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FAM153B family with sequence similarity 153 member B [ Homo sapiens (human) ]

Gene ID: 202134, updated on 25-Oct-2022

Summary

Official Symbol
FAM153Bprovided by HGNC
Official Full Name
family with sequence similarity 153 member Bprovided by HGNC
Primary source
HGNC:HGNC:27323
See related
AllianceGenome:HGNC:27323
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Biased expression in testis (RPKM 19.5), ovary (RPKM 5.2) and 5 other tissues See more
Orthologs
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Genomic context

See FAM153B in Genome Data Viewer
Location:
5q35.2
Exon count:
27
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (176063055..176127142)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (176606717..176670819)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (175490058..175554145)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene protein FAM83G-like Neighboring gene uncharacterized LOC100996385 Neighboring gene PLCR-B recombination region Neighboring gene uncharacterized LOC107986487 Neighboring gene Sharpr-MPRA regulatory region 12759 Neighboring gene selenophosphate synthetase 1 pseudogene 3

Genomic regions, transcripts, and products

Expression

  • 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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Clone Names

  • FLJ30444, DKFZp434D115

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

RNA

  1. NR_169299.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC139491

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    176063055..176127142
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    176606717..176670819
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001079529.2: Suppressed sequence

    Description
    NM_001079529.2: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
  2. NM_001265615.2: Suppressed sequence

    Description
    NM_001265615.2: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.
  3. NR_038402.1: Suppressed sequence

    Description
    NR_038402.1: This RefSeq was removed because the transcript is 5'' partial.