유전자
FGFR1
fibroblast growth factor receptor 1
요약
- 세포유전학적 위치
- 8p11.23
- 좌표
- 염색체 8: 38,411,143–38,468,635 (GRCh38)
- 엑손
- 엑손 18개, 57.5 kb에 걸쳐
- 단백질
- 아미노산 822개
- 다른 이름
- H2, H3, H4, H5, CEK, FLG, BFGFR, N-SAM, CD331
- 이전 기호
- FLT2, KAL2
- MANE Select 전사체
- ENST00000447712.7NM_023110.3
- 유전자좌 유형
- gene with protein product
- Very high
- Confident
- Low
- Very low
기준 게놈GRCh38hg38
유전자 및 변이 페이지의 위치 정보는 이 브라우저에서 선택한 설정을 따릅니다.
이 유전자와 관련된 큐레이션 보고서
저성선자극호르몬성 성선기능저하증
시상하부-뇌하수체 축에서 호르몬 자극이 부족하여 난소 또는 고환의 기능에 이상이 생기는 상태입니다.
- 4명의 GenCC 제출자가 확정적 또는 강함으로 평가합니다
증후군성 두개골유합증
조기 두개골 봉합선 폐쇄와 함께 다른 특징이 나타나는 질환으로, Apert, Crouzon, Pfeiffer, Muenke, Saethre-Chotzen 증후군이 포함되며 FGFR2, FGFR3, FGFR1, TWIST1, TCF12, ERF 등의 유전자에 의해 발생합니다.
- ClinGen의 이 연관성 평가: 확정적
- 5명의 GenCC 제출자가 확정적 또는 강함으로 평가합니다
알면 달라지는 점
조기에 진단받으면 적시에 수술을 받고 머리 성장, 시력 및 청력을 지속적으로 관찰할 수 있습니다. Muenke 증후군과 같은 경미한 형태는 성인이 되어서도 알아차리지 못할 수 있으며, 이는 가족계획과 관련이 있습니다.
FGFR1의 구조
- 코딩 서열
- 비번역 영역
- 인트론
- 전사 방향
- 알려진 질병 유발 부위
- 짧은 리드가 판독하기 어려운 구간
v1.5 릴리스 기준, 이 유전자의 MANE Select 전사체 엑손이며 NCBI와 EMBL-EBI 자료를 바탕으로 하고 GRCh38 참조 게놈에 기반합니다.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
유전자 전체 57.5 kb 중 엑손이 5.7 kb를 차지하며, 이 중 2,469개의 염기가 단백질을 암호화합니다.
전장 유전체 검사가 FGFR1 유전자를 읽는 방법
171
FGFR1 내 위치 중 ClinVar가 병원성 또는 가능성 높은 병원성으로 분류하는 위치
이 중 어느 곳도 짧은 리드가 판독하기 어려운 구간에 있지 않습니다.
전장 유전체 검사는 인트론을 포함해 FGFR1의 전체 57.5kb를 모두 포함하며, 엑손 5.7kb만 보는 것이 아닙니다.
같은 질환과 연관된 유전자
- TCF12transcription factor 12질환 2개 공유
- ANOS1anosmin 1질환 1개 공유
- ARHGAP35Rho GTPase activating protein 35질환 1개 공유
- CHD7chromodomain helicase DNA binding protein 7질환 1개 공유
- CPEcarboxypeptidase E질환 1개 공유
- CYP26B1cytochrome P450 family 26 subfamily B member 1질환 1개 공유
- DCAF17DDB1 and CUL4 associated factor 17질환 1개 공유
- ERFETS2 repressor factor질환 1개 공유
- FEZF1FEZ family zinc finger 1질환 1개 공유
- FGF17fibroblast growth factor 17질환 1개 공유
- FGF8fibroblast growth factor 8질환 1개 공유
- FGFR2fibroblast growth factor receptor 2질환 1개 공유
Traits linked to FGFR1
The Human Phenotype Ontology lists these as features of the rare conditions FGFR1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Deformity of the skull
- Eye folds
- Failure of development of more than six teeth
- High, narrow palate
- Long philtrum
- Metopic synostosis
- Short nose
- Triangular head shape
Show 86 more traits
- Upward slanting of the opening between the eyelids
- Wide nasal bridge
- Zygomatic flattening
- Bicoronal synostosis
- Blockage of the rear opening of the nasal cavity
- Broad head shape
- Chewing difficulties
- Cleft palate
- Corners of eye widely separated
- Decreased number of teeth
- Depressed nasal bridge
- Downward slanting of the opening between the eyelids
- Encephalocele
- High forehead
- High palate
- Hyposmia
- Lost smell
- Midface retrusion
- Midnasal stenosis
- Multiple unerupted teeth
- Non-midline cleft of the upper lip
- Only one upper front tooth
- Abnormal eyelashes
- Abnormal nasolacrimal system morphology
- Abnormality of the eyelid
- Abnormality of the face
- Abnormality of the skull
- Abnormally small head
- Absence of premolar
- Absence of six year molar
- Absence of upper lateral incisor
- Absent central incisor
- Bad bite
- Bifid uvula
- Big calvaria
- Big lower jaw
- Central cleft upper lip
- Cleft eyelid
- Cleft upper lip
- Decreased length of dental roots
- Decreased size of maxilla
- Decreased size of tooth
- Delayed eruption of permanent teeth
- Delayed eruption of teeth
- Enlargement of craniofacial bones
- Failure of eruption of tooth
- Flat nose
- Frontal bossing
- Highly arched eyebrow
- Little lower jaw
- Monobrow
- Narrow forehead
- Narrow nasal bridge
- Nasal tip, upturned
- Prominent brow
- Short neck
- Short philtrum
- Tented mouth
- Widely spaced teeth
- Abnormal dentition
- Abnormality of canine
- Abnormality of dental shape
- Abnormality of shape of baby molar
