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SNX18P4 sorting nexin 18 pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 100418976, updated on 10-Oct-2023

Summary

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Official Symbol
SNX18P4provided by HGNC
Official Full Name
sorting nexin 18 pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:39612
See related
AllianceGenome:HGNC:39612
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

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Location:
9q21.11
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (66082385..66083772, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (77851970..77853357, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (43062963..43064350, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene zinc finger protein 114 pseudogene Neighboring gene family with sequence similarity 95 member B1-like Neighboring gene cytochrome P450 family 4 subfamily F member 59, pseudogene Neighboring gene ankyrin repeat domain 20 family member A3, pseudogene Neighboring gene RNA, U6 small nuclear 538, pseudogene Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:43133708-43134468 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:43134469-43135229 Neighboring gene general transcription factor II, i pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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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_023820.1 

    Range
    101..1488
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    66082385..66083772 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    77851970..77853357 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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