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List of genes:

Pubmed

Gene: 

TULP2 (official gene symbol)

Other symbol: 

TULP2

CT family: 

CT65 

CT identifier: 

CT65

Aliases from NCBI:

TUBL2

6 records found.

ARTICLE DATE PUBMED ID TITLE GENES
1 07/01/2004 15220211 Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19q.
  To ascertain whether distinct chromosomal loci existed that were linked to severe obesity, as well as to utilize the increased heritability of this excessive phenotype, we performed a genome-wide scan...
2 01/01/2004 14708010 Tubby proteins: the plot thickens.
  The tubby mouse, which shows late-onset obesity and neurosensory deficits, arises from a mutation in the Tub gene. Tub shares homology with the genes for tubby-like proteins Tulp1, Tulp2 and Tulp3. Ab...
3 07/25/2001 11483369 Molecular cloning, expression and regulation of the avian tubby-like protein 1 (tulp1) gene.
  The tubby-like protein 1 (tulp1) gene is a member of the tubby multigene family which includes tub, tulp1, tulp2 and tulp3. Human and mouse tulp1 genes were cloned and mutations in tulp1 have been imp...
4 09/30/2000 11000483 GFP-tagged expression and immunohistochemical studies to determine the subcellular localization of the tubby gene family members.
  The tubby gene family consists of four members, TUB, TULP1, TULP2 and TULP3, with unknown function. However, a splice junction mutation within the mouse tub gene leads to retinal and cochlear degenera...
5 12/01/1998 9828123 Molecular characterization of a novel tubby gene family member, TULP3, in mouse and humans.
  Tubby and related proteins are derived from a small family of novel genes. The carboxytermini of this family are highly conserved across a number of species including humans, mice, Caenorhabditis eleg...
6 04/01/1997 9096357 Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases.
  Tubby, an autosomal recessive mutation, mapping to mouse chromosome 7, was recently found to be the result of a splicing defect in a novel gene with unknown function. Database searches revealed that s...