HFE (Q14890978): Difference between revisions

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@@ Property / genetic association: cardiovascular disease / reference @@
+reference URL: https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1287&ncbiId=3077
reference URL: http://www.genome.gov/gwastudies/index.cfm?gene=HFE
stated in: Phenocarta
stated in: Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits
retrieved: 20 November 2018Timestamp +2018-11-20T00:00:00Z
Zeitzone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2018-11-20T00:00:00Z
-Zeitzone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / genetic association: cardiovascular disease / reference @@
-reference URL: https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1287&ncbiId=3077
reference URL: http://www.genome.gov/gwastudies/index.cfm?gene=HFE
stated in: Phenocarta
stated in: Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits
retrieved: 22 May 2018Timestamp +2018-05-22T00:00:00Z
Zeitzone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2018-05-22T00:00:00Z
-Zeitzone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / genetic association: arterial hypertension / reference @@
+reference URL: https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10763&ncbiId=3077
reference URL: http://www.genome.gov/gwastudies/index.cfm?gene=HFE
stated in: Phenocarta
stated in: Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
retrieved: 20 November 2018Timestamp +2018-11-20T00:00:00Z
Zeitzone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2018-11-20T00:00:00Z
-Zeitzone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / genetic association: arterial hypertension / reference @@
-reference URL: https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10763&ncbiId=3077
reference URL: http://www.genome.gov/gwastudies/index.cfm?gene=HFE
stated in: Phenocarta
stated in: Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
retrieved: 22 May 2018Timestamp +2018-05-22T00:00:00Z
Zeitzone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2018-05-22T00:00:00Z
-Zeitzone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After

Revision as of 19:22, 20 November 2018

protein-coding gene in the species Homo sapiens

HFE1
HH
HLA-H
MVCD7
TFQTL2
HFE gene
hemochromatosis
homeostatic iron regulator

Sprache	Label	Description	Also known as
Englisch	HFE	protein-coding gene in the species Homo sapiens	HFE1 HH HLA-H MVCD7 TFQTL2 HFE gene hemochromatosis homeostatic iron regulator

Statements

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000010704

Protein HFE PDB 1a6z.png
994 × 374; 279 KB

0 references

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

homeostatic iron regulator

1 reference

6 July 2017

UniProt protein ID

genetic association

cardiovascular disease

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1287&ncbiId=3077

http://www.genome.gov/gwastudies/index.cfm?gene=HFE

Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits

20 November 2018

arterial hypertension

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10763&ncbiId=3077

http://www.genome.gov/gwastudies/index.cfm?gene=HFE

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

20 November 2018

human chromosome 6

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

26087281

human chromosome 6

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

26087509

human chromosome 6

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

26098343

human chromosome 6

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

26098571

human chromosome 6

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

cytogenetic location

6p22.2

1 reference

12 October 2018

88330

1 reference

12 October 2018

Gene Atlas image

PBB GE HFE 206086 x at fs.png
732 × 530; 12 KB

0 references

PBB GE HFE 206087 x at fs.png
732 × 530; 12 KB

0 references

PBB GE HFE 211330 s at fs.png
732 × 530; 12 KB

0 references

1 reference

HomoloGene build68

88330

1 reference

HomoloGene build68

88330

http://identifiers.org/ncbigene/3077

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

Identifiers

MeSH descriptor ID

0 references

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

1 reference

12 October 2018

Ensembl gene ID

ENSG00000010704

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

Ensembl transcript ID

ENST00000488199

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000309234

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000317896

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000336625

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000349999

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000352392

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000353147

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000357618

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000397022

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000461397

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000470149

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000483782

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000485729

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

ENST00000486147

1 reference

ensembl Release 94

Ensembl gene ID

ENSG00000010704

HGNC gene symbol

1 reference

12 October 2018

1 reference

12 October 2018

Sitelinks

Wikipedia(6 entries)

cywiki HFE
dewiki Hereditäre-Hämochromatose-Protein
enwiki HFE (gene)
frwiki HFE (protéine)
slwiki Gen HFE
ukwiki HFE

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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