MARK2P10 MARK2 pseudogene 10 [Homo sapiens (human)] - Gene

Summary

Official Symbol: MARK2P10provided by HGNC
Official Full Name: MARK2 pseudogene 10provided by HGNC
Primary source: HGNC:HGNC:39801
See related: Ensembl:ENSG00000227284 AllianceGenome:HGNC:39801
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:: 7q21.3

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	7	NC_000007.14 (96858164..96859671)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	7	NC_060931.1 (98087782..98089289)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	7	NC_000007.13 (96487476..96488983)

Chromosome 7 - NC_000007.14 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?

Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

General gene information

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Markers

D7S1796 (e-PCR), detects polymorphism
- UniSTS:36097

D7S491 (e-PCR), detects polymorphism
- UniSTS:13829

RH47418 (e-PCR)
- UniSTS:21003

WI-21635 (e-PCR)
- UniSTS:70929

D7S1796 (e-PCR), detects polymorphism
- UniSTS:30336

AFM284ZC1 (e-PCR)
- UniSTS:15015

A004Q32 (e-PCR)
- UniSTS:56774

RH119216 (e-PCR)
- UniSTS:138725

D7S624 (e-PCR)
- UniSTS:44024

Other Names

MAP/microtubule affinity-regulating kinase 2 pseudogene 10
microtubule affinity regulating kinase 2 pseudogene 10

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.