Gen
FIG4
FIG4 phosphoinositide 5-phosphatase
- HGNC 16873↗(åbnes i en ny fane)
- Ensembl-gen ENSG00000112367↗(åbnes i en ny fane)
- NCBI Gene 9896↗(åbnes i en ny fane)
Oversigt
- Cytogenetisk placering
- 6q21
- Koordinater
- Kromosom 6: 109.691.296–109.825.426 (GRCh38)
- Exoner
- 23 exoner fordelt over 134,1 kb
- Protein
- 907 aminosyrer
- Også kendt som
- SAC3, hSac3, dJ249I4.1, ALS11, CMT4J
- Tidligere symboler
- KIAA0274
- MANE Select-transkript
- ENST00000230124.8NM_014845.6
- 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
Amyotrofisk lateral sklerose (ALS)
- Amyotrofisk lateral sklerose
En neurodegenerativ sygdom i de øvre og nedre motoriske neuroner, som forekommer i sporadiske og familiære former.
- 1 GenCC-indsender vurderer den som definitiv eller stærk
Hvad viden ændrer
Tofersen (Qalsody, FDA 2023) til SOD1-ALS; ASO-forsøg for C9orf72 og FUS; riluzol; edaravon; AMX0035 (natriumphenylbutyrat-tauroursodiol); tværfaglig ALS-klinik; respiratorisk støtte; genetisk rådgivning til familiemedlemmer
Bredere grupperinger
Charcot-Marie-Tooth-sygdom
Et af 62 gener, der er knyttet til det
En gruppe arvelige perifere neuropatier, der forårsager progressiv svaghed og tab af muskelmasse i de distale muskler samt nedsat følesans, hovedsagelig i fødder og hænder.
- ClinGen vurderer forbindelsen som definitivt
- 6 GenCC-indsendere vurderer den som definitiv eller stærk
Hvad viden ændrer
Genetisk rådgivning, undersøgelser tilpasset undertypen, fysioterapi, ortopædiske hjælpemidler, undgåelse af neurotoksiske lægemidler, genspecifikke kliniske forsøg og overvågning for tilhørende symptomer
Sådan er FIG4 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 kb af genets 134,1 kb; 2.724 af disse baser koder for proteinet.
Sådan læser en genomtest FIG4
107
positioner i FIG4, 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 134,1 kb af FIG4, inklusive introner, og ikke kun de 3 kb eksoner.
Gener knyttet til de samme sygdomme
- SPG11SPG11 vesicle trafficking associated, spatacsinDeler 2 sygdomme
- VCPvalosin containing proteinDeler 2 sygdomme
- AARS1alanyl-tRNA synthetase 1Deler 1 sygdom
- AIFM1apoptosis inducing factor mitochondria associated 1Deler 1 sygdom
- ALS2alsin Rho guanine nucleotide exchange factor ALS2Deler 1 sygdom
- ANGangiogeninDeler 1 sygdom
- ANXA11annexin A11Deler 1 sygdom
- ATP1A1ATPase Na+/K+ transporting subunit alpha 1Deler 1 sygdom
- C9orf72C9orf72-SMCR8 complex subunitDeler 1 sygdom
- CADM3cell adhesion molecule 3Deler 1 sygdom
- CCNFcyclin FDeler 1 sygdom
- CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10Deler 1 sygdom
Træk knyttet til FIG4
Human Phenotype Ontology angiver disse som kendetegn ved de sjældne tilstande, FIG4 kan forårsage. Hvert træks side viser de andre gener, der er knyttet til det.
