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    MLECP1 malectin pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 106480317, updated on 10-Oct-2023

    Summary

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    Official Symbol
    MLECP1provided by HGNC
    Official Full Name
    malectin pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:51122
    See related
    Ensembl:ENSG00000277899 AllianceGenome:HGNC:51122
    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

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    See MLECP1 in Genome Data Viewer
    Location:
    18q12.3
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (44522366..44523074)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (44713557..44714265)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (42102331..42103039)

    Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1478 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr18:41921090-41922289 Neighboring gene uncharacterized LOC124904291 Neighboring gene keratin 8 pseudogene 5 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr18:42003750-42004339 Neighboring gene long intergenic non-protein coding RNA 1601 Neighboring gene NANOG hESC enhancer GRCh37_chr18:42132670-42133206 Neighboring gene uncharacterized LOC124904290 Neighboring gene NANOG hESC enhancer GRCh37_chr18:42159022-42159523

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    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)

    General gene information

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    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_044402.1 

      Range
      101..809
      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_000018.10 Reference GRCh38.p14 Primary Assembly

      Range
      44522366..44523074
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060942.1 Alternate T2T-CHM13v2.0

      Range
      44713557..44714265
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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