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ADAM1B ADAM metallopeptidase domain 1B (pseudogene) [ Homo sapiens (human) ]

Gene ID: 100420505, updated on 13-May-2022

Summary

Official Symbol
ADAM1Bprovided by HGNC
Official Full Name
ADAM metallopeptidase domain 1B (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:44366
See related
Ensembl:ENSG00000226469 AllianceGenome:HGNC:44366
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

See ADAM1B in Genome Data Viewer
Location:
12q24.13
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (111927194..111928934)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (111904099..111905839)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (112364998..112366738)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene MAPK activated protein kinase 5 Neighboring gene ribosomal protein S2 pseudogene 41 Neighboring gene transmembrane protein 116 Neighboring gene ADAM metallopeptidase domain 1A (pseudogene) Neighboring gene solute carrier family 25 member 3 pseudogene 2 Neighboring gene immediate early response 3 interacting protein 1 pseudogene

Genomic regions, transcripts, and products

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_024129.1 

    Range
    101..1841
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    111927194..111928934
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    111904099..111905839
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)