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  • Trisomy 13, also called Patau syndrome, is a chromosomal condition associated with severe
  • Partial monosomy and partial trisomy of chromosome 13 occur when a portion of the long (q) arm of
  • Trisomy 18, also called Edwards syndrome, is a chromosomal condition associated with abnormalities
  • The KRT13 gene provides instructions for making a protein called keratin 13. Keratins are a group
  • A common form of aneuploidy is trisomy, or the presence of an extra chromosome in cells. "Tri-" is
  • Found in name or synonym: IL-13
  • Found in name or synonym: MMP-13
  • Found in name or synonym: XXY trisomy
  • Found in name or synonym: FGF-13
  • Found in name or synonym: HUCEP-13
  • Most cases of Down syndrome result from trisomy 21, which means each cell in the body has three
  • Found in name or synonym: Trisomy Xq28
  • Found in name or synonym: cadherin family member 13
  • Found in name or synonym: protein unc-13 homolog D
  • Triple X syndrome, also called trisomy X or 47,XXX, is characterized by the presence of an
  • Found in name or synonym: ADAMTS-13
  • Found in name or synonym: TCF-13
  • Found in name or synonym: trisomy 7q11.23
  • Found in name or synonym: vacuolar protein sorting 13 homolog B (yeast)
  • Found in name or synonym: vacuolar protein sorting 13 homolog A (S. cerevisiae)
  • Found in name or synonym: solute carrier family 25 (aspartate/glutamate carrier), member 13
  • Found in name or synonym: 13S golgi transport complex 1 90 kDa subunit
  • trisomy 13, trisomy 21, or trisomy 9. This condition can also be associated with missing (deletions) or
  • Found in name or synonym: serine-threonine-protein kinase 13
  • Found in name or synonym: antigen NY-CO-13
  • Trisomy 8 occurs when cells have three copies of chromosome 8 instead of the usual two copies. Full
  • This gene encodes a member of the vacuolar protein sorting-associated 13 gene family. Alternate
  • arrhythmogenic right ventricular dysplasia, familial 13. Alternative splicing results in multiple transcript
  • this gene are found on chromosome 7, 10, 13 and 16. Multiple transcript variants encoding different
  • border microvilli. Mutations in this gene are associated with primary ciliary dyskinesia-13. Alternative
  • multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]
  • non-receptor type 13. Two nearly identical copies of this gene exist within a palindromic region. This
  • in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been
  • non-receptor type 13. Two nearly identical copies of this gene exist within a palindromic region. This
  • This gene encodes a protein belonging to the solute carrier family 13 group of proteins. This
  • with Syntaxin 13 which mediates intracellular membrane fusion. Mutations in this gene cause symptoms
  • Trisomy 18 occurs when each cell in the body has three copies of chromosome 18 instead of the usual
  • congenital amaurosis type 13 and Retinitis Pigmentosa 53. [provided by RefSeq, Sep 2015]
  • the basal body. A mutation in this gene was found in a family with Joubert syndrome-13. Alternative
  • hyperplasia (CLAH), also called lipoid CAH. A pseudogene of this gene is located on chromosome 13. [provided
  • upstream 13 kDa protein that is a member of the TCL1 family. This protein may be involved in leukemogenesis
  • phosphorylation deficiency-13 and autosomal recessive nonsyndromic deafness-70. Related pseudogenes are found on
  • syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing
  • to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13
  • to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X
  • transcript variants. A related pseudogene has been identified on chromosome 13. Read-through transcription
  • pseudogenes have been identified on chromosomes 5 and 13. [provided by RefSeq, Apr 2015]
  • on chromosomes 2, 13, and 22. [provided by RefSeq, Jan 2014]
  • and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been
  • for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13

Viewing: Health Conditions

  • Trisomy 13, also called Patau syndrome, is a chromosomal condition associated with severe
  • Trisomy 18, also called Edwards syndrome, is a chromosomal condition associated with abnormalities
  • Found in name or synonym: XXY trisomy
  • Most cases of Down syndrome result from trisomy 21, which means each cell in the body has three
  • Found in name or synonym: Trisomy Xq28
  • Triple X syndrome, also called trisomy X or 47,XXX, is characterized by the presence of an
  • Found in name or synonym: trisomy 7q11.23
  • trisomy 13, trisomy 21, or trisomy 9. This condition can also be associated with missing (deletions) or

Viewing: Genes

  • Partial monosomy and partial trisomy of chromosome 13 occur when a portion of the long (q) arm of
  • The KRT13 gene provides instructions for making a protein called keratin 13. Keratins are a group
  • Found in name or synonym: IL-13
  • Found in name or synonym: MMP-13
  • Found in name or synonym: FGF-13
  • Found in name or synonym: HUCEP-13
  • Found in name or synonym: cadherin family member 13
  • Found in name or synonym: protein unc-13 homolog D
  • Found in name or synonym: ADAMTS-13
  • Found in name or synonym: TCF-13
  • Found in name or synonym: vacuolar protein sorting 13 homolog B (yeast)
  • Found in name or synonym: vacuolar protein sorting 13 homolog A (S. cerevisiae)
  • Found in name or synonym: solute carrier family 25 (aspartate/glutamate carrier), member 13
  • Found in name or synonym: 13S golgi transport complex 1 90 kDa subunit
  • Found in name or synonym: serine-threonine-protein kinase 13
  • Found in name or synonym: antigen NY-CO-13
  • Trisomy 8 occurs when cells have three copies of chromosome 8 instead of the usual two copies. Full
  • This gene encodes a member of the vacuolar protein sorting-associated 13 gene family. Alternate
  • arrhythmogenic right ventricular dysplasia, familial 13. Alternative splicing results in multiple transcript
  • this gene are found on chromosome 7, 10, 13 and 16. Multiple transcript variants encoding different
  • border microvilli. Mutations in this gene are associated with primary ciliary dyskinesia-13. Alternative
  • multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]
  • non-receptor type 13. Two nearly identical copies of this gene exist within a palindromic region. This
  • in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been
  • non-receptor type 13. Two nearly identical copies of this gene exist within a palindromic region. This
  • This gene encodes a protein belonging to the solute carrier family 13 group of proteins. This
  • with Syntaxin 13 which mediates intracellular membrane fusion. Mutations in this gene cause symptoms
  • Trisomy 18 occurs when each cell in the body has three copies of chromosome 18 instead of the usual
  • congenital amaurosis type 13 and Retinitis Pigmentosa 53. [provided by RefSeq, Sep 2015]
  • the basal body. A mutation in this gene was found in a family with Joubert syndrome-13. Alternative
  • hyperplasia (CLAH), also called lipoid CAH. A pseudogene of this gene is located on chromosome 13. [provided
  • upstream 13 kDa protein that is a member of the TCL1 family. This protein may be involved in leukemogenesis
  • phosphorylation deficiency-13 and autosomal recessive nonsyndromic deafness-70. Related pseudogenes are found on
  • syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing
  • to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13
  • to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X
  • transcript variants. A related pseudogene has been identified on chromosome 13. Read-through transcription
  • pseudogenes have been identified on chromosomes 5 and 13. [provided by RefSeq, Apr 2015]
  • on chromosomes 2, 13, and 22. [provided by RefSeq, Jan 2014]
  • and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been
  • for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13

Viewing: Help Me Understand Genetics