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MYCLP1 MYCL pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 4611, updated on 10-Oct-2023

Summary

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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

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Location:
Xq22.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (107272464..107276556)
RS_2023_10 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 ReSE screen-validated silencer GRCh37_chrX:106399301-106399461 Neighboring gene dynein axonemal assembly factor 6 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:106598330-106599265 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:106607772-106608400 Neighboring gene DnaJ heat shock protein family (Hsp40) member A1 pseudogene 3 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:106640109-106640292 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20927 Neighboring gene keratin 18 pseudogene 49

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Phylogenetic analysis of the human basic helix-loop-helix proteins. Ledent V, et al. Genome Biol, 2002. PMID 12093377, Free PMC Article
  2. Mapping and characterization of an X-linked processed gene related to MYCL1. Morton CC, et al. Genomics, 1989 Apr. PMID 2541066
  3. Testis-specific expression of the human MYCL2 gene. Robertson NG, et al. Nucleic Acids Res, 1991 Jun 11. PMID 1711681, Free PMC Article
  4. Mapping of the MYCL2 processed gene to Xq22-23 and identification of an additional L MYC-related sequence in Xq27.2. Redolfi E, et al. FEBS Lett, 1999 Mar 12. PMID 10100857
  5. The human L-myc gene encodes multiple nuclear phosphoproteins from alternatively processed mRNAs. De Greve J, et al. Mol Cell Biol, 1988 Oct. PMID 3054516, Free PMC Article

See all (8) citations in PubMed

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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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: 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_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.
Nucleotide Protein
Heading Accession and Version

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