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RNU7-106P RNA, U7 small nuclear 106 pseudogene [ Homo sapiens (human) ]

Gene ID: 106479066, updated on 10-Oct-2023

Summary

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Official Symbol
RNU7-106Pprovided by HGNC
Official Full Name
RNA, U7 small nuclear 106 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:45640
See related
AllianceGenome:HGNC:45640
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:
12q21.31
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (80068710..80068754, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (80047474..80047518, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (80462490..80462534, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene heat shock protein family D (Hsp60) member 1 pseudogene 20 Neighboring gene ribosomal protein L7 pseudogene 38 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:80477061-80477602 Neighboring gene ribosomal protein L26 pseudogene 32 Neighboring gene otogelin like Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:80543056-80543602 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4684 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:80643124-80643716 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:80643717-80644308 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:80713982-80714515 Neighboring gene RN7SK pseudogene 261

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_044631.1 

    Range
    101..145
    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
    80068710..80068754 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    80047474..80047518 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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