1. Gene
  2. FOXL1 - forkhead box L1 Gene

FOXL1 - forkhead box L1 Gene

中文名称:叉头盒 L1

种属: Homo sapiens

同用名: FKH6; FKHL11; FREAC7

基因 ID: 2300 | 基因类型: protein coding

关于 FOXL1

Cytogenetic location: 16q24.1 Genomic coordinates (GRCh38): 16:86,578,549-86,583,478 (from NCBI)

This gene has 2 transcripts (splice variants), 169 orthologues and 42 paralogues.

功能概要

该基因编码叉头/翼状螺旋盒 (FOX) 转录因子家族的成员。 FOX 转录因子的特点是具有独特的 DNA 结合叉头结构域,并且在个体发育过程中的多个过程 (包括代谢、细胞增殖和基因表达) 的调节中发挥关键作用。[RefSeq 提供,2012 年 11 月]

This gene encodes a member of the forkhead/winged helix-box (FOX) family of transcription factors. FOX transcription factors are characterized by a distinct DNA-binding forkhead domain and play critical roles in the regulation of multiple processes including metabolism, cell proliferation and gene expression during ontogenesis. [provided by RefSeq, Nov 2012]

FOXL1 基因产物(1)

mRNA Protein Name
NM_005250.3 NP_005241.1 forkhead box protein L1
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 DNA binding IDA
IDA: 通过直接分析推断
7957066 GOA
enables sequence-specific DNA binding IDA
IDA: 通过直接分析推断
7957066 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in heart development IMP
IMP: 通过突变表型推断
21457232 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in nucleus IDA
IDA: 通过直接分析推断
34633540 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

FOXL1 蛋白结构

Forkhead

Forkhead: Forkhead domain (49 - 143)

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

forkhead box protein L1

forkhead-like 11

关联疾病

疾病名称 别名
Lymphedema-Distichiasis Syndrome

Lymphedema With Distichiasis

Lymphedema-Distichiasis Syndrome With Renal Disease And Diabetes Mellitus

LPHDST

Distichiasis-Lymphedema Syndrome

Lymphedema Distichiasis Syndrome

Hereditary Lymphedema-Distichiasis Syndrome

Lymphedema Distichiasis

Hypoplastic Left Heart Syndrome

Hlhs

Heart, Hypoplastic Left, Syndrome

Hypoplasia Of The Left Heart

Left Heart Hypoplasia Syndrome

Hlhs - [Hypoplastic Left Heart Syndrome]

Hypoplasia Of Aortic Valve, In Hypoplastic Left Heart Syndrome

Atresia Of Mitral Valve, In Hypoplastic Left Heart Syndrome

Atresia Or Marked Hypoplasia Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle

Atresia Or Marked Hypoplasia, Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle With Mitral Valve Atresia

Aortic Valve Atresia, In Hypoplastic Left Heart Syndrome

Ascending Aorta Hypoplasia, In Hypoplastic Left Heart Syndrome

Otosclerosis

Otospongiosis

Vacterl Association

Vater Association

Vater Syndrome

Pancreas, Annular

Annular Pancreas

Pancreas Annulare

Congenital Annular Pancreas

Microphthalmia, Syndromic 3

MCOPS3

Aeg Syndrome

Microphthalmia And Esophageal Atresia Syndrome

Anophthalmia/Microphthalmia-Esophageal Atresia Syndrome

Anophthalmia-Esophageal-Genital Syndrome

Optic Nerve Hypoplasia And Abnormalities Of The Central Nervous System

Syndromic Microphthalmia 3

Sox2 Anophthalmia Syndrome

Anophthalmia Clinical With Associated Anomalies

Anophthalmia Esophageal Genital Syndrome

Anophthalmia Microphthalmia Esophageal Atresia

Syndromic Microphthalmia Type 3

Sox2-Related Eye Disorders

Anophthalmia, Clinical, With Associated Anomalies

Syndromic Microphthalmia, Type 3

Microphthalmia, Syndromic, 3

Anophthalmia/Microphthalmia-Esophageal Atresia

Microphthalmia Syndromic, Type 3

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
Canis familiaris FOXL1 VGNC VGNC:40958
Rattus norvegicus FOXL1 RGD RGD:1584212
Bos taurus FOXL1 VGNC VGNC:29092
Mus musculus FOXL1 MGD MGI:1347469