2. Gene
  3. ATG13 - autophagy related 13 Gene

ATG13 - autophagy related 13 Gene

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

Also known as KIAA0652; PARATARG8

Gene ID: 9776 | Gene type: protein coding

About ATG13

Cytogenetic location: 11p11.2 Genomic coordinates (GRCh38): 11:46,617,553-46,674,518 (from NCBI)

This gene has 31 transcripts (splice variants) and 217 orthologues. Ubiquitous expression in testis (RPKM 17.3), brain (RPKM 12.2) and 25 other tissues.

Summary

The protein encoded by this gene is an Autophagy factor and a target of the TOR kinase signaling pathway. The encoded protein is essential for autophagosome formation and Mitophagy. [provided by RefSeq, Oct 2016]

ATG13 Products(51)

mRNA Protein Name
NM_001142673.3 NP_001136145.1 autophagy-related protein 13 isoform c
NM_001205119.2 NP_001192048.1 autophagy-related protein 13 isoform a
NM_001205120.2 NP_001192049.1 autophagy-related protein 13 isoform c
NM_001205121.2 NP_001192050.1 autophagy-related protein 13 isoform f
NM_001205122.2 NP_001192051.1 autophagy-related protein 13 isoform h
NM_001346311.2 NP_001333240.1 autophagy-related protein 13 isoform a
NM_001346312.2 NP_001333241.1 autophagy-related protein 13 isoform a
NM_001346313.2 NP_001333242.1 autophagy-related protein 13 isoform a
NM_001346314.2 NP_001333243.1 autophagy-related protein 13 isoform a
NM_001346315.2 NP_001333244.1 autophagy-related protein 13 isoform a
NM_001346316.2 NP_001333245.1 autophagy-related protein 13 isoform a
NM_001346317.2 NP_001333246.1 autophagy-related protein 13 isoform b
NM_001346318.2 NP_001333247.1 autophagy-related protein 13 isoform b
NM_001346319.2 NP_001333248.1 autophagy-related protein 13 isoform c
NM_001346320.2 NP_001333249.1 autophagy-related protein 13 isoform c
NM_001346321.2 NP_001333250.1 autophagy-related protein 13 isoform c
NM_001346322.2 NP_001333251.1 autophagy-related protein 13 isoform c
NM_001346323.2 NP_001333252.1 autophagy-related protein 13 isoform c
NM_001346324.2 NP_001333253.1 autophagy-related protein 13 isoform c
NM_001346325.2 NP_001333254.1 autophagy-related protein 13 isoform c
NM_001346326.2 NP_001333255.1 autophagy-related protein 13 isoform c
NM_001346327.2 NP_001333256.1 autophagy-related protein 13 isoform c
NM_001346328.2 NP_001333257.1 autophagy-related protein 13 isoform c
NM_001346329.2 NP_001333258.1 autophagy-related protein 13 isoform c
NM_001346330.2 NP_001333259.1 autophagy-related protein 13 isoform c
NM_001346331.2 NP_001333260.1 autophagy-related protein 13 isoform c
NM_001346332.2 NP_001333261.1 autophagy-related protein 13 isoform c
NM_001346333.2 NP_001333262.1 autophagy-related protein 13 isoform d
NM_001346334.2 NP_001333263.1 autophagy-related protein 13 isoform d
NM_001346335.2 NP_001333264.1 autophagy-related protein 13 isoform d
NM_001346336.2 NP_001333265.1 autophagy-related protein 13 isoform d
NM_001346337.2 NP_001333266.1 autophagy-related protein 13 isoform d
NM_001346338.2 NP_001333267.1 autophagy-related protein 13 isoform e
NM_001346340.2 NP_001333269.1 autophagy-related protein 13 isoform e
NM_001346342.2 NP_001333271.1 autophagy-related protein 13 isoform f
NM_001346344.2 NP_001333273.1 autophagy-related protein 13 isoform f
NM_001346346.2 NP_001333275.1 autophagy-related protein 13 isoform f
NM_001346348.2 NP_001333277.1 autophagy-related protein 13 isoform f
NM_001346349.2 NP_001333278.1 autophagy-related protein 13 isoform f
NM_001346350.2 NP_001333279.1 autophagy-related protein 13 isoform f
NM_001346351.2 NP_001333280.1 autophagy-related protein 13 isoform f
NM_001346352.2 NP_001333281.1 autophagy-related protein 13 isoform f
NM_001346353.2 NP_001333282.1 autophagy-related protein 13 isoform f
NM_001346354.2 NP_001333283.1 autophagy-related protein 13 isoform f
NM_001346355.2 NP_001333284.1 autophagy-related protein 13 isoform g
NM_001346356.2 NP_001333285.1 autophagy-related protein 13 isoform g
NM_001346357.2 NP_001333286.1 autophagy-related protein 13 isoform i
NM_001346358.2 NP_001333287.1 autophagy-related protein 13 isoform i
NM_001346359.2 NP_001333288.1 autophagy-related protein 13 isoform i
NM_001346360.2 NP_001333289.1 autophagy-related protein 13 isoform j
NM_014741.5 NP_055556.2 autophagy-related protein 13 isoform f

