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H-InvDB_8.3 released on March 26, 2013.
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H-Invitational ID: HIT000098026_03 Accession number: BC045533 Created date: 26-Mar-2013 Last modified: 26-Mar-2013
Definition: Golgi resident protein GCP60.

Transcript original information
Accession number BC045533.1
Clone Number MGC:57123 IMAGE:5259930
Experimental resources NBRC: NITE Biological Resource Center  NBRC ; HGPD: Human Gene and Protein Database HGPD ; Antibody: searching human antibodies at "BIO-kaimono.com" Antibody (ACBD3) ; Catalog: searching experimental product catalogs at "BIO-kaimono.com" Catalog (ACBD3);
Sequence data provider NA
Annotation project NA
Length of cDNA 3560[bp] (No. of exon:8)[A:1059 T:1020 G:820 C:661]
Devision NA
Molecular type NA
Library origin Cell type NA
Tissue type Brain, hippocampus
Develpmental stage NA
Sequence quality information
CDS feature Complete CDS
Kozak sequence NA
PolyA Site: 3546(+) Signal: 3527-3531(+)
Vector/adapter sequence NA
Frame shift NA
Remaining intron NA
Splice site acceptor (NAGNAG) CAGGAG; 
Transcript quality feature NA
Notes NA

Gene structure information  G-integra H-DBAS cDNA-genome alignment
H-Inv cluster ID HIX0001643
Genomic location  G-integra Help Chromosome 1
Location 1q42.12
Position 226332382- 226374409
Strand -
Possible duplicated location(s) NA
Gene structure 8 exon(s)
Database links RefSeq NM_022735
Ensembl ENST00000366812ENST00000464927
Entrez Gene Entrez Gene ID:64746
GeneCard GeneCardACBD3*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 HIP000024076
Predicted CDS 34..1620;  528[aa];  Orientation:+1; 
Codon Adaptation Index (CAI). 0.743
Database links RefSeq NP_073572
UniProt Q9H3P7

Gene function information  Gene family PPI viewer Similarity Search Tool TACT
H-Inv ID HIT000098026_03
H-Inv cluster ID Locus viewHIX0001643
Accession number BC045533.1
Transcript feature  Help NO; 
Coding potential  Help Protein coding; 
Definition Golgi resident protein GCP60.
Similarity category  Help Category: Identical to known human protein(Category I).
Identical to known human protein (NP_073572)  [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 ACBD3
HGNC aliases "golgi complex associated protein 1, 60kDa", "acyl-Coenzyme A binding domain containing 3"
HGNC name acyl-CoA binding domain containing 3
UniProt NA
EC number NA
(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 HIP000024076
No. of interaction 3
Interaction partner(s) HIP000040279HIP000100876HIP000246796
BIND 150193; 
MINT MINT-61799; 
HPRD 03933;  03990;  06901; 
IntAct EBI-1791788; 
Database links RefSeq NM_022735
Ensembl ENST00000366812ENST00000464927
Entrez Gene Entrez Gene ID:64746
GeneCard GeneCardACBD3*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. 

Subcellular localization information  Last modified:26-Mar-2013
WoLF PSORT nuclear;  cytosol; 
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:26-Mar-2013
Disease relation Disease name:NA
Related information in OMIM OMIM ID:NA Title:NA
Co-localized orphan diseases OMIM ID:  115665116600155600600975605225605606606788606852606928607317607671608543608553608995610320612367612596
Disease related mutation NA
Literature-Extracted GENe-Disease Associations (LEGENDA) LEGENDA Gene name Entrez Gene ID:(64746)
Disease Entrez Gene ID:(64746)
Substance Entrez Gene ID:(64746)
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
54 .. 54 A/T rs77797743 - CDS Synonymous[Ala7Ala]
593 ^ 594 -/C rs111701159 - CDS
594 .. 594 A/C rs2306120 - CDS Nonsynonymous[Glu187Asp]
612 .. 612 A/T rs9730340 - CDS Nonsynonymous[Glu193Asp]
673 .. 673 C/G rs112143123 - CDS Nonsynonymous[Arg214Gly]
718 .. 718 A/C rs78919255 - CDS Synonymous[Arg229Arg]
719 .. 719 G/C rs77727776 - CDS Nonsynonymous[Arg229Thr]
1212 .. 1212 C/T rs114674626 - CDS Synonymous[Ser393Ser]
1451 .. 1451 A/G rs17855715 - CDS Nonsynonymous[Lys473Arg]
1503 .. 1503 G/T rs3211100 + CDS Nonsynonymous[Glu490Asp]
1564 .. 1564 T/C rs113333885 - CDS Nonsynonymous[Ser511Pro]
1641 .. 1641 G/A rs41304002 - 3'UTR
1647 .. 1647 A/T rs1062716 + 3'UTR
1846 .. 1846 A/G rs111803808 - 3'UTR
2002 .. 2002 G/A rs61835249 - 3'UTR
2165 .. 2165 C/A rs61835248 - 3'UTR
2381 .. 2385 TTTTG/- rs72264515 - 3'UTR
2562 .. 2562 A/G rs41314288 - 3'UTR
2726 .. 2726 C/T rs41304004 - 3'UTR
2933 .. 2933 G/A rs1043641 + 3'UTR
3222 ^ 3223 -/T rs35794165 - 3'UTR
3231 ^ 3232 -/T rs71746173 - 3'UTR
3295 .. 3296 AT/- rs71728926 - 3'UTR
3455 .. 3455 T/C rs115185049 - 3'UTR
 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