CLN8

CLN8
Identifikatori
Aliasi	CLN8
Vanjski ID-jevi	OMIM: 607837 MGI: 1349447 HomoloGene: 10340 GeneCards: CLN8
Lokacija gena (čovjek) Hrom. Hromosom 8 (čovjek)[1] Bend 8p23.3 Početak 1,755,778 bp[1] Kraj 1,801,711 bp[1]
Lokacija gena (miš) Hrom. Hromosom 8 (miš)[2] Bend 8 A1.1|8 7.59 cM Početak 14,931,335 bp[2] Kraj 14,951,720 bp[2]
Ortolozi
Vrste	Čovjek	Miš
Entrez	2055	26889
Ensembl	ENSG00000182372 ENSG00000278220	ENSMUSG00000026317
UniProt	Q9UBY8	Q9QUK3
RefSeq (mRNK)	NM_001034061 NM_018941	NM_012000
RefSeq (bjelančevina)	NP_061764	NP_036130
Lokacija (UCSC)	Chr 8: 1.76 – 1.8 Mb	Chr 8: 14.93 – 14.95 Mb
PubMed pretraga	[3]	[4]
Wikipodaci
Pogledaj/uredi – čovjek Pogledaj/uredi – miš

Protein CLN8 je protein koji je kod ljudi kodiran genom CLN8.^[5][6]

1. ^ ^{a b c} ENSG00000278220 GRCh38: Ensembl release 89: ENSG00000182372, ENSG00000278220 - Ensembl, maj 2017
2. ^ ^{a b c} GRCm38: Ensembl release 89: ENSMUSG00000026317 - Ensembl, maj 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. ^ Ranta S, Zhang Y, Ross B, Lonka L, Takkunen E, Messer A, Sharp J, Wheeler R, Kusumi K, Mole S, Liu W, Soares MB, Bonaldo MF, Hirvasniemi A, de la Chapelle A, Gilliam TC, Lehesjoki AE (Oct 1999). "The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8". Nat Genet. 23 (2): 233–6. doi:10.1038/13868. PMID 10508524. S2CID 23920094.
6. ^ "Entrez Gene: CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)".