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Protein-coding gene in the species Homo sapiens
Homeobox protein Hox-A2 is a protein that in humans is encoded by the HOXA2 gene. In vertebrates, the genes encoding the class of transcription factors
HOXA2
Group of genes
Cluster Human Chromosome Genes HOXA@ chromosome 7 HOXA1, HOXA2, HOXA3, HOXA4, HOXA5, HOXA6, HOXA7, HOXA9, HOXA10, HOXA11, HOXA13 HOXB@ chromosome 17 HOXB1
Hox_gene
Part of the temporal bone
Kazuhiro; Miyagawa-Tomita, Sachiko (2015-06-15). "Distinct effects of Hoxa2 overexpression in cranial neural crest populations reveal that the mammalian
Temporal_styloid_process
ENSG00000106031 Homeodomain Known motif – High-throughput in vitro [375] DTTTTATKRS HOXA2 ENSG00000105996 Homeodomain Known motif – High-throughput in vitro [376]
List of human transcription factors
List_of_human_transcription_factors
DNA pattern affecting anatomy development
name chromosome gene HOXA (or sometimes HOX1) - HOXA@ chromosome 7 HOXA1, HOXA2, HOXA3, HOXA4, HOXA5, HOXA6, HOXA7, HOXA9, HOXA10, HOXA11, HOXA13 HOXB -
Homeobox
Protein-coding gene in humans
defects associated with mutations in Hoxa1 restore normal palatogenesis to Hoxa2 mutants". Development. 126 (22): 5011–26. doi:10.1242/dev.126.22.5011. PMID 10529419
Homeobox_A1
Non-coding RNA in the species Homo sapiens
long non-coding RNA gene. In humans, it is located between the HOXA1 and HOXA2 genes. HOTAIRM1 is expressed in cells of a myeloid lineage, and may play
HOTAIRM1
Portion of the cranium that is derived from pharyngeal arches
Kazuhiro; Miyagawa-Tomita, Sachiko (2015-06-15). "Distinct effects of Hoxa2 overexpression in cranial neural crest populations reveal that the mammalian
Splanchnocranium
Transient structure in animal development
origins of vestibular projection neurons assessed using rhombomere-specific Hoxa2 enhancer elements in the mouse embryo". The Journal of Neuroscience. 27
Rhombomere
Protein-coding gene in humans
Maconochie MK, Neun R, Pattyn A, Chambon P, Krumlauf R, Rijli FM (Apr 1999). "Hoxa2 and Hoxb2 control dorsoventral patterns of neuronal development in the rostral
HOXB2
9; 601186; STRA6 Microtia, hearing impairment, and cleft palate; 612290; HOXA2 Microvillus inclusion disease; 251850; MYO5B Migraine, familial basilar;
List_of_OMIM_disorder_codes
Protein-coding gene in humans
Yates JA, Menon T, Thompson BA, Bochar DA (February 2010). "Regulation of HOXA2 gene expression by the ATP-dependent chromatin remodeling enzyme CHD8".
CHD8
Q86X24 7192 HORMAD2 HGNC:28383; Q8N7B1 7193 HOXA1 HGNC:5099; P49639 7194 HOXA2 HGNC:5103; O43364 7195 HOXA3 HGNC:5104; O43365 7196 HOXA4 HGNC:5105; Q00056
List of human protein-coding genes 4
List_of_human_protein-coding_genes_4
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