1. Gene
  2. UBIAD1 - UbiA prenyltransferase domain containing 1 Gene

UBIAD1 - UbiA prenyltransferase domain containing 1 Gene

中文名称:含 UbiA 异戊二烯基转移酶结构域 1

种属: Homo sapiens

同用名: SCCD; TERE1

基因 ID: 29914 | 基因类型: protein coding

关于 UBIAD1

Cytogenetic location: 1p36.22 Genomic coordinates (GRCh38): 1:11,273,198-11,299,574 (from NCBI)

This gene has 4 transcripts (splice variants), 197 orthologues and is associated with 3 phenotypes. Ubiquitous expression in testis (RPKM 2.8), ovary (RPKM 2.6) and 25 other tissues.

功能概要

该基因编码一种被认为参与胆固醇和磷脂代谢的蛋白质。该基因的突变与 Schnyder 结晶性角膜营养不良有关。[RefSeq 提供,2008 年 10 月]

This gene encodes a protein thought to be involved in Cholesterol and phospholipid metabolism. Mutations in this gene are associated with Schnyder crystalline corneal dystrophy. [provided by RefSeq, Oct 2008]

UBIAD1 基因产物(3)

mRNA Protein Name
NM_001330349.2 NP_001317278.1 ubiA prenyltransferase domain-containing protein 1 isoform 2
NM_001330350.2 NP_001317279.1 ubiA prenyltransferase domain-containing protein 1 isoform 3
NM_013319.3 NP_037451.1 ubiA prenyltransferase domain-containing protein 1 isoform 1
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables antioxidant activity IMP
IMP: 通过突变表型推断
23374346 GOA
enables prenyltransferase activity EXP
EXP: 通过实验结果推断
20953171 GOA
enables prenyltransferase activity IDA
IDA: 通过直接分析推断
20953171 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
23169578 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in menaquinone biosynthetic process IMP
IMP: 通过突变表型推断
23169578 GOA
involved in ubiquinone biosynthetic process IMP
IMP: 通过突变表型推断
23374346 GOA
involved in vitamin K biosynthetic process IDA
IDA: 通过直接分析推断
20953171 GOA
involved in vitamin K biosynthetic process IMP
IMP: 通过突变表型推断
23169578 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in Golgi membrane IDA
IDA: 通过直接分析推断
23374346 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
11314041 GOA
located in endoplasmic reticulum IDA
IDA: 通过直接分析推断
20953171 GOA
located in membrane IDA
IDA: 通过直接分析推断
11314041 GOA
located in nucleus IDA
IDA: 通过直接分析推断
11314041 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

UBIAD1 蛋白结构

UbiA

UbiA: UbiA prenyltransferase family (59 - 321)

