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Mendeliome

Gene: HP

Red List (low evidence)

HP (haptoglobin)
EnsemblGeneIds (GRCh38): ENSG00000257017
EnsemblGeneIds (GRCh37): ENSG00000257017
OMIM: 140100, Gene2Phenotype
HP is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Mendelian variable rather than disease association.
Created: 4 May 2022, 6:21 a.m. | Last Modified: 4 May 2022, 6:21 a.m.
Panel Version: 0.13708

Phenotypes
[Anhaptoglobinemia] 614081; [Hypohaptoglobinemia] 614081

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • [Anhaptoglobinemia] 614081
  • [Hypohaptoglobinemia] 614081
OMIM
140100
Clinvar variants
Variants in HP
Penetrance
None
Panels with this gene

History Filter Activity

4 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: hp has been classified as Red List (Low Evidence).

4 May 2022, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: HP were changed from to [Anhaptoglobinemia] 614081; [Hypohaptoglobinemia] 614081

4 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: hp has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: HP was added gene: HP was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: HP was set to Unknown