parathyroid hormone responsive B1 gene

Introduction

7p14

Pathology

• chromosomal aberration involving PTHB1 translocation t(1;7)(q42;p15) with OBSCN is found in Wilms tumor 5
• defects in PTHB1 are a cause of Bardet-Biedl syndrome type 9

More general terms

• unclassified gene

Database

• OMIM: https://mirror.omim.org/entry/607968
• Entrez gene: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=27241