2. Gene
  3. FITM2 - fat storage inducing transmembrane protein 2 Gene

FITM2 - fat storage inducing transmembrane protein 2 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：脂肪储存诱导跨膜蛋白 2

种属: Homo sapiens

同用名: Fit2; SIDDIS; C20orf142; dJ881L22.2

基因 ID: 128486 | 基因类型: protein coding

关于 FITM2

Cytogenetic location: 20q13.12 Genomic coordinates (GRCh38): 20:44,302,840-44,311,202 (from NCBI)

This gene has 1 transcript (splice variant), 205 orthologues, 1 paralogue and is associated with 1 phenotype. Broad expression in heart (RPKM 23.3), fat (RPKM 9.0) and 21 other tissues.

功能概要

FIT2 属于参与脂肪储存的进化保守蛋白家族 (Kadereit 等人，2008 [PubMed 18160536]) 。[OMIM 提供，2008 年 5 月]

FIT2 belongs to an evolutionarily conserved family of proteins involved in fat storage (Kadereit et al., 2008 [PubMed 18160536]).[supplied by OMIM, May 2008]

FITM2 基因产物(1)

mRNA Protein Name
NM_001080472.4 NP_001073941.1 acyl-coenzyme A diphosphatase FITM2

FITM2 蛋白结构

Scs3p

Scs3p: Inositol phospholipid synthesis and fat-storage-inducing TM (45 - 234)

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

acyl-coenzyme A diphosphatase FITM2

fat-inducing protein 2

FITM2 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
FITM2 Q8N6M3 HTATIP2 Homo sapiens Q9BUP3-3
Validated Y2H
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
Siddiqi Syndrome

SIDDIS

Deafness, Dystonia, Developmental Delay, And Poor Growth
Sexual Sadism

Sadism
Dystonia

Dystonic Disease

Dystonic Disorder

Dystonia Disorders

Neuroleptic Dyskinesia
Mohr-Tranebjaerg Syndrome

Deafness-Dystonia-Optic Neuronopathy Syndrome

Jensen Syndrome

Deafness Dystonia Syndrome

MTS

Dds

Deafness-Dystonia-Optic Atrophy Syndrome

Deafness Syndrome, Progressive, With Blindness, Dystonia, Fractures, And Mental Deficiency

Opticoacoustic Nerve Atrophy With Dementia

Dystonia-Deafness Syndrome

Ddp

Ddon Syndrome

Mohr-Tranebjærg Syndrome

Deafness Dystonia Optic Atrophy Syndrome

Deafness Dystonia Optic Neuronopathy Syndrome

Dystonia Deafness Syndrome

Ddon

Deafness - Dystonia - Optic Neuronopathy Syndrome

Deafness-Dystonia-Optic Neuronopathy Syndrome

Hearing Loss-Dystonia-Optic Neuronopathy Syndrome

Dfn-1

X-Linked Progressive Deafness Type 1
Ichthyosis

Ichthyoses

Non-Syndromic Ichthyosis

Congenital Ichthyosis
Congenital Generalized Lipodystrophy

Berardinelli-Seip Congenital Lipodystrophy

Berardinelli-Seip Syndrome

Brunzell Syndrome

Bscl

Generalized Lipodystrophy

Lipodystrophy, Congenital Generalized

Seip Syndrome

Total Lipodystrophy

Cgl

Lipoatrophic Diabetes

Lipodystrophy, Generalized, Congenital

Familial Generalized Lipodystrophy

Congenital Generalized Lipodystrophy Type 2

Lipoatrophic Diabetes Mellitus

Familial Partial Lipodystrophy, Type 2
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS04953 FITM2 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Felis catus FITM2 VGNC VGNC:80100
Rattus norvegicus FITM2 RGD RGD:1307696
Bos taurus FITM2 VGNC VGNC:29016
Canis familiaris FITM2 VGNC VGNC:54304
Mus musculus FITM2 MGD MGI:2444508
Macaca mulatta FITM2 VGNC VGNC:84768
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