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FAM78B family with sequence similarity 78 member B [ Homo sapiens (human) ]

Gene ID: 149297, updated on 23-Nov-2021

Summary

Official Symbol
FAM78Bprovided by HGNC
Official Full Name
family with sequence similarity 78 member Bprovided by HGNC
Primary source
HGNC:HGNC:13495
See related
Ensembl:ENSG00000188859
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
Broad expression in brain (RPKM 1.6), testis (RPKM 1.0) and 21 other tissues See more
Orthologs
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Genomic context

See FAM78B in Genome Data Viewer
Location:
1q24.1
Exon count:
3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (166055918..166167001, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (166025155..166136238, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene RPS3A pseudogene 10 Neighboring gene RNA, 5S ribosomal pseudogene 64 Neighboring gene FAM78B antisense RNA 1 Neighboring gene uncharacterized LOC112268276 Neighboring gene microRNA 921 Neighboring gene EWS RNA binding protein 1 pseudogene Neighboring gene long intergenic non-protein coding RNA 1675 Neighboring gene flavin containing dimethylaniline monoxygenase 7, pseudogene

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

  • MGC131653

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.

mRNA and Protein(s)

  1. NM_001017961.5NP_001017961.1  protein FAM78B isoform 1

    See identical proteins and their annotated locations for NP_001017961.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) encodes the longer isoform (1).
    Source sequence(s)
    AB593134, AK299946, AL596087, AL626787, BM663586
    Consensus CDS
    CCDS30931.1
    UniProtKB/Swiss-Prot
    Q5VT40
    UniProtKB/TrEMBL
    F1T0K0
    Related
    ENSP00000346404.3, ENST00000354422.4
  2. NM_001320302.2NP_001307231.1  protein FAM78B isoform 2

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) contains an alternate 3' terminal exon, resulting in novel 3' coding region and 3' UTR, compared to variant 1. It encodes isoform 2, which is shorter and has a distinct C-terminus, compared to isoform 1.
    Source sequence(s)
    AB593134, AL596087, AL626787, H15427
    UniProtKB/TrEMBL
    F1T0K0

RNA

  1. NR_135199.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) contains a different 3' exon structure, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AB593134, AK299946, AL596087, AL626787, BX387125, H15427
  2. NR_163271.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL596087, AL626787

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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
    166055918..166167001 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_017000417.2XP_016855906.1  protein FAM78B isoform X1

    UniProtKB/Swiss-Prot
    Q5VT40
    Related
    ENSP00000412766.1, ENST00000435676.2
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