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LOC387761 similar to hCG1816027 [ Homo sapiens (human) ]

Gene ID: 387761, discontinued on 20-Jun-2009
  • This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.

Summary

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Gene symbol
LOC387761
Gene description
similar to hCG1816027
Gene type
protein coding
RefSeq status
WITHDRAWN
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
DISCONTINUED: This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.
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Genomic context

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Location:
11p12
Exon count:
7
Sequence:
Chromosome: 11; NC_000011.8 (42165869..42232128, complement)

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. LOC387761 is more likely to represent the genuine signals of T2DM in the Tunisian population.
    Title: Association of genetic variations in TCF7L2, SLC30A8, HHEX, LOC387761, and EXT2 with Type 2 diabetes mellitus in Tunisia.
  2. Observational study of gene-disease association, gene-gene interaction, and gene-environment interaction. (HuGE Navigator)
    Title: Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. men and women of European ancestry.
  3. Data show that SNPs in LOC387761 did not confer a significant risk for type 2 diabetes in Pima Indians.
    Title: Association analysis of variation in/near FTO, CDKAL1, SLC30A8, HHEX, EXT2, IGF2BP2, LOC387761, and CDKN2B with type 2 diabetes and related quantitative traits in Pima Indians.
  4. Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)
    Title: Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men.
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Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

General protein information

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Names
similar to hCG1816027

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Build 36.3 (NOTE: not current)

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference assembly

Genomic

  1. NC_000011.8 Reference assembly

    Range
    42165869..42232128 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_373495.4 → XP_373495.4  

Alternate assembly (based on HuRef)

Genomic

  1. AC_000143.1 Alternate assembly (based on HuRef)

    Range
    41919111..41985335
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_001716771.1 → XP_001716823.1