LOC646214 p21 (RAC1) activated kinase 2 pseudogene [Homo sapiens (human)] - Gene

Summary

Gene symbol: LOC646214
Gene description: p21 (RAC1) activated kinase 2 pseudogene
Gene type: pseudo
RefSeq status: VALIDATED
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:: 15q11.2

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	15	NC_000015.10 (21289604..21297829, complement)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	15	NC_060939.1 (18632546..18640775, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	15	NC_000015.9 (21932514..21940739, 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?

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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

RH121965 (e-PCR)
- UniSTS:95010

GDB:595844 (e-PCR)
- UniSTS:158033

NoName (e-PCR)
- UniSTS:482146

G30964 (e-PCR)
- UniSTS:5011

G32566 (e-PCR)
- UniSTS:117150

D11S2766 (e-PCR)
- UniSTS:151969

NoName (e-PCR)
- UniSTS:62643

D11S3270 (e-PCR)
- UniSTS:152513

D11S1053 (e-PCR)
- UniSTS:74951

RH11274 (e-PCR)
- UniSTS:84185

RH67257 (e-PCR)
- UniSTS:92894

RH70587 (e-PCR)
- UniSTS:92150

Other Names

p21 protein (Cdc42/Rac)-activated kinase 2 pseudogene
p21-activated kinase 2 pseudogene

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.