MYO1D - myosin ID Gene

Homo sapiens

Also known as myr4; PPP1R108

Gene ID: 4642 | Gene type: protein coding

About MYO1D

Cytogenetic location: 17q11.2 Genomic coordinates (GRCh38): 17:32,492,522-32,877,124 (from NCBI)

This gene has 16 transcripts (splice variants), 204 orthologues and 43 paralogues. Broad expression in colon (RPKM 49.5), small intestine (RPKM 32.7) and 22 other tissues.

Summary

Enables protein domain specific binding activity. Predicted to be involved in actin filament organization; early endosome to recycling endosome transport; and vesicle transport along actin filament. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

MYO1D Products(4)

mRNA	Protein	Name
NM_001303279.2	NP_001290208.1	unconventional myosin-Id isoform 2
NM_001303280.2	NP_001290209.1	unconventional myosin-Id isoform 3
NM_001411088.1	NP_001398017.1	unconventional myosin-Id isoform 4
NM_015194.3	NP_056009.1	unconventional myosin-Id isoform 1

MYO1D Protein Structure

Myosin_head

Myosin_TH1

0
200
400
600
800
1006 a.a.

Protein Preferred Names

Protein Names

unconventional myosin-Id

myosin-I gamma

Related Diseases

Diseases

Alias

Canavan Disease

Aspartoacylase Deficiency	Aminoacylase 2 Deficiency
Spongy Degeneration Of Central Nervous System	Aspa Deficiency
Acy2 Deficiency	Canavan-Van Bogaert-Bertrand Disease
Mild Canavan Disease	Asp Deficiency
Spongy Degeneration Of The Central Nervous System	Severe Canavan Disease
Von Bogaert-Bertrand Disease	Canavan'S Disease
Spongy Degeneration Of The Brain	Juvenile Canavan Disease
Infantile Canavan Disease	Neonatal Canavan Disease
CAND	Disease, Canavan
Canavan Disease, Juvenile	Canavan Disease, Infantile
Canavan Disease, Neonatal

Visceral Heterotaxy

Situs Ambiguus	Heterotaxia
Heterotaxy Syndrome	Heterotaxy
Lateralization Defect	Situs Ambiguous
Left Isomerism	Htx
Ivemark Syndrome	Right Isomerism
Situs Ambiguus Viscerum	Incomplete Situs Inversus
Partial Situs Inversus	Heterotaxy, Visceral
Asplenia Syndrome	Bilateral Left-Sidedness
Polysplenia Syndrome	Moller Syndrome

Situs Inversus

Situs Inversus Viscerum	Laterality Sequence
Complete Transposition	Siv

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-RS08940	MYO1D Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	MYO1D	VGNC	VGNC:68391
Canis familiaris	MYO1D	VGNC	VGNC:43563
Mus musculus	MYO1D	MGD	MGI:107728
Rattus norvegicus	MYO1D	RGD	RGD:621321
Macaca mulatta	MYO1D	VGNC	VGNC:75113
Bos taurus	MYO1D	VGNC	VGNC:31819

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