1. Gene
  2. MINAR2 - membrane integral NOTCH2 associated receptor 2 Gene

MINAR2 - membrane integral NOTCH2 associated receptor 2 Gene

中文名称:膜积分 NOTCH2 相关受体 2

种属: Homo sapiens

同用名: KIAA1024L

基因 ID: 100127206 | 基因类型: protein coding

关于 MINAR2

This gene has 1 transcript (splice variant), 194 orthologues and 1 paralogue. Low expression observed in reference dataset.

功能概要

预计是膜的组成部分。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

MINAR2 基因产物(1)

mRNA Protein Name
NM_001257308.2 NP_001244237.1 major intrinsically disordered NOTCH2-binding receptor 1-like
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 cholesterol binding IDA
IDA: 通过直接分析推断
36317962 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
32954300 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in angiogenesis IMP
IMP: 通过突变表型推断
35727972 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in endoplasmic reticulum IDA
IDA: 通过直接分析推断
32954300 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

MINAR2 蛋白结构

UPF0258

UPF0258: Uncharacterised protein family (UPF0258) (47 - 187)

  • 0
  • 100
  • 190 a.a.
蛋白主名 其他名称

major intrinsically disordered NOTCH2-binding receptor 1-like

KIAA1024 like

关联疾病

疾病名称 别名
Contractural Arachnodactyly, Congenital

Congenital Contractural Arachnodactyly

Beals Syndrome

CCA

Beals-Hecht Syndrome

Distal Arthrogryposis Type 9

Arthrogryposis, Distal, Type 9

Da9

Arachnodactyly, Contractural Beals Type

Contractures, Multiple With Arachnodactyly

Ear Anomalies-Contractures-Dysplasia Of Bone With Kyphoscoliosis

Arthrogyroposis, Distal, Type 9

Distal Arthrogyropsis Type 9

Cca Syndrome

Arachnodactyly

Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant

ADLD

Adult-Onset Autosomal Dominant Demyelinating Leukodystrophy

Leukodystrophy, Adult-Onset, Autosomal Dominant

Adult-Onset Autosomal Dominant Leukodystrophy

Autosomal Dominant Leukodystrophy With Autonomic Disease

Autosomal Dominant Adult-Onset Demyelinating Leukodystrophy

Multiple Sclerosis-Like Disorder

Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type, Formerly

Autosomal-Dominant Or Late-Onset Type Pelizaeus-Merzbacher Disease

Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type

Adult-Onset Autosomal Dominant Leukodystrophy With Autonomic Symptoms

Lmnb1-Related Adult-Onset Autosomal Dominant Leukodystrophy

Leukodystrophy, Demyelinating, Autosomal Dominant, Adult-Onset

Pelizaeus-Merzbacher Disease Autosomal Dominant

Pelizaeus-Merzbacher Disease Late-Onset Type

Adult Onset Autosomal Dominant Leukodystrophy

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
Rattus norvegicus MINAR2 RGD RGD:1312005
Macaca mulatta MINAR2 VGNC VGNC:84441
Mus musculus MINAR2 MGD MGI:2442934
Felis catus MINAR2 VGNC VGNC:63509
Canis familiaris MINAR2 VGNC VGNC:58317
Bos taurus MINAR2 VGNC VGNC:30562