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MYO5BP3 myosin VB pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 441442, updated on 10-Oct-2023

Summary

Official Symbol
MYO5BP3provided by HGNC
Official Full Name
myosin VB pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:38497
See related
Ensembl:ENSG00000228656 AllianceGenome:HGNC:38497
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See MYO5BP3 in Genome Data Viewer
Location:
9q13
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (63761345..63762818, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (47797104..47798577)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (68357079..68358552, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC100419925 Neighboring gene CDRT15 pseudogene 7 Neighboring gene cyclin dependent kinase 2 associated protein 2 pseudogene 3 Neighboring gene prostaglandin E receptor 4 pseudogene 3

Genomic regions, transcripts, and products

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.

Genomic

  1. NG_021621.2 

    Range
    101..1574
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    63761345..63762818 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    47797104..47798577
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)