- Absence of lower premolar
- Cleft of the mouth
- Cloverleaf cranium shape
- Coronal craniosynostosis
- Decreased size of teeth
- Mono nostril
- Outward turned lips
- Peg-shaped maxillary lateral incisors
- Proboscis
- Prominent forehead
- Short face
- Taurodontia
- Thin dental enamel
- Benign eye tumor
- Blockage of nose
- Dandy-Walker malformation
- Decreased depth of eye sockets
- Decreased size of bone of forehead
- Dental crowding
- High, prominent forehead
- Narrowing of the rear opening of the nasal cavity
- Skin tag in front of the ear
- Wide nose
Abnormality of the nervous system
- Agenesis of corpus callosum
- Delayed speech and language development
- Global developmental delay
- Aplasia/Hypoplasia of the corpus callosum
- Epilepsy
- Intellectual disability
- Lobar holoprosencephaly
- Neurodevelopmental abnormality
Show 59 more traits
- Abnormal central motor function
- Abnormal morphology of the olfactory bulb
- Abnormal shape of brainstem
- Abnormal speech pattern
- Abnormality of the autonomic nervous system
- Absent septum pellucidum
- Absent speech development
- Anxiety
- Aplasia of the falx cerebri
- Astrocytoma
- Attention deficit
- Behavioral abnormality
- Decrease in size of the outer layer of the brain due to loss of brain cells
- Degeneration of cerebrum
- Depression
- Difficulty finding words
- Echoing another person's speech
- Inability to speak
- Inability to walk
- Irritability
- Lack of feeling, emotion, interest
- Lethargy
- Limb dystonia
- Neural tube defect
- Oromotor apraxia
- Paralysis or weakness of one side of body
- Poor speech
- Sleep-wake cycle disturbance
- Specific learning disability
- Subcortical cerebral atrophy
- Ventriculomegaly
- Abnormal gait
- Absent/small cerebellum
- Alobar holoprosencephaly
- Aplasia of the olfactory bulb
- Aqueductal stenosis
- Ataxia
- Autism
- Difficulty articulating speech
- Difficulty sleeping
- Extreme thirst
- Grand mal seizures
- Hand mirror movements
- Holoprosencephaly
- Leg paralysis
- Paralysis
- Paralysis of all four limbs
- Paralysis on one side of body
- Semilobar holoprosencephaly
- Too much cerebrospinal fluid in the brain
- Tremor
- Weakness of one side of body
- Rise in pressure inside skull
- Cavity within brain
- Chiari malformation
- Cortical dysplasia
- Fluid-filled sac located in membrane surrounding brain or spinal cord
- Small cerebellum
- Underdevelopment of part of brain called corpus callosum
Abnormality of limbs
- Absent/small thumb
- Broad bone of big toe
- Broad thumb
- Cleft hand
- Hallux varus
- Short big toe
- Wide 1st long bone of foot
- Aplasia/Hypoplasia of the radius
Show 36 more traits
- Broad innermost bone of the big toe
- Broad outermost bone of big toe
- Disproportionately short upper portion of limb
- Finger syndactyly
- Fused toes
- Short 1st long bone of foot
- Short fingers or toes
- Short foot
- Short palm
- Short thumb
- Split hand
- Webbed 2nd and 3rd toes
- 3-4 toe cutaneous syndactyly
- Abnormality of limbs
- Calcaneonavicular fusion
- Curvature of digit
- Dropped arches
- High-arched foot
- Hip dislocation
- Permanent flexion of the finger
- Bowing of the long bones
- Broad big toe
- Broad foot
- Broad palm
- Elbow ankylosis
- Fusion of upper and lower arm bones
- Limb undergrowth
- Short finger bones
- Short long bone of foot
- Short middle bones (feet)
- Shortened long bone of hand
- Shortening of all middle phalanges of the fingers
- Webbed fingers or toes
- Wide digital bones
- Wide long bone of foot
- Wide long bones of hand
Abnormality of the musculoskeletal system
- Abnormal vertebral body morphology
- Delayed bone maturation
- Inability to make and keep healthy fat tissue
- Multiple fatty lumps
- Abnormal collarbone
- Abnormal deposits of calcium in the brain
- Bone cyst
- Breakdown of bone
