1. Gene
  2. PRPF39 - pre-mRNA processing factor 39 Gene

PRPF39 - pre-mRNA processing factor 39 Gene

Homo sapiens
Gene ID: 55015 | Gene type: protein coding

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
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference 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 Reference
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