Gene
CD151
CD151 molecule (Raph blood group)
- HGNC 1630↗(opens in a new tab)
- Ensembl gene ENSG00000177697↗(opens in a new tab)
- NCBI Gene 977↗(opens in a new tab)
Summary
- Cytogenetic location
- 11p15.5
- Coordinates
- Chromosome 11: 832,952–838,831 (GRCh38)
- Exons
- 9 exons across 5.9 kb
- Protein
- 253 amino acids
- Also known as
- SFA-1, PETA-3, TSPAN24, RAPH
- MANE Select transcript
- ENST00000397420.9NM_004357.5
- 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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Epidermolysis Bullosa
- Inherited epidermolysis bullosa
All inherited forms of skin fragility with blistering, including simplex, junctional and dystrophic epidermolysis bullosa and Kindler syndrome.
- 1 GenCC submitter rates it definitive or strong
What knowing changes
Recessive dystrophic forms need regular skin cancer surveillance, and gene-based wound therapy is now available for dystrophic EB.
How CD151 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 1.5 kb of the gene's 5.9 kb; 762 of those bases code for the protein.
How a genome test reads CD151
9
positions in CD151 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 5.9 kb of CD151, introns included, not only the 1.5 kb of exons.
Genes linked to the same conditions
- COL17A1collagen type XVII alpha 1 chainShares 1 condition
- COL7A1collagen type VII alpha 1 chainShares 1 condition
- DSPdesmoplakinShares 1 condition
- DSTdystoninShares 1 condition
- EXPH5exophilin 5Shares 1 condition
- FERMT1FERM domain containing kindlin 1Shares 1 condition
- ITGA3integrin subunit alpha 3Shares 1 condition
- ITGA6integrin subunit alpha 6Shares 1 condition
- ITGB4integrin subunit beta 4Shares 1 condition
- JUPjunction plakoglobinShares 1 condition
- KLHL24kelch like family member 24Shares 1 condition
- KRT14keratin 14Shares 1 condition
Traits linked to CD151
The Human Phenotype Ontology lists these as features of the rare conditions CD151 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.). CD151 gene: CD151 molecule (Raph blood group). Retrieved 16 October 2026, from https://dantelabs.com/genes/cd151
Dante Labs. CD151 gene: CD151 molecule (Raph blood group) [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/cd151
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