MID1IP1 - MID1 interacting protein 1 Gene

Homo sapiens

Also known as S14R; MIG12; THRSPL; G12-like; STRAIT11499

Gene ID: 58526 | Gene type: protein coding

About MID1IP1

Cytogenetic location: Xp11.4 Genomic coordinates (GRCh38): X:38,801,459-38,806,532 (from NCBI)

This gene has 4 transcripts (splice variants), 183 orthologues and 1 paralogue. Ubiquitous expression in bone marrow (RPKM 21.2), fat (RPKM 16.5) and 25 other tissues.

Summary

Predicted to enable identical protein binding activity and protein C-terminus binding activity. Predicted to be involved in several processes, including negative regulation of microtubule depolymerization; positive regulation of fatty acid biosynthetic process; and protein polymerization. Predicted to be located in cytoplasm and microtubule Cytoskeleton. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Apr 2022]

MID1IP1 Products(3)

mRNA	Protein	Name
NM_001098790.2	NP_001092260.1	mid1-interacting protein 1
NM_001098791.2	NP_001092261.1	mid1-interacting protein 1
NM_021242.6	NP_067065.1	mid1-interacting protein 1

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	Reference	Source
enables protein binding	IPI IPI: Inferred from physical interaction	16189514	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

MID1IP1 Protein Structure

Spot_14

0
100
183 a.a.

Protein Preferred Names

Protein Names

mid1-interacting protein 1

MID1 interacting G12-like protein

Recombinant MID1IP1 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P76497	MID1IP1 Protein, Human (His)	Q9NPA3 (M1-H183)	≥95%

Related Diseases

Diseases

Alias

Developmental And Epileptic Encephalopathy 28

DEE28	Epileptic Encephalopathy, Early Infantile, 28
Eiee28	Developmental And Epileptic Encephalopathy, 28
Early Infantile Epileptic Encephalopathy 28	Encephalopathy, Epileptic, Early Infantile, Type 28

Gluten Allergy

Allergy To Gluten

Gluten Allergic Reaction

Spinocerebellar Ataxia, Autosomal Recessive 12

Autosomal Recessive Spinocerebellar Ataxia 12	SCAR12
Spinocerebellar Ataxia With Mental Retardation And Epilepsy	Autosomal Recessive Cerebellar Ataxia-Epilepsy-Intellectual Disability Syndrome Due To Wwox Deficiency
Autosomal Recessive Spinocerebellar Ataxia Type 12	Spinocerebellar Ataxia, Autosomal Recessive, 12
Ataxia, Spinocerebellar, Autosomal Recessive, Type 12

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS08435	MID1IP1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Macaca mulatta	MID1IP1	VGNC	VGNC:74549
Rattus norvegicus	MID1IP1	RGD	RGD:1303258
Bos taurus	MID1IP1	VGNC	VGNC:31465
Felis catus	MID1IP1	VGNC	VGNC:63497
Canis familiaris	MID1IP1	VGNC	VGNC:43223
Mus musculus	MID1IP1	MGD	MGI:1915291
Others	MID1IP1	NCBI

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