abnormal seminal vesicle development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant or incomplete differentiation of either of the paired sac-like glandular structures situated posterolateral to the urinary bladder in the male and functioning as part of the reproductive system; seminal vesicles develop from the segments of the Wolffian ducts immediately adjacent to the urogenital sinus (Mammalian Phenotype Ontology, MP_0013317)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013317
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Genes

8 gene mutations causing the abnormal seminal vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
FGFR2 fibroblast growth factor receptor 2
GDF7 growth differentiation factor 7
HOXA10 homeobox A10
HOXA13 homeobox A13
KISS1 KiSS-1 metastasis-suppressor
LACTB2 lactamase, beta 2
SAFB scaffold attachment factor B