OCA2

OCA2 melanosomal transmembrane protein
OMIM: 611409, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green OCA2 in Ocular and Oculocutaneous Albinism


Level 2: Ophthalmological disorders
Version 1.11

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Albinism, brown oculocutaneous, MIM# 203200
  • Albinism, oculocutaneous, type II, MIM# 203200

Green OCA2 in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Albinism, brown oculocutaneous 203200
  • Albinism, oculocutaneous, type II 203200
  • autosomal dominant Albinism, oculocutaneous
Tags
  • SV/CNV

Green OCA2 in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 0.109

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Albinism, brown oculocutaneous, 203200 (3)

Green OCA2 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Albinism, oculocutaneous

Green OCA2 in Congenital nystagmus


Level 2: Ophthalmological disorders
Version 1.21

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • NHS Genomic Medicine Service
  • Victorian Clinical Genetics Services
Phenotypes
  • Albinism, brown oculocutaneous, MIM# 203200
  • Albinism, oculocutaneous, type II, MIM# 203200

Red OCA2 in Prepair 1000+


Level 2: Screening
Version 1.9

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Mackenzie's Mission
Phenotypes
  • Albinism, oculocutaneous, type II (MIM#203200)

Red OCA2 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.114

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BabySeq Category A gene
Phenotypes
  • Albinism, oculocutaneous, type II, MIM# 203200
  • Albinism, brown oculocutaneous, MIM# 203200