KCNMB3P1 KCNMB3 pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: KCNMB3P1provided by HGNC
Official Full Name: KCNMB3 pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:6288
See related: AllianceGenome:HGNC:6288
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: KCNMB2L; KCNMB3L; KCNMBLP; KCNMB3L1
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Genomic context

Location:: 22q11.1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	22	NC_000022.11 (16580766..16582707, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	22	NC_060946.1 (17257312..17259255, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	22	NC_000022.10 (17061656..17063597, complement)

Chromosome 22 - NC_000022.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Observational study of gene-disease association. (HuGE Navigator)
Title: L-type voltage-dependent calcium channel alpha subunit 1C is a novel candidate gene associated with secondary hyperparathyroidism: an application of haplotype-based analysis for multiple linked single nucleotide polymorphisms.

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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

RH65790 (e-PCR)
- UniSTS:68910

KCNMB3_1988 (e-PCR)
- UniSTS:280807

Other Names

potassium calcium-activated channel subfamily M regulatory beta subunit 3 pseudogene 1
potassium channel subfamily M regulatory beta subunit 3 pseudogene 1
potassium large conductance calcium-activated channel, subfamily M, beta member 3 pseudogene 1

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.