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HOXD13 gene

Known as: Homeobox D13 Gene, HOMEOBOX D13, HOX4I 
This gene plays a role in the development of limbs and appendages.
National Institutes of Health

Related topics

Related topics

9 relations
Cell Differentiation processHomeobox Protein Hox-D13Homo sapiensPattern Formation

Narrower (1)

HOXD13 wt Allele

Broader (1)

HOXD@ gene cluster

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A Nonsense Mutation in HOXD13 Gene from A Chinese Family with Non-Syndromic Synpolydactyly.
Synpolydactyly is a congenital limb malformation characterized by incomplete separation and duplication in fingers and/or toes… 
2017
2017
Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing.
Syndactyly is one of the most common hereditary limb malformations, and is characterized by the fusion of specific fingers and/or… 
2017
2017
Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly
Synpolydactyly (SPD) is an autosomal dominant limb malformation with a distinctive combination of syndactyly and polydactyly. SPD… 
2014
2014
Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families
Background Syndactyly type 1 (SD1) is an autosomal dominant limb malformation characterized in its classical form by complete or… 
2012
2012
HOXA13 and HOXD13 expression during development of the syndactylous digits in the marsupial Macropus eugenii
Kangaroos and wallabies have specialised limbs that allow for their hopping mode of locomotion. The hindlimbs differentiate much… 
2011
2011
Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly.
2005
2005
Mutation analysis of HOXD13 gene in a Chinese pedigree with synpolydactyly.
OBJECTIVE To study the clinical features and to identify homeobox D13 (HOXD13) gene mutation of the affected individuals in a… 
2005
2005
Sensorineural deafness, abnormal genitalia, synostosis of metacarpals and metatarsals 4 and 5, and mental retardation: Description of a second patient and exclusion of HOXD13
In 1988 Pfeiffer and Kapferer reported on a patient with sensorineural deafness, psychomotor delay, hypospadias, cerebral… 
2003
2003
An acceptor splice site mutation in HOXD13 results in variable hand, but consistent foot malformations
HOXD13 is the most 5′ of the HOXD cluster of homeobox genes in chromosome band 2q31.1. Heterozygous expansions of a polyalanine… 
1997
1997
Transcriptional regulation of the HOX4C gene by basic fibroblast growth factor on rheumatoid synovial fibroblasts.
OBJECTIVE To examine the expression of genes of the HOX D cluster in the synovial tissue of patients with rheumatoid arthritis… 
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