1. Gene
  2. MINAR2 - membrane integral NOTCH2 associated receptor 2 Gene

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

MINAR2 Protein Structure

UPF0258

UPF0258: Uncharacterised protein family (UPF0258) (47 - 187)

  • 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

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