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HPFH2 hereditary persistence of fetal hemoglobin, heterocellular, Indian type [ Homo sapiens (human) ]

Gene ID: 3247, updated on 31-Aug-2024

Summary

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Official Symbol
HPFH2provided by HGNC
Official Full Name
hereditary persistence of fetal hemoglobin, heterocellular, Indian typeprovided by HGNC
Primary source
MIM:142335
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
7q36

Bibliography

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Related articles in PubMed

  1. Fetal hemoglobin in sickle cell anemia. Akinsheye I, et al. Blood, 2011 Jul 7. PMID 21490337, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
hereditary persistence of fetal hemoglobin, heterocellular, Indian type
OMIM: 142335GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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