Show 33 more traits
- Decreased muscle tone in infant
- Involuntary muscle stiffness, contraction, or spasm
- Low solidness and mass of the bones
- Muscle stiffness
- Osteopenia
- Osteoporosis
- Rigidity
- Skeletal tumor
- Spasticity and rigidity of muscles
- Abnormal bone maturation
- Abnormal shape of cartilage
- Abnormal skeletal development
- Abnormality of the skeletal system
- Dysostosis multiplex
- EMG: myopathic abnormalities
- Flexed joint that cannot be straightened
- Funnel chest
- Hypermobility of all joints
- Low muscle tone
- Low muscle tone in trunk
- Muscle weakness
- Osteochondrosis
- Permanent flexion of the finger or toe
- Recurrent fractures
- Scoliosis
- Fatty lump
- Flattened vertebrae
- Increased susceptibility to fractures
- Low muscle tone, in neonatal onset
- Lumbar hemivertebrae
- Multiple central nervous system lipomas
- Pseudoarthrosis
- Small shoulder blade
Abnormality of the genitourinary system
- Decreased testicular size
- Primary amenorrhea
- Short penis
- Abnormal erection
- Absent sperm in semen
- Decreased fertility
- Difficulty getting a full erection
- Increased female sex drive
Show 17 more traits
- Non-obstructive azoospermia
- Underdeveloped penis
- Undescended testes
- Previous menstrual periods stop
- Small uterus
- Underdeveloped ovary
- Abnormal morphology of female internal genitalia
- Abnormality of the genitourinary system
- Absent kidney
- Ambiguous external genitalia
- Dyspareunia
- Infertility
- Chordee
- Hydronephrosis
- Hypospadias
- Long penis
- Pelvic kidney
Abnormality of the endocrine system
- Hypogonadotropic hypogonadism
- Absence of pubertal development
- Absence of secondary sex characteristics
- Anterior hypopituitarism
- Decreased function of male gonad
- Decreased serum testosterone level
- Delayed puberty
- Female hypogonadism
Show 11 more traits
- Gonadotropin-releasing hormone deficiency
- Abnormal hypothalamus physiology
- Abnormality of the endocrine system
- Abnormality of the hypothalamus-pituitary axis
- Diabetes insipidus
- Underdeveloped pituitary gland
- Central hypothyroidism
- Decreased response to growth hormone stimulation test
- Panhypopituitarism
- Underactive thyroid
- Gonadotropin deficiency
Abnormality of the cardiovascular system
- Increased blood pressure in blood vessels of lungs
- Strawberry birthmark
- Tricuspid valve prolapse
- Visceral angiomatosis
- Abnormal aortic morphology
- Abnormal cardiovascular system morphology
- Abnormal heart rate variability
- Abnormality of the heart
Show 9 more traits
- Interrupted aortic arch
- Narrowing of aorta
- Narrowing of aortic valve
- Strawberry mark
- Tetralogy of Fallot
- An opening in the wall separating the top two chambers of the heart
- Hole in heart wall separating two lower heart chambers
- Narrowing of blood vessel below aortic heart valve
- Narrowing of peripheral lung artery
Growth abnormality
- Growth delay
- Severe short stature
- Eunuchoid habitus
- Faltering weight
- Prenatal growth deficiency
- Short stature
- Abnormality of body height
- Faltering weight in infancy
Show 1 more traits
외부 링크
단백질
이 정보의 출처
- HGNC: 유전자의 기호, 명칭, 다른 기호 및 위치입니다.
- NCBI와 EMBL-EBI의 MANE Select v1.5: 전사체, 엑손 및 코딩 서열입니다.
- GenCC와 ClinGen, 2026-10-16 공개본: 해당 유전자와 연관된 질환과 그 연관성의 강도입니다.
- ACMG 이차 소견 목록, SF v3.2입니다.
- ClinVar와 GIAB 층화 자료: 알려진 질병 유발 부위와 짧은 리드(short read)로 분석하기 어려운 영역입니다.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- 데이터 릴리스 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). FGFR1 gene: fibroblast growth factor receptor 1. Retrieved 2026년 10월 16일, from https://dantelabs.com/ko/genes/fgfr1
Dante Labs. FGFR1 gene: fibroblast growth factor receptor 1 [Internet]. [cited 2026년 10월 16일]. Available from: https://dantelabs.com/ko/genes/fgfr1
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