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

Gene ID: 106481193, updated on 10-Oct-2023

Summary

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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 AllianceGenome:HGNC:47003
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:
12p12.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (25404285..25404428, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (25276828..25276971, complement)
105.20220307 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 uncharacterized LOC124902899 Neighboring gene KRAS proto-oncogene, GTPase Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_26705 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4293 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4294 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6116 Neighboring gene NFE2L2 motif-containing MPRA enhancer 301/302 Neighboring gene uncharacterized LOC105369701 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr12:25517951-25518546 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:25522046-25522546 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:25522547-25523047 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:25538426-25539295 Neighboring gene ribosomal protein L39 pseudogene 27 Neighboring gene family with sequence similarity 133 member A pseudogene

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)

General gene information

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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_043254.1 

    Range
    101..244
    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_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    25404285..25404428 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    25276828..25276971 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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