transcription factor 1-beta, also known as LMX1B, is a protein which in humans is encoded by the LMX1B gene. LMX1B is a LIM homeobox transcription factor...
8 KB (1,074 words) - 19:29, 2 December 2023
the ABO blood group locus. It is associated with random mutations in the LMX1B gene. Studies have been conducted and 83 mutations of this gene have been...
11 KB (1,134 words) - 14:38, 25 May 2025
not always recognized if it is not contained in a Kozak-like sequence. Lmx1b is an example of a gene with a weak Kozak consensus sequence. For initiation...
30 KB (3,674 words) - 01:19, 25 May 2025
HGNC:17880 Q8IWU2 8799 LMTK3 HGNC:19295 Q96Q04 8800 LMX1A HGNC:6653 Q8TE12 8801 LMX1B HGNC:6654 O60663 8802 LNP1 HGNC:28014 A1A4G5 8803 LNPEP HGNC:6656 Q9UIQ6...
277 KB (17 words) - 18:41, 6 October 2024
expression of Shh. Wnt7a also causes Lmx1b, a LIM Homeobox gene (and thus a transcription factor), to be expressed. Lmx1b is involved in dorsalization of the...
36 KB (4,234 words) - 18:27, 25 May 2025
LIM-class: ISL1, ISL2; LHX1, LHX2, LHX3, LHX4, LHX5, LHX6, LHX8, LHX9; LMX1A, LMX1B POU-class: HDX; POU1F1; POU2F1; POU2F2; POU2F3; POU3F1; POU3F2; POU3F3;...
41 KB (4,386 words) - 22:42, 24 May 2025
Lissencephaly X2 MNX1 Currarino syndrome HOXD13 SPD1 synpolydactyly PDX1 MODY 4 LMX1B Nail–patella syndrome MSX1 Tooth and nail syndrome OFC5 PITX2 Axenfeld syndrome...
19 KB (1,902 words) - 22:07, 30 May 2025
neurons, expressing βIII-tubulin, tyrosine hydroxylase, AADC, DAT, ChAT, LMX1B, and MAP2. The presence of catecholamine-associated enzymes may indicate...
92 KB (10,517 words) - 16:41, 2 June 2025
ENSG00000162761 Homeodomain Known motif – High-throughput in vitro [497] BTAATTA LMX1B ENSG00000136944 Homeodomain Known motif – High-throughput in vitro [498]...
374 KB (81 words) - 11:17, 3 January 2025
PMID 10640831. S2CID 23735189. Dreyer SD, Morello R, German MS, et al. (2000). "LMX1B transactivation and expression in nail-patella syndrome". Hum. Mol. Genet...
9 KB (1,074 words) - 19:29, 23 April 2024
1387/ijdb.041964hn. Matsunaga, E., Katahira, T., and Nakamura, H. "Role of Lmx1b and Wnt1 in mesencephalon and metencephalon development""Development" (2002)...
5 KB (513 words) - 05:25, 4 January 2020
eyelids) that lead to vision loss or blindness. There is some evidence that LMX1B plays a role in periocular mesenchymal survival. Optic cup and choroidal...
16 KB (1,919 words) - 17:18, 12 July 2024
Lissencephaly X2 MNX1 Currarino syndrome HOXD13 SPD1 synpolydactyly PDX1 MODY 4 LMX1B Nail–patella syndrome MSX1 Tooth and nail syndrome OFC5 PITX2 Axenfeld syndrome...
8 KB (1,003 words) - 00:05, 2 September 2024
Lissencephaly X2 MNX1 Currarino syndrome HOXD13 SPD1 synpolydactyly PDX1 MODY 4 LMX1B Nail–patella syndrome MSX1 Tooth and nail syndrome OFC5 PITX2 Axenfeld syndrome...
6 KB (524 words) - 02:48, 26 May 2025
syndrome LEMD3 Buschke–Ollendorff syndrome Lewis Y Infantile hemangioma LMX1B Nail–patella syndrome MATP Membrane-associated transporter protein Oculocutaneous...
12 KB (108 words) - 02:46, 17 September 2022
Naegeli–Franceschetti–Jadassohn syndrome; 161000; KRT14 Nail–patella syndrome; 161200; LMX1B Nance–Horan syndrome; 302350; NHS Narcolepsy 1; 161400; HCRT Nasopharyngeal...
234 KB (18,877 words) - 18:07, 24 March 2025