ACCS - 1-aminocyclopropane-1-carboxylate synthase homolog (inactive) Gene

Also Known as ACS; PHACS

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84680

About ACCS

Cytogenetic location: 11p11.2 Genomic coordinates (GRCh38): 11:44,066,270-44,084,237 (from NCBI)

This gene has 13 transcripts (splice variants), 149 orthologues and 7 paralogues. Ubiquitous expression in spleen (RPKM 11.2), gall bladder (RPKM 7.3) and 25 other tissues.

Summary

Enables identical protein binding activity. Predicted to be involved in biosynthetic process. [provided by Alliance of Genome Resources, Apr 2022]

ACCS Products (2)

mRNA Protein Name
NM_001127219.2 NP_001120691.1 1-aminocyclopropane-1-carboxylate synthase-like protein 1
NM_032592.4 NP_115981.1 1-aminocyclopropane-1-carboxylate synthase-like protein 1
Molecular Function GO Annotation Evidence References Source
NOT enables 1-aminocyclopropane-1-carboxylate synthase activity IDA
IDA: Inferred from direct assay
11470512 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ACCS Protein Structure

Aminotran_1_2

Aminotran_1_2: Aminotransferase class I and II (98 - 460)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 501 a.a.
Protein Preferred Names Protein Names

1-aminocyclopropane-1-carboxylate synthase-like protein 1

  • ACC synthase-like protein 1

ACCS Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ACCS Q96QU6 UQCRB Homo sapiens P14927 25416956
Intra
ACCS Q96QU6 ACCS Homo sapiens Q96QU6 31515488
Intra
ACCS Q96QU6 ACCS Homo sapiens Q96QU6 32296183
Intra
ACCS Q96QU6 ACCS Homo sapiens Q96QU6-1 31515488
Intra
ACCS Q96QU6 ACCS Homo sapiens Q96QU6 32296183
Intra
ACCS Q96QU6 ACCS Homo sapiens Q96QU6 25416956
Intra
ACCS Q96QU6 ACCS Homo sapiens Q96QU6 32296183
Intra
ACCS Q96QU6 ACCS Homo sapiens Q96QU6 16189514
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Thyroid Dyshormonogenesis 5
  • TDH5

  • Hypothyroidism, Congenital, Due To Dyshormonogenesis, 5

  • Thyroid Hormonogenesis, Genetic Defect In, 5

  • Genetic Defect In Thyroid Hormonogenesis 5

  • Chdh5

  • Congenital Hypothyroidism Due To Dyshormonogenesis Type 5

  • Genetic Defect In Thyroid Hormonogenesis Type 5

Granulomatous Amebic Encephalitis
  • Granulomatous Amoebic Encephalitis

  • Acanthamoeba Encephalitis

  • Acanthamoeba Granulomatous Encephalitis

  • Granulomatous Amebic Encephalitis Due To Acanthamoeba

Twin-To-Twin Transfusion Syndrome
  • Twin To Twin Transfusion Syndrome

  • Twin Twin Transfusion Syndrome

  • Fetal Blood Loss From Fetal Hemorrhage Into Co-Twin

  • Fetal Hemorrhage Into Co-Twin

  • Twin To Twin Transfusion

  • Twin-To-Twin Blood Transfer

  • Fetal Transfusion Syndrome

  • Fetofetal Transfusion Syndrome

  • Ttts

  • Feto-Fetal Transfusion Syndrome

  • Fetofetal Transfusion

  • Fetus-To-Fetus Placental Transfusion Syndrome

Primary Amebic Meningoencephalitis
  • Pam

  • Naegleria Fowleri Infection

  • Meningoencephalitis Caused By Naegleria Fowleri

  • Primary Amoebic Meningoencephalitis

Thyroid Dyshormonogenesis 4
  • Deiodinase Deficiency

  • TDH4

  • Iodotyrosine Dehalogenase Deficiency

  • Thyroid Hormonogenesis, Genetic Defect In, 4

  • Hypothyroidism, Congenital, Due To Dyshormonogenesis, 4

  • Genetic Defect In Thyroid Hormonogenesis 4

  • Chdh4

  • Congenital Hypothyroidism Due To Dyshormonogenesis Type 4

  • Genetic Defect In Thyroid Hormonogenesis Type 4

Aplasia Of Lacrimal And Salivary Glands
  • ALSG

  • Congenital Absence Of Lacrimal Puncta And Salivary Glands

  • Xerostomia

  • Absence Of Salivary Glands

  • Parotid Aplasia Or Hypoplasia

  • Congenital Absence Of Lacrimal Puncta Or Salivary Glands

  • Alsg - [Aplasia Of Lacrimal Or Salivary Glands]

Mucopolysaccharidosis, Type Ix
  • Mucopolysaccharidosis Type Ix

  • Hyaluronidase Deficiency

  • MPS9

  • Mps Ix

  • Mucopolysaccharidosis Ix

  • Mpsix

  • Mucopolysaccharidosis Type 9

  • Mucopolysaccharidosis 9

Neonatal Anemia
  • Anemia Neonatal

  • Anemia, Neonatal

  • Anaemia Neonatal

  • Neonatal Anaemia

Familial Thyroid Dyshormonogenesis
  • Thyroid Dyshormonogenesis

  • Familial Dyshormonogenetic Goiter

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 ACCS RGD RGD:1309314
Mus musculus ACCS MGD MGI:1919717
Others ACCS NCBI