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LOC100506772 hypothetical LOC100506772 [ Homo sapiens (human) ]

Gene ID: 100506772, 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  • This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.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
LOC100506772
Gene description
hypothetical LOC100506772
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WITHDRAWN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DISCONTINUED: This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.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: 17
Exon count:
2
Sequence:
Chromosome: 17; NC_000017.10 (7186087..7187390, 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

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

General gene information

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Markers

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_000017.10 GRCh37.p2 Reference primary assembly

    Range
    7186087..7187390 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_109360.1 RNA Sequence

Alternate assembly HuRef

Genomic

  1. AC_000149.1 Alternate assembly HuRef

    Range
    7077445..7078748 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_111663.1 RNA Sequence