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RNU4-35P RNA, U4 small nuclear 35, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481182, updated on 4-Mar-2025

Summary

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Official Symbol
RNU4-35Pprovided by HGNC
Official Full Name
RNA, U4 small nuclear 35, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46971
See related
Ensembl:ENSG00000199458 AllianceGenome:HGNC:46971
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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See RNU4-35P in Genome Data Viewer
Location:
6q22.31
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (121453981..121454121, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (122641035..122641175, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (121775127..121775267, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene high mobility group nucleosomal binding domain 2 pseudogene 29 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89339 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:121751780-121752762 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:121759052-121759929 Neighboring gene uncharacterized LOC124901515 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:121768314-121768814 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:121768815-121769315 Neighboring gene gap junction protein alpha 1 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89387 Neighboring gene transcription factor A, mitochondrial pseudogene Neighboring gene RNA, U4 small nuclear 76, 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_043154.1 

    Range
    101..241
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    121453981..121454121 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    122641035..122641175 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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