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ANKRD33BP2 ANKRD33B pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100129384, updated on 10-Dec-2024

Summary

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Official Symbol
ANKRD33BP2provided by HGNC
Official Full Name
ANKRD33B pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:56294
See related
AllianceGenome:HGNC:56294
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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See ANKRD33BP2 in Genome Data Viewer
Location:
11p11.12
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (48900218..48901263, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (49068113..49069158, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (48921770..48922815, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 4 subfamily A member 42 pseudogene Neighboring gene olfactory receptor family 4 subfamily A member 44 pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr11:48827442-48828219 Neighboring gene NANOG hESC enhancer GRCh37_chr11:48837141-48837722 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:48838603-48839148 Neighboring gene OCT4 hESC enhancer GRCh37_chr11:48842688-48843189 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:48849408-48849948 Neighboring gene NANOG hESC enhancer GRCh37_chr11:48858585-48859086 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:48866441-48867079 Neighboring gene OCT4 hESC enhancer GRCh37_chr11:48895908-48896723 Neighboring gene tripartite motif containing 48 pseudogene Neighboring gene tripartite motif-containing 51C, 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_028803.2 

    Range
    94..1139
    Download
    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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    48900218..48901263 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    49068113..49069158 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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