sternebra fusion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description appearance of one or more sternebrae as a single structure (Mammalian Phenotype Ontology, MP_0010082)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010082
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Genes

14 gene mutations causing the sternebra fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
COL27A1 collagen, type XXVII, alpha 1
DERL2 derlin 2
DLL3 delta-like 3 (Drosophila)
EFNB1 ephrin-B1
GLI3 GLI family zinc finger 3
HOXA4 homeobox A4
HOXA5 homeobox A5
KMT2A lysine (K)-specific methyltransferase 2A
PAX1 paired box 1
RPL38 ribosomal protein L38
SOX11 SRY (sex determining region Y)-box 11
SULF1 sulfatase 1
SULF2 sulfatase 2