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FITM2 - fat storage inducing transmembrane protein 2 Gene

Also Known as Fit2; SIDDIS; C20orf142; dJ881L22.2

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 128486

About 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.

Summary

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 Products (1)

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

FITM2 Protein Structure

Scs3p

0
100
200
262 a.a.

Protein Preferred Names	Protein Names
acyl-coenzyme A diphosphatase FITM2	fat-inducing protein 2

FITM2 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	Verweise
Intra	FITM2	Q8N6M3	HTATIP2	Homo sapiens	Q9BUP3-3	Validated Y2H	32296183

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
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

Diseases	Alias
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

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

Art. -Nr.	Produktname	Wirkung	Reinheit	Rare Diseases
HY-RS04953	FITM2 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	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
Others	FITM2	NCBI