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OCLM oculomedin [ Homo sapiens (human) ]

Gene ID: 10896, discontinued on 17-Nov-2019
  • This record was withdrawn in collaboration with EMBL-EBI and HGNC. It was defined by AF142063.1, which lacks sufficient support to meet our criteria for representation as a distinct gene.

Summary

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Official Symbol
OCLMprovided by HGNC
Official Full Name
oculomedinprovided by HGNC
Primary source
HGNC:HGNC:8103
See related
MIM:604301
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WITHDRAWN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
Also known as
TISR
Summary
DISCONTINUED: This record was withdrawn in collaboration with EMBL-EBI and HGNC. It was defined by AF142063.1, which lacks sufficient support to meet our criteria for representation as a distinct gene.
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Genomic context

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See OCLM in Genome Data Viewer
Location:
1q31.1
Annotation release Status Assembly Chr Location
109.20190905 latest, but not current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (186400578..186401449)

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000001.11 Chromosome 1 Reference GRCh38.p13 Primary Assembly

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. There was no evidence that the oculomedin gene participates in the etiology of glaucoma.
    Title: Evaluation of the Oculomedin gene in the etiology of primary open angle and exfoliative glaucoma.
Submit: New GeneRIF Correction

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See Variation Viewer (GRCh38)

Genotypes

Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

General protein information

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Names
oculomedin
trabecular meshwork inducible stretch response protein

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905 (NOTE: not current)

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    186400578..186401449
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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.

Chemical Information
Molecular Biology Databases
Research Materials
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