ATG13 Protein Structure

ATG13

ATG13: Autophagy-related protein 13 (17 - 195)

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  • 517 a.a.
Protein Preferred Names Protein Names

autophagy-related protein 13

ATG13 autophagy related 13 homolog

Related Diseases

Diseases Alias
Neurodegeneration With Brain Iron Accumulation

Nbia

Neurodegeneration With Brain Iron Accumulation Disorders

Neurodegeneration, With Brain Iron Accumulation
Liver Carcinoma In Situ

Carcinoma In Situ Of Liver And Biliary System

Carcinoma In Situ Of Liver, Gallbladder And Bile Ducts
Charcot-Marie-Tooth Disease, Axonal, Type 2e

Charcot-Marie-Tooth Disease Type 2

CMT2E

CMT2S

CMT2Y

Charcot-Marie-Tooth Disease Type 2e

Charcot-Marie-Tooth Disease Type 2y

Charcot-Marie-Tooth Disease Axonal Type 2s

Charcot-Marie-Tooth Disease, Axonal, Type 2s

Charcot-Marie-Tooth Disease, Type 2e

Hereditary Motor And Sensory Neuropathy Type 2

Charcot-Marie-Tooth Neuropathy, Type 2s

Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s

Charcot-Marie-Tooth Disease, Axonal, Type 2y

Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y

Charcot-Marie-Tooth Neuropathy, Type 2y

Charcot-Marie-Tooth Disease, Type 2y

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e

Charcot-Marie-Tooth Neuropathy Type 2e

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation

Cmt2 Due To Vcp Mutation

Charcot-Marie-Tooth Disease Type 2s

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2

Autosomal Dominant Axonal Charcot-Marie-Tooth Disease

Cmt2

Charcot-Marie-Tooth Neuropathy, Type 2e

Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type

Hereditary Motor And Sensory Neuropathy Okinawa Type

Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y

Charcot-Marie-Tooth Neuropathy Type 2y

Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s

Charcot-Marie-Tooth Neuropathy Type 2s

Charcot-Marie-Tooth Type 2

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y

Charcot-Marie-Tooth Disease 2e

Charcot-Marie-Tooth Disease Axonal Type 2e

Charcot-Marie-Tooth Disease Neuronal Type 2e

Charcot-Marie-Tooth Disease 2s

Charcot-Marie-Tooth Neuropathy Axonal Type 2s

Charcot-Marie-Tooth Disease 2y

Charcot-Marie-Tooth Disease, Type 2

Hereditary Motor And Sensory-Neuropathy Type Ii
Amyotrophic Lateral Sclerosis 1

Amyotrophic Lateral Sclerosis

ALS

Lou Gehrig Disease

Amyotrophic Lateral Sclerosis Type 1

Charcot Disease

ALS1

Amyotrophic Lateral Sclerosis, Susceptibility To

Fals

Lou Gehrig'S Disease

Mnd

Motor Neuron Disease

Familial Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis 1, Familial

Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

Motor Neuron Disease, Bulbar

Motor Neurone Disease

Amyotrophic Lateral Sclerosis With Dementia

Dementia With Amyotrophic Lateral Sclerosis

Motor Neuron Disease, Amyotrophic Lateral Sclerosis

Sclerosis, Lateral, Amyotrophic

Sclerosis, Lateral, Amyotrophic, Type 1

Amyotrophic Sclerosis

Als - [Amyotrophic Lateral Sclerosis]

Wasting Palsy

Amyotrophic Paralysis

Amyotrophy Lateral Sclerosis

Wasting Paralysis

Spinal Progressive Amyotrophy

Progressive Atrophic Paralysis
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-RS01141 ATG13 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris ATG13 VGNC VGNC:38217
Macaca mulatta ATG13 VGNC VGNC:70148
Bos taurus ATG13 VGNC VGNC:26251
Rattus norvegicus ATG13 RGD RGD:1310685
Felis catus ATG13 VGNC VGNC:59996
Mus musculus ATG13 MGD MGI:1196429