Description
This panel was developed and is maintained by VCGS.

9 reviewers

  • Manny Jacobs (Victorian Clinical Genetics Services)

  • John Coleman (Murdoch Children's Research Institute)

  • Teresa Zhao (Victorian Clinical Genetics Services)

  • Chirag Patel (Genetic Health Queensland)

  • Ain Roesley (Victorian Clinical Genetics Services)

  • Elena Savva (Victorian Clinical Genetics Services)

  • Bryony Thompson (Royal Melbourne Hospital)

  • Paul De Fazio (Victorian Clinical Genetics Services)

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

24 Entities

24 reviewed, 19 green

List Entity Reviews Mode of inheritance Details
24 Entitiess
Green Green List (high evidence)
AP3B1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hermansky-Pudlak syndrome 2, MIM# 608233
  • MONDO:0011997
Tags
  • clinical trial
  • treatable
Green Green List (high evidence)
BLOC1S3
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hermansky-Pudlak syndrome 8, MIM# 614077
  • MONDO:0013560
Tags
Green Green List (high evidence)
BLOC1S5
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Hermansky–Pudlak syndrome type 11, 619172
Tags
Green Green List (high evidence)
BLOC1S6
2 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hermansky-Pudlak syndrome 9, MIM# 614171
Tags
Green Green List (high evidence)
DCT
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Oculocutaneous albinism, type VIII, MIM# 619165
Tags
Green Green List (high evidence)
DTNBP1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hermansky-Pudlak syndrome 7, MIM# 614076
  • MONDO:0013559
Tags
Green Green List (high evidence)
GPR143
2 reviews
2 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ocular albinism, type I, Nettleship-Falls type, MIM# 300500
  • MONDO:0021019
Tags
Green Green List (high evidence)
HPS1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hermansky-Pudlak syndrome 1, MIM# 203300
  • MONDO:0008748
Tags
Green Green List (high evidence)
HPS3
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hermansky-Pudlak syndrome 3, MIM# 614072
  • MONDO:0013555
Tags
Green Green List (high evidence)
HPS4
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hermansky-Pudlak syndrome 4, MIM# 614073
  • MONDO:0013556
Tags
Green Green List (high evidence)
HPS5
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hermansky-Pudlak syndrome 5 (MIM#614074)
Tags
Green Green List (high evidence)
HPS6
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hermansky-Pudlak syndrome 6, MIM# 614075
  • MONDO:0013558
Tags
Green Green List (high evidence)
LRMDA
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Albinism, oculocutaneous, type VII, MIM# 615179
  • MONDO:0014070
Tags
Green Green List (high evidence)
LYST
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Chediak-Higashi syndrome, MIM# 214500
Tags
Green Green List (high evidence)
OCA2
2 reviews
2 green
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
Tags
Green Green List (high evidence)
SLC24A5
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Albinism, oculocutaneous, type VI, MIM# 113750
Tags
Green Green List (high evidence)
SLC45A2
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Albinism, oculocutaneous, type IV, MIM# 606574
  • MONDO:0011683
Tags
Green Green List (high evidence)
TYR
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Albinism, oculocutaneous, type IA, MIM# 203100
  • MONDO:0008745
  • Albinism, oculocutaneous, type IB, MIM# 606952
Tags
Green Green List (high evidence)
TYRP1
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Albinism, oculocutaneous, type III, MIM# 203290
  • MONDO:0008747
Tags
Amber Amber List (moderate evidence)
AP3D1
2 reviews
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Amber
  • Literature
  • NHS GMS
Phenotypes
  • Hermansky-Pudlak syndrome 10, MIM# 617050
Tags
Amber Amber List (moderate evidence)
CLCN7
1 review
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Hypopigmentation, organomegaly, and delayed myelination and development, MIM# 618541
Tags
Amber Amber List (moderate evidence)
MC1R
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • {Albinism, oculocutaneous, type II, modifier of}, MIM# 203200
Tags
Amber Amber List (moderate evidence)
TPCN2
1 review
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Hypopigmentation of the skin MONDO:0019290
Tags
Red Red List (low evidence)
PMEL
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Cculocutaneous albinism, PMEL-related MONDO:0018910
Tags

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