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) - 04:21, 10 July 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) - 07:06, 25 July 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) - 05:52, 28 February 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
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
trigonocephaly, turricephaly Usually considered nonsyndromic. Craniosynostosis (ALX4) Susceptible cause; usually considered nonsyndromic. Craniosynstosis (ZIC1)...
52 KB (2,779 words) - 19:17, 14 October 2023
HGNC:20605 Q60I27 606 ALX1 HGNC:1494 Q15699 607 ALX3 HGNC:449 O95076 608 ALX4 HGNC:450 Q9H161 609 ALYREF HGNC:19071 Q86V81 610 AMACR HGNC:451 Q9UHK6 611...
277 KB (17 words) - 23:17, 27 April 2024
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