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SNX18P12 sorting nexin 18 pseudogene 12 [ Homo sapiens (human) ]

Gene ID: 131183826, updated on 12-Sep-2024

Summary

Official Symbol
SNX18P12provided by HGNC
Official Full Name
sorting nexin 18 pseudogene 12provided by HGNC
Primary source
HGNC:HGNC:39620
See related
AllianceGenome:HGNC:39620
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Annotation information
Annotation category: not annotated on reference assembly
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Genomic context

See SNX18P12 in Genome Data Viewer
Location:
chromosome: 21
Annotation release Status Assembly Chr Location
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (1568255..1569592, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (10202804..10204141, complement)

Chromosome 14 - NC_060938.1Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124907360 Neighboring gene double homeobox 5 Neighboring gene uncharacterized LOC124900640 Neighboring gene uncharacterized LOC124907362 Neighboring gene putative ankyrin repeat domain-containing protein 20A2 Neighboring gene collagen alpha-1(III) chain-like

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_203421.1 

    Range
    101..1438
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    1568255..1569592 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)