H-InvDB x AHG DB
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H-InvDB_8.3 released on March 26, 2013.
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H-Invitational ID: HIT000330374 Accession number: AK222594 Created date: 26-Mar-2013 Last modified: 20-Apr-2012
Definition: Ribosomal protein S4, Y-linked 1 Y isoform variant; Fragment;
 
 

Gene function information  Gene family PPI viewer Similarity Search Tool TACT
H-Inv ID HIT000330374
H-Inv cluster ID Locus viewHIX0017179
Accession number AK222594.1
CAGE tag ID NA
EST ID NA
Transcript feature  Help NO; 
Coding potential  Help Protein coding; 
Definition Ribosomal protein S4, Y-linked 1 Y isoform variant; Fragment;
Similarity category  Help Category: Identical to known human protein(Category I).
Identical to known human protein (Q53HI6)  [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Experimental evidence Protein evidence
PubMed ID 81252989373149ALL
Gene family/group Gene family H-Inv gene family/group ID HIF0000406
Gene family/group name Ribosomal protein S4e (IPR000876).
Evidence motif (InterPro) ID IPR000876
Gene symbol/name HGNC symbol RPS4Y1
HGNC aliases "ribosomal protein S4, Y-linked"
HGNC name ribosomal protein S4, Y-linked 1
DDBJ NA
UniProt NA
EC number NA
GGDB
(GlycoGene Database)
Gene symbol NA
Familly NA
Designation NA
Expression NA
KEGG metabolic pathway NA
Protein-protein interaction (PPI) PPI viewer H-Inv protein ID HIP000145418
No. of interaction 5
Interaction partner(s) HIP000057276HIP000068244HIP000091191HIP000257150HIP000381737
BIND 177539; 
DIP NA
MINT MINT-64176; 
HPRD 00129;  00559; 
IntAct EBI-2826885;  EBI-735516; 
Database links RefSeq NM_001008
Ensembl ENST00000250784ENST00000430575ENST00000477725ENST00000515575
Entrez Gene Entrez Gene ID:6192
KEGG GENES KEGG GENES(6192)
GeneCard GeneCardRPS4Y1*GeneCards is provided free to academic non-profit institutions.
etc H-GOLDHuman-Gene diversity Of Life-style related Diseases
Curation status Auto-annotated
Notes NA
Related H-InvDB links Ribosomal protein S4e (IPR000876). Similarity Search ToolSimilarity Search Tool;  TACTTACT
fRNAdb (The functional RNA database) : overlapping fRNAdb entries with H-InvDB transcripts based on the location of the genome. 
NA