molekularna funkcija • stretch-activated, cation-selective, calcium channel activity Ćelijska komponenta • membrana • integral component of membrane • ćelijska membrana Biološki proces • calcium ion import across plasma membrane Izvori:Amigo / QuickGO
Ortolozi
Vrste	Čovjek	Miš
Entrez	728215	270028
Ensembl	ENSG00000204442	ENSMUSG00000079157
UniProt	B1AL88	Q8CCS2
RefSeq (mRNK)	NM_001080396	NM_173446 NM_001347127
RefSeq (bjelančevina)	NP_001073865	NP_001334056 NP_775622
Lokacija (UCSC)	Chr 13: 107.16 – 107.87 Mb	Chr 8: 9.26 – 9.82 Mb
PubMed pretraga
Wikipodaci
Pogledaj/uredi – čovjek Pogledaj/uredi – miš

Član A porodice proteina sa sličnošću sekvence 155 je protein koji je kod ljudi kodiran genom FAM155A.

Aminokiselinska sekvenca

Dužina polipeptidnog lanca je 458 aminokiselina, a molekulska težina 51.493 Da.

Simboli

C: Cistein
D: Asparaginska kiselina
E: Glutaminska kiselina
F: Fenilalanin
G: Glicin
H: Histidin
I: Izoleucin
K: Lizin
L: Leucin
M: Metionin
N: Asparagin
P: Prolin
Q: Glutamin
R: Arginin
S: Serin
T: Treonin
V: Valin
W: Triptofan
Y: Tirozin

10		20		30		40		50
MTRGAWMCRQ		YDDGLKIWLA		APRENEKPFI		DSERAQKWRL		SLASLLFFTV
LLSDHLWFCA		EAKLTRARDK		EHQQQQRQQQ		QQQQQQRQRQ		QQQQQRRQQE
PSWPALLASM		GESSPAAQAH		RLLSASSSPT		LPPSPGDGGG		GGGKGNRGKD
DRGKALFLGN		SAKPVWRLET		CYPQGASSGQ		CFTVENADAV		CARNWSRGAA
GGDGQEVRSK		HPTPLWNLSD		FYLSFCNSYT		LWELFSGLSS		PNTLNCSLDV
VLKEGGEMTT		CRQCVEAYQD		YDHHAQEKYE		EFESVLHKYL		QSEEYSVKSC
PEDCKIVYKA		WLCSQYFEVT		QFNCRKTIPC		KQYCLEVQTR		CPFILPDNDE
VIYGGLSSFI		CTGLYETFLT		NDEPECCDVR		REEKSNNPSK		GTVEKSGSCH
RTSLTVSSAT		RLCNSRLKLC		VLVLILLHTV		LTASAAQNTA		GLSFGGINTL
EENSTNEE

Dopunska literatura

• Anney, R. J. L.; Lasky-Su, J.; ó'Dúshláine, C.; Kenny, E.; Neale, B. M.; Mulligan, A.; Franke, B.; Zhou, K.; Chen, W.; Christiansen, H.; Arias-Vásquez, A.; Banaschewski, T.; Buitelaar, J.; Ebstein, R.; Miranda, A.; Mulas, F.; Oades, R. D.; Roeyers, H.; Rothenberger, A.; Sergeant, J.; Sonuga-Barke, E.; Steinhausen, H.; Asherson, P.; Faraone, S. V.; Gill, M. (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. 147B (8): 1369–1378. doi:10.1002/ajmg.b.30871. PMID 18951430.
• Cross-Disorder Group of the Psychiatric Genomics Consortium; Genetic Risk Outcome of Psychosis (GROUP) Consortium (2013). "Identification of risk loci with shared effects on five major psychiatric disorders: A genome-wide analysis". The Lancet. 381 (9875): 1371–1379. doi:10.1016/S0140-6736(12)62129-1. PMC 3714010. PMID 23453885.
• Wang, K.; Zhang, H.; Bloss, C. S.; Duvvuri, V.; Kaye, W.; Schork, N. J.; Berrettini, W.; Hakonarson, H. (2010). "A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa" (PDF). Molecular Psychiatry. 16 (9): 949–959. doi:10.1038/mp.2010.107. PMC 3859494. PMID 21079607.
• Li, S. H.; McInnis, M. G.; Margolis, R. L.; Antonarakis, S. E.; Ross, C. A. (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, A. R.; Sanna, S.; Deiana, B.; Lai, S.; Uda, M.; Schlessinger, D.; Abecasis, G. A. R.; Ferrucci, L.; Costa Jr, P. T. (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.