Gene
CD55
CD55 molecule (Cromer blood group)
- HGNC 2665↗(opens in a new tab)
- Ensembl gene ENSG00000196352↗(opens in a new tab)
- NCBI Gene 1604↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q32.2
- Coordinates
- Chromosome 1: 207,321,678–207,360,966 (GRCh38)
- Exons
- 10 exons across 39.3 kb
- Protein
- 381 amino acids
- Inheritance
- Autosomal recessive
- Also known as
- CR, TC, CROM
- Previous symbols
- DAF
- MANE Select transcript
- ENST00000367064.9NM_000574.5
- 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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CHAPLE Disease (CD55 Deficiency)
- CHAPLE disease (CD55-deficient protein-losing enteropathy)Autosomal recessive
Complement hyperactivation, angiopathic thrombosis and protein-losing enteropathy caused by loss of CD55.
- 1 GenCC submitter rates it definitive or strong
What knowing changes
Complement-blocking treatment, including pozelimab, which the FDA approved for this condition in 2023, can control the disease.
Inheritance
- Autosomal recessive
- It takes a changed copy from each parent. With one, you are a carrier and usually unaffected; when both parents are carriers, each child has a one-in-four chance of inheriting two.
How CD55 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- 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 2.6 kb of the gene's 39.3 kb; 1,146 of those bases code for the protein.
How a genome test reads CD55
6
positions in CD55 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 39.3 kb of CD55, introns included, not only the 2.6 kb of exons.
Traits linked to CD55
The Human Phenotype Ontology lists these as features of the rare conditions CD55 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
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.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). CD55 gene: CD55 molecule (Cromer blood group). Retrieved 17 October 2026, from https://dantelabs.com/genes/cd55
Dante Labs. CD55 gene: CD55 molecule (Cromer blood group) [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/cd55
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