Free for academic non-profit institutions. Other users need a Commercial license

Aliases for HTC2 Gene

Aliases for HTC2 Gene

  • Hypertrichosis 2 (Generalized, Congenital) 2 3
  • Hypertrichosis 2 (Generalised, Congenital) 2 3
  • CXINSq27.1 3
  • HCG 3
  • CGH 3

External Ids for HTC2 Gene

Summaries for HTC2 Gene

GeneCards Summary for HTC2 Gene

HTC2 (Hypertrichosis 2 (Generalized, Congenital)) is a Genetic Locus. Diseases associated with HTC2 include Hypertrichosis Universalis Congenita, Ambras Type and X-Linked Congenital Generalized Hypertrichosis.

Additional gene information for HTC2 Gene

No data available for Entrez Gene Summary , CIViC summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for HTC2 Gene

Genomics for HTC2 Gene

Genomic Locations for HTC2 Gene

Genomic Locations for HTC2 Gene
Unknown strand

Genomic View for HTC2 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for HTC2 Gene

Function for HTC2 Gene

Animal Model Products

Clone Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Phenotypes From GWAS Catalog , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for HTC2 Gene

Localization for HTC2 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS , Subcellular locations from the Human Protein Atlas (HPA) and Gene Ontology (GO) - Cellular Components for HTC2 Gene

Pathways & Interactions for HTC2 Gene

No Data Available

Interacting Proteins for HTC2 Gene

Gene Ontology (GO) - Biological Process for HTC2 Gene


No data available for Pathways by source and SIGNOR curated interactions for HTC2 Gene

Drugs & Compounds for HTC2 Gene

No Compound Related Data Available

Transcripts for HTC2 Gene

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for HTC2 Gene

No ASD Table

Relevant External Links for HTC2 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for HTC2 Gene

Expression for HTC2 Gene

NURSA nuclear receptor signaling pathways regulating expression of HTC2 Gene:

No Expression Related Data Available

No data available for mRNA expression in normal human tissues , mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein differential expression in normal tissues , Protein expression , Protein tissue co-expression partners , mRNA Expression by UniProt/SwissProt , Evidence on tissue expression from TISSUES and Phenotype-based relationships between genes and organs from Gene ORGANizer for HTC2 Gene

Orthologs for HTC2 Gene

No data available for Orthologs and Evolution for HTC2 Gene

Paralogs for HTC2 Gene

No data available for Paralogs for HTC2 Gene

Variants for HTC2 Gene

Additional Variant Information for HTC2 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Sequence variations from dbSNP and Humsavar , Structural Variations from Database of Genomic Variants (DGV) and Variation tolerance for HTC2 Gene

Disorders for HTC2 Gene

MalaCards: The human disease database

(2) MalaCards diseases for HTC2 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
hypertrichosis universalis congenita, ambras type
  • htc1
x-linked congenital generalized hypertrichosis
  • hypertrichosis, congenital generalized
- elite association - COSMIC cancer census association via MalaCards
Search HTC2 in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with HTC2: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for HTC2 Gene

Publications for HTC2 Gene

  1. Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis. (PMID: 23603273) DeStefano GM … Christiano AM (Proceedings of the National Academy of Sciences of the United States of America 2013) 2 3 58
  2. X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3. (PMID: 21636067) Zhu H … Zhang X (American journal of human genetics 2011) 2 3 58
  3. Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait. (PMID: 12752576) Tadin-Strapps M … Christiano AM (Clinical genetics 2003) 2 3 58

Products for HTC2 Gene

Sources for HTC2 Gene

Loading form....