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: HIT000425447 Accession number: AK292650 Created date: 26-Mar-2013 Last modified: 20-Apr-2012
Definition: Sorting nexin-20 isoform 3.
 
 

Transcript original information
Accession number AK292650.1
CAGE tag ID NA
EST ID NA
Clone Number THYMU2039124
Experimental resources NBRC: NITE Biological Resource Center  NBRC ; HGPD: Human Gene and Protein Database HGPD ; Antibody: searching human antibodies at "BIO-kaimono.com" Antibody (SNX20) ; Catalog: searching experimental product catalogs at "BIO-kaimono.com" Catalog (SNX20);
Sequence data provider NA
Annotation project NA
Length of cDNA 549[bp] (No. of exon:4)[A:129 T:89 G:152 C:179]
Devision HUM
Molecular type mRNA
Library origin Cell type NA
Tissue type thymus
Develpmental stage NA
Mini-G
Sequence quality information
CDS feature Complete CDS
Kozak sequence NA
PolyA NA
Vector/adapter sequence NA
Frame shift NA
Remaining intron NA
Splice site acceptor (NAGNAG) NA
Transcript quality feature NA
Notes NA

Gene structure information  G-integra H-DBAS cDNA-genome alignment
H-Inv cluster ID HIX0019600
Genomic location  G-integra Help Chromosome 16
Location 16q12.1
Position 50701818- 50715223
Strand -
Possible duplicated location(s) NA
Gene structure 4 exon(s)
Database links RefSeq NM_153337NM_182854NM_001144972
Ensembl ENST00000300590ENST00000330943ENST00000413750ENST00000423026
Entrez Gene Entrez Gene ID:124460
KEGG GENES KEGG GENES(124460)
GeneCard GeneCardSNX20*GeneCards is provided free to academic non-profit institutions.
Related H-InvDB links H-DBASH-DBAS G-integraG-integra cDNA-genome alignmentcDNA-genome alignment

Predicted CDS information
HIP ID HIP000193117
Predicted CDS 133..441;  102[aa];  Orientation:+1; 
Codon Adaptation Index (CAI). 0.812
Database links RefSeq NP_001138444
UniProt NA
CCDS CCDS45481

Gene function information  Gene family PPI viewer Similarity Search Tool TACT
H-Inv ID HIT000425447
H-Inv cluster ID Locus viewHIX0019600
Accession number AK292650.1
CAGE tag ID NA
EST ID NA
Transcript feature  Help NO; 
Coding potential  Help Protein coding; 
Definition Sorting nexin-20 isoform 3.
Similarity category  Help Category: Identical to known human protein(Category I).
Identical to known human protein (NP_001138444)  [Identity/coverage = 100.0%/100.0%] to Homo sapiens protein.
Experimental evidence Protein evidence
PubMed ID NA
Gene family/group Gene family H-Inv gene family/group ID NA
Gene family/group name NA
Evidence motif (InterPro) ID NA
Gene symbol/name HGNC symbol SNX20
HGNC aliases NA
HGNC name sorting nexin 20
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 HIP000193117
No. of interaction 4
Interaction partner(s) HIP000161494HIP000259349HIP000259349HIP000349427
BIND NA
DIP 132844E;  43036E; 
MINT NA
HPRD NA
IntAct EBI-2005282;  EBI-341732; 
Database links RefSeq NM_153337NM_182854NM_001144972
Ensembl ENST00000300590ENST00000330943ENST00000413750ENST00000423026
Entrez Gene Entrez Gene ID:124460
KEGG GENES KEGG GENES(124460)
GeneCard GeneCardSNX20*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 Gene familyGene family;  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


Subcellular localization information  Last modified:20-Apr-2012
WoLF PSORT extracellular;  cytosol;  nuclear;  Other; 
Target P Other
SOSUI soluble protein
TMHMM soluble protein
PTS1 Not targeted
Related H-InvDB links LIFEdb LIFEdb; 
JRE-1.4.0 or later is required. Download JRE at Sun's web site.

Disease/pathology information  DiseaseInfo Viewer LEGENDA Last modified:20-Apr-2012
Disease relation Disease name:NA
Related information in OMIM OMIM ID:NA Title:NA
Co-localized orphan diseases OMIM ID:  156850605013605021606668607339608558608903610260
Disease related mutation NA
Literature-Extracted GENe-Disease Associations (LEGENDA) LEGENDA Gene name Entrez Gene ID:(124460)
Disease Entrez Gene ID:(124460)
Substance Entrez Gene ID:(124460)
Related H-InvDB links DiseaseInfo ViewerDiseaseInfo ViewerLEGENDALEGENDA

Polymorphism (SNP, indel), microsatellite (Short Tandem Repeat, STR) and repeat information  VaryGene Repeat mask viewer
 Single Nucleotide Polymorphism (SNP) and indel  VaryGene
Location Variation dbSNP ID Strand CDS/UTR Translation
39 .. 39 C/T rs2066848 - 5'UTR
229 .. 229 G/A rs34428900 - CDS Nonsynonymous[Asp33Asn]
235 .. 235 C/T rs17846633 - CDS Nonsynonymous[Pro35Ser]
236 .. 236 C/T rs1131716 + CDS Nonsynonymous[Pro35Leu]
262 .. 262 G/A rs35973532 - CDS Nonsynonymous[Asp44Asn]
303 .. 303 G/A rs35435054 - CDS Synonymous[Thr57Thr]
372 .. 372 C/T rs6596 + CDS Synonymous[Ile80Ile]
 Microsatellite (Short Tandem Repeat, STR)
No data available
 Microsatellite: Human-Gene diversity Of Life-style related Diseases (H-GOLD)
No data available
 Repeat  Repeat mask viewer
No data available
Database links H-GOLDHuman-Gene diversity Of Life-style related Diseases(H-GOLD)
Related H-InvDB links VaryGeneVaryGene;  Repeat mask viewerRepeat Mask Viewer