CNOT6LP1 CNOT6L pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: CNOT6LP1provided by HGNC
Official Full Name: CNOT6L pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:32355
See related: AllianceGenome:HGNC:32355
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

Location:: 15q21.3

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	15	NC_000015.10 (56003305..56007179, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	15	NC_060939.1 (53806751..53810624, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	15	NC_000015.9 (56295503..56299377, complement)

Chromosome 15 - NC_000015.10 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?

FUS driven circCNOT6L biogenesis in mouse and human spermatozoa supports zygote development.
Title: FUS driven circCNOT6L biogenesis in mouse and human spermatozoa supports zygote development.

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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

SHGC-145013 (e-PCR)
- UniSTS:174377

NoName (e-PCR)
- UniSTS:235228

SHGC-5880 (e-PCR)
- UniSTS:70121

CNOT6L (e-PCR)
- UniSTS:519156

Other Names

CCR4-NOT transcription complex subunit 6-like 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.