  • 0
  • 100
  • 200
  • 300
  • 338 a.a.
蛋白主名 其他名称

ubiA prenyltransferase domain-containing protein 1

transitional epithelia response protein

UBIAD1 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
Intra UBIAD1 Q9Y5Z9 RETREG3 Homo sapiens Q86VR2
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 RETREG3 Homo sapiens Q86VR2
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 NCAPH2 Homo sapiens Q6IBW4-4
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 NCAPH2 Homo sapiens Q6IBW4-4
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 MRM3 Homo sapiens Q9HC36
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 MRM3 Homo sapiens Q9HC36
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 CYB5R3 Homo sapiens P00387
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 CYB5R3 Homo sapiens P00387
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 TMEFF2 Homo sapiens Q9UIK5
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 TMEFF2 Homo sapiens Q9UIK5
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 HIBADH Homo sapiens P31937
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 HIBADH Homo sapiens P31937
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 KCNJ6 Homo sapiens P48051
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 KCNJ6 Homo sapiens P48051
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 AHNAK2 Homo sapiens Q8IVF2-3
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 AHNAK2 Homo sapiens Q8IVF2-3
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 FNDC9 Homo sapiens Q8TBE3
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 FNDC9 Homo sapiens Q8TBE3
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 ASGR2 Homo sapiens P07307-3
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 ASGR2 Homo sapiens P07307-3
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 GPR152 Homo sapiens Q8TDT2
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 GPR152 Homo sapiens Q8TDT2
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 CRB3 Homo sapiens Q9BUF7-2
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 CRB3 Homo sapiens Q9BUF7-2
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 SCN3B Homo sapiens Q9NY72
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 SCN3B Homo sapiens Q9NY72
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 PIGP Homo sapiens P57054
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 PIGP Homo sapiens P57054
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 EVI2B Homo sapiens P34910-2
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 EVI2B Homo sapiens P34910-2
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 CPLX4 Homo sapiens Q7Z7G2
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 CPLX4 Homo sapiens Q7Z7G2
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 FAM209A Homo sapiens Q5JX71
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 FAM209A Homo sapiens Q5JX71
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 LHFPL5 Homo sapiens Q8TAF8
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 LHFPL5 Homo sapiens Q8TAF8
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 EVI2A Homo sapiens P22794
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 EVI2A Homo sapiens P22794
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 HRAS Homo sapiens P01112
Anti Tag CoIP
30518913
Intra UBIAD1 Q9Y5Z9 HRAS Homo sapiens P01112
FRET
30518913
Intra UBIAD1 Q9Y5Z9 HRAS Homo sapiens P01112
IF
30518913
Intra UBIAD1 Q9Y5Z9 HRAS Homo sapiens P01112
BiFC
30518913
Intra UBIAD1 Q9Y5Z9 CD33 Homo sapiens P20138
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 CD33 Homo sapiens P20138
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 EBP Homo sapiens Q15125
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 EBP Homo sapiens Q15125
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 FKBP7 Homo sapiens Q9Y680
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 FKBP7 Homo sapiens Q9Y680
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 FKBP7 Homo sapiens Q9Y680
Validated Y2H
32296183
Intra UBIAD1 Q9Y5Z9 SAR1A Homo sapiens Q9NR31
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 SAR1A Homo sapiens Q9NR31
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 HMGCR Homo sapiens P04035
Anti Tag CoIP
33961781
Intra UBIAD1 Q9Y5Z9 HMGCR Homo sapiens P04035
Anti Tag CoIP
23169578
Intra UBIAD1 Q9Y5Z9 SLC7A14 Homo sapiens Q8TBB6
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 SLC7A14 Homo sapiens Q8TBB6
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 SYT1 Homo sapiens P21579
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 SYT1 Homo sapiens P21579
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 SOAT1 Homo sapiens P35610
Anti Tag CoIP
23169578
Intra UBIAD1 Q9Y5Z9 CD53 Homo sapiens P19397
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 CD53 Homo sapiens P19397
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 CREB3L1 Homo sapiens Q96BA8
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 CREB3L1 Homo sapiens Q96BA8
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 BIK Homo sapiens Q13323
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 BIK Homo sapiens Q13323
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 PHACTR3 Homo sapiens Q96KR7
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 PHACTR3 Homo sapiens Q96KR7
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 TMEM139 Homo sapiens Q8IV31
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 TMEM139 Homo sapiens Q8IV31
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 MGST3 Homo sapiens O14880
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 MGST3 Homo sapiens O14880
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 CLDN7 Homo sapiens O95471
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 CLDN7 Homo sapiens O95471
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 REEP4 Homo sapiens Q9H6H4
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 REEP4 Homo sapiens Q9H6H4
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 CD79A Homo sapiens P11912
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 CD79A Homo sapiens P11912
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 ERGIC3 Homo sapiens Q9Y282
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 ERGIC3 Homo sapiens Q9Y282
Y2H Prey Pooling
32296183
Intra UBIAD1 Q9Y5Z9 TMEM14B Homo sapiens Q9NUH8
Y2H Array
32296183
Intra UBIAD1 Q9Y5Z9 TMEM14B Homo sapiens Q9NUH8
Y2H Prey Pooling
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Schnyder Corneal Dystrophy

