1. Gene
  2. ANKRD37 - ankyrin repeat domain 37 Gene

ANKRD37 - ankyrin repeat domain 37 Gene

中文名称:锚蛋白重复结构域 37

种属: Homo sapiens

同用名: Lrp2bp

基因 ID: 353322 | 基因类型: protein coding

关于 ANKRD37

Cytogenetic location: 4q35.1 Genomic coordinates (GRCh38): 4:185,396,841-185,400,723 (from NCBI)

This gene has 6 transcripts (splice variants), 140 orthologues and 1 paralogue. Ubiquitous expression in esophagus (RPKM 19.3), prostate (RPKM 17.2) and 25 other tissues.

功能概要

位于胞质溶胶中;线粒体;和核质。 [由基因组资源联盟提供,2022 年 4 月]

Located in cytosol; mitochondrion; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

ANKRD37 基因产物(1)

mRNA Protein Name
NM_181726.4 NP_859077.1 ankyrin repeat domain-containing protein 37
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
32296183 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

ANKRD37 蛋白结构

Ank_2

Ank_2: Ankyrin repeats (3 copies) (11 - 92)

  • 0
  • 100
  • 158 a.a.
蛋白主名 其他名称

ankyrin repeat domain-containing protein 37

low density lipoprotein receptor-related protein binding protein

ANKRD37 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
种属内
ANKRD37 Q7Z713 HIF1AN Homo sapiens Q9NWT6 32296183
种属内
ANKRD37 Q7Z713 HIF1AN Homo sapiens Q9NWT6 32296183
种属内
ANKRD37 Q7Z713 HIF1AN Homo sapiens Q9NWT6 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
Donnai-Barrow Syndrome

Faciooculoacousticorenal Syndrome

Dbs/Foar Syndrome

Foar Syndrome

Diaphragmatic Hernia-Exomphalos-Hypertelorism Syndrome

Facio-Oculo-Acoustico-Renal Syndrome

Diaphragmatic Hernia, Exomphalos, Absent Corpus Callosum, Hypertelorism, Myopia, Sensorineural Deafness, And Proteinuria

Diaphragmatic Hernia-Hypertelorism-Myopia-Deafness Syndrome

Holmes-Schepens Syndrome

Syndrome Of Ocular And Facial Anomalies, Telecanthus And Deafness

DBS

Diaphragmatic Hernia Exomphalos Absent Corpus Callosum Hypertelorism Myopia Sensorineural Deafness And Proteinuria

Diaphragmatic Hernia-Exomphalos-Corpus Callosum Agenesis

Diaphragmatic Hernia-Hypertelorism-Myopia-Hearing Loss Syndrome

Syndrome Of Ocular And Facial Anomalies, Telecanthus And Hearing Loss

Donnai Barrow Syndrome

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
Felis catus ANKRD37 VGNC VGNC:59811
Macaca mulatta ANKRD37 VGNC VGNC:106544
Mus musculus ANKRD37 MGD MGI:3603344
Canis familiaris ANKRD37 VGNC VGNC:37901
Bos taurus ANKRD37 VGNC VGNC:25928
Rattus norvegicus ANKRD37 RGD RGD:1565715