MINAR2 - membrane integral NOTCH2 associated receptor 2 Gene

Homo sapiens

Also known as KIAA1024L

Gene ID: 100127206 | Gene type: protein coding

About MINAR2

This gene has 1 transcript (splice variant), 194 orthologues and 1 paralogue. Low expression observed in reference dataset.

Summary

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

MINAR2 Products(1)

mRNA	Protein	Name
NM_001257308.2	NP_001244237.1	major intrinsically disordered NOTCH2-binding receptor 1-like

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables cholesterol binding	IDA IDA: Inferred from direct assay	36317962	GOA
enables protein binding	IPI IPI: Inferred from physical interaction	32954300	GOA

Biological Process GO Annotation	Evidence	Reference	Source
involved in angiogenesis	IMP IMP: Inferred from mutant phenotype	35727972	GOA

Cellular Component GO Annotation	Evidence	Reference	Source
located in endoplasmic reticulum	IDA IDA: Inferred from direct assay	32954300	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

MINAR2 Protein Structure

UPF0258

0
100
190 a.a.

Protein Preferred Names

Protein Names

major intrinsically disordered NOTCH2-binding receptor 1-like

KIAA1024 like

Related Diseases

Diseases

Alias

Contractural Arachnodactyly, Congenital

Congenital Contractural Arachnodactyly	Beals Syndrome
CCA	Beals-Hecht Syndrome
Distal Arthrogryposis Type 9	Arthrogryposis, Distal, Type 9
Da9	Arachnodactyly, Contractural Beals Type
Contractures, Multiple With Arachnodactyly	Ear Anomalies-Contractures-Dysplasia Of Bone With Kyphoscoliosis
Arthrogyroposis, Distal, Type 9	Distal Arthrogyropsis Type 9
Cca Syndrome	Arachnodactyly

Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant

ADLD	Adult-Onset Autosomal Dominant Demyelinating Leukodystrophy
Leukodystrophy, Adult-Onset, Autosomal Dominant	Adult-Onset Autosomal Dominant Leukodystrophy
Autosomal Dominant Leukodystrophy With Autonomic Disease	Autosomal Dominant Adult-Onset Demyelinating Leukodystrophy
Multiple Sclerosis-Like Disorder	Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type, Formerly
Autosomal-Dominant Or Late-Onset Type Pelizaeus-Merzbacher Disease	Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type
Adult-Onset Autosomal Dominant Leukodystrophy With Autonomic Symptoms	Lmnb1-Related Adult-Onset Autosomal Dominant Leukodystrophy
Leukodystrophy, Demyelinating, Autosomal Dominant, Adult-Onset	Pelizaeus-Merzbacher Disease Autosomal Dominant
Pelizaeus-Merzbacher Disease Late-Onset Type	Adult Onset Autosomal Dominant Leukodystrophy

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-RS08450	MINAR2 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	MINAR2	RGD	RGD:1312005
Macaca mulatta	MINAR2	VGNC	VGNC:84441
Mus musculus	MINAR2	MGD	MGI:2442934
Felis catus	MINAR2	VGNC	VGNC:63509
Canis familiaris	MINAR2	VGNC	VGNC:58317
Bos taurus	MINAR2	VGNC	VGNC:30562

Name
Email *

	Sorry, but the email address you supplied was invalid.