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BIN2P2 bridging integrator 2 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 644601, updated on 10-Oct-2023

Summary

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Official Symbol
BIN2P2provided by HGNC
Official Full Name
bridging integrator 2 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:43661
See related
Ensembl:ENSG00000248684 AllianceGenome:HGNC:43661
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:
5q13.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (75910582..75912168)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (76391687..76393238)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (75206407..75207993)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene solute carrier family 25 member 5 pseudogene 9 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22685 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22686 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22687 Neighboring gene karyopherin subunit alpha 7 pseudogene Neighboring gene synaptic vesicle glycoprotein 2C Neighboring gene ReSE screen-validated silencer GRCh37_chr5:75212667-75212925 Neighboring gene aconitate hydratase, mitochondrial-like Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:75332902-75333626 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:75333627-75334351 Neighboring gene SAP18 pseudogene 1

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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Markers

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_021885.3 

    Range
    101..1687
    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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    75910582..75912168
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    76391687..76393238
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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