ALX4
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 11[13]
- Cytogenetic location
- 11p11.2[19]
- Encodes
- ALX homeobox 4[11]
- Expressed in
- gonad, olfactory zone of nasal mucosa, tendon, muscle of thigh, Achilles tendon, ganglionic eminence, skin of abdomen, skin of leg, skeletal muscle tissue, prefrontal cortex[20][21][22][23][24][25][26][27][28][29]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- frontonasal dysplasia with alopecia and genital anomaly, Potocki–Shaffer syndrome, craniosynostosis 5, susceptibility to, parietal foramina[14][15][16][17]
- HomoloGene ID
- 7229[3]
- Strand orientation
- reverse strand[18]
🏷️ Also known as
en ALX4
en ALX homeobox 4
en CRS5
en FND2
ar ALX٤
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000052850
- Ensembl transcript ID
- ENST00000652299
- Entrez Gene ID
- 60529
- Exact match
- identifiers.org
- Freebase ID
- /m/03hmg7x
- HGNC ID
- 450
- HGNC gene symbol
- ALX4
- OMIM ID
- 605420
- RefSeq RNA ID
- NM_021926
- UMLS CUI
- C1412373
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