Gen
ROR2
ROR family WNT receptor 2
- HGNC 10257↗(åbnes i en ny fane)
- Ensembl-gen ENSG00000169071↗(åbnes i en ny fane)
- NCBI Gene 4920↗(åbnes i en ny fane)
Oversigt
- Cytogenetisk placering
- 9q22.31
- Koordinater
- Kromosom 9: 91.722.601–91.950.228 (GRCh38)
- Exoner
- 9 exoner fordelt over 227,6 kb
- Protein
- 943 aminosyrer
- Tidligere symboler
- NTRKR2, BDB, BDB1
- MANE Select-transkript
- ENST00000375708.4NM_004560.4
- Lokustype
- gene with protein product
- Meget høj
- Sikker
- Lav
- Meget lav
ReferencegenomGRCh38hg38
Positioner på gen- og variantsider følger dette valg i denne browser.
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Bestil min Genome TestKurerede rapporter relevant for dette gen
Ingen Genome Test-rapport læser ROR2 endnu. Testen sekventerer hele dit genom, så dine data omfatter det alligevel.
Sådan er ROR2 opbygget
- Kodende sekvens
- Utranslateret region
- Intron
- Transkriptionsretning
- Kendte sygdomsfremkaldende steder
- Regioner, som korte læsninger har svært ved
Eksoner i genets MANE Select-transkript (udgave v1.5), fra NCBI og EMBL-EBI, på referencegenomet GRCh38.
Kromosombånd fra UCSC's GRCh38-ideogram (2022-10-29).
Gener i nærheden fra Ensembl-udgivelse 116, på GRCh38.
Eksoner udgør 4,2 kb af genets 227,6 kb; 2.832 af disse baser koder for proteinet.
Sådan læser en genomtest ROR2
25
positioner i ROR2, hvor ClinVar klassificerer en ændring som patogen eller sandsynligvis patogen
Ingen af dem ligger i en region, som korte læsninger har svært ved.
En helgenomsanalyse dækker alle 227,6 kb af ROR2, inklusive introner, og ikke kun de 4,2 kb eksoner.
Træk knyttet til ROR2
Human Phenotype Ontology angiver disse som kendetegn ved de sjældne tilstande, ROR2 kan forårsage. Hvert træks side viser de andre gener, der er knyttet til det.
Abnormality of head or neck
- Short nose
- Abnormal dentition
- Downturned corners of mouth
- Midface retrusion
- Nasal tip, upturned
- Open bite
- Prominent forehead
- Wide mouth
Vis 36 træk mere
- Wide nasal bridge
- Abnormally small tongue
- Big calvaria
- Broad opening between the eyelids
- Cleft tongue
- Decreased number of teeth
- Depressed nasal bridge
- Downward slanting of the opening between the eyelids
- Eye folds
- Frontal bossing
- Gum enlargement
- Little lower jaw
- Long eyelashes
- Long philtrum
- Narrow palate
- Receding chin
- Short neck
- Tented mouth
- Thin red part of the upper lip
- Tongue tied
- Triangular mouth
- Upward slanting of the opening between the eyelids
- Abnormality of the palate
- Cleft of the mouth
- Exaggerated cupid's bow
- Extra teeth
- Failure of development of between one and six teeth
- Short philtrum
- Abnormally large tongue
- Absent uvula
- Delayed cranial suture closure
- Delayed eruption of permanent teeth
- Dental crowding
- Flat face
- Wider-than-typical soft spot of skull
- Zygomatic flattening
Abnormality of limbs
- Disproportionately short middle portion of limb
- Fused innermost and middle bones of little finger
- Short fingers or toes
- Absent/small outermost finger bone of the hand
- Curvature of digit
- Curvature of little finger
- Short outermost finger bone
- Short palm
Vis 34 træk mere
- Bilateral ulnar hypoplasia
- Bowing of outer large bone of the forearm
- Broad big toe
- Broad bone of big toe
- Broad thumb
- Dislocated radial head
- Elbow dislocation
- Limited pronation/supination of forearm
- Mesomelic arm shortening
- Single interphalangeal crease of fifth finger
- Underdeveloped outer large forearm bone
- Bilateral single transverse palmar creases
- Finger syndactyly
- Fused toes
- Fusion of wrist bones
- Gap between 1st and 2nd toes
- Hip dislocation
- Permanent flexion of the finger
- Single transverse palmar crease
- Split hand
- Webbed fingers
- Webbed fingers or toes
- Absent/small long bones of hand
- Absent/small outermost bones of toe
- Broad toe
- Duplication of the outermost bone of hand
- Joint contracture of the hand
- Notched outermost bones of toes
- Radial deviation of finger
- Short digit
- Short middle bone of finger
- Short middle bone of the little finger
- Small hand
- Type B brachydactyly
Abnormality of the integument
- Small nail
- Abnormal fingernail development
- Atypical nail growth
- Beauty mark
- Hair loss
- port-wine stain
- Spinal dimple
- Absent nails
Vis 1 træk mere
Abnormality of the cardiovascular system
- Abnormal aortic morphology
- Abnormal pulmonary valve morphology
- Abnormal tricuspid valve morphology
- Abnormality of the heart
- An opening in the wall separating the top two chambers of the heart
- Hole in heart wall separating two lower heart chambers
- Tetralogy of Fallot
- Right ventricular outlet tract obstruction
Eksterne links
Genposter
Transkript
Protein
Hvor oplysningerne kommer fra
- HGNC: genets symbol, navn, andre symboler og placering.
- MANE Select v1.5, fra NCBI og EMBL-EBI: transkriptet, dets exoner og kodende sekvens.
- ClinVar og GIAB-stratifikationerne: kendte sygdomsfremkaldende positioner og de regioner, som korte læsninger har svært ved at aflæse.
- Human Phenotype Ontology, version 2026-09-01: de træk, der er knyttet til genet. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.16-c6eea6bf.
Citér denne side
Dante Labs. (u.d.). ROR2-genet: ROR family WNT receptor 2. Hentet 17. oktober 2026, fra https://dantelabs.com/da/genes/ror2
Dante Labs. ROR2-genet: ROR family WNT receptor 2 [Internet]. [citeret 17. oktober 2026]. Tilgængelig fra: https://dantelabs.com/da/genes/ror2
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