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TBX6

TBX6

Protein-coding gene in the species Homo sapiens

T-box 6 is a protein that in humans is encoded by the TBX6 gene. This gene is a member of a phylogenetically conserved family of genes that share a common

TBX6

Myogenesis

Formation of muscular tissue, particularly during embryonic development

by a gene regulatory network that includes a member of the T-box family, tbx6, ripply1, and mesp-ba. Skeletal myogenesis depends on the strict regulation

Myogenesis

16p11.2 deletion syndrome

Rare condition caused by a microdeletion on the short arm of chromosome 16

ASPHD1 KCTD13 TMEM219 TAOK2 HIRIP3 INO80E DOC2A C16orf92 FAM57B ALDOA PPP4C TBX6 YPEL3 GDPD3 MAPK3 CORO1A BOLA2 SLX1A SLX1B SULT1A3 SULT1A4 Nearby regions

16p11.2 deletion syndrome

16p11.2_deletion_syndrome

T-box

Genes that affect limb and heart development

TBR1 (TBR1) TBX1 (TBX1) TBX2 (TBX2) TBX3 (TBX3) TBX4 (TBX4) TBX5 (TBX5) TBX6 (TBX6) TBX10 (TBX10) TBX15 (TBX15) TBX18 (TBX18) TBX19 (TBX19) TBX20 (TBX20)

T-box

MESP2

Protein-coding gene in the species Homo sapiens

Nelson AC, Valentin G, Tan H, Oates AC, Wardle FC, Devoto SH (Mar 2015). "Tbx6, Mesp-b and Ripply1 regulate the onset of skeletal myogenesis in zebrafish"

MESP2

List of human transcription factors

ENSG00000089225 T-box Known motif – High-throughput in vitro [910] TVACACCT TBX6 ENSG00000149922 T-box Known motif – High-throughput in vitro [911] TVACACSY

List of human transcription factors

List_of_human_transcription_factors

TBX3

Protein-coding gene in the species Homo sapiens

five subfamilies, namely Brachyury (T), T-brain (Tbr1), TBX1, TBX2, and TBX6. Tbx3 is a member of the Tbx2 subfamily which includes Tbx2, Tbx4 and Tbx5

TBX3

Fibroblast growth factor and mesoderm formation

Brachyury (frogs) or No tail (fish) (10), VegT (frog) or Spadetail (fish), and Tbx6 (fish and frogs) (11) are important FGF targets that play a key role in mesoderm

Fibroblast growth factor and mesoderm formation

Fibroblast_growth_factor_and_mesoderm_formation

Transmembrane protein 268

Protein-coding gene in the species Homo sapiens

"Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6". Human Molecular Genetics. 22 (8): 1625–31. doi:10.1093/hmg/ddt012. PMID 23335591

Transmembrane protein 268

Transmembrane_protein_268

Spondylocostal dysostosis

Axial skeleton growth disorder

608681 MESP2 15q26.1 SCDO3 609813 LFNG 7p22.3 SCDO4 613686 HES7 17p13.1 SCDO5 122600 TBX6 16p11.2 SCDO6 616566 RIPPLY2 6q14.2 SCDO7 621523 DMRT2 9p24.3

Spondylocostal dysostosis

Spondylocostal_dysostosis

List of human protein-coding genes 8

O15119 16413 TBX4 HGNC:11603; P57082 16414 TBX5 HGNC:11604; Q99593 16415 TBX6 HGNC:11605; O95947 16416 TBX10 HGNC:11593; O75333 16417 TBX15 HGNC:11594;

List of human protein-coding genes 8

List_of_human_protein-coding_genes_8

Gastruloid

Embryonic Stem Cells

near the region expressing T/Bra, cells expressing the mesodermal marker tbx6 are extruded from the similar to cells in the gastrulating embryo; it is

Gastruloid

TBX19

Protein-coding gene in the species Homo sapiens

phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19". Genomics. 55 (1): 10–20. doi:10.1006/geno.1998.5632.

TBX19

Spliceman

Morin-Papunen, Laure; Rosenberg, Carla; Aittomäki, Kristiina (2013-08-16). "TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia"

Spliceman

TMEM61

Protein and coding gene in humans

473 682 + E2F6\ 376 528 - TFAP2B\ 58 514 - KLF4\ 170 522 - NFIC\ 564 548 + Tbx6\ 488 537 + PLAG1\ 235 512 - THAP1\ 376 510 + TFAP2C\ 59 494 + KLF10\ 376

TMEM61