MAPK8IP1P2 mitogen-activated protein kinase 8 interacting protein 1 pseudogene 2 [Homo sapiens (human)] - Gene

Summary

Official Symbol: MAPK8IP1P2provided by HGNC
Official Full Name: mitogen-activated protein kinase 8 interacting protein 1 pseudogene 2provided by HGNC
Primary source: HGNC:HGNC:52402
See related: AllianceGenome:HGNC:52402
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:: 17q21.31

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	17	NC_000017.11 (45600101..45601862, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	17	NC_060941.1 (46461784..46463545, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	17	NC_000017.10 (43677467..43679228, complement)

Chromosome 17 - NC_000017.11 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?

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 studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

SHGC-144940 (e-PCR)
- UniSTS:174341

RH78669 (e-PCR)
- UniSTS:43621

RH64899 (e-PCR)
- UniSTS:26727

RH12593 (e-PCR)
- UniSTS:72050

BCD2335 (e-PCR)
- UniSTS:26507

D11S946E (e-PCR)
- UniSTS:147371

RH103702 (e-PCR)
- UniSTS:98027

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.