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HOXA13

HOXA13

Protein-coding gene in the species Homo sapiens

Homeobox protein Hox-A13 is a protein that in humans is encoded by the HOXA13 gene. In vertebrates, the genes encoding the class of transcription factors

HOXA13

Human penis size

Measurement of the human penis

in an embryo is controlled by some of the same Hox genes (in particular HOXA13 and HOXD13) as those that control the development of the limbs. Mutations

Human penis size

Human_penis_size

Esophageal cancer

Malignant neoplastic disease of the esophagus

hormonal factors. At a mechanistic level, in the esophagus there is a small HOXA13 expressing compartment that is more resistant to bile and acids as the normal

Esophageal cancer

Esophageal_cancer

Hand–foot–genital syndrome

Medical condition

imaging studies of the kidneys, bladder, and female reproductive tract. HOXA13 is the only gene known to be associated with HFGS. Approximately 60% of

Hand–foot–genital syndrome

Hand–foot–genital_syndrome

Barrett's esophagus

Precancerous tissue formation in the esophagus

cells that are more resistant to these corrosive substances. In particular, HOXA13-expressing stem cells that are characterised by distal (intestinal) characteristics

Barrett's esophagus

Barrett's_esophagus

Hox gene

Group of genes

Nesteruk K, Spaander MC, Verhaar AP, Yu B, Silva RA, et al. (June 2021). "HOXA13 in etiology and oncogenic potential of Barrett's esophagus". Nature Communications

Hox gene

Hox_gene

Paramesonephric duct

Paired ducts in the mammalian embryo in the primitive urogenital structures

the uterus and cervix, in the MDM. Two additional Hox genes, HoxA9 and HoxA13, specify the development of the Fallopian tube and the upper vagina. The

Paramesonephric duct

Paramesonephric_duct

HOXD13

Protein

2019-11-18. Chew KY, Yu H, Pask AJ, Shaw G, Renfree MB (January 2012). "HOXA13 and HOXD13 expression during development of the syndactylous digits in the

HOXD13

Hoxa

Topics referred to by the same term

the following genes associated with it: HOXA9 HOXA11 HOXA11-AS1 (gene) HOXA13 HOXA, the Hazaribagh Old Xaverians Association, the official alumni organization

Hoxa

Homeobox

DNA pattern affecting anatomy development

HOXA1, HOXA2, HOXA3, HOXA4, HOXA5, HOXA6, HOXA7, HOXA9, HOXA10, HOXA11, HOXA13 HOXB - HOXB@ chromosome 17 HOXB1, HOXB2, HOXB3, HOXB4, HOXB5, HOXB6, HOXB7

Homeobox

List of animals by number of legs

Koryu; Wagner, Günter P.; Kohlsdorf, Tiana (2015). "Molecular evolution of HoxA13 and the multiple origins of limbless morphologies in amphibians and reptiles"

List of animals by number of legs

List_of_animals_by_number_of_legs

Limb development

Development of limbs in vertebrates

family) Bmp2, Bmp4, Bmp7 Dach1 En1 Fgf4, Fgf8, Fgf9, Fgf10, Fgf17, Fgfr1 Gli3 Gremlin1 Hand2 Hoxa13, Hoxd13 Msx1, Msx2 Pitx1 Shh Tbx4, Tbx5 Wnt3, Wnt5a

Limb development

Limb_development

List of human transcription factors

ENSG00000005073 Homeodomain Known motif – High-throughput in vitro [374] DWTTTACGACB HOXA13 ENSG00000106031 Homeodomain Known motif – High-throughput in vitro [375]

List of human transcription factors

List_of_human_transcription_factors

Triphalangeal thumbs-brachyectrodactyly syndrome

Medical condition

Kofman-Alfaro, S.; Zenteno, J. C. (2002-09-01). "Mutational analysis of HOXD13 and HOXA13 genes in the triphalangeal thumb-brachyectrodactyly syndrome". Journal of

Triphalangeal thumbs-brachyectrodactyly syndrome

Triphalangeal_thumbs-brachyectrodactyly_syndrome

Microsatellite

Repeating sequences of 2–13 base pairs of DNA

range of Carnivora species. Length changes in polyalanine tracts within the HOXA13 gene are linked to hand-foot-genital syndrome, a developmental disorder

Microsatellite

Müllerian anomalies

Medical condition

with Müllerian anomalies. Mutations of homeobox genes HOXA10, HOXA11 and HOXA13 in uterus malformations are also responsible for renal and skeletal developmental

Müllerian anomalies

Müllerian_anomalies

HOXA11

Protein-coding gene in the species Homo sapiens

transcripts: detection of NUP98-HOXA9 in myeloid leukemias with HOXA11 or HOXA13 breaks of the chromosomal translocation t(7;11)(p15;p15)". Blood. 99 (4):

HOXA11

List of human protein-coding genes 4

P31269 7201 HOXA10 HGNC:5100; P31260 7202 HOXA11 HGNC:5101; P31270 7203 HOXA13 HGNC:5102; P31271 7204 HOXB1 HGNC:5111; P14653 7205 HOXB2 HGNC:5113; P14652

List of human protein-coding genes 4

List_of_human_protein-coding_genes_4

HOTTIP

Diederichs, S; Cillo, C; Terracciano, LM (2014). "Long noncoding RNA HOTTIP/HOXA13 expression is associated with disease progression and predicts outcome in

HOTTIP

Alan Edward Guttmacher

Director of the National Institute of Child Health (NICHD)

Williams TM, Mortlock DP, Sateesh P, Scambler PJ, McKinnon W, Guttmacher AE. A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion

Alan Edward Guttmacher

Alan_Edward_Guttmacher

List of OMIM disorder codes

coarse facies, and early death; 612938; FTO Guttmacher syndrome; 176305; HOXA13 Gyrate atrophy of choroid and retina with or without ornithinemia; 258870;

List of OMIM disorder codes

List_of_OMIM_disorder_codes

WTAP (gene)

Protein that in humans is encoded by the WTAP gene

S2CID 21813024. Utsch B, Kaya A, Ozburun A, et al. (2004). "Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadias". Scand. J. Urol. Nephrol. 37

WTAP (gene)

WTAP_(gene)

Development, Growth & Differentiation

Academic journal

Suzuki. Tatsuya Takemoto, Yo-ichi Shiraishi,Atsushi Kuroiwa 61 228-251 2019 Hoxa13 regulates expression of common Hox target genes involved in cartilage development

Development, Growth & Differentiation

Development,_Growth_&_Differentiation

Schmitt Gillenwater Kelly syndrome

Medical condition

male external genitalia, Shh acts as a central cue, indirectly activating Hoxa13 and Hoxd13 by binding to the Patched receptor, and directly activating BMP2

Schmitt Gillenwater Kelly syndrome

Schmitt_Gillenwater_Kelly_syndrome