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TIMM23 - translocase of inner mitochondrial membrane 23 Gene

Also Known as TIM23

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 100287932

About TIMM23

Cytogenetic location: 10q11.22 Genomic coordinates (GRCh38): 10:45,972,489-46,003,742 (from NCBI)

This gene has 1 transcript (splice variant), 234 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 39.1), heart (RPKM 22.4) and 25 other tissues.

Summary

The protein encoded by this gene is part of a complex located in the inner mitochondrial membrane that mediates the transport of transit peptide-containing proteins across the membrane. Multiple transcript variants, one protein-coding and Others not protein-coding, have been found for this gene. [provided by RefSeq, Jul 2012]

TIMM23 Products (1)

mRNA	Protein	Name
NM_006327.4	NP_006318.1	mitochondrial import inner membrane translocase subunit Tim23

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	References	Source
enables protein binding	IPI IPI: Inferred from physical interaction	15044455	GOA

Biological Process GO Annotation	Evidence	References	Source
involved in type 2 mitophagy	IMP IMP: Inferred from mutant phenotype	37160114	GOA

Cellular Component GO Annotation	Evidence	References	Source
part of TIM23 mitochondrial import inner membrane translocase complex	IDA IDA: Inferred from direct assay	10339406	GOA
located in mitochondrial inner membrane	IDA IDA: Inferred from direct assay	10339406	GOA
located in mitochondrial intermembrane space	IDA IDA: Inferred from direct assay	15044455	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TIMM23 Protein Structure

Tim17

0
100
209 a.a.

Protein Preferred Names	Protein Names
mitochondrial import inner membrane translocase subunit Tim23	translocase of inner mitochondrial membrane 23 homolog

TIMM23 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	TIMM23	O14925	JAGN1	Homo sapiens	Q8N5M9	Validated Y2H	32296183
Intra	TIMM23	O14925	JAGN1	Homo sapiens	Q8N5M9	Y2H Array	32296183
Intra	TIMM23	O14925	JAGN1	Homo sapiens	Q8N5M9	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	FXYD3	Homo sapiens	Q14802-3	Validated Y2H	32296183
Intra	TIMM23	O14925	FXYD3	Homo sapiens	Q14802-3	Y2H Array	32296183
Intra	TIMM23	O14925	FXYD3	Homo sapiens	Q14802-3	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	TLCD4	Homo sapiens	Q96MV1	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	TLCD4	Homo sapiens	Q96MV1	Validated Y2H	32296183
Intra	TIMM23	O14925	TLCD4	Homo sapiens	Q96MV1	Y2H Array	32296183
Intra	TIMM23	O14925	AQP6	Homo sapiens	Q13520	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	AQP6	Homo sapiens	Q13520	Validated Y2H	32296183
Intra	TIMM23	O14925	AQP6	Homo sapiens	Q13520	Y2H Array	32296183
Intra	TIMM23	O14925	TMEM88	Homo sapiens	Q6PEY1	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	TMEM88	Homo sapiens	Q6PEY1	Y2H Array	32296183
Intra	TIMM23	O14925	TMEM88	Homo sapiens	Q6PEY1	Validated Y2H	32296183
Intra	TIMM23	O14925	GOLT1A	Homo sapiens	Q6ZVE7	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	GOLT1A	Homo sapiens	Q6ZVE7	Validated Y2H	32296183
Intra	TIMM23	O14925	GOLT1A	Homo sapiens	Q6ZVE7	Y2H Array	32296183
Intra	TIMM23	O14925	SCN3B	Homo sapiens	Q9NY72	Validated Y2H	32296183
Intra	TIMM23	O14925	SCN3B	Homo sapiens	Q9NY72	Y2H Array	32296183
Intra	TIMM23	O14925	SCN3B	Homo sapiens	Q9NY72	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	HSD17B13	Homo sapiens	Q7Z5P4	Validated Y2H	32296183
Intra	TIMM23	O14925	HSD17B13	Homo sapiens	Q7Z5P4	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	HSD17B13	Homo sapiens	Q7Z5P4	Y2H Array	32296183
Intra	TIMM23	O14925	RNASEK	Homo sapiens	Q6P5S7	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	RNASEK	Homo sapiens	Q6P5S7	Validated Y2H	32296183
Intra	TIMM23	O14925	RNASEK	Homo sapiens	Q6P5S7	Y2H Array	32296183
Intra	TIMM23	O14925	FAM210B	Homo sapiens	Q96KR6	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	FAM210B	Homo sapiens	Q96KR6	Y2H Array	32296183
Intra	TIMM23	O14925	FAM210B	Homo sapiens	Q96KR6	Validated Y2H	32296183
Intra	TIMM23	O14925	LAMP2	Homo sapiens	P13473-2	Validated Y2H	32814053
Intra	TIMM23	O14925	LAMP2	Homo sapiens	P13473-2	Y2H Array	32814053
Intra	TIMM23	O14925	LAMP2	Homo sapiens	P13473-2	Y2H Pooling	32814053
Intra	TIMM23	O14925	TIMM17B	Homo sapiens	O60830	Validated Y2H	32296183
Intra	TIMM23	O14925	TMEM86B	Homo sapiens	Q8N661	Validated Y2H	32296183
Intra	TIMM23	O14925	TMEM86B	Homo sapiens	Q8N661	Y2H Array	32296183
Intra	TIMM23	O14925	TMEM86B	Homo sapiens	Q8N661	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	SH3GLB1	Homo sapiens	Q9Y371	Validated Y2H	32814053
Intra	TIMM23	O14925	SH3GLB1	Homo sapiens	Q9Y371	Y2H Pooling	32814053
Intra	TIMM23	O14925	SH3GLB1	Homo sapiens	Q9Y371	Y2H Array	32814053
Intra	TIMM23	O14925	EBP	Homo sapiens	Q15125	Y2H Array	32296183
Intra	TIMM23	O14925	EBP	Homo sapiens	Q15125	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	EBP	Homo sapiens	Q15125	Validated Y2H	32296183
Intra	TIMM23	O14925	SLC16A7	Homo sapiens	O60669	Y2H Array	32296183
Intra	TIMM23	O14925	SLC16A7	Homo sapiens	O60669	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	SLC16A7	Homo sapiens	O60669	Validated Y2H	32296183
Intra	TIMM23	O14925	TSPAN8	Homo sapiens	P19075	Y2H Array	32296183
Intra	TIMM23	O14925	TSPAN8	Homo sapiens	P19075	Validated Y2H	32296183
Intra	TIMM23	O14925	TSPAN8	Homo sapiens	P19075	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	CREB3L1	Homo sapiens	Q96BA8	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	CREB3L1	Homo sapiens	Q96BA8	Validated Y2H	32296183
Intra	TIMM23	O14925	CREB3L1	Homo sapiens	Q96BA8	Y2H Array	32296183
Intra	TIMM23	O14925	TMEM14B	Homo sapiens	Q9NUH8	Y2H Prey Pooling	32296183
Intra	TIMM23	O14925	TMEM14B	Homo sapiens	Q9NUH8	Validated Y2H	32296183
Intra	TIMM23	O14925	TMEM14B	Homo sapiens	Q9NUH8	Y2H Array	32296183

