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SNX3P1X sorting nexin 3 pseudogene 1 X-linked [ Homo sapiens (human) ]

Gene ID: 100873884, updated on 29-Apr-2018

Summary

Official Symbol
SNX3P1Xprovided by HGNC
Official Full Name
sorting nexin 3 pseudogene 1 X-linkedprovided by HGNC
Primary source
HGNC:HGNC:41516
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See SNX3P1X in Genome Data Viewer
Location:
Xq21.31
Annotation release Status Assembly Chr Location
109 current GRCh38.p12 (GCF_000001405.38) X NC_000023.11 (92515326..92515497, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (91770325..91770496, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene protocadherin 11 X-linked Neighboring gene eukaryotic translation initiation factor 4A1 pseudogene 10 Neighboring gene keratin 18 pseudogene 11 Neighboring gene ribosomal protein L26 pseudogene 36 Neighboring gene adaptor related protein complex 2 subunit beta 1 pseudogene

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

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_032372.1 

    Range
    101..272
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109 details...Open this link in a new tab

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

Reference GRCh38.p12 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p12 Primary Assembly

    Range
    92515326..92515497 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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