Gene
FAM89A
family with sequence similarity 89 member A
- HGNC 25057↗(opens in a new tab)
- Ensembl gene ENSG00000182118↗(opens in a new tab)
- NCBI Gene 375061↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q42.2
- Coordinates
- Chromosome 1: 231,018,958–231,040,254 (GRCh38)
- Exons
- 2 exons across 21.3 kb
- Protein
- 184 amino acids
- Also known as
- MGC15887
- Previous symbols
- C1orf153
- MANE Select transcript
- ENST00000366654.5NM_198552.3
- 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 FAM89A 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 1.5 kb of the gene's 21.3 kb; 555 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.). FAM89A gene: family with sequence similarity 89 member A. Retrieved 16 October 2026, from https://dantelabs.com/genes/fam89a
Dante Labs. FAM89A gene: family with sequence similarity 89 member A [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/fam89a
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