U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

LOC100129500 hypothetical LOC100129500 [ Homo sapiens (human) ]

Gene ID: 100129500, 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  • This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.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

Go to the top of the page Help
Gene symbol
LOC100129500
Gene description
hypothetical LOC100129500
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WITHDRAWN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DISCONTINUED: This record has been withdrawn by NCBI because the model on which it was based was not predicted in a later annotation.
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

Go to the top of the page Help
Location:
19q13.32
Exon count:
2
Sequence:
Chromosome: 19; NC_000019.9 (45411802..45431701, complement)

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to nucleotide: Graphics FASTA GenBank

Bibliography

Go to the top of the pageHelp

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

Go to the top of the page Help

Review eQTL and phenotype association data in this region using PheGenI

General gene information

Go to the top of the page Help

Markers

General protein information

Go to the top of the page Help
Names
hypothetical LOC100129500

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

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_000019.9 Genome Reference Consortium Human Build 37 (GRCh37), Primary_Assembly

    Range
    45411802..45431701 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_001722946.2 → XP_001722998.1  

Alternate assembly (HuRef)

Genomic

  1. AC_000151.1 Alternate assembly (HuRef)

    Range
    41842588..41862249 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_001724653.2 → XP_001724705.1  

  2. XM_001724655.2 → XP_001724707.1  

Gene LinkOut

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