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ABHD17AP9 ABHD17A pseudogene 9 [ Homo sapiens (human) ]

Gene ID: 100132251, updated on 10-Oct-2023

Summary

Official Symbol
ABHD17AP9provided by HGNC
Official Full Name
ABHD17A pseudogene 9provided by HGNC
Primary source
HGNC:HGNC:38510
See related
AllianceGenome:HGNC:38510
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
FAM108A10P
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Genomic context

Location:
16p11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (33140868..33144023)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (33140823..33143978, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (33152189..33155344)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene HERC2 pseudogene 8 Neighboring gene COX assembly mitochondrial protein 2 homolog Neighboring gene TP53 target 3C Neighboring gene uncharacterized LOC124903683

Genomic regions, transcripts, and products

General gene information

Other Names

  • abhydrolase domain containing 17A pseudogene 9
  • family with sequence similarity 108, member A10, pseudogene

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_028293.1 

    Range
    101..3256
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    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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    33140868..33144023
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    33140823..33143978 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)