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PRAMEF16 PRAME family member 16 [ Homo sapiens (human) ]

Gene ID: 654348, discontinued on 7-Jan-2016
  • This record has been withdrawn by NCBI and HGNC. It represents a duplicate gene copy that has been removed in the GRCh38 reference genome assembly.

Summary

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Official Symbol
PRAMEF16provided by HGNC
Official Full Name
PRAME family member 16provided by HGNC
Primary source
HGNC:HGNC:25767
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WITHDRAWN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DISCONTINUED: This record has been withdrawn by NCBI and HGNC. It represents a duplicate gene copy that has been removed in the GRCh38 reference genome assembly.
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Genomic context

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See PRAMEF16 in Genome Data Viewer
Location:
1p36.21
Exon count:
3
Annotation release Status Assembly Chr Location
105 latest, but not current GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (13495254..13498260)

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000001.10 chromosome 1 reference GRCh37.p13 Primary Assembly

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

Variation

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See variants in ClinVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General protein information

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Names
PRAME family member 16

NCBI Reference Sequences (RefSeq)

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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_000001.10 Reference GRCh37.p13 Primary Assembly

    Range
    13495254..13498260
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001045480.1 → NP_001038945.1  

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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