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ALX4

ALX4

Protein-coding gene in the species Homo sapiens

protein aristaless-like 4 is a protein that in humans is encoded by the ALX4 gene. Alx4 belongs to the group-1 aristaless-related genes, a majority of which

ALX4

Omphalocele

Congenital defect

myotubules that form muscle fibers. Mutations in homeobox genes such as Alx4, that direct the formation of body structures during early embryonic development

Omphalocele

Dun gene

Dilution gene

non-dun2 is predicted to include binding sites for the transcription factors ALX4 and MSX2, which are both known to be involved in hair follicle development

Dun gene

Dun_gene

Lymphoid enhancer-binding factor 1

Protein-coding gene in the species Homo sapiens

with: ALX4, AML-1, Catenin beta-1/β-catenin/CTNNB1, including transgenically, EP300, MITF PIAS4, SMAD2, and SMAD3. ALX4, a protein encoded by the ALX4 gene

Lymphoid enhancer-binding factor 1

Lymphoid_enhancer-binding_factor_1

List of human transcription factors

ENSG00000156150 Homeodomain Known motif – High-throughput in vitro [18] TAATTR ALX4 ENSG00000052850 Homeodomain Known motif – High-throughput in vitro [19] TAATYNRRTTA

List of human transcription factors

List_of_human_transcription_factors

Homeobox

DNA pattern affecting anatomy development

ZEB2; ZFHX2, ZFHX3, ZFHX4; ZHX1, HOMEZ; PRD-class: ALX1 (CART1), ALX3, ALX4; ARGFX; ARX; DMBX1; DPRX; DRGX; DUXA, DUXB, DUX (1, 2, 3, 4, 4c, 5); ESX1;

Homeobox

Parietal foramina

largely an autosomal dominant heritable condition associated with the MSX2 or ALX4 genes. FPP is often asymptomatic, but it is also associated with headaches

Parietal foramina

Parietal_foramina

Zone of polarizing activity

expresses a TF called ALX4 at the anterior part of the mesoderm, with the TF HOXB8 being expressed at the posterior portion. The Alx4 region, the medial

Zone of polarizing activity

Zone_of_polarizing_activity

Ciliopathy

Genetic disease resulting in abnormal formation or function of cilia

Focal dermal hypoplasia 305600 PORCN Frontonasal dysplasia 136760 ALX3, ALX4, ALX1 Fryns microphthalmia syndrome 600776 Fryns syndrome 229850 Genitopatellar

Ciliopathy

List of conditions with craniosynostosis

List of medical conditions involving craniosynostosis

trigonocephaly, turricephaly Usually considered nonsyndromic. Craniosynostosis (ALX4) Susceptible cause; usually considered nonsyndromic. Craniosynstosis (ZIC1)

List of conditions with craniosynostosis

List_of_conditions_with_craniosynostosis

List of human protein-coding genes 1

HGNC:20605; Q60I27 607 ALX1 HGNC:1494; Q15699 608 ALX3 HGNC:449; O95076 609 ALX4 HGNC:450; Q9H161 610 ALYREF HGNC:19071; Q86V81 611 AMACR HGNC:451; Q9UHK6

List of human protein-coding genes 1

List_of_human_protein-coding_genes_1

List of OMIM disorder codes

Frontometaphyseal dysplasia; 305620; FLNA Frontonasal dysplasia 2; 613451; ALX4 Frontonasal dysplasia 3; 613456; ALX1 Frontorhiny; 136760; ALX3 Frontotemporal

List of OMIM disorder codes

List_of_OMIM_disorder_codes

ALX1

Protein-coding gene in humans

deCrombrugghe B, Wisdom R (Jan 1999). "Physical and genetic interactions between Alx4 and Cart1". Development. 126 (2): 359–69. doi:10.1242/dev.126.2.359. PMID 9847249

ALX1

Adams–Oliver syndrome

Medical condition

associated with chromosomal translocations. A panel of candidate genes (including ALX4, ALX1, MSX1, MSX2, P63, RUNX2 and HOXD13) were tested but no disease-causing

Adams–Oliver syndrome

Adams–Oliver_syndrome

TBX15

Human protein and coding gene

the scapula itself. Tbx15 appears to play a synergistic role with Gli3 and Alx4 in the formation of the skeletal features of the shoulder girdle, with more

TBX15

2019 in archosaur paleontology

volumes. A study on the expression patterns of the anterior genes Gli3 and Alx4 in limb buds of emu, chicken and zebra finch embryos, and on their implications

2019 in archosaur paleontology

2019_in_archosaur_paleontology