FAM223B family with sequence similarity 223 member B [Homo sapiens (human)] - Gene

Summary

Official Symbol: FAM223Bprovided by HGNC
Official Full Name: family with sequence similarity 223 member Bprovided by HGNC
Primary source: HGNC:HGNC:34048
See related: Ensembl:ENSG00000272681 AllianceGenome:HGNC:34048
Gene type: ncRNA
RefSeq status: PREDICTED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: CXorf52; CXorf52B; LINC00204B; NCRNA00204B
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Genomic context

Location:: Xq28

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	X	NC_000023.11 (154632470..154633182, complement)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	X	NC_060947.1 (152868903..152869615, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	X	NC_000023.10 (153860736..153861448, complement)

Chromosome X - NC_000023.11 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?

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 variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

stSG604151 (e-PCR)
- UniSTS:447488

stSG604197 (e-PCR)
- UniSTS:447525

ECD23031 (e-PCR)
- UniSTS:304016

ECD23833 (e-PCR)
- UniSTS:304817

ECD22602 (e-PCR)
- UniSTS:303588

RH44897 (e-PCR)
- UniSTS:27388

Other Names

family with sequence similarity 223 member B (non-protein coding)
long intergenic non-protein coding RNA 204B
non-protein coding RNA 204B

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.

RNA

NR_027402.1 RNA Sequence

Status: PREDICTED

Source sequence(s)

AC244107

Related

ENST00000598177.2

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

NC_000023.11 Reference GRCh38.p14 Primary Assembly

Range

154632470..154633182 complement

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GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

NC_060947.1 Alternate T2T-CHM13v2.0

Range

152868903..152869615 complement

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GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

NM_173168.1: Suppressed sequence

Description

NM_173168.1: This RefSeq was suppressed temporarily based on the calculation that the annotated protein was shorter than a protein or proteins from a putative ortholog.