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  2. ATG9A - autophagy related 9A Gene

ATG9A - autophagy related 9A Gene

Homo sapiens

Also known as mATG9; APG9L1; MGD3208

Gene ID: 79065 | Gene type: protein coding

About ATG9A

Cytogenetic location: 2q35 Genomic coordinates (GRCh38): 2:219,219,380-219,229,636 (from NCBI)

This gene has 21 transcripts (splice variants), 206 orthologues and 1 paralogue. Broad expression in testis (RPKM 45.2), brain (RPKM 19.5) and 25 other tissues.

Summary

Acts upstream of or within autophagosome assembly. Located in endosome; phagophore assembly site; and trans-Golgi network. [provided by Alliance of Genome Resources, Apr 2022]

ATG9A Products(2)

mRNA Protein Name
NM_001077198.3 NP_001070666.1 autophagy-related protein 9A
NM_024085.5 NP_076990.4 autophagy-related protein 9A

ATG9A Protein Structure

APG9

APG9: Autophagy protein Apg9 (174 - 532)

  • 0
  • 200
  • 400
  • 600
  • 839 a.a.
Protein Preferred Names Protein Names

autophagy-related protein 9A

APG9 autophagy 9-like 1

Related Diseases

Diseases Alias
Spastic Paraplegia 52, Autosomal Recessive

SPG52

Hereditary Spastic Paraplegia 52

Cpsq6

Cerebral Palsy, Spastic Quadriplegic, 6, Formerly

Cpsq6, Formerly

Autosomal Recessive Spastic Paraplegia 52

Spastic Quadriplegic Cerebral Palsy 6

Cerebral Palsy, Spastic Quadriplegic 6

Spastic Paraplegia 50, Autosomal Recessive

Hereditary Spastic Paraplegia 50

SPG50

Ap-4 Deficiency Syndrome

Ap-4-Associated Hereditary Spastic Paraplegia

Adaptor Protein Complex 4 Deficiency

Cerebral Palsy, Spastic Quadriplegic, 3, Formerly

Cpsq3, Formerly

Autosomal Recessive Spastic Paraplegia 50

Cpsq3

Spastic Quadriplegic Cerebral Palsy 3

Ap-4 Deficiency

Ap-4-Associated Hsp

Paraplegia, Spastic, Autosomal Recessive, Type 50

Spastic Paraplegia-50, Autosomal Recessive

Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia

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
Felis catus ATG9A VGNC VGNC:80143
Macaca mulatta ATG9A VGNC VGNC:81180
Canis familiaris ATG9A VGNC VGNC:38228
Rattus norvegicus ATG9A RGD RGD:1310450
Mus musculus ATG9A MGD MGI:2138446
Bos taurus ATG9A VGNC VGNC:26262