1. Genes and Genomic Entities
  2. ARHGAP35

ARHGAP35

Rho GTPase activating protein 35
OMIM: 605277, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Green ARHGAP35 in Hypogonadotropic hypogonadism (GMS)


Level 2: Endocrinology
Version 5.2
Latest signed off version: v5.0 (6 May 2026)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
  • Literature
Phenotypes
  • hypogonadotropic hypogonadism, MONDO:0018555
Tags
  • gene-checked
Green ARHGAP35 in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • ARHGAP35-related developmental disorder (monoallelic)
    Tags
    • gene-checked
    Amber ARHGAP35 in Intellectual disability


    Level 2: Developmental disorders
    Version 10.17
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Developmental disorder
    Tags
    • watchlist
    • gene-checked
    Green ARHGAP35 in Structural eye disease


    Level 2: Ophthalmology
    Version 5.6
    Latest signed off version: v5.0 (6 May 2026)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Anophthalmia
    • microphthalmia
    • coloboma
    Tags
    • gene-checked