Format

Send to:

Choose Destination

RNU4-67P RNA, U4 small nuclear 67, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481193, updated on 23-Nov-2021

Summary

Official Symbol
RNU4-67Pprovided by HGNC
Official Full Name
RNA, U4 small nuclear 67, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47003
See related
Ensembl:ENSG00000201439
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See RNU4-67P in Genome Data Viewer
Location:
12p12.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (25404285..25404428, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (25557219..25557362, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene NFE2L2 motif-containing MPRA enhancer 301/302 Neighboring gene uncharacterized LOC105369701 Neighboring gene ribosomal protein L39 pseudogene 27 Neighboring gene family with sequence similarity 133 member A pseudogene

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_043254.1 

    Range
    101..244
    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
    25404285..25404428 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center