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SNX18P9 sorting nexin 18 pseudogene 9 [ Homo sapiens (human) ]

Gene ID: 644576, updated on 12-Oct-2019

Summary

Official Symbol
SNX18P9provided by HGNC
Official Full Name
sorting nexin 18 pseudogene 9provided by HGNC
Primary source
HGNC:HGNC:39617
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 SNX18P9 in Genome Data Viewer
Location:
9q13
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (64439032..64440151)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (69451450..69452569)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene ANKRD20A4-ANKRD20A20P readthrough Neighboring gene ankyrin repeat domain 20 family member A4, pseudogene Neighboring gene RNA, U6 small nuclear 1193, pseudogene Neighboring gene ankyrin repeat domain 20 family member A20, pseudogene Neighboring gene cytochrome P450 family 4 subfamily F member 45, pseudogene Neighboring gene cytochrome P450 family 4 subfamily F member 25, pseudogene

Genomic regions, transcripts, and products

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_006123.3 

    Range
    101..1220
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p13 Primary Assembly

    Range
    64439032..64440151
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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