1. Gene
  2. PPAN - peter pan homolog Gene

PPAN - peter pan homolog Gene

Homo sapiens

Also known as SSF; SSF1; SSF2; BXDC3; SSF-1

Gene ID: 56342 | Gene type: protein coding

About PPAN

Cytogenetic location: 19p13.2 Genomic coordinates (GRCh38): 19:10,106,223-10,112,012 (from NCBI)

This gene has 8 transcripts (splice variants) and 191 orthologues. Ubiquitous expression in appendix (RPKM 9.7), spleen (RPKM 9.5) and 25 other tissues.

Summary

The protein encoded by this gene is an evolutionarily conserved protein similar to yeast SSF1 as well as to the gene product of the Drosophila gene peter pan (ppan). SSF1 is known to be involved in the second step of mRNA splicing. Both SSF1 and ppan are essential for cell growth and proliferation. Exogenous expression of this gene was reported to reduce the anchorage-independent growth of some tumor cells. Read-through transcription of this gene with P2RY11/P2Y(11), an adjacent downstream gene that encodes an ATP receptor, has been found. These read-through transcripts are ubiquitously present and up-regulated during granulocyte differentiation. [provided by RefSeq, Nov 2010]

PPAN Products(3)

mRNA Protein Name
NM_001346139.1 NP_001333068.1 suppressor of SWI4 1 homolog isoform 2
NM_001346141.1 NP_001333070.1 suppressor of SWI4 1 homolog isoform 4
NM_020230.7 NP_064615.3 suppressor of SWI4 1 homolog isoform 1

PPAN Protein Structure

Brix

Brix: Brix domain (33 - 286)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 473 a.a.
Protein Preferred Names Protein Names

suppressor of SWI4 1 homolog

brix domain-containing protein 3

Related Diseases

Diseases Alias
Narcolepsy

Paroxysmal Sleep

Gelineau Syndrome

Narcoleptic Syndrome

Narcolepsy-Cataplexy Syndrome

Cataplexy And Narcolepsy

Narcolepsy, Without Cataplexy

Gelineau'S Syndrome

Narcolepsy With Or Without Cataplexy

Narcolepsy Nos

Neurodegeneration With Brain Iron Accumulation 4

NBIA4

Mpan

Mitochondrial Protein-Associated Neurodegeneration

Nbia Due To C19orf12 Mutation

Neurodegeneration With Brain Iron Accumulation Due To C19orf12 Mutation

Neurodegeneration With Brain Iron Accumulation Type 4

Mitochondrial Membrane Protein Associated Neurodegeneration

Neurodegeneration, With Brain Iron Accumulation, Type 4

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 PPAN MGD MGI:2178445
Rattus norvegicus PPAN RGD RGD:1306325