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
Cardiomyopathy, Familial Hypertrophic, 16	Hypertrophic Cardiomyopathy 16 CMH16 Cardiomyopathy, Hypertrophic, 16 Cardiomyopathy Familial Hypertrophic 16 Cardiomyopathy, Familial Hypertrophic 16 Cardiomyopathy, Hypertrophic, Familial, Type 16
Cardiomyopathy, Familial Hypertrophic, 18	Hypertrophic Cardiomyopathy 18 CMH18 Cardiomyopathy, Hypertrophic, 18 Cardiomyopathy Familial Hypertrophic 18 Cardiomyopathy, Familial Hypertrophic 18 Cardiomyopathy, Hypertrophic, Familial, Type 18
Cardiomyopathy, Familial Hypertrophic, 17	Hypertrophic Cardiomyopathy 17 CMH17 Cardiomyopathy, Hypertrophic, 17 Cardiomyopathy Familial Hypertrophic 17 Cardiomyopathy, Familial Hypertrophic 17 Cardiomyopathy, Hypertrophic, Familial, Type 17
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
3-Methylglutaconic Aciduria, Type V	3-Methylglutaconic Aciduria Type 5 Mga5 MGCA5 Dcma Dcma Syndrome Dilated Cardiomyopathy With Ataxia 3-Methylglutaconic Aciduria Type V Mga Type V Cardiomyopathy, Dilated, With Ataxia Mga, Type V Dilated Cardiomyopathy With Ataxia Syndrome Dnajc19 Defect 3-Methylglutaconic Aciduria 5 3-Alpha-Methylglutaconic Aciduria Type 5 3-@Methylglutaconic Aciduria, Type V
Developmental And Epileptic Encephalopathy 12	Epileptic Encephalopathy, Early Infantile, 12 DEE12 Eiee12 Early Infantile Epileptic Encephalopathy 12 Developmental And Epileptic Encephalopathy, 12 Encephalopathy, Epileptic, Early Infantile, Type 12
3-Methylglutaconic Aciduria	3-Methyl Glutaconic Aciduria
Sengers Syndrome	Mitochondrial Dna Depletion Syndrome 10 Cardiomyopathy And Cataract Cataract And Cardiomyopathy MTDPS10 Congenital Cataract-Hypertrophic Cardiomyopathy-Mitochondrial Myopathy Syndrome Cardiomyopathic Mitochondrial Dna Depletion Syndrome 10 Senger Syndrome

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)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS14531	TIMM23 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	TIMM23	MGD	MGI:1858317
Others	TIMM23	NCBI