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LOC100505968 hypothetical LOC100505968 [ Homo sapiens (human) ]

Gene ID: 100505968, discontinued on 29-Jun-2011
  • This record has been withdrawn by NCBI staff. This record was defined by AK027209.1, which is not sufficient evidence to define a distinct locus.

Summary

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Gene symbol
LOC100505968
Gene description
hypothetical LOC100505968
Gene type
unknown
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WITHDRAWN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DISCONTINUED: This record has been withdrawn by NCBI staff. This record was defined by AK027209.1, which is not sufficient evidence to define a distinct locus.

Genomic context

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Location:
10q25.2
Sequence:
Chromosome: 10; NC_000010.10 (114830990..114831726)

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000010.10 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

General gene information

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Clone Names

  • FLJ23556

NCBI Reference Sequences (RefSeq)

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NEW Try the new Transcript table

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_000010.10 GRCh37.p2 Reference primary assembly

    Range
    114830990..114831726
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version