Gene
FAM47B
family with sequence similarity 47 member B
- HGNC 26659↗(opens in a new tab)
- Ensembl gene ENSG00000189132↗(opens in a new tab)
- NCBI Gene 170062↗(opens in a new tab)
Summary
- Cytogenetic location
- Xp21.1
- Coordinates
- Chromosome X: 34,942,796–34,944,915 (GRCh38)
- Exons
- 1 exon across 2.1 kb
- Protein
- 645 amino acids
- Also known as
- FLJ35782
- MANE Select transcript
- ENST00000329357.6NM_152631.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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How FAM47B is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 2.1 kb of the gene's 2.1 kb; 1,938 of those bases code for the protein.
External links
Gene records
Transcript
Protein
Clinical
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
Cite this page
Dante Labs. (n.d.). FAM47B gene: family with sequence similarity 47 member B. Retrieved 17 October 2026, from https://dantelabs.com/genes/fam47b
Dante Labs. FAM47B gene: family with sequence similarity 47 member B [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/fam47b
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