2. Gene
  3. ACBD3 - acyl-CoA binding domain containing 3 Gene

ACBD3 - acyl-CoA binding domain containing 3 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as PAP7; GCP60; GOCAP1; GOLPH1

Gene ID: 64746 | Gene type: protein coding

About ACBD3

Cytogenetic location: 1q42.12 Genomic coordinates (GRCh38): 1:226,144,679-226,186,741 (from NCBI)

This gene has 2 transcripts (splice variants), 229 orthologues and 1 paralogue. Ubiquitous expression in thyroid (RPKM 19.9), esophagus (RPKM 18.2) and 25 other tissues.

Summary

The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. The protein encoded by this gene is involved in the maintenance of Golgi structure and function through its interaction with the integral membrane protein giantin. It may also be involved in the hormonal regulation of steroid formation. [provided by RefSeq, Jul 2008]

ACBD3 Products(1)

mRNA Protein Name
NM_022735.4 NP_073572.2 Golgi resident protein GCP60

ACBD3 Protein Structure

ACBP

ACBP: Acyl CoA binding protein (84 - 171)

GOLD_2

GOLD_2: Golgi-dynamics membrane-trafficking (397 - 527)

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  • 528 a.a.
Protein Preferred Names Protein Names

Golgi resident protein GCP60

PBR- and PKA-associated protein 7

Related Diseases

Diseases Alias
Nonparalytic Poliomyelitis

Acute Nonparalytic Poliomyelitis

Non-Paralytic Aseptic Meningitis
Schizophrenia 14

Sczd14

Schizophrenia, Susceptibility To, 14

Schizophrenia Susceptibility Locus, Chromosome 2q32-Related
Nasal Cavity Lymphoma

Lymphoma Of Nasal Cavity

Lymphoma Of The Nasal Cavity
Acute Flaccid Myelitis
Poliomyelitis

Polio

Infantile Paralysis
Acute Hemorrhagic Conjunctivitis

Viral Conjunctivitis

Conjunctivitis, Acute Hemorrhagic

Apollo Disease

Epidemic Hemorrhagic Conjunctivitis

Viral Conjunctiva Disorder

Viral Conjunctivitis Nos
Primary Pigmented Nodular Adrenocortical Disease

Ppnad

Primary Pigmented Nodular Adrenal Dysplasia

Pigmented Nodular Adrenocortical Disease, Primary, 2

Pigmented Nodular Adrenocortical Disease, Primary, 1
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS00142 ACBD3 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus ACBD3 VGNC VGNC:59500
Bos taurus ACBD3 VGNC VGNC:25531
Canis familiaris ACBD3 VGNC VGNC:37500
Mus musculus ACBD3 MGD MGI:2181074
Rattus norvegicus ACBD3 RGD RGD:727851
Macaca mulatta ACBD3 VGNC VGNC:69408