(Q14888283)

English

THBD

protein-coding gene in the species Homo sapiens

AHUS6
BDCA3
CD141
THPH12
THRM
TM
thrombomodulin
BDCA-3

In more languages

default values for all languages

No label defined

No description defined

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

class of disease

0 references

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000178726

rare thrombotic disorder due to a constitutional coagulation factors defect

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Protein THBD PDB 1adx.png
672 × 391; 118 KB

0 references

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

1 reference

6 July 2017

UniProt protein ID

human chromosome 20

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

23045633

human chromosome 20

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

23026270

human chromosome 20

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

23030378

human chromosome 20

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

23049672

human chromosome 20

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

cytogenetic location

20p11.21

1 reference

15 May 2022

308

1 reference

15 May 2022

Gene Atlas image

PBB GE THBD 203888 at fs.png
732 × 530; 11 KB

0 references

PBB GE THBD 203887 s at fs.png
732 × 530; 11 KB

0 references

2 references

HomoloGene build68

308

Orthologous MAtrix

https://omabrowser.org/oma/vps/P07204/

2 references

HomoloGene build68

308

Orthologous MAtrix

https://omabrowser.org/oma/vps/P07204/

gingival epithelium

1

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

2

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

3

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

4

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

skin of abdomen

5

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

6

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

periodontal fiber

7

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

lower lobe of lung

8

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

upper lobe of left lung

9

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

left coronary artery

10

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000178726

http://identifiers.org/ncbigene/7056

1 reference

Identifiers.org

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

http://www.orpha.net/ORDO/Orphanet_3324

0 references

Identifiers

1 reference

15 May 2022

1 reference

15 May 2022

Ensembl gene ID

ENSG00000178726

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

Ensembl transcript ID

ENST00000377103

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000178726

GARD rare disease ID

0 references

HGNC gene symbol

1 reference

15 May 2022

1 reference

15 May 2022

mapping relation type

2 references

Monarch Disease Ontology release 2018-06-29

28 July 2018

Online Mendelian Inheritance in Man

19 August 2019

0 references

1 reference

based on heuristic

inferred by common HGNC mappings on source and on Wikidata

15 June 2023

Sitelinks

Wikipedia(0 entries)

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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