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LOC100506729 hypothetical LOC100506729 [ Homo sapiens (human) ]

Gene ID: 100506729, discontinued on 3-Aug-2011
  • This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.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
LOC100506729
Gene description
hypothetical LOC100506729
Gene type
ncRNA
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WITHDRAWN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DISCONTINUED: This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.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:
chromosome: 19
Exon count:
4
Sequence:
Chromosome: 19; NC_000019.9 (204014..205946, complement)

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000019.9 chromosome

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Build 37.2 (NOTE: not current)

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

GRCh37.p2 Reference primary assembly

Genomic

  1. NC_000019.9 GRCh37.p2 Reference primary assembly

    Range
    204014..205946 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_109549.1 RNA Sequence

  2. XR_109550.1 RNA Sequence