Schnyder Crystalline Corneal Dystrophy

SCCD

Corneal Dystrophy, Crystalline, Of Schnyder

Corneal Dystrophy, Schnyder Type

Corneal Dystrophy Crystalline Of Schnyder

Crystalline Stromal Dystrophy

Hereditary Crystalline Stromal Dystrophy Of Schnyder

Scd

Corneal Dystrophy, Schnyder

Schnyder Crystalline Dystrophy Sine Crystals

Dystrophy, Corneal, Crystalline, Schnyder

Corneal Dystrophy
Transitional Cell Carcinoma

Transitional Cell Neoplasm

Carcinoma, Transitional Cell

Transitional Carcinoma

Transitional Cell Tumor

Urothelial Cell Carcinoma

Carcinoma Transitional Cell

Transitional Cell Carcinoma Of Bladder

Stromal Dystrophy
Stromal Corneal Dystrophy

Stromal Dystrophies Corneal

Corneal Deposit

Deposits - Cornea

Corneal Dystrophy, Thiel-Behnke Type

Thiel-Behnke Corneal Dystrophy

Tbcd

CDTB

Cdb2

Corneal Dystrophy Of Bowman Layer Type Ii

Anterior Limiting Membrane Dystrophy Type Ii

Waardenburg-Jonker Corneal Dystrophy

Corneal Dystrophy Of Bowman Layer, Type Ii

Corneal Dystrophy, Honeycomb-Shaped

Corneal Dystrophy Honeycomb-Shaped

Corneal Dystrophy Thiel Behnke Type

Corneal Dystrophy Honeycomb Shaped

Corneal Dystrophy Of The Bowman Layer Type 2

Thiel Behnke Corneal Dystrophy

Anterior Limiting Membrane Dystrophy Type 2

Corneal Dystrophy Of Bowman Layer Type 2

Curly Fiber Corneal Dystrophy

Honeycomb Corneal Dystrophy

Honeycomb-Shaped Corneal Dystrophy

Dystrophy, Corneal, Thiel-Behnke Type

Corneal Dystrophy, Posterior Polymorphous, 1

Posterior Polymorphous Corneal Dystrophy

Ppcd

Maumenee Corneal Dystrophy

Posterior Polymorphous Corneal Dystrophy 1

PPCD1

Corneal Dystrophy, Hereditary Polymorphous Posterior

Corneal Endothelial Dystrophy 1, Autosomal Dominant

Schlichting Dystrophy

Ched1

Corneal Endothelial Dystrophy 1, Autosomal Dominant, Formerly

Ched1, Formerly

Hereditary Polymorphus Posterior Corneal Dystrophy

Posterior Polymorphous Dystrophy

Hereditary Polymorphous Posterior Corneal Dystrophy

Dystrophy, Corneal, Posterior Polymorphous

Dystrophy, Corneal, Posterior Polymorphous, Type 1

Polymorphous Corneal Dystrophy

Corneal Endothelial Dystrophy 2

Macular Dystrophy, Corneal

Macular Corneal Dystrophy

MCD

Corneal Dystrophy, Macular Type

Groenouw Type Ii Corneal Dystrophy

Fehr Corneal Dystrophy

Macular Dystrophy, Corneal Type 1

Mcdc1

Macular Corneal Dystrophy Type Ii

Macular Corneal Dystrophy, Type Ii

Macular Corneal Dystrophy, Type I

Mcdc1, Formerly

