UNC13D
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 17[12]
- Cytogenetic location
- 17q25.1[16]
- Encodes
- Unc-13 homolog D, Protein unc-13 homolog D[9][10]
- Expressed in
- granulocyte, bone marrow cell, spleen, right lung, upper lobe of left lung, monocyte, sural nerve, blood, appendix, lymph node[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- familial hemophagocytic lymphohistiocytosis 3, familial hemophagocytic lymphohistiocytosis[13][14]
- HomoloGene ID
- 26714[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en HPLH3
en FHL3
en HLH3
en unc-13 homolog D
en Munc13-4
en UNC13D
ar UNC١٣D
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000092929
- Ensembl transcript ID
- ENST00000592386, ENST00000207549, ENST00000412096, ENST00000585574, ENST00000586108, ENST00000586147, ENST00000586519, ENST00000586930, ENST00000587105, ENST00000587495, ENST00000587504, ENST00000588774, ENST00000589670, ENST00000590762, ENST00000590856, ENST00000591563, ENST00000591616
- Entrez Gene ID
- 201294
- Exact match
- identifiers.org
- Freebase ID
- /m/02vxw7l
- HGNC ID
- 23147
- HGNC gene symbol
- UNC13D
- Microsoft Academic ID (discontinued)
- 2779057471
- OMIM ID
- 608897
- RefSeq RNA ID
- NM_199242
- UMLS CUI
- C1427947
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Instance of 1
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Summary
UNC13D is a gene[1].