PRPF39 - pre-mRNA processing factor 39 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 55015

About PRPF39

Cytogenetic location: 14q21.2 Genomic coordinates (GRCh38): 14:45,084,116-45,116,282 (from NCBI)

This gene has 12 transcripts (splice variants) and 210 orthologues. Ubiquitous expression in skin (RPKM 15.3), prostate (RPKM 14.2) and 25 other tissues.

Summary

Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP; U2-type prespliceosome; and commitment complex. [provided by Alliance of Genome Resources, Apr 2022]

PRPF39 Products (1)

mRNA Protein Name
NM_017922.4 NP_060392.3 pre-mRNA-processing factor 39
Molecular Function GO Annotation Evidence Verweise Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 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
Protein Preferred Names Protein Names

pre-mRNA-processing factor 39

  • PRP39 homolog

PRPF39 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
PRPF39 Q86UA1 ATN1 Homo sapiens Q86V38 32814053
Intra
PRPF39 Q86UA1 ATN1 Homo sapiens Q86V38 32814053
Intra
PRPF39 Q86UA1 ATN1 Homo sapiens Q86V38 32814053
Intra
PRPF39 Q86UA1 FGFR3 Homo sapiens P22607 32814053
Intra
PRPF39 Q86UA1 FGFR3 Homo sapiens P22607 32814053
Intra
PRPF39 Q86UA1 FGFR3 Homo sapiens P22607 32814053
Intra
PRPF39 Q86UA1 SMN1 Homo sapiens Q16637 32814053
Intra
PRPF39 Q86UA1 SMN1 Homo sapiens Q16637 32814053
Intra
PRPF39 Q86UA1 SMN1 Homo sapiens Q16637 32814053
Intra
PRPF39 Q86UA1 TOLLIP Homo sapiens Q9H0E2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Schindler Disease
  • Alpha-N-Acetylgalactosaminidase Deficiency

  • Naga Deficiency

  • Alpha-Galactosidase B Deficiency

  • Alpha-Galnac Deficiency, Schindler Type

  • Alpha-Naga Deficiency

  • Angiokeratoma Corporis Diffusum-Glycopeptiduria

  • Galb Deficiency

  • Kanzaki Disease

  • Lysosomal Glycoaminoacid Storage Disease-Angiokeratoma Corporis Diffusum

  • Neuroaxonal Dystrophy, Schindler Type

  • Neuronal Axonal Dystrophy, Schindler Type

  • Schindler Disease, Type I

  • Schindler Disease, Type Ii

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
Bos taurus PRPF39 VGNC VGNC:33377
Mus musculus PRPF39 MGD MGI:104602
Felis catus PRPF39 VGNC VGNC:64373
Rattus norvegicus PRPF39 RGD RGD:1308702
Macaca mulatta PRPF39 VGNC VGNC:76292
Canis familiaris PRPF39 VGNC VGNC:45024
Others PRPF39 NCBI