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CALM2P4 calmodulin 2 pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 643193, updated on 10-Oct-2023

Summary

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Official Symbol
CALM2P4provided by HGNC
Official Full Name
calmodulin 2 pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:39661
See related
Ensembl:ENSG00000233662 AllianceGenome:HGNC:39661
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 CALM2P4 in Genome Data Viewer
Location:
13q32.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (98640809..98641307, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (97850792..97851290, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (99293063..99293561, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene NUS1 pseudogene 4 Neighboring gene CYCS pseudogene 35 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7921 Neighboring gene RNA, 7SL, cytoplasmic 60, pseudogene Neighboring gene solute carrier family 15 member 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5461 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:99390337-99390879

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)

See Variation Viewer (GRCh38)

General gene information

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Markers

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_011335.2 

    Range
    101..599
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    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    98640809..98641307 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    97850792..97851290 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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