Trait
Slender long bone
Reduced diameter of a long bone.
Summary
- Also called
- Long bones slender, Slender long bones, Thin long bones, Gracile long bones, Slender, gracile long tubular bones, Thin, gracile long bones
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test47 genes linked to Slender long bone
Changes in these genes cause rare conditions in which Slender long bone 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 |
|---|---|---|
| BRF1BRF1 general transcription factor IIIB subunit | Always | In 2 conditions |
| CCDC134coiled-coil domain containing 134 | Always | In 1 condition |
| CDC6cell division cycle 6 | Always | In 2 conditions |
| CUL7cullin 7 | Always | In 2 conditions |
| DONSONDNA replication fork stabilization factor DONSON | Always | In 1 condition |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Always | In 1 condition |
| ITCHitchy E3 ubiquitin protein ligase | Always | In 1 condition |
| ORC1origin recognition complex subunit 1 | Always | In 2 conditions |
| ORC4origin recognition complex subunit 4 | Always | In 2 conditions |
| ORC6origin recognition complex subunit 6 | Always | In 2 conditions |
| POLR3ARNA polymerase III subunit A | Always | In 1 condition |
| PPP3CAprotein phosphatase 3 catalytic subunit alpha | Always | In 1 condition |
| TMEM38Btransmembrane protein 38B | Always | In 1 condition |
| TOMM7translocase of outer mitochondrial membrane 7 | Always | In 1 condition |
| CCDC8coiled-coil domain containing 8 subunit of 3M complex | Very often (80–99%) | In 2 conditions |
| CDC45cell division cycle 45 | Very often (80–99%) | In 1 condition |
| CDT1chromatin licensing and DNA replication factor 1 | Very often (80–99%) | In 2 conditions |
| GMNNgeminin DNA replication inhibitor | Very often (80–99%) | In 1 condition |
| MAFBMAF bZIP transcription factor B | Very often (80–99%) | In 1 condition |
| NFIXnuclear factor I X | Very often (80–99%) | In 3 conditions |
| OBSL1obscurin like cytoskeletal adaptor 1 | Very often (80–99%) | In 2 conditions |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Very often (80–99%) | In 1 condition |
| FDFT1farnesyl-diphosphate farnesyltransferase 1 | Often (30–79%) | In 1 condition |
| GLE1GLE1 RNA export mediator | Often (30–79%) | In 1 condition |
| LRP5LDL receptor related protein 5 | Often (30–79%) | In 1 condition |
| PIGUphosphatidylinositol glycan anchor biosynthesis class U | Often (30–79%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Often (30–79%) | In 1 condition |
| RSPRY1ring finger and SPRY domain containing 1 | Often (30–79%) | In 1 condition |
| FBXO11F-box protein 11 | Sometimes (5–29%) | In 1 condition |
| HARS1histidyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| LARP7La ribonucleoprotein 7, transcriptional regulator | Sometimes (5–29%) | In 1 condition |
| PDGFRBplatelet derived growth factor receptor beta | Sometimes (5–29%) | In 1 condition |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Sometimes (5–29%) | In 1 condition |
| SONSON DNA and RNA binding protein | Sometimes (5–29%) | In 1 condition |
| ATP6V0A2ATPase H+ transporting V0 subunit a2 | Not recorded | In 1 condition |
| B3GALT6beta-1,3-galactosyltransferase 6 | Not recorded | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Not recorded | In 1 condition |
| COL1A2collagen type I alpha 2 chain | Not recorded | In 1 condition |
| FAM111AFAM111 trypsin like peptidase A | Not recorded | In 1 condition |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Not recorded | In 1 condition |
Show 7 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| MGAT2alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Not recorded | In 1 condition |
| MUSKmuscle associated receptor tyrosine kinase | Not recorded | In 1 condition |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Not recorded | In 1 condition |
| P3H1prolyl 3-hydroxylase 1 | Not recorded | In 1 condition |
| PCNTpericentrin | Not recorded | In 1 condition |
| SCARF2scavenger receptor class F member 2 | Not recorded | In 1 condition |
| TBCEtubulin folding cofactor E | 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.
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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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