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MTFR1P1 MTFR1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100128171, updated on 10-Oct-2023

Summary

Official Symbol
MTFR1P1provided by HGNC
Official Full Name
MTFR1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:54981
See related
AllianceGenome:HGNC:54981
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

See MTFR1P1 in Genome Data Viewer
Location:
Xq12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (66359581..66361865, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (64787352..64789636, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (65579423..65581707, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene eukaryotic translation initiation factor 4B pseudogene 9 Neighboring gene hephaestin Neighboring gene G protein-coupled receptor 165, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:65709355-65709854 Neighboring gene pyruvate kinase M1/2 pseudogene 2

Genomic regions, transcripts, and products

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_011583.1 

    Range
    101..2385
    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
    66359581..66361865 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    64787352..64789636 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)