1. Gene
  2. ACY3 - aminoacylase 3 Gene

ACY3 - aminoacylase 3 Gene

Homo sapiens

Also known as ACY-3; HCBP1

Gene ID: 91703 | Gene type: protein coding

About ACY3

Cytogenetic location: 11q13.2 Genomic coordinates (GRCh38): 11:67,642,555-67,650,730 (from NCBI)

This gene has 2 transcripts (splice variants), 232 orthologues and 1 paralogue. Biased expression in kidney (RPKM 28.0), duodenum (RPKM 26.6) and 8 other tissues.

Summary

Predicted to enable aminoacylase activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

ACY3 Products(1)

mRNA Protein Name
NM_080658.2 NP_542389.1 N-acyl-aromatic-L-amino acid amidohydrolase (carboxylate-forming)

ACY3 Protein Structure

AstE_AspA

AstE_AspA: Succinylglutamate desuccinylase / Aspartoacylase family (11 - 300)

  • 0
  • 100
  • 200
  • 300
  • 319 a.a.
Protein Preferred Names Protein Names

N-acyl-aromatic-L-amino acid amidohydrolase (carboxylate-forming)

HCV core-binding protein 1

Recombinant ACY3 Proteins

Cat. No. Product Name Accession Purity
HY-P7457 ACY3 Protein, Human (His) Q96HD9 (M1-S319) ≥95%

Related Diseases

Diseases Alias
Hepatitis C Virus

Hepatitis C Virus, Susceptibility To

Hepatitis C Virus Infection, Response To Therapy Of

Hcv

Hcv, Susceptibility To

Hepatitis C Virus, Resistance To

Hepatitis C Virus, Response To Therapy Of

Resistance To Hepatitis C Virus

Canavan Disease

Aspartoacylase Deficiency

Aminoacylase 2 Deficiency

Spongy Degeneration Of Central Nervous System

Aspa Deficiency

Acy2 Deficiency

Canavan-Van Bogaert-Bertrand Disease

Mild Canavan Disease

Asp Deficiency

Spongy Degeneration Of The Central Nervous System

Severe Canavan Disease

Von Bogaert-Bertrand Disease

Canavan'S Disease

Spongy Degeneration Of The Brain

Juvenile Canavan Disease

Infantile Canavan Disease

Neonatal Canavan Disease

CAND

Disease, Canavan

Canavan Disease, Juvenile

Canavan Disease, Infantile

Canavan Disease, Neonatal

Leukodystrophy, Hypomyelinating, 2

Pmld1

Hypomyelinating Leukodystrophy 2

HLD2

Pelizaeus-Merzbacher-Like Disease 1

Pelizaeus-Merzbacher-Like Disease Due To Gjc2 Mutation

Pelizaeus-Merzbacher-Like Disease Type 1

Pelizaeus-Merzbacher-Like Disease, 1

Pelizaeus Merzbacher Like Disease

Pelizaeus-Merzbacher-Like Disease

Pmld - Pelizaeus Merzbacher Like Disease

Pelizaeus-Merzbacher-Like Disease Autosomal Recessive Type 1

Pmldar1

Leukodystrophy, Hypomyelinating, Type 2

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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus ACY3 RGD RGD:1305394
Macaca mulatta ACY3 VGNC VGNC:99538
Mus musculus ACY3 MGD MGI:1918920
Others ACY3 NCBI