Format

Send to:

Choose Destination

PHB1P19 PHB1 pseudogene 19 [ Homo sapiens (human) ]

Gene ID: 494150, updated on 23-Nov-2021

Summary

Official Symbol
PHB1P19provided by HGNC
Official Full Name
PHB1 pseudogene 19provided by HGNC
Primary source
HGNC:HGNC:51552
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
PHBP19
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See PHB1P19 in Genome Data Viewer
Location:
12q13.13
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (51124435..51125468, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (51518218..51519251, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene LETM1 domain containing 1 Neighboring gene cysteine and serine rich nuclear protein 2 Neighboring gene transcription factor CP2 Neighboring gene ribosomal protein L35a pseudogene 29 Neighboring gene RNA, U6 small nuclear 199, pseudogene Neighboring gene POU class 6 homeobox 1

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_004766.4 

    Range
    101..1134
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    51124435..51125468 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center