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MORF4L1P6 mortality factor 4 like 1 pseudogene 6 [ Homo sapiens (human) ]

Gene ID: 100873878, updated on 10-Oct-2023

Summary

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Official Symbol
MORF4L1P6provided by HGNC
Official Full Name
mortality factor 4 like 1 pseudogene 6provided by HGNC
Primary source
HGNC:HGNC:39258
See related
AllianceGenome:HGNC:39258
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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Location:
Xq13.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (73474536..73475030)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (71907916..71908410)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (72694372..72694866)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 1044, pseudogene Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chrX:72666583-72667248 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:72667249-72667913 Neighboring gene NANOG hESC enhancer GRCh37_chrX:72673827-72674431 Neighboring gene caudal type homeobox 4 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:72701495-72702694 Neighboring gene mitogen-activated protein kinase kinase 4 pseudogene 1 Neighboring gene ribosomal protein L7 pseudogene 53 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:72775946-72776585 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20905 Neighboring gene cysteine rich hydrophobic domain 1 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:72891741-72891916

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)

See Variation Viewer (GRCh38)

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_032238.2 

    Range
    101..595
    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
    73474536..73475030
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    71907916..71908410
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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