LTN1 - listerin E3 ubiquitin protein ligase 1 Gene

Also Known as RNF160; ZNF294; C21orf10; C21orf98

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 26046

About LTN1

Cytogenetic location: 21q21.3 Genomic coordinates (GRCh38): 21:28,928,144-28,992,877 (from NCBI)

This gene has 7 transcripts (splice variants) and 213 orthologues. Ubiquitous expression in thyroid (RPKM 7.5), placenta (RPKM 7.3) and 25 other tissues.

Summary

Like most RING finger proteins, LTN1 functions as an E3 ubiquitin Ligase (Chu et al., 2009 [PubMed 19196968]).[supplied by OMIM, Nov 2010]

LTN1 Products (2)

mRNA Protein Name
NM_001320766.2 NP_001307695.2 E3 ubiquitin-protein ligase listerin isoform 2
NM_015565.3 NP_056380.3 E3 ubiquitin-protein ligase listerin isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
21903422 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
25578875 GOA
Biological Process GO Annotation Evidence References Source
involved in rescue of stalled ribosome IDA
IDA: Inferred from direct assay
25578875 GOA
involved in ribosome-associated ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
25578875 GOA
Cellular Component GO Annotation Evidence References Source
part of RQC complex IDA
IDA: Inferred from direct assay
25578875 GOA
located in cytosol IDA
IDA: Inferred from direct assay
25578875 GOA
is active in cytosolic ribosome IDA
IDA: Inferred from direct assay
25578875 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

LTN1 Protein Structure

FANCL_C

FANCL_C: FANCL C-terminal domain (1714 - 1756)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1500
  • 1766 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase listerin

  • RING-type E3 ubiquitin transferase listerin

LTN1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
LTN1 O94822 STING1 Homo sapiens Q86WV6 21903422
Intra
LTN1 O94822 TIRAP Homo sapiens P58753 21903422
Intra
LTN1 O94822 IRF7 Homo sapiens Q92985 21903422
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
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

Parkinson Disease, Late-Onset
  • Parkinson Disease

  • Parkinson'S Disease

  • PD

  • PARK

  • Parkinson Disease, Susceptibility To

  • Late Onset Parkinson'S Disease

  • Late Onset Parkinson Disease

  • Paralysis Agitans

  • Primary Parkinsonism

  • Idiopathic Parkinson Disease

  • Parkinson'S

  • Parkinson Disease, Late-Onset, Susceptibility To

  • Parkinson Disease, Age Of Onset, Modifier

  • Lewy Body Parkinson Disease

  • Idiopathic Parkinson'S Disease

  • Pd - [Parkinson Disease]

  • Parkinson Disease Nos

  • Parkinson, Nos

  • Primary Parkinson Disease

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
Mus musculus LTN1 MGD MGI:1926163
Macaca mulatta LTN1 VGNC VGNC:74275
Canis familiaris LTN1 VGNC VGNC:42862
Bos taurus LTN1 VGNC VGNC:31078
Rattus norvegicus LTN1 RGD RGD:1311238
Felis catus LTN1 VGNC VGNC:63327
Others LTN1 NCBI