Trait
Winged shoulder blade
Clinical name: Scapular winging
Abnormal protrusion of the scapula away from the surface of the back.
Summary
- Also called
- Scapula alata, Winged scapulae, Winged scapulas
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test110 genes linked to Winged shoulder blade
Changes in these genes cause rare conditions in which Winged shoulder blade is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ANXA11annexin A11 | Always | In 1 condition |
| CRPPACDP-L-ribitol pyrophosphorylase A | Always | In 2 conditions |
| CSGALNACT1chondroitin sulfate N-acetylgalactosaminyltransferase 1 | Always | In 1 condition |
| FBN1fibrillin 1 | Always | In 1 condition |
| FHL1four and a half LIM domains 1 | Always | In 3 conditions |
| FILIP1filamin A interacting protein 1 | Always | In 1 condition |
| GYG1glycogenin 1 | Always | In 1 condition |
| LGI4leucine rich repeat LGI family member 4 | Always | In 1 condition |
| LRIF1ligand dependent nuclear receptor interacting factor 1 | Always | In 1 condition |
| POGLUT1protein O-glucosyltransferase 1 | Always | In 1 condition |
| RFC4replication factor C subunit 4 | Always | In 1 condition |
| RYR3ryanodine receptor 3 | Always | In 1 condition |
| SGCAsarcoglycan alpha | Always | In 2 conditions |
| SGCDsarcoglycan delta | Always | In 2 conditions |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Always | In 2 conditions |
| SYNE2spectrin repeat containing nuclear envelope protein 2 | Always | In 2 conditions |
| TGFB3transforming growth factor beta 3 | Always | In 1 condition |
| TUBA4Atubulin alpha 4a | Always | In 1 condition |
| ACTA1actin alpha 1, skeletal muscle | Very often (80–99%) | In 2 conditions |
| BICD2BICD cargo adaptor 2 | Very often (80–99%) | In 1 condition |
| CCDC8coiled-coil domain containing 8 subunit of 3M complex | Very often (80–99%) | In 1 condition |
| CUL7cullin 7 | Very often (80–99%) | In 2 conditions |
| DNMT3BDNA methyltransferase 3 beta | Very often (80–99%) | In 1 condition |
| DUX4double homeobox 4 | Very often (80–99%) | In 1 condition |
| DUX4L1double homeobox 4 like 1 (pseudogene) | Very often (80–99%) | In 1 condition |
| FRG1FSHD region gene 1 | Very often (80–99%) | In 2 conditions |
| HMGCS13-hydroxy-3-methylglutaryl-CoA synthase 1 | Very often (80–99%) | In 1 condition |
| HSPB8heat shock protein family B (small) member 8 | Very often (80–99%) | In 1 condition |
| OBSL1obscurin like cytoskeletal adaptor 1 | Very often (80–99%) | In 2 conditions |
| BAG3BAG cochaperone 3 | Often (30–79%) | In 1 condition |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Often (30–79%) | In 1 condition |
| CAPN3calpain 3 | Often (30–79%) | In 3 conditions |
| COL13A1collagen type XIII alpha 1 chain | Often (30–79%) | In 1 condition |
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Often (30–79%) | In 1 condition |
| EMDemerin | Often (30–79%) | In 1 condition |
| EMILIN1elastin microfibril interfacer 1 | Often (30–79%) | In 1 condition |
| LAMB2laminin subunit beta 2 | Often (30–79%) | In 1 condition |
| LMNAlamin A/C | Often (30–79%) | In 3 conditions |
| MYBPC1myosin binding protein C1 | Often (30–79%) | In 1 condition |
| MYH7myosin heavy chain 7 | Often (30–79%) | In 1 condition |
Show 70 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| PAX1paired box 1 | Often (30–79%) | In 1 condition |
| PRR12proline rich 12 | Often (30–79%) | In 1 condition |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Often (30–79%) | In 2 conditions |
| PUS1pseudouridine synthase 1 | Often (30–79%) | In 1 condition |
| PYROXD1pyridine nucleotide-disulphide oxidoreductase domain 1 | Often (30–79%) | In 1 condition |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Often (30–79%) | In 1 condition |
| RYR1ryanodine receptor 1 | Often (30–79%) | In 2 conditions |
| SEPTIN9septin 9 | Often (30–79%) | In 1 condition |
| SGCGsarcoglycan gamma | Often (30–79%) | In 1 condition |
| SMPXsmall muscle protein X-linked | Often (30–79%) | In 1 condition |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Often (30–79%) | In 1 condition |
| SQSTM1sequestosome 1 | Often (30–79%) | In 1 condition |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Often (30–79%) | In 1 condition |
