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...
9 KB (1,078 words) - 22:21, 13 October 2022
myotubules that form muscle fibers. Mutations in homeobox genes such as Alx4, that direct the formation of body structures during early embryonic development...
27 KB (3,063 words) - 17:50, 17 August 2024
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;...
41 KB (4,385 words) - 21:28, 21 August 2024
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...
20 KB (2,643 words) - 17:52, 2 September 2024
Focal dermal hypoplasia 305600 PORCN Frontonasal dysplasia 136760 ALX3, ALX4, ALX1 Fryns microphthalmia syndrome 600776 Fryns syndrome 229850 Genitopatellar...
35 KB (2,499 words) - 18:40, 12 July 2024
ENSG00000156150 Homeodomain Known motif – High-throughput in vitro [18] TAATTR ALX4 ENSG00000052850 Homeodomain Known motif – High-throughput in vitro [19] TAATYNRRTTA...
374 KB (81 words) - 02:10, 23 September 2023
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...
15 KB (2,078 words) - 01:03, 24 November 2022
target. Lymphoid enhancer-binding factor 1 has been shown to interact with: ALX4, AML-1, Catenin beta-1/β-catenin/CTNNB1, including transgenically, EP300...
15 KB (1,797 words) - 07:24, 15 January 2024
HGNC:20605 Q60I27 605 ALX1 HGNC:1494 Q15699 606 ALX3 HGNC:449 O95076 607 ALX4 HGNC:450 Q9H161 608 ALYREF HGNC:19071 Q86V81 609 AMACR HGNC:451 Q9UHK6 610...
277 KB (17 words) - 18:34, 6 October 2024
associated with chromosomal translocations. A panel of candidate genes (including ALX4, ALX1, MSX1, MSX2, P63, RUNX2 and HOXD13) were tested but no disease-causing...
18 KB (1,952 words) - 19:51, 23 August 2024
trigonocephaly, turricephaly Usually considered nonsyndromic. Craniosynostosis (ALX4) Susceptible cause; usually considered nonsyndromic. Craniosynstosis (ZIC1)...
52 KB (2,779 words) - 23:07, 7 October 2024
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...
6 KB (822 words) - 07:32, 7 June 2023
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...
12 KB (1,474 words) - 06:58, 20 December 2023
Frontometaphyseal dysplasia; 305620; FLNA Frontonasal dysplasia 2; 613451; ALX4 Frontonasal dysplasia 3; 613456; ALX1 Frontorhiny; 136760; ALX3 Frontotemporal...
234 KB (18,877 words) - 06:16, 6 November 2024
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...
341 KB (35,610 words) - 23:16, 15 November 2024