유전자
RERE
arginine-glutamic acid dipeptide repeats
요약
- 세포유전학적 위치
- 1p36.23
- 좌표
- 염색체 1: 8,352,404–8,817,640 (GRCh38)
- 엑손
- 엑손 23개, 465.2 kb에 걸쳐
- 단백질
- 아미노산 1,566개
- 다른 이름
- KIAA0458, ARP, ARG, DNB1, ATN2
- 이전 기호
- ATN1L
- MANE Select 전사체
- ENST00000400908.7NM_001042681.2
- 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
No Genome Test report reads RERE yet. The test sequences your whole genome, so your data includes it all the same.
RERE의 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 465.2 kb 중 엑손이 8 kb를 차지하며, 이 중 4,701개의 염기가 단백질을 암호화합니다.
전장 유전체 검사가 RERE 유전자를 읽는 방법
42
RERE 내 위치 중 ClinVar가 병원성 또는 가능성 높은 병원성으로 분류하는 위치
이 중 6곳(14%)은 짧은 리드가 판독하기 어려운 구간에 있습니다.
- Segmental duplications (6곳)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.
전장 유전체 검사는 인트론을 포함해 RERE의 전체 465.2kb를 모두 포함하며, 엑손 8kb만 보는 것이 아닙니다.
Traits linked to RERE
The Human Phenotype Ontology lists these as features of the rare conditions RERE can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Autism spectrum disorder
- Focal impaired awareness seizure
- Global developmental delay
- Abnormal gait
- Abnormal speech pattern
- Absent speech development
- Agenesis of corpus callosum
- Decrease in size of the outer layer of the brain due to loss of brain cells
Show 28 more traits
- Delayed speech and language development
- EEG abnormality
- Intellectual disability
- Poor speech
- Ventriculomegaly
- Autism
- Behavioral abnormality
- Brain imaging abnormality
- Cerebellar vermis hypoplasia
- Epilepsy
- Reduced cerebral white matter volume
- Repetitive movements
- Self-injurious behavior
- Thin corpus callosum
- Underdevelopment of part of brain called corpus callosum
- Abnormal cranial nerve physiology
- Attention deficit
- Cancer of early nerve cells
- CNS demyelination
- Cranial nerve paralysis
- Delayed CNS myelination
- Difficulty articulating speech
- Head-banging
- Hypoplasia of the pons
- Hypoplastic anterior commissure
- Increased appetite
- Paralysis or weakness of one side of body
- Pauses in breathing while sleeping
Abnormality of head or neck
- Horizontal eyebrow
- Long philtrum
- Midface retrusion
- Pointed chin
- Wide nasal bridge
- Abnormality of the eyebrow
- Abnormally small head
- Broad head shape
Show 25 more traits
- Delayed cranial suture closure
- Depressed nasal bridge
- Eye folds
- Flat nose
- Narrow mouth
- Abnormal facial shape
- Abnormality of the neck
- Big calvaria
- Blockage of the rear opening of the nasal cavity
- Broad eyebrow
- Bulbous nose
- Cleft lip
- Downward slanting of the opening between the eyelids
- Frontal bossing
- Grooved tongue
- High palate
- Little lower jaw
- Narrow opening between the eyelids
- Nasal tip, upturned
- Pit in front of the ear
- Smooth philtrum
- Triangular face
- Upward slanting of the opening between the eyelids
- Wide gum ridges
- Widow's peak
Abnormality of the eye
- Anisometropia
- Astigmatism
- Cerebral visual impairment
- Optic nerve hypoplasia
- Deeply set eye
- Abnormality of the eye
- Abnormality of vision
- Cross-eyed
Show 17 more traits
- Severe farsightedness
- Abnormally close eyes
- Abnormally small eyeball
- Absent pigmentation in the eye
- Birth defect that causes a hole in the innermost layer at the back of the eye
- Cat eye
- Close sighted
- Clouding of the lens of the eye
- Drooping upper eyelid
- Involuntary, rapid, rhythmic eye movements
- Inward turning cross eyed
- Notched pupil
- Optic atrophy
- Outward facing eye ball
- Peters anomaly
- Visual impairment
- Wide-set eyes
Abnormality of the musculoskeletal system
- Low muscle tone
- 11 pairs of ribs
- Abnormal formation of the hip
- Cleft ribs
- Excessive inward curvature of lower spine
- Hunched back
- Joint stiffness
- Muscle tissue disease
Show 4 more traits
Abnormality of the genitourinary system
- Chordee
- Small kidneys
- Vesicoureteral reflux
- Abnormal female external genitalia
- Abnormality of the genitourinary system
- Abnormality of the kidney
- Cystic kidney disease
- Hydronephrosis
Show 3 more traits
Abnormality of limbs
- Broad thumb
- Single transverse palmar crease
- Permanent flexion of the finger
- Short fingers or toes
- Short foot
- Curvature of little finger
- Duplication of bones of the toes
- Left and right leg differ in length or width
Show 2 more traits
Abnormality of the ear
- Ears rotated toward back of head
- Conductive deafness
- Earlobe crease
- Hearing impairment
- Low-set ears
- Prominent stem of antihelix
- Sensorineural hearing impairment
- Simple ear
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.
- 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.). RERE gene: arginine-glutamic acid dipeptide repeats. Retrieved 2026년 10월 17일, from https://dantelabs.com/ko/genes/rere
Dante Labs. RERE gene: arginine-glutamic acid dipeptide repeats [Internet]. [cited 2026년 10월 17일]. Available from: https://dantelabs.com/ko/genes/rere
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