| TK2thymidine kinase 2 | Often (30–79%) | In 2 conditions |
| TMEM43transmembrane protein 43 | Often (30–79%) | In 1 condition |
| TTNtitin | Often (30–79%) | In 2 conditions |
| VCPvalosin containing protein | Often (30–79%) | In 3 conditions |
| ALG14ALG14 UDP-N-acetylglucosaminyltransferase subunit | Sometimes (5–29%) | In 1 condition |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Sometimes (5–29%) | In 2 conditions |
| ANO5anoctamin 5 | Sometimes (5–29%) | In 1 condition |
| ASH1LASH1 like histone lysine methyltransferase | Sometimes (5–29%) | In 1 condition |
| BIN1bridging integrator 1 | Sometimes (5–29%) | In 2 conditions |
| COL12A1collagen type XII alpha 1 chain | Sometimes (5–29%) | In 2 conditions |
| COL6A1collagen type VI alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| COL6A2collagen type VI alpha 2 chain | Sometimes (5–29%) | In 1 condition |
| COL6A3collagen type VI alpha 3 chain | Sometimes (5–29%) | In 1 condition |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Sometimes (5–29%) | In 1 condition |
| DSTYKdual serine/threonine and tyrosine protein kinase | Sometimes (5–29%) | In 1 condition |
| DYSFdysferlin | Sometimes (5–29%) | In 1 condition |
| FLNCfilamin C | Sometimes (5–29%) | In 1 condition |
| GDF11growth differentiation factor 11 | Sometimes (5–29%) | In 1 condition |
| GFPT1glutamine--fructose-6-phosphate transaminase 1 | Sometimes (5–29%) | In 1 condition |
| GMPPBGDP-mannose pyrophosphorylase B | Sometimes (5–29%) | In 1 condition |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Sometimes (5–29%) | In 1 condition |
| JPH1junctophilin 1 | Sometimes (5–29%) | In 1 condition |
| KBTBD13kelch repeat and BTB domain containing 13 | Sometimes (5–29%) | In 1 condition |
| KLHL41kelch like family member 41 | Sometimes (5–29%) | In 1 condition |
| MYH2myosin heavy chain 2 | Sometimes (5–29%) | In 1 condition |
| MYPNmyopalladin | Sometimes (5–29%) | In 2 conditions |
| NEBnebulin | Sometimes (5–29%) | In 1 condition |
| NEFLneurofilament light chain | Sometimes (5–29%) | In 1 condition |
| POLGDNA polymerase gamma, catalytic subunit | Sometimes (5–29%) | In 2 conditions |
| POMT2protein O-mannosyltransferase 2 | Sometimes (5–29%) | In 1 condition |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Sometimes (5–29%) | In 2 conditions |
| SPEGstriated muscle enriched protein kinase | Sometimes (5–29%) | In 1 condition |
| SPRED2sprouty related EVH1 domain containing 2 | Sometimes (5–29%) | In 1 condition |
| TNNT1troponin T1, slow skeletal type | Sometimes (5–29%) | In 1 condition |
| TPM2tropomyosin 2 | Sometimes (5–29%) | In 2 conditions |
| TPM3tropomyosin 3 | Sometimes (5–29%) | In 1 condition |
| TRIOtrio Rho guanine nucleotide exchange factor | Sometimes (5–29%) | In 1 condition |
| TWNKtwinkle mtDNA helicase | Sometimes (5–29%) | In 1 condition |
| VWA1von Willebrand factor A domain containing 1 | Sometimes (5–29%) | In 1 condition |
| DNM1Ldynamin 1L | Rarely (1–4%) | In 1 condition |
| EBF3EBF transcription factor 3 | Rarely (1–4%) | In 1 condition |
| OPA1OPA1 mitochondrial dynamin like GTPase | Rarely (1–4%) | In 1 condition |
| PPIBpeptidylprolyl isomerase B | Rarely (1–4%) | In 1 condition |
| RRM1ribonucleotide reductase catalytic subunit M1 | Rarely (1–4%) | In 1 condition |
| TOP3ADNA topoisomerase III alpha | Rarely (1–4%) | In 1 condition |
| ATP6V0A2ATPase H+ transporting V0 subunit a2 | Not recorded | In 1 condition |
| C19orf12chromosome 19 open reading frame 12 | Not recorded | In 1 condition |
| EYA1EYA transcriptional coactivator and phosphatase 1 | Not recorded | In 1 condition |
| FLNAfilamin A | Not recorded | In 1 condition |
| FLNBfilamin B | Not recorded | In 1 condition |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Not recorded | In 1 condition |
| PAX3paired box 3 | Not recorded | In 1 condition |
| PLIN4perilipin 4 | Not recorded | In 1 condition |
| SGCBsarcoglycan beta | Not recorded | In 1 condition |
| TNPO3transportin 3 | Not recorded | In 1 condition |
| TRPS1transcriptional repressor GATA binding 1 | Not recorded | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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