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COL4A1
COL4A1 유전자에 관한 페이지입니다. 이 사이트에는 이 유전자 안쪽에 공개 변이 147개, 근처에 1개가 있으며, 모두 발표된 유전 연구에서 나왔습니다. 이 유전자는 질환 페이지 17개와 이어집니다.
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AI·크롤러가 읽은 횟수
Claude 0 ChatGPT 0 Google · Gemini 0 Perplexity 0 Meta AI 1 Microsoft · Copilot 1 Amazon 0 Apple 0 중국 (ByteDance, Huawei, Baidu…) 0 Others 0 합계 2 크롤러가 밝힌 이름 기준입니다. 사칭으로 확인된 요청은 세지 않습니다. Google · Gemini에는 Google 검색 크롤러인 Googlebot이 포함되며, Google은 그 색인을 자체 AI 기능에도 사용합니다. 다른 검색엔진과 봇은 Others에 있습니다.
연결된 질환
COL4A1 안쪽의 변이 (147)
rs1057523354 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs112314120 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs113994104 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs113994105 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs113994106 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs1877185960 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs1877832657 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs1877834934 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs1878411691 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs2139163150 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs2139179173 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs2501770861 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs2501783763 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs2501787905 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs2501791888 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs2501800825 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs267606743 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs267606744 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs672601346 · Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome rs1057518654 · Brain small vessel disease 1 with or without ocular anomalies rs1057523325 · Brain small vessel disease 1 with or without ocular anomalies rs1064794777 · Brain small vessel disease 1 with or without ocular anomalies rs1131691834 · Brain small vessel disease 1 with or without ocular anomalies rs113994103 · Brain small vessel disease 1 with or without ocular anomalies rs113994109 · Brain small vessel disease 1 with or without ocular anomalies rs113994111 · Brain small vessel disease 1 with or without ocular anomalies rs113994112 · Brain small vessel disease 1 with or without ocular anomalies rs113994113 · Brain small vessel disease 1 with or without ocular anomalies rs113994114 · Brain small vessel disease 1 with or without ocular anomalies rs121912857 · Brain small vessel disease 1 with or without ocular anomalies rs1555302922 · Brain small vessel disease 1 with or without ocular anomalies rs1555303720 · Brain small vessel disease 1 with or without ocular anomalies rs1566351456 · Brain small vessel disease 1 with or without ocular anomalies rs1594535661 · Brain small vessel disease 1 with or without ocular anomalies rs1594555106 · Brain small vessel disease 1 with or without ocular anomalies rs1876543576 · Brain small vessel disease 1 with or without ocular anomalies rs1877518903 · Brain small vessel disease 1 with or without ocular anomalies rs1877796592 · Brain small vessel disease 1 with or without ocular anomalies rs1877796698 · Brain small vessel disease 1 with or without ocular anomalies rs1877889898 · Brain small vessel disease 1 with or without ocular anomalies rs1877963897 · Brain small vessel disease 1 with or without ocular anomalies rs1878012979 · Brain small vessel disease 1 with or without ocular anomalies rs1878013473 · Brain small vessel disease 1 with or without ocular anomalies rs1878142219 · Brain small vessel disease 1 with or without ocular anomalies rs1878248687 · Brain small vessel disease 1 with or without ocular anomalies rs1879717674 · Brain small vessel disease 1 with or without ocular anomalies rs2139146298 · Brain small vessel disease 1 with or without ocular anomalies rs2139146303 · Brain small vessel disease 1 with or without ocular anomalies rs2139149392 · Brain small vessel disease 1 with or without ocular anomalies rs2139154554 · Brain small vessel disease 1 with or without ocular anomalies rs2139154591 · Brain small vessel disease 1 with or without ocular anomalies rs2139156007 · Brain small vessel disease 1 with or without ocular anomalies rs2139160332 · Brain small vessel disease 1 with or without ocular anomalies rs2139162416 · Brain small vessel disease 1 with or without ocular anomalies rs2139162750 · Brain small vessel disease 1 with or without ocular anomalies rs2139162773 · Brain small vessel disease 1 with or without ocular anomalies rs2139162781 · Brain small vessel disease 1 with or without ocular anomalies rs2139162955 · Brain small vessel disease 1 with or without ocular anomalies rs2139163058 · Brain small vessel disease 1 with or without ocular anomalies rs2139164265 · Brain small vessel disease 1 with or without ocular anomalies rs2139164302 · Brain small vessel disease 1 with or without ocular anomalies rs2139165584 · Brain small vessel disease 1 with or without ocular anomalies rs2139165606 · Brain small vessel disease 1 with or without ocular anomalies rs2139169623 · Brain small vessel disease 1 with or without ocular anomalies rs2139187455 · Brain small vessel disease 1 with or without ocular anomalies rs2139207389 · Brain small vessel disease 1 with or without ocular anomalies rs2501568764 · Brain small vessel disease 1 with or without ocular anomalies rs2501584950 · Brain small vessel disease 1 with or without ocular anomalies rs2501590784 · Brain small vessel disease 1 with or without ocular anomalies rs2501608143 · Brain small vessel disease 1 with or without ocular anomalies rs2501741449 · Brain small vessel disease 1 with or without ocular anomalies rs2501741661 · Brain small vessel disease 1 with or without ocular anomalies rs2501749906 · Brain small vessel disease 1 with or without ocular anomalies rs2501752012 · Brain small vessel disease 1 with or without ocular anomalies rs2501770185 · Brain small vessel disease 1 with or without ocular anomalies rs2501779394 · Brain small vessel disease 1 with or without ocular anomalies rs2501779644 · Brain small vessel disease 1 with or without ocular anomalies rs2501780568 · Brain small vessel disease 1 with or without ocular anomalies rs2501791898 · Brain small vessel disease 1 with or without ocular anomalies rs587777379 · Brain small vessel disease 1 with or without ocular anomalies rs606231465 · Brain small vessel disease 1 with or without ocular anomalies rs672601347 · Brain small vessel disease 1 with or without ocular anomalies rs672601348 · Brain small vessel disease 1 with or without ocular anomalies rs672601349 · Brain small vessel disease 1 with or without ocular anomalies rs797045034 · Brain small vessel disease 1 with or without ocular anomalies rs2139156247 · COL4A1 or COL4A2-related cerebral small vessel disease rs2501780064 · COL4A1 or COL4A2-related cerebral small vessel disease rs1555305593 · COL4A1-related disorder rs1879237220 · COL4A1-related disorder rs2139154447 · COL4A1-related disorder rs2501538404 · COL4A1-related disorder rs2501757578 · COL4A1-related disorder rs2501780562 · COL4A1-related disorder rs766209938 · Colpocephaly rs2139163073 · Congenital anomaly of kidney and urinary tract rs11838776 · 관상동맥질환 rs9521678 · 관상동맥질환 rs11617955 · 관상동맥질환 (심근경색, 경피적 관상동맥성형술, 관상동맥우회술, 협심증 또는 만성 허혈성 심장병) rs113994108 · Developmental cataract rs6492257 · Diastolic blood pressure (BMI adjusted) rs751749 · Diastolic blood pressure (UKB data field 4079) rs4142040 · 추정 사구체 여과율 (크레아티닌) rs7329411 · 키(신장) rs75372280 · BMI 보정 엉덩이둘레 rs2847468 · 엉덩이 지수 rs1064795935 · Inborn genetic diseases rs1555302454 · Inborn genetic diseases rs1555302735 · Inborn genetic diseases rs1555302942 · Inborn genetic diseases rs1555303010 · Inborn genetic diseases rs1879015838 · Inborn genetic diseases rs2501757966 · Inborn genetic diseases rs2501780336 · Inborn genetic diseases rs797044867 · Inborn genetic diseases rs587780588 · Intracranial hemorrhage rs766346293 · Irido-corneo-trabecular dysgenesis rs638634 · Ischemic heart disease (PheCode 411) rs761712661 · 원추각막 rs2501580028 · Melanoma rs1085307709 · Microangiopathy and leukoencephalopathy, pontine, autosomal dominant rs1876438936 · Microangiopathy and leukoencephalopathy, pontine, autosomal dominant rs1876439052 · Microangiopathy and leukoencephalopathy, pontine, autosomal dominant rs1877904298 · Microangiopathy and leukoencephalopathy, pontine, autosomal dominant rs2138415342 · Microangiopathy and leukoencephalopathy, pontine, autosomal dominant rs2501592907 · Microangiopathy and leukoencephalopathy, pontine, autosomal dominant rs780492563 · Microangiopathy and leukoencephalopathy, pontine, autosomal dominant rs1877701802 · 소두증 rs16975420 · 단핵구 (절대 수, 최댓값, 역정규 변환) rs2501600650 · Nonpapillary renal cell carcinoma rs1555303073 · Optic nerve hypoplasia rs61963337 · 혈소판 분포폭 rs9588131 · 혈소판용적률 rs2139160399 · 공뇌증 rs61963301 · Primary open angle glaucoma (MTAG) rs13260 · 맥압 rs1877827904 · Retinal arterial tortuosity rs1363290269 · Sarcoma rs2139187383 · Seizure rs7326444 · Spontaneous coronary artery dissection rs616008 · TINAGL1 단백질 수치 rs1085307816 · Uterine corpus endometrial carcinoma rs1878014262 · 혈관성 치매 rs72655742 · 정점별 뇌고랑 깊이 rs61963358 · 허리-엉덩이 지수 rs73617438 · 허리-엉덩이 지수 rs664532 · 허리-엉덩이 둘레비 rs552125 · 체질량지수 보정 허리엉덩이비율
COL4A1 근처의 변이 (1)
유전자 바깥에 있지만 가장 가까운 유전자라서 이 이름으로 기록된 위치입니다. 유전자 근처의 변이가 늘 그 유전자를 통해 작용하는 것은 아닙니다.
유전자 지식 그래프 에서 COL4A1 유전자와 이어진 모든 것을 보거나, /ko/api/v1/genes/COL4A1 에서 데이터로 볼 수 있습니다.
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COL4A1 유전자. MyGeneLog™. https://www.mygenelog.com/ko/genes/COL4A1
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