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LOC100131540 uncharacterized LOC100131540 [ Homo sapiens (human) ]

Gene ID: 100131540, discontinued on 30-Mar-2017
  • This record has been withdrawn by NCBI staff. This record represented a gene that is not currently annotated by NCBI.

Summary

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Gene symbol
LOC100131540
Gene description
uncharacterized LOC100131540
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WITHDRAWN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DISCONTINUED: This record has been withdrawn by NCBI staff.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 represented a gene that is not currently annotated by NCBI.

Genomic context

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Location:
9q22.1
Exon count:
1
Annotation release Status Assembly Chr Location
105 latest, but not current GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (91619549..91623358)

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000009.11 chromosome 9 reference GRCh37.p13 Primary Assembly

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
    Title: Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
  2. Observational study of gene-disease association. (HuGE Navigator)
    Title: Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

NCBI Reference Sequences (RefSeq)

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NEW Try the new Transcript table

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 105 (NOTE: not current)

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

Reference GRCh37.p13 Primary Assembly

Genomic

  1. NC_000009.11 Reference GRCh37.p13 Primary Assembly

    Range
    91619549..91623358
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_242637.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.