Gen
GJA1
gap junction protein alpha 1
- HGNC 4274↗(åbnes i en ny fane)
- Ensembl-gen ENSG00000152661↗(åbnes i en ny fane)
- NCBI Gene 2697↗(åbnes i en ny fane)
Oversigt
- Cytogenetisk placering
- 6q22.31
- Koordinater
- Kromosom 6: 121.435.646–121.449.727 (GRCh38)
- Exoner
- 2 exoner fordelt over 14,1 kb
- Protein
- 382 aminosyrer
- Også kendt som
- CX43, ODD, ODOD, SDTY3
- Tidligere symboler
- ODDD, GJAL
- MANE Select-transkript
- ENST00000282561.4NM_000165.5
- Lokustype
- gene with protein product
- Meget høj
- Sikker
- Lav
- Meget lav
ReferencegenomGRCh38hg38
Positioner på gen- og variantsider følger dette valg i denne browser.
Læs GJA1 og resten af dit genom med én test.
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Bestil min Genome TestKurateret rapport relevant for dette gen
Arvelige palmoplantar keratodermier og pachyonychia congenita
- Arvelig palmoplantar keratoderm
Arvelig fortykkelse af håndflader og fodsåler, herunder pachyonychia congenita, mal de Meleda, Nagashima-type og bothnisk keratoderm, keratitis-ichthyosis-døvhedssyndrom samt de CTSC-relaterede Papillon-Lefèvre- og Haim-Munk-syndromer.
- 2 GenCC-indsendere vurderer den som definitiv eller stærk
Hvad viden ændrer
Diagnosen vejleder fodpleje og smertebehandling. For CTSC-relaterede former beskytter tidlig tandbehandling tænderne, og GJB2-relaterede former bør få tjekket hørelsen.
Sådan er GJA1 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 3,1 kb af genets 14,1 kb; 1.149 af disse baser koder for proteinet.
Sådan læser en genomtest GJA1
38
positioner i GJA1, hvor ClinVar klassificerer en ændring som patogen eller sandsynligvis patogen
38 af dem (100 %) ligger i regioner, som korte læsninger har svært ved.
- Low mappability (8 steder)Regions where 100 bp or 250 bp reads cannot be placed uniquely.
- Segmental duplications (38 steder)Copies of at least 1 kb sharing at least 90% identity with another part of the genome (paralogues, pseudogenes); reads may align to the wrong copy.
En helgenomsanalyse dækker alle 14,1 kb af GJA1, inklusive introner, og ikke kun de 3,1 kb eksoner.
Gener knyttet til de samme sygdomme
- AAGABalpha and gamma adaptin binding proteinDeler 1 sygdom
- AP1B1adaptor related protein complex 1 subunit beta 1Deler 1 sygdom
- AQP5aquaporin 5Deler 1 sygdom
- CTSCcathepsin CDeler 1 sygdom
- DSG1desmoglein 1Deler 1 sygdom
- DSPdesmoplakinDeler 1 sygdom
- GJB2gap junction protein beta 2Deler 1 sygdom
- GJB3gap junction protein beta 3Deler 1 sygdom
- GJB4gap junction protein beta 4Deler 1 sygdom
- GJB6gap junction protein beta 6Deler 1 sygdom
- GRHL2grainyhead like transcription factor 2Deler 1 sygdom
- KDSR3-ketodihydrosphingosine reductaseDeler 1 sygdom
Træk knyttet til GJA1
Human Phenotype Ontology angiver disse som kendetegn ved de sjældne tilstande, GJA1 kan forårsage. Hvert træks side viser de andre gener, der er knyttet til det.
