DCX
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human X chromosome[11]
- Cytogenetic location
- Xq23[15]
- Encodes
- Doublecortin[9]
- Expressed in
- ganglionic eminence, ventricular zone, tail of epididymis, endothelial cell, Brodmann area 23, middle temporal gyrus, secondary oocyte, primary visual cortex, Brodmann area 10, Brodmann area 46[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- lissencephaly, lissencephaly type 1 due to doublecortin gene mutation[12][13]
- HomoloGene ID
- 7683[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en DBCN
en DC
en DCX
en doublecortin
en LISX
en SCLH
en XLIS
it Doublecortina
ru Даблкортин
🔖 Identifiers · 13
- OpenAlex ID
- C2781461022
- Image (Wikimedia Commons)
- Protein DCX PDB 1mjd.png ↗
- Ensembl gene ID
- ENSG00000077279
- Ensembl transcript ID
- ENST00000496551, ENST00000356220, ENST00000358070, ENST00000371993, ENST00000468911, ENST00000488120, ENST00000635795, ENST00000636035, ENST00000636381, ENST00000637453, ENST00000637570, ENST00000680476
- Entrez Gene ID
- 1641
- Exact match
- identifiers.org
- Freebase ID
- /m/02qt9md
- HGNC ID
- 2714
- HGNC gene symbol
- DCX
- Microsoft Academic ID (discontinued)
- 2781461022
- OMIM ID
- 300121
- RefSeq RNA ID
- NM_000555, NM_001195553, NM_178151, NM_178152, NM_178153, XM_011530879, NM_001369370, NM_001369371, NM_001369372, NM_001369373, NM_001369374
Show all 13 identifiers +1
- UMLS CUI
- C1413938
🔗 Connections
Expressed in 4
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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