HID1 - HID1 domain containing Gene

Homo sapiens

Also known as DMC1; HID-1; DEE105; 17orf28; C17orf28

Gene ID: 283987 | Gene type: protein coding

About HID1

Cytogenetic location: 17q25.1 Genomic coordinates (GRCh38): 17:74,950,742-74,972,759 (from NCBI)

This gene has 14 transcripts (splice variants) and 259 orthologues. Broad expression in stomach (RPKM 20.2), prostate (RPKM 17.0) and 21 other tissues.

Summary

Located in Golgi cisterna; cytoplasmic microtubule; and cytosol. Is extrinsic component of Golgi membrane. [provided by Alliance of Genome Resources, Apr 2022]

HID1 Products(1)

mRNA	Protein	Name
NM_030630.3	NP_085133.1	protein HID1

HID1 Protein Structure

Hid1

0
200
400
600
788 a.a.

Protein Preferred Names

Protein Names

protein HID1

HID1 domain-containing protein

Related Diseases

Diseases

Alias

Developmental And Epileptic Encephalopathy 105 With Hypopituitarism

DEE105

Palmoplantar Keratoderma, Nonepidermolytic, Focal 1

Focal Nonepidermolytic Palmoplantar Keratoderma	Isolated Focal Non-Epidermolytic Palmoplantar Keratoderma
FNEPPK1	Ppkfne
Keratoderma, Focal Nonepidermolytic Palmoplantar	Palmoplantar Keratoderma, Nonepidermolytic, Focal
Hyperkeratosis Of The Palms And Soles And Esophageal Papillomas	Fneppk
Focal Nonepidermolytic Palmoplantar Keratoderma 1	Keratoderma, Palmoplantar, Non-Epidermolytic, Focal 1
Keratoderma, Palmoplantar, Nonepidermolytic, Focal, Type 1

Visual Epilepsy

Seizures	Epilepsy, Visual
Visual Seizure	Acute Symptomatic Seizure
Provoked Seizure	Nonepileptic Seizure Disorder
Uncontrolled Seizures	Seizure Nos
Fits Nos	Onset Seizure Nos
Seizure Disturbance

Developmental And Epileptic Encephalopathy 4

DEE4	Epileptic Encephalopathy, Early Infantile, 4
Eiee4	Early Infantile Epileptic Encephalopathy 4
Stxbp1-Related Early-Onset Encephalopathy	Early Myoclonic Encephalopathy
Developmental And Epileptic Encephalopathy, 4	Stxbp1 Disorders
Stxbp1 Encephalopathy	Developmental And Epileptic Encephalopathy, Type 4
Early-Infantile Epileptic Encephalopathy 4	Stxbp1 Encephalopathy With Epilepsy
Stxbp1 Epileptic Encephalopathy	Stxbp1-Related Developmental And Epileptic Encephalopathy
Stxbp1-Related Epileptic Encephalopathy	Eme
Neonatal Epilepsy With Suppression-Burst Pattern	Encephalopathy, Epileptic, Early Infantile, Type 4

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-RS06167	HID1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	HID1	VGNC	VGNC:41685
Rattus norvegicus	HID1	RGD	RGD:1311422
Felis catus	HID1	VGNC	VGNC:62813
Mus musculus	HID1	MGD	MGI:2445087
Bos taurus	HID1	VGNC	VGNC:29847
Macaca mulatta	HID1	VGNC	VGNC:73394
Others	HID1	NCBI

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