absent proamniotic cavity Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the cavity of the developing embryo that is formed within the epiblast tissue prior to the closing of the proamniotic canal by the amniotic folds (Mammalian Phenotype Ontology, MP_0011198)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011198
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11 gene mutations causing the absent proamniotic cavity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GADD45GIP1 growth arrest and DNA-damage-inducible, gamma interacting protein 1
HNF1B HNF1 homeobox B
HSP90B1 heat shock protein 90kDa beta (Grp94), member 1
LIMS1 LIM and senescent cell antigen-like domains 1
NBN nibrin
PPP1R8 protein phosphatase 1, regulatory subunit 8
PRMT1 protein arginine methyltransferase 1
SBDS Shwachman-Bodian-Diamond syndrome
TRAIP TRAF interacting protein
USP7 ubiquitin specific peptidase 7 (herpes virus-associated)
ZBTB17 zinc finger and BTB domain containing 17