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HCC thyroid carcinoma, Hurthle cell [ Homo sapiens (human) ]

Gene ID: 619501, discontinued on 13-Sep-2024

Summary

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Official Symbol
HCCprovided by HGNC
Official Full Name
thyroid carcinoma, Hurthle cellprovided by HGNC
Primary source
MIM:607464
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:
17p13

Bibliography

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Related articles in PubMed

  1. High resolution loss of heterozygosity mapping of 17p13 in thyroid cancer: Hurthle cell carcinomas exhibit a small 411-kilobase common region of allelic imbalance, probably containing a novel tumor suppressor gene. Farrand K, et al. J Clin Endocrinol Metab, 2002 Oct. PMID 12364463

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
thyroid carcinoma, Hurthle cell
OMIM: 607464GeneReviews: Not available

General gene information

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Markers

Property

  • phenotype only

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