Macular Dystrophy, Corneal, 1

Macular Corneal Dystrophy Type 1

Corneal Dystrophy Groenouw Type Ii

Corneal Dystrophy Macular Type

Macular Corneal Dystrophy Type I

Dystrophy, Macular, Corneal

Corneal Dystrophy, Reis-Bucklers Type

Reis-Bucklers Corneal Dystrophy

Rbcd

CDRB

Cdb1

Corneal Dystrophy Of Bowman Layer Type I

Geographic Corneal Dystrophy

Granular Corneal Dystrophy Type Iii

Reis-Bucklers' Corneal Dystrophy

Anterior Limiting Membrane Dystrophy Type I

Corneal Dystrophy Of Bowman Layer Type 1

Corneal Dystrophy Of Bowman Layer, Type I

Corneal Dystrophy, Geographic

Granular Corneal Dystrophy, Type Iii

Corneal Dystrophy Reis Bucklers Type

Corneal Dystrophy Geographic

Reis Bucklers Corneal Dystrophy

Reis Bucklers Dystrophy

Anterior Limiting Membrane Dystrophy Type 1

Atypical Granular Corneal Dystrophy

Granular Corneal Dystrophy Type 3

Superficial Granular Corneal Dystrophy

Corneal Dystrophy Of Bowman Layer, Type 1

Dystrophy, Corneal, Reis-Bucklers Type

Granular Corneal Dystrophy

Granular Dystrophy Corneal

Corneal Dystrophies, Hereditary

Hereditary Corneal Dystrophy

Corneal Dystrophy Nos

Familial Hereditary Corneal Degeneration

Hereditary Corneal Opacity

Arcus Corneae

Arcus Senilis

Corneal Arcus

Arcus Of Cornea

Corneal Endothelial Dystrophy

Congenital Hereditary Endothelial Dystrophy Of Cornea

Chandler Syndrome

CHED

Chandler'S Syndrome

Endothelial Corneal Dystrophy

Ched2

Maumenee Corneal Dystrophy

Corneal Dystrophy, Congenital Hereditary Endothelial

Dystrophy Of Corneal Endothelium

Corneal Endothelial Dystrophy 2

Corneal Endothelial Dystrophy 2, Autosomal Recessive, Formerly

Ched2, Formerly

Corneal Endothelial Dystrophy, Autosomal Recessive

Endothelial Dystrophy

Posterior Membrane Corneal Dystrophy

Corneal Endothelial Dystrophy Type 2

Congenital Hereditary Endothelial Dystrophy Of The Cornea

Congenital Hereditary Endothelial Dystrophy Type Ii

Autosomal Recessive Ched

Autosomal Recessive Congenital Hereditary Endothelial Dystrophy

Chedii

Congenital Hereditary Endothelial Dystrophy Type 2

Infantile Hereditary Endothelial Dystrophy

Congenital Hereditary Endothelial Corneal Dystrophy

Corneal Endothelial Dystrophy 2, Autosomal Recessive

Iridocorneal Endothelial Syndrome

Dystrophy, Corneal, Endothelial

Corneal Endothelial Dystrophy 1, Autosomal Dominant

Epithelial And Subepithelial Dystrophy
Corneal Dystrophy, Posterior Polymorphous, 3

