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MYCLP3 MYCL pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 9964, updated on 17-Sep-2024

Summary

Official Symbol
MYCLP3provided by HGNC
Official Full Name
MYCL pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:7557
See related
AllianceGenome:HGNC:7557
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MYCL3
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Genomic context

See MYCLP3 in Genome Data Viewer
Location:
Xq27.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (143594883..143596013, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (141904167..141905296, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (142682694..142683823, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene MT-ND2 pseudogene 39 Neighboring gene SPANX family member N3 Neighboring gene SLIT and NTRK like family member 4 Neighboring gene heterogeneous nuclear ribonucleoprotein H1 pseudogene 2

Genomic regions, transcripts, and products

General gene information

Other Names

  • v-myc avian myelocytomatosis viral oncogene homolog 3 (pseudogene)
  • v-myc myelocytomatosis viral oncogene homolog 1, lung carcinoma derived pseudogene
  • v-myc myelocytomatosis viral oncogene homolog 3 pseudogene

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_001222.5 

    Range
    101..1231
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    143594883..143596013 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    141904167..141905296 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)