1. Gene
  2. STOML3 - stomatin like 3 Gene

STOML3 - stomatin like 3 Gene

中文名称:气孔样 3

种属: Homo sapiens

同用名: SRO; Epb7.2l

基因 ID: 161003 | 基因类型: protein coding

关于 STOML3

Cytogenetic location: 13q13.3 Genomic coordinates (GRCh38): 13:38,965,925-38,990,831 (from NCBI)

This gene has 2 transcripts (splice variants), 276 orthologues and 4 paralogues. Biased expression in lung (RPKM 1.0), endometrium (RPKM 0.3) and 2 other tissues.

功能概要

预测作用于信号转导的上游或内部。预测位于纤毛和膜筏。预计是膜的组成部分。预计在质膜上有活性。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to act upstream of or within signal transduction. Predicted to be located in cilium and membrane raft. Predicted to be integral component of membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

STOML3 基因产物(2)

mRNA Protein Name
NM_001144033.2 NP_001137505.1 stomatin-like protein 3 isoform 2
NM_145286.3 NP_660329.1 stomatin-like protein 3 isoform 1
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

STOML3 蛋白结构

Band_7

Band_7: SPFH domain / Band 7 family (52 - 224)

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

stomatin-like protein 3

EPB72-like 3

STOML3 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
STOML3 Q8TAV4 SEC22A Homo sapiens Q96IW7 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
Overhydrated Hereditary Stomatocytosis

Ohs

Potassium Sodium Disorder Of Erythrocyte

OHST

Stomatocytosis I

Potassium-Sodium Disorder Of Erythrocyte

Stomatocytosisiohst

Hereditary, Overhydrated, Cation-Leak Stomatocytosis

Overhydrated Cation Leak Stomatocytosis

Stomatocytosis, Overhydrated Hereditary

Oculomotor Nerve Paralysis

Iii Nerve Palsy

Iiird Nerve Paralysis

Third Cranial Nerve Paralysis

Herpes Zoster Oticus

Nervus Intermedius Neuralgia

Ramsay Hunt Syndrome Type 2

Geniculate Herpes Zoster

Geniculate Neuralgia

Herpes Zoster Auricularis

Herpetic Geniculate Ganglionitis

Ramsay Hunt Syndrome Type Ii

Ramsey Hunt Syndrome

Facial Nerve Palsy Due To Vzv

Facial Nerve Palsy Due To Herpes Zoster Infection

Facial Nerve Paralysis Due To Vzv

Hunt Syndrome

Hunt'S Syndrome

Ramsay Hunt Syndrome

Myoclonus And Ataxia

Gliosarcoma

Glioblastoma With Sarcomatous Component

Sarcomatous Glioblastoma

Abducens Palsy

Sixth Nerve Palsy

Abducens Nerve Palsy

Abducens Nerve Disease

Abducens Nerve Weakness

Lateral Rectus Muscle Denervation Paresis

Lateral Rectus Muscle Innervation Disorder

Sixth Cranial Nerve Disorder

6th Nerve Palsy

Abducens Nerve Diseases

Vith Nerve Disorder

Vith Nerve Paralysis

Cranial Mononeuropathy Vi

Cranial Nerve Vi Palsy

Sixth Cranial Nerve Palsy

Vi Nerve Palsy

Abducens Nerve Disorder

Abducens Sixth Nerve Palsy

Abducens Nerve Paralysis

Disease Or Disorder Of Abducent Nerve

Sixth Cranial Nerve Disease

Sixth Cranial Nerve Weakness

Disorder Of Sixth Cranial Nerve

Isolated Abducent Nerve Palsy

Atrophy Of Sixth Cranial Nerve

Paralysis Of Sixth Cranial Nerve

Facial Neuralgia
Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema

Dehydrated Hereditary Stomatocytosis

Hereditary Xerocytosis

Xerocytosis, Hereditary

Pshk1

Pseudohyperkalemia Edinburgh

Dehydrated Hereditary Stomatocytosis With Or Without Pseudohyperkalemia And/Or Perinatal Edema

DHS1

Dhs

Hereditary Desiccytosis

Dehydrated Hereditary Stomatocytosis 1

Desiccytosis, Hereditary

Pseudohyperkalemia, Familial, 1, Due To Red Cell Leak

Pseudohyperkalemia Familial 1, Due To Red Cell Leak

Desiccytosis Hereditary

Xerocytosis Hereditary

Familial Pseudohyperkalemia 1 Due To Red Cell Leak

Stomatocytosis, Dehydrated, Hereditary, With/Without Pseudohyperkalemia And/Or Perinatal Edema

Xerocytosis

Third Cranial Nerve Disease

Disorder Of Oculomotor Nerve

Oculomotor Nerve Disorder

Oculomotor Nerve Paralysis

Third Cranial Nerve Disorder

Intracranial Hypotension
Brooke-Spiegler Syndrome

Cyld Cutaneous Syndrome

Spiegler-Brooke Syndrome

Familial Cylindromatosis

BRSS

Bss

Sbs

Multiple Familial Trichoepithelioma

Ancell-Spiegler Cylindromas

Familial Multiple Trichoepithelioma

Trichoepithelioma

Fc

Mft

Multiple Familial Trichoepitheliomas

Ccs

Turban Tumor Syndrome

Schilbach-Rott Syndrome

Eccrine Dermal Cylindroma

Familial Multiple Trichoepitheliomata

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
Mus musculus STOML3 MGD MGI:2388072
Rattus norvegicus STOML3 RGD RGD:1311090
Bos taurus STOML3 VGNC VGNC:35412
Macaca mulatta STOML3 VGNC VGNC:78170
Canis familiaris STOML3 VGNC VGNC:46932
Felis catus STOML3 VGNC VGNC:65795