Abnormality of head or neck
- Decreased width of baby teeth
- Delayed eruption of teeth
- Enlargement of facial bones
- Flat nose
- Little lower jaw
- Sparse eyebrow
- Underdeveloped tissue around nostril
- Wide fontanelles
Vis 57 træk mere
- Abnormal tooth enamel
- Abnormality of the nose
- Abnormally small head
- Broad columella
- Cleft palate
- Decreased number of teeth
- Dental cavities
- Depressed nasal bridge
- Early loss of baby teeth
- Enlargement of craniofacial bones
- Narrow nasal bridge
- Sparse eyelashes
- Sparse scalp hair
- Wide nasal bridge
- Big lower jaw
- Central cleft upper lip
- Corners of eye widely separated
- Enlargement of skull bones
- High forehead
- High palate
- Large cranial suture
- Nasal tip, upturned
- Short nose
- Wide gum ridges
- Absent eyebrow
- Bell's palsy
- Eye folds
- Non-midline cleft of the upper lip
- Taurodontia
- Upward slanting of the opening between the eyelids
- Abnormal nasopharynx morphology
- Absence of a tooth
- Bad bite
- Big calvaria
- Blockage of nose
- Bony paranasal bossing
- Broad head shape
- Cleft upper lip
- Coarse facial features
- Decreased size of maxilla
- Decreased size of teeth
- Decreased size of tooth
- Decreased volume of lip
- Delayed eruption of permanent teeth
- Dental crowding
- Downward slanting of the opening between the eyelids
- Early tooth loss
- Frontal bossing
- Long nose
- Long philtrum
- Low hanging columella
- Macrodontia of permanent maxillary central incisor
- Narrow mouth
- Narrow nose
- Narrow opening between the eyelids
- Short opening between the eyelids
- Thin dental enamel
Abnormality of limbs
- Plantar hyperkeratosis
- Thickening of palms and soles
- Webbed 4th-5th finger
- Abnormality of the wide portion of a long bone
- Curvature of little finger
- Finger syndactyly
- Fused toes
- Joint contracture of the 5th finger
Vis 28 træk mere
- 3-4 finger cutaneous syndactyly
- Absent/small middle finger bone of the hand
- Curvature of digit
- Flexion contracture of finger
- Patchy palmoplantar hyperkeratosis
- Permanent flexion of the finger
- Abnormal shape of shaft of long bone
- Extra finger
- Extra thumb
- Madelung deformity
- Short big toe
- Short fingers or toes
- Short toe
- Tapered finger
- Absent middle bone of little finger
- Club-shaped outermost end of thighbone
- Curvature of outermost bone of little finger
- Flared wide portion of long bone
- Hip dislocation
- Metaphyseal dysplasia
- Outward turned elbows
- Short 5th finger
- Short foot
- Short middle bone of the little finger
- Small hand
- Uneven increase in bone density in finger bone
- Webbed 2nd, 3rd and 4th toes
- Webbed 3rd-4th toes
Abnormality of the integument
- Atypical nail growth
- Brittle hair
- Chicken skin
- Fine hair
- Hair loss
- Hypergranulosis
- Hyperkeratosis
- Orthokeratosis
Vis 28 træk mere
- Patchy darkened skin
- Sparse hair
- Thickening of upper layer of skin
- White discoloration of nails
- Abnormal blistering of the skin
- Abnormality of the nail
- Flat, discolored area of skin
- Hyperpigmented skin patches
- Photosensitive skin
- Poor nail formation
- Abnormal fingernails
- Abnormality of the hair
- Curly hair
- Dry skin
- Generalized hypotrichosis
- Grooved nails
- Irregular hyperpigmentation
- Sclerodactyly
- Slow-growing hair
- Absent hair
- Cracked skin
- Dry hair
- Excessive hairiness over body
- Poor wound healing
- Scaling skin
- Skin cancer
- Trichorrhexis nodosa
- Brittle nails
Abnormality of the eye
- Abnormally small eyeball
- Glaucoma
- Uveitis
- Wide-set eyes
- Cornea of eye less than 10mm in diameter
- Abnormality of the eye
- Abnormality of vision
- Abnormally close eyes
Vis 13 træk mere
Abnormality of the ear
- Abnormality of the ear
- Abnormally shaped ears
- Conductive deafness
- Deafness in one ear
- Hearing impairment
- Prominent ear
- Sensorineural hearing impairment
- Large earlobe
Vis 2 træk mere
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.
- GenCC og ClinGen, udgivet 2026-10-16: hvilke sygdomme genet er knyttet til, og hvor stærkt.
- ACMG-listen over sekundære fund, SF v3.2.
- 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.). GJA1-genet: gap junction protein alpha 1. Hentet 17. oktober 2026, fra https://dantelabs.com/da/genes/gja1
Dante Labs. GJA1-genet: gap junction protein alpha 1 [Internet]. [citeret 17. oktober 2026]. Tilgængelig fra: https://dantelabs.com/da/genes/gja1
Én test. Svar for hele livet.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger