1. Gene
  2. OPALIN - oligodendrocytic myelin paranodal and inner loop protein Gene

OPALIN - oligodendrocytic myelin paranodal and inner loop protein Gene

Homo sapiens

Also known as TMP10; HTMP10; TMEM10

Gene ID: 93377 | Gene type: protein coding

About OPALIN

Cytogenetic location: 10q24.1 Genomic coordinates (GRCh38): 10:96,343,221-96,359,002 (from NCBI)

This gene has 6 transcripts (splice variants) and 91 orthologues. Restricted expression toward brain (RPKM 29.7).

Summary

Predicted to be involved in regulation of oligodendrocyte differentiation. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Apr 2022]

OPALIN Products(10)

mRNA Protein Name
NM_001040102.3 NP_001035191.1 opalin isoform b
NM_001040103.3 NP_001035192.1 opalin isoform c
NM_001284320.2 NP_001271249.1 opalin isoform d
NM_001284321.2 NP_001271250.1 opalin isoform e
NM_001284322.2 NP_001271251.1 opalin isoform c
NM_001284323.2 NP_001271252.1 opalin isoform c
NM_001284324.2 NP_001271253.1 opalin isoform c
NM_001284326.2 NP_001271255.1 opalin isoform f
NM_001284327.2 NP_001271256.1 opalin isoform f
NM_033207.5 NP_149984.1 opalin isoform a
Protein Preferred Names Protein Names

opalin

transmembrane protein 10

Recombinant OPALIN Proteins

Cat. No. Product Name Accession Purity
HY-P77113 OPALIN Protein, Human (HEK293, Fc) Q96PE5 (T51-E141) ≥95%

Related Diseases

Diseases Alias
Fucosidosis

Alpha-L-Fucosidase Deficiency

Fucosidase Deficiency Disease

A-Fucosidase Deficiency

Alpha Fucosidase Deficiency

Lysosomal Storage Disease Caused By Defective Alpha-L-Fucosidase With Accumulation Of Fucose In The Tissues

Alpha-Fucosidase Deficiency

Fucosidase Deficiency

FUCA1D

Multiple Sclerosis

MS

Multiple Sclerosis, Susceptibility To

Disseminated Sclerosis

Multiple Sclerosis, Disease Progression, Modifier Of

Insular Sclerosis

Multiple Sclerosis Modifier Of Disease Progression

Multiple Sclerosis, Susceptibility To 1

Multiple Sclerosis, Susceptibility To, 1

Multiple Sclerosis 1

Generalized Multiple Sclerosis

Multiple Sclerosis Variant

Multiple Sclerosis Susceptibility To

Cerebrospinal Sclerosis

Generalised Multiple Sclerosis

Ms - [Multiple Sclerosis]

Disseminated Cerebrospinal Sclerosis

Disseminated Multiple Sclerosis

Disseminated Nervous System Myelosclerosis

Multiple Cerebrospinal Sclerosis

Multiple Combined Sclerosis

Multiple Sclerosis Generalised

Disseminated Brain Sclerosis

Disseminated Spinal Sclerosis

Insular Brain Sclerosis

Miliary Brain Sclerosis

Multiple Combined Sclerosis Of Spinal Cord

Multiple Ascending Sclerosis

Multiple Brain Sclerosis

Multiple Sclerosis Of Brain Stem

Multiple Sclerosis Of The Brain Stem

Multiple Sclerosis Of Cord

Sclérose En Plaques

Plaque Sclerosis

Multiple Sclerosis Of The Spinal Cord

Pelizaeus-Merzbacher Disease

PMD

HLD1

Pelizaeus-Merzbacher Brain Sclerosis

Leukodystrophy, Hypomyelinating, 1

Diffuse Familial Brain Sclerosis

Pelizaeus Merzbacher Brain Sclerosis

Sudanophilic Leukodystrophy, Paelizeus-Merzbacher Type

Cockayne-Pelizaeus-Merzbacher Disease

Hypomyelinating Leukodystrophy 1

Leukodystrophy, Sudanophilic

Pelizaeus Merzbacher Disease

Hypomyelinating Leukodystrophy, 1

Sudanophilic Leukodystrophy

Pelizaeus-Merzbacher Disease, Connatal Form

Connatal Pmd

Pelizaeus-Merzbacher Disease Type Ii

Severe Pmd

Null Syndrome

Plp1 Null Syndrome

Pelizaeus-Merzbacher Disease, Null Syndrome

Brain Sclerosis Diffuse Familial

Sudanophilic Leukodystrophy Paelizeus-Merzbacher Type

Leukodystrophy Hypomyelinating 1

Diffuse Cerebral Sclerosis Of Schilder

Hypomyelinating Leukodystrophy

Hld

Leukodystrophy, Hypomyelinating

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
Canis familiaris OPALIN VGNC VGNC:44127
Bos taurus OPALIN VGNC VGNC:32434
Rattus norvegicus OPALIN RGD RGD:1307776
Macaca mulatta OPALIN VGNC VGNC:75443
Mus musculus OPALIN MGD MGI:2657025