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ABCD1P2 ATP binding cassette subfamily D member 1 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 26983, updated on 10-Dec-2024

Summary

Official Symbol
ABCD1P2provided by HGNC
Official Full Name
ATP binding cassette subfamily D member 1 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:63
See related
Ensembl:ENSG00000215151 AllianceGenome:HGNC:63
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
bA453N3.6
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Genomic context

See ABCD1P2 in Genome Data Viewer
Location:
10p11.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (38601416..38605602)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (38660168..38664354)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (38894547..38898733)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene septin 14 pseudogene 10 Neighboring gene capicua transcriptional repressor pseudogene 9 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr10:38815532-38816393 Neighboring gene NANOG hESC enhancer GRCh37_chr10:38876229-38876730 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr10:38877019-38877912 Neighboring gene NANOG hESC enhancer GRCh37_chr10:38888420-38888921 Neighboring gene poly(A) binding protein cytoplasmic 1 pseudogene 12 Neighboring gene solute carrier family 9 member B1 pseudogene 3

Genomic regions, transcripts, and products

General gene information

Other Names

  • ATP-binding cassette, sub-family D (ALD), member 1 pseudogene
  • ATP-binding cassette, sub-family D (ALD), member 1, pseudogene 2

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_001270.5 

    Range
    101..4287
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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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    38601416..38605602
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_021160000.1 Reference GRCh38.p14 PATCHES

    Range
    274483..278669
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    38660168..38664354
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    GenBank, FASTA, Sequence Viewer (Graphics)