FZD10-AS1 FZD10 antisense divergent transcript [Homo sapiens (human)] - Gene

Summary

Official Symbol: FZD10-AS1provided by HGNC
Official Full Name: FZD10 antisense divergent transcriptprovided by HGNC
Primary source: HGNC:HGNC:48632
See related: Ensembl:ENSG00000250208 AllianceGenome:HGNC:48632
Gene type: ncRNA
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: FZD10-DT
Expression: Broad expression in endometrium (RPKM 2.0), prostate (RPKM 1.6) and 21 other tissues See more
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Genomic context

Location:: 12q24.33

Exon count:: 4

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	12	NC_000012.12 (130151593..130161678, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	12	NC_060936.1 (130188718..130198821, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	12	NC_000012.11 (130636138..130646223, complement)

Chromosome 12 - NC_000012.12 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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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 variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Interactions

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Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

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Markers

FZD10_7998 (e-PCR)
- UniSTS:468058

G64711 (e-PCR)
- UniSTS:163679

SHGC-144822 (e-PCR)
- UniSTS:172439

Other Names

FZD10 antisense RNA 1 (head to head)
FZD10 divergent transcript

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.