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IFITM3P7 IFITM3 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 391020, updated on 13-May-2022

Summary

Official Symbol
IFITM3P7provided by HGNC
Official Full Name
IFITM3 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:54546
See related
AllianceGenome:HGNC:54546
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 IFITM3P7 in Genome Data Viewer
Location:
1p36.11
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (25124893..25125457, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (24961179..24961743, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (25451384..25451948, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene enhancer 2 sub-fragment of super enhancer upstream of RUNX3 Neighboring gene microRNA 4425 Neighboring gene long intergenic non-protein coding RNA 2793 Neighboring gene uncharacterized LOC124903880 Neighboring gene SYF2 pre-mRNA splicing factor

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_006227.1 

    Range
    101..665
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    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    25124893..25125457 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    24961179..24961743 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)