TMEM258P1 TMEM258 pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: TMEM258P1provided by HGNC
Official Full Name: TMEM258 pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:56321
See related: AllianceGenome:HGNC:56321
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:: 11p15.4

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	11	NC_000011.10 (5362575..5362966)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	11	NC_060935.1 (5421896..5422269)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	11	NC_000011.9 (5383805..5384196)

Chromosome 11 - NC_000011.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Go to reference sequence details

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

stSG610923 (e-PCR)
- UniSTS:449035

SHGC-142587 (e-PCR)
- UniSTS:171537

ECD09024 (e-PCR)
- UniSTS:290070

ECD09545 (e-PCR)
- UniSTS:290586

REN97909 (e-PCR)
- UniSTS:422706

REN97910 (e-PCR)
- UniSTS:422707

REN97911 (e-PCR)
- UniSTS:422708

REN97912 (e-PCR)
- UniSTS:422709

REN97913 (e-PCR)
- UniSTS:422710

REN97914 (e-PCR)
- UniSTS:422711

REN97915 (e-PCR)
- UniSTS:422712

REN97916 (e-PCR)
- UniSTS:422713

REN97917 (e-PCR)
- UniSTS:422714

D11S1760 (e-PCR), detects polymorphism
- UniSTS:45739

ECD07195 (e-PCR)
- UniSTS:288252

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.