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JTBP1 jumping translocation breakpoint pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100874254, updated on 13-May-2022

Summary

Official Symbol
JTBP1provided by HGNC
Official Full Name
jumping translocation breakpoint pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:39180
See related
Ensembl:ENSG00000233603 AllianceGenome:HGNC:39180
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 JTBP1 in Genome Data Viewer
Location:
22q13.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (40798039..40798285)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (41270229..41270475)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (41194043..41194289)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 1401 Neighboring gene solute carrier family 25 member 17 Neighboring gene RFK pseudogene 4 Neighboring gene microRNA 4766 Neighboring gene ST13 Hsp70 interacting protein

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_032231.1 

    Range
    101..347
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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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    40798039..40798285
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    41270229..41270475
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)