Abnormality of the nervous system
- Bilateral tonic-clonic seizure with focal onset
- Cerebellar vermis hypoplasia
- Focal impaired awareness seizure
- Global developmental delay
- Lou Gehrig's disease
- More grooves in brain
- Severe global developmental delay
- Underdeveloped frontal lobe
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- Underdevelopment of part of brain called corpus callosum
- Ventriculomegaly
- Visual hallucinations
- Cortical dysplasia
- Delayed fine motor development
- Delayed motor skills
- Delayed speech and language development
- Motor neuron atrophy
- Ongoing loss of nerve cells
- Agenesis of corpus callosum
- Aggressive behavior
- Anxiety
- Arrhinencephaly
- Babinski sign
- Behavioral abnormality
- Bulbar signs
- Can't control feelings
- Cognitive impairment
- Delirium
- Depression
- Difficulty articulating speech
- Epilepsy
- Fewer and broader ridges in brain
- Grand mal seizures
- Hoffmann sign
- Increased reflexes
- Intellectual disability
- Irritability
- Loss of brain cells
- Muscle twitch
- Paralysis
- Repeated seizures without recovery between them
- Abnormal fear-induced behavior
- Difficulty sleeping
- Frontotemporal dementia
- Hallucinations of sound
- High stepping
- Jaw hyperreflexia
- Language impairment
- Motor delay
- Psychotic mentation
- Small cerebellum
- Suicidal ideation
- Too much cerebrospinal fluid in the brain
- Abnormal gait
- Absent reflexes
- Axonal loss
- Decreased motor nerve conduction velocity
- Decreased nerve conduction velocity
- Decreased reflex response
- Decreased sensation in extremities
- Onion bulb formation
- Peripheral hypomyelination
- Upper motor neuron dysfunction
Abnormality of head or neck
- Decreased volume of lip
- Eye folds
- Flat back of skull
- Parietal bossing
- Upward slanting of the opening between the eyelids
- Abnormality of cranium
- Craniofacial disproportion
- Little lower jaw
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- Redundant neck skin
- Short upper lip
- Sparse scalp hair
- Wide fontanelles
- Abnormal occipital bone morphology
- Abnormal parietal bone morphology
- Abnormality of tooth part
- Abnormally small head
- Broad secondary alveolar ridge
- Decreased bone formation of skull
- Decreased salivary flow
- Drooling
- Early loss of baby teeth
- High forehead
- High palate
- High, narrow palate
- Large cranial suture
- Long, narrow head
- Nasal tip, upturned
- Short chin
- Short philtrum
- Small head present at birth
- Soft skullcap
- Sparse eyebrow
- Sparse eyelashes
- Thin red part of the upper lip
- Wasting of the tongue
- Abnormal facial shape
- Abnormality of the palate
- Big calvaria
- Gingival recession
- Increased nuchal translucency
- Narrow nasal base
- Retraction of the tongue
- Tongue twitching
- Decreased size of facial bones
- Wide gum ridges
Abnormality of limbs
- Absent thumb
- Absent/small big toe
- Curvature of digit
- Short index finger
- Short outermost finger bone
- Short thumb
- Tapered finger
- Tapered toe
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- Absent outermost bone of big toe
- Absent outermost hand bone
- Absent/small middle finger bone of the hand
- Absent/small outermost finger bone of the hand
- Short finger
- Short innermost big toe bone
- Short toe
- Abnormalities of the fingers
- Absent 1st long bone of hand
- Absent big toe
- Absent middle bone of index finger
- Absent outermost index finger bone
- Absent/small 1st long bone of foot
- Bilateral single transverse palmar creases
- Cutaneous syndactyly
- Decreased arm strength
- Dislocated hip since birth
- Flat acetabular roof
- Front half of foot turns inward
- Hip dislocation
- Lower limb muscle weakness
- Rocker bottom foot
- Short long bone of foot
- Short middle bone of finger
- Shortening of all outermost bone of the toes
- Single transverse palmar crease
- Thickening of the outer layer of the skin of the palms and soles
- Webbed fingers or toes
- Abnormality of fingers or toes
- Flared wide portion of long bone
- Foot drop
- Slender long bones with narrow shaft
- Ankle flexion contracture
- Fused toes
Abnormality of the musculoskeletal system
- Delayed ossification of pubic rami
- Hunched back
- Small shoulder blade
- Absent collarbone
- Generalized muscle weakness
- Low muscle tone
- Abnormal shape of pelvis bone
- Absent bone maturation in sternum
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- Absent/small collarbone
- Anterior concavity of thoracic vertebrae
- Distal muscle wasting
- Fatigable weakness of bulbar muscles
- Fatigable weakness of respiratory muscles
- Fatigable weakness of swallowing muscles
- Generalized low muscle tone in neonate
- Involuntary muscle stiffness, contraction, or spasm
- Muscle degeneration
- Muscle spasm
- Progressive distal muscular atrophy
- Rounded shoulders
- Short collarbone
- Absent/small shoulder blade
- Short ribs
- Spastic paraparesis
- Distal arthrogryposis
- Frequent falls
- Weakness of outermost muscles
Growth abnormality
- Growth delay
- Birth length less than 3rd percentile
- Faltering weight in infancy
- Growth delay as children
- Severe faltering weight
- Short stature
- Small for gestational age
- Weight loss
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Abnormality of the ear
- Low-set ears
- Abnormally shaped ears
- Cupped ear
- Prominent antihelix
- Prominent ear
- Sensorineural hearing impairment
- Small ears
- Hearing impairment
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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.). FIG4-genet: FIG4 phosphoinositide 5-phosphatase. Hentet 17. oktober 2026, fra https://dantelabs.com/da/genes/fig4
Dante Labs. FIG4-genet: FIG4 phosphoinositide 5-phosphatase [Internet]. [citeret 17. oktober 2026]. Tilgængelig fra: https://dantelabs.com/da/genes/fig4
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