Early Detection Research Network

PQBP1

Aliases:
This biomarker is also known as:
  • Npw38,
  • MRXS8,
  • RENS1,
  • NPW38,
  • 38 kDa nuclear protein containing a WW domain,
  • nuclear protein containing WW domain 38 kD,
  • Polyglutamine tract-binding protein 1,
  • Sutherland-Haan X-linked mental retardation syndrome,
  • SHS,
  • MRXS3,
  • polyglutamine binding protein 1,
  • mental retardation, X-linked 55,
  • MRX55,
  • polyglutamine tract-binding protein 1,
  • PQBP1,
  • polyglutamine-binding protein 1,
  • PQBP-1,

Description…

From NCBI Gene: This gene encodes a nuclear polyglutamine-binding protein that is involved with transcription activation. The encoded protein contains a WW domain. Mutations in this gene have been found in patients with Renpenning syndrome 1 and other syndromes with X-linked mental retardation. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.[provided by RefSeq, Nov 2009]

Datasets

There are no datasets associated with this biomarker.

Attributes
QA State: Curated
Type: Gene
HGNC Name: PQBP1

The following organs have data associated with this biomarker…

Attributes

Phase: One
QA State: Curated
Organ-specific information for this biomarker is currently being annotated or is under review. You must be logged in or do not have permission to view any additional information. Contact the Informatics Center if you should have access to this biomarker.

This biomarker is currently being annotated or is under review. You must be logged in or do not have permission to view any additional information. Contact the Informatics Center if you should have access to this biomarker.