1. Gene
  2. PELI1 - pellino E3 ubiquitin protein ligase 1 Gene

PELI1 - pellino E3 ubiquitin protein ligase 1 Gene

Homo sapiens
Gene ID: 57162 | Gene type: protein coding

About PELI1

Cytogenetic location: 2p14 Genomic coordinates (GRCh38): 2:64,092,652-64,144,420 (from NCBI)

This gene has 4 transcripts (splice variants), 279 orthologues and 2 paralogues. Broad expression in bone marrow (RPKM 57.0), esophagus (RPKM 14.7) and 19 other tissues.

Summary

Enables ubiquitin protein Ligase activity. Involved in several processes, including negative regulation of necroptotic process; protein polyubiquitination; and response to lipopolysaccharide. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]

PELI1 Products(1)

mRNA Protein Name
NM_020651.4 NP_065702.2 E3 ubiquitin-protein ligase pellino homolog 1

PELI1 Protein Structure

Pellino

Pellino: Pellino (4 - 418)

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

E3 ubiquitin-protein ligase pellino homolog 1

RING-type E3 ubiquitin transferase pellino homolog 1

Recombinant PELI1 Proteins

Cat. No. Product Name Accession Purity
HY-P75970 Pellino-1 Protein, Human (sf9, His-GST) Q96FA3 (M1-D418) ≥95%

Related Diseases

Diseases Alias
Tyrosinemia, Type Iii

Tyrosinemia Type Iii

4-Hydroxyphenylpyruvate Dioxygenase Deficiency

TYRSN3

4-Hydroxyphenylpyruvic Acid Oxidase Deficiency

Tyrosinemia Type 3

4-Alpha Hydroxyphenylpyruvate Dioxygenase Deficiency

4-Alpha Hydroxyphenylpyruvic Acid Oxidase Deficiency

Tyrosinemia Due To 4-Hydroxyphenylpyruvate Dioxygenase Deficiency

Tyrosinemia Due To 4-Hydroxyphenylpyruvic Acid Oxidase Deficiency

Tyrosinemia Due To Hpd Deficiency

Tyrosinemia 3

Noonan Syndrome 1

Noonan Syndrome

NS1

Male Turner Syndrome

Female Pseudo-Turner Syndrome

Turner Phenotype With Normal Karyotype

Noonan Syndrome With Pigmented Villonodular Synovitis

Turner'S Phenotype, Karyotype Normal

Familial Turner Syndrome

Noonan'S Syndrome

Noonan-Ehmke Syndrome

Ns

Pseudo-Ullrich-Turner Syndrome

Turner Syndrome In Female With X Chromosome

Turner-Like Syndrome

Ullrich-Noonan Syndrome

Noonan-Like/Multiple Giant Cell Lesion Syndrome

Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions

Pterygium Colli Syndrome

Noonan Syndrome, Type 1

Turner Syndrome, Male

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 PELI1 VGNC VGNC:68783
Macaca mulatta PELI1 VGNC VGNC:106195
Mus musculus PELI1 MGD MGI:1914495
Bos taurus PELI1 VGNC VGNC:32740
Canis familiaris PELI1 VGNC VGNC:44414
Rattus norvegicus PELI1 RGD RGD:1311199
Others PELI1 NCBI