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LOC100132767 hypothetical LOC100132767 [ Homo sapiens (human) ]

Gene ID: 100132767, discontinued on 29-Oct-2010
  • This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.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
LOC100132767
Gene description
hypothetical LOC100132767
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WITHDRAWN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DISCONTINUED: This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.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:
16p11.2
Exon count:
1
Sequence:
Chromosome: 16; NC_000016.9 (29606400..29607450)

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 protein information

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Names
hypothetical LOC100132767

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Build 37.1 (NOTE: not current)

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

Genome Reference Consortium Human Build 37 (GRCh37), Primary_Assembly

Genomic

  1. NC_000016.9 Genome Reference Consortium Human Build 37 (GRCh37), Primary_Assembly

    Range
    29606400..29607450
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    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_001725561.2 → XP_001725613.1  

Alternate assembly (HuRef)

Genomic

  1. AC_000148.1 Alternate assembly (HuRef)

    Range
    27267625..27268675 complement
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    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_001720251.2 → XP_001720303.1