Posterior Polymorphous Corneal Dystrophy 3

PPCD3

Dystrophy, Corneal, Posterior Polymorphous, Type 3

Corneal Dystrophy, Meesmann, 1

Meesmann Corneal Dystrophy

Mecd

Corneal Dystrophy, Meesmann Epithelial

Juvenile Hereditary Epithelial Dystrophy

Corneal Dystrophy, Juvenile Epithelial Of Meesmann

MECD1

Meesmann Corneal Dystrophy 1

Meesmann Corneal Epithelial Dystrophy

Meesmann Epithelial Corneal Dystrophy

Corneal Dystrophy, Juvenile Epithelial, Of Meesmann

Stocker-Holt Dystrophy

Meesman Dystrophy

Meesman'S Corneal Dystrophy

Juvenile Hereditary Epithelial Dystrophy Of Meesmann

Corneal Dystrophy, Meesmann 1

Juvenile Epithelial Corneal Dystrophy Of Meesmann

Mcd

Dystrophy, Corneal, Meesmann

Epithelial Recurrent Erosion Dystrophy

ERED

Corneal Erosions, Recurring Hereditary

Col17a1

Dystrophia Helsinglandica

Dystrophia Smolandiensis

Recurrent Hereditary Corneal Erosions

Rces

Recurrent Corneal Erosion Syndrome

Recurrent Erosion Of Cornea

Corneal Degeneration

Degenerative Corneal Opacity

Corneal Dystrophy, Avellino Type

Avellino Corneal Dystrophy

CDA

Combined Granular-Lattice Corneal Dystrophy

Cgd2

Granular Corneal Dystrophy Type 2

Acd

Granular Corneal Dystrophy 2

Corneal Dystrophy Avellino Type

Granular Corneal Dystrophy Type Ii

Granular Corneal Dystrophy, Type Ii

Combined Granular-Lattice Corneal Dystrophies

Granular And Lattice Corneal Dystrophies

Granular-Lattice Corneal Dystrophy

Gcd2

Gcdii

Granular-Lattice Corneal Dystrophy

Corneal Dystrophy, Lisch Epithelial

Lisch Epithelial Corneal Dystrophy

LECD

Band-Shaped And Whorled Microcystic Corneal Epithelial Dystrophy

Band-Shaped And Whorled Microcystic

Band-Shaped And Whorled Microcystic Dystrophy Of The Corneal Epithelium

Corneal Dystrophy, Groenouw Type I

CDGG1

Gcd1

Groenouw Corneal Dystrophy Type I

Granular Corneal Dystrophy 1

Granular Corneal Dystrophy Type I

Corneal Dystrophy Groenouw Type I

Granular Corneal Dystrophy, Type I

Corneal Dystrophy, Punctate Or Nodular

Groenouw Type I Corneal Dystrophy

Corneal Dystrophy Granular Type

Corneal Dystrophy Punctate Or Nodular

Classic Gcd

Classic Granular Corneal Dystrophy

Gcdi

Granular Corneal Dystrophy Type 1

Corneal Dystrophy, Groenouw Type 1

Mesh

D003317

Punctate Or Nodular Corneal Dystrophy

Dystrophy, Corneal, Groenouw Type I

Corneal Dystrophy, Gelatinous Drop-Like

Gelatinous Drop-Like Corneal Dystrophy

GDLD

Cdgdl

Corneal Amyloidosis

Lattice Corneal Dystrophy Type Iii

Amyloidosis, Corneal

Amyloid Corneal Dystrophy, Japanese Type

Gdcd

Primary Familial Amyloidosis Of The Cornea

Subepithelial Amyloidosis Of The Cornea

Corneal Dystrophy, Lattice Type 3

Corneal Dystrophy, Lattice Type Iii

Lattice Corneal Dystrophy, Type Iii

Amyloidosis Corneal

Lattice Corneal Dystrophy Type3

Amyloid Corneal Dystrophy Japanese Type

Dystrophy, Corneal, Gelatinous Drop-Like

Amyloid Of Cornea

Lecithin:Cholesterol Acyltransferase Deficiency

Norum Disease

Lcat Deficiency

Familial Lcat Deficiency

Fld

Lecithin Acyltransferase Deficiency

Complete Lcat Deficiency

Lecithin Cholesterol Acyltransferase Deficiency

Lecithin-Cholesterol Acyltransferase Deficiency

Familial Lecithin-Cholesterol Acyltransferase Deficiency

Norum'S Disease

LCATD

Deficiency, Lecithin:Cholesterol Acyltransferase

Vitamin K Deficiency Bleeding

Vitamin K Deficiency

Deficiency Of Vitamin K

Vitamin K

Vitamin K Deficiency Hemorrhagic Disease

Corneal Disease

Corneal Diseases

Corneal Disorders

Epithelial Basement Membrane Dystrophy

Ebmd

Corneal Dystrophy, Epithelial Basement Membrane

Cogan Corneal Dystrophy

Microcystic Corneal Dystrophy

Anterior Basement Membrane Dystrophy

Cogan Microcystic Epithelial Dystrophy

Map-Dot-Fingerprint Dystrophy

Microscopic Cystic Corneal Dystrophy

Corneal Dystrophy, Subepithelial Mucinous

Subepithelial Mucinous Corneal Dystrophy

SMCD

Epithelial-Stromal Tgfbi Dystrophy
Fuchs' Endothelial Dystrophy

Fuchs Endothelial Corneal Dystrophy

Fuchs Endothelial Dystrophy

Fuchs Dystrophy

Fced

Fuchs' Corneal Dystrophy

Fuchs' Endothelial Corneal Dystrophy

Fuchs Atrophy

Fuchs Corneal Dystrophy

Endoepithelial Corneal Dystrophy

Fecd

Late Hereditary Endothelial Dystrophy

Corneal Dystrophy, Fuchs Endothelial

Dystrophy, Corneal, Fuchs Endothelial

Corneal Dystrophy, Fuchs' Endothelial, 1

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta UBIAD1 VGNC VGNC:79881
Rattus norvegicus UBIAD1 RGD RGD:1309588
Bos taurus UBIAD1 VGNC VGNC:36606
Mus musculus UBIAD1 MGD MGI:1918957
Canis familiaris UBIAD1 VGNC VGNC:48075