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FAM153DP family with sequence similarity 153 member D, pseudogene [ Homo sapiens (human) ]

Gene ID: 102724062, updated on 17-Sep-2024

Summary

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Official Symbol
FAM153DPprovided by HGNC
Official Full Name
family with sequence similarity 153 member D, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:55022
See related
AllianceGenome:HGNC:55022
Gene type
pseudo
RefSeq status
MODEL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
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Genomic context

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See FAM153DP in Genome Data Viewer
Location:
16p11.2
Exon count:
15
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (32600346..32626108)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (33014797..33040542)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene poly(A) binding protein cytoplasmic 1 pseudogene 13 Neighboring gene ATP binding cassette subfamily D member 1 pseudogene 3 Neighboring gene uncharacterized LOC107984013 Neighboring gene TP53 target 3

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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Related articles in PubMed

  1. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560, Free PMC Article

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 studies and variants in dbVar

See Variation Viewer (GRCh38)

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    32600346..32626108
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_004837542.2 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    33014797..33040542
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007087058.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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