THBD
protein-coding gene in the species Homo sapiens
Facts
14 properties- Subclass of
- protein-coding gene, rare thrombotic disorder due to a constitutional coagulation factors defect[3][4]
- Chromosome
- human chromosome 20[13]
- Cytogenetic location
- 20p11.21[15]
- Encodes
- thrombomodulin[11]
- Expressed in
- gingival epithelium, vena cava, right lung, skin of hip, skin of abdomen, skin of thigh, periodontal fiber, lower lobe of lung, upper lobe of left lung, left coronary artery[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- HomoloGene ID
- 308[5]
- On focus list of Wikimedia project
- concrete/abstract disjunction anomalies[16]
- P14914
- D03324[27]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en AHUS6
en BDCA-3
en BDCA3
en CD141
en THBD
en THPH12
en THRM
en thrombomodulin
en TM
he תרומבומודולין
it Trombomodulina
ru Тромбомодулин
🔖 Identifiers · 12
- Image (Wikimedia Commons)
- Protein THBD PDB 1adx.png ↗
- Ensembl gene ID
- ENSG00000178726
- Ensembl transcript ID
- ENST00000377103
- Entrez Gene ID
- 7056
- Exact match
- identifiers.org, www.orpha.net
- GARD rare disease ID
- 5195
- HGNC ID
- 11784
- HGNC gene symbol
- THBD
- OMIM ID
- 188040
- Orphanet ID
- 3324
- RefSeq RNA ID
- NM_000361
- UMLS CUI
- C1420720
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Summary
THBD is a gene[1].