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NUFIP1P1 NUFIP1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 89761, updated on 10-Dec-2019

Summary

Official Symbol
NUFIP1P1provided by HGNC
Official Full Name
NUFIP1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:8058
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
NUFIP1P

Genomic context

See NUFIP1P1 in Genome Data Viewer
Location:
6q12
Annotation release Status Assembly Chr Location
109.20191205 current GRCh38.p13 (GCF_000001405.39) 6 NC_000006.12 (66091475..66094945, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (66801368..66804838, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377838 Neighboring gene uncharacterized LOC105377840 Neighboring gene uncharacterized LOC105377839 Neighboring gene uncharacterized LOC105377841 Neighboring gene transcription elongation regulator 1 pseudogene

Genomic regions, transcripts, and products

General gene information

Other Names

  • NUFIP1P, FMR1 interacting protein 1 pseudogene
  • nuclear fragile X mental retardation protein interacting protein 1 pseudogene

NCBI Reference Sequences (RefSeq)

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_001030.2 

    Range
    101..3571
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000006.12 Reference GRCh38.p13 Primary Assembly

    Range
    66091475..66094945 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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