H-InvDB - Transcript view HIT000454139

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H-Invitational ID:	HIT000454139	Accession number:	DQ587608	Created date:	26-Mar-2013	Last modified:	27-May-2015
Definition:	Non-protein-coding transcript, uncharacterized transcript.

[CDS]
provide predicted CDS, orientation, codon adaptation
index (CAI) and translation.

[Motif]
provide location, ID and descriptions of functional motifs (InterPro)

[GO]
provide gene ontology (GO) annotation of molecular
function, biological process and cellular component.

[Subcellular loc.]
provide subcellular localization prediction by
WolfPSORT, Target P, SOSUI, TMHMM and PTS1

[Protein structure]
provide assigned PDB and SCOP IDs by reverse
PSI-BLAST, and summary prediction of 3D structure by GTOP

[Expression]
provide tissue-specific expression in 10 tissue
categories determined by iAFLP data (JBIRC)

[Disease info.]
provide known disease-related genes and co-localized
orphan pathology with the name of the disease
and OMIM ID

[Evolutionary info.]
provide orthologs relationships, phylogenic
trees and sequence alignments

Disease/pathology information

Last modified:27-May-2015

Disease relation		Disease name: Combined SAP deficiency (611721); Disease name: Gaucher disease, atypical (610539); Disease name: Krabbe disease, atypical (611722); Disease name: Metachromatic leukodystrophy due to SAP-b deficiency (249900);
Related information in OMIM		OMIM ID: 176801; Title: PROSAPOSIN
Co-localized orphan diseases		NA
Disease related mutation		MutationView: 176801; JRE-1.4.0 or later is required.Download JRE at Sun's web site.
Literature-Extracted GENe-Disease Associations (LEGENDA)	Gene name	NA
	Disease	NA
	Substance	NA
Related H-InvDB links		DiseaseInfo Viewer; LEGENDA;