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MYCLP1 MYCL pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 4611, updated on 13-May-2022

Summary

Official Symbol
MYCLP1provided by HGNC
Official Full Name
MYCL pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:7556
See related
MIM:310310; AllianceGenome:HGNC:7556
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
MYCL2; L-MYC2; MYCL1P1; bHLHe38
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See MYCLP1 in Genome Data Viewer
Location:
Xq22.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (107272464..107276556)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (105708864..105712925)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (106515694..106519786)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene nucleoporin 62 C-terminal like Neighboring gene GTF3C6 pseudogene 2 Neighboring gene dynein axonemal assembly factor 6 Neighboring gene DnaJ heat shock protein family (Hsp40) member A1 pseudogene 3 Neighboring gene keratin 18 pseudogene 49

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • MYCL-related processed
  • v-myc avian myelocytomatosis viral oncogene homolog 1 pseudogene 1
  • v-myc avian myelocytomatosis viral oncogene homolog 2
  • v-myc myelocytomatosis viral oncogene homolog 1 pseudogene 1
  • v-myc myelocytomatosis viral oncogene homolog 2

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_009866.3 

    Range
    101..4193
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    107272464..107276556
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    105708864..105712925
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_005377.2: Suppressed sequence

    Description
    NM_005377.2: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.