2. Gene
  3. MICALL1 - MICAL like 1 Gene

MICALL1 - MICAL like 1 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as MIRAB13; MICAL-L1

Gene ID: 85377 | Gene type: protein coding

About MICALL1

Cytogenetic location: 22q13.1 Genomic coordinates (GRCh38): 22:37,906,297-37,942,822 (from NCBI)

This gene has 12 transcripts (splice variants), 215 orthologues and 7 paralogues. Ubiquitous expression in placenta (RPKM 11.0), esophagus (RPKM 10.9) and 25 other tissues.

Summary

Enables identical protein binding activity; phosphatidic acid binding activity; and small GTPase binding activity. Involved in several processes, including plasma membrane tubulation; protein localization to endosome; and slow endocytic recycling. Located in late endosome and recycling endosome membrane. Is extrinsic component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

MICALL1 Products(4)

mRNA Protein Name
NM_001410818.1 NP_001397747.1 MICAL-like protein 1 isoform 1
NM_001410819.1 NP_001397748.1 MICAL-like protein 1 isoform 2
NM_001410820.1 NP_001397749.1 MICAL-like protein 1 isoform 4
NM_033386.4 NP_203744.1 MICAL-like protein 1 isoform 3

MICALL1 Protein Structure

CH

CH: Calponin homology (CH) domain (7 - 107)

LIM

LIM: LIM domain (164 - 217)

DUF3585

DUF3585: Protein of unknown function (DUF3585) (678 - 817)

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  • 800
  • 863 a.a.
Protein Preferred Names Protein Names

MICAL-like protein 1

molecule interacting with Rab13

Related Diseases

Diseases Alias
Bardet-Biedl Syndrome 5

BBS5

Bardet-Biedl Syndrome, Type 5
Microvillus Inclusion Disease

Congenital Microvillous Atrophy

Intractable Diarrhea Of Infancy

Congenital Familial Protracted Diarrhea With Enterocyte Brush-Border Abnormalities

Davidson Disease

Microvillous Inclusion Disease

Congenital Microvillus Atrophy

Mvid

Diarrhea 2 With Microvillus Atrophy

Mvd

Congenital Familial Protracted Diarrhea

Davidson'S Disease

Familial Enteropathy, Microvillus

Microvillus Atrophy, Congenital

Congenital Enteropathy

Familial Protracted Enteropathy

Microvillous Atrophy

Microvillus Atrophy With Diarrhea 2

Idi
Robinow Syndrome, Autosomal Dominant 1

Autosomal Dominant Robinow Syndrome 1

DRS1

Robinow Dwarfism

Fetal Face Syndrome

Acral Dysostosis With Facial And Genital Abnormalities

Robinow, Autosomal Dominant Syndrome, Type 1
Retinitis Pigmentosa 39

RP39

Retinitis Pigmentosa, Type 39
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-RS08428 MICALL1 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris MICALL1 VGNC VGNC:54528
Bos taurus MICALL1 VGNC VGNC:52803
Macaca mulatta MICALL1 VGNC VGNC:107801
Felis catus MICALL1 VGNC VGNC:97508
Mus musculus MICALL1 MGD MGI:105870
Rattus norvegicus MICALL1 RGD RGD:1305415