SPRY4

sprouty RTK signaling antagonist 4
OMIM: 607984, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Amber SPRY4 in Hypogonadotropic hypogonadism

Level 3: Hypothalamic and pituitary disorders
Level 2: Endocrine disorders
Version 1.41

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Literature
  • Radboud University Medical Center, Nijmegen
  • Expert list
Phenotypes
  • Hypogonadotropic hypogonadism 17 with or without anosmia, OMIM:615266
Tags
  • monogenic-polygenic
Amber SPRY4 in Hypogonadotropic hypogonadism (GMS)


Version 3.18
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
  • Expert list
  • Radboud University Medical Center, Nijmegen
  • Expert Review Amber
Phenotypes
  • Hypogonadotropic hypogonadism 17 with or without anosmia, OMIM:615266
Tags
  • monogenic-polygenic
Red SPRY4 in Fetal anomalies


Version 4.1
Latest signed off version: v4.0 (1 May 2024)

review Unknown
Sources
  • Expert Review Red
  • PAGE Additional Gene List
Phenotypes
  • Hypogonadotropic hypogonadism 17 with or without anosmia 615266
Red SPRY4 in Rare syndromic craniosynostosis or isolated multisuture synostosis

Level 3: Craniosynostosis syndromes
Level 2: Skeletal disorders
Version 5.1
Latest signed off version: v5.0 (1 May 2024)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
Phenotypes
  • craniosynostosis, MONDO:0015469