1. Gene
  2. HCG25 - HLA complex group 25 Gene

HCG25 - HLA complex group 25 Gene

Homo sapiens

Also known as dJ1033B10.16

Gene ID: 414765 | Gene type: ncRNA

About HCG25

This gene has 9 transcripts (splice variants) and 1 gene allele. Ubiquitous expression in skin (RPKM 11.4), prostate (RPKM 11.1) and 25 other tissues.

Related Diseases

Diseases Alias
Immunodeficiency 32a

Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Irf8 Deficiency

IMD32A

Immunodeficiency 32a, Mycobacteriosis, Autosomal Dominant

Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Interferon Regulatory Factor 8 Deficiency

Msmd Due To Partial Interferon Regulatory Factor 8 Deficiency

Msmd Due To Partial Irf8 Deficiency

Irf8 Deficiency, Autosomal Dominant

Cd11c-Positive/Cd1c-Positive Dendritic Cell Deficiency, Autosomal Dominant

Autosomal Dominant Cd11c-Positive/Cd1c-Positive Dendritic Cell Deficiency

Autosomal Dominant Immunodeficiency 32a, Mycobacteriosis

Autosomal Dominant Irf8 Deficiency

Immunodeficiency, Type 32a

Hypotrichosis 12

HYPT12

Hypotrichosis, Type 12

Pthirus Pubis Infestation

Infestation By Phthirus Pubis

Crabs

Pediculosis Pubis

Pediculus Pubis

Phthiriasis Pubis

Phthirus Pubis

Phthirus/Pediculus Pubis - Pubic Lice - Crabs

Monocyte, Dendritic Cell, And Nk Cell Deficiency
Immunodeficiency 32b

IMD32B

Immunodeficiency 32b, Monocyte And Dendritic Cell Deficiency, Autosomal Recessive

Immunodeficiency 32b, Monocyte, Dendritic Cell, And Natural Killer Cell Deficiency, Autosomal Recessive

Irf8 Deficiency, Autosomal Recessive

Epstein-Barr Virus Chronic Infection By

Epstein-Barr Virus, Susceptibility To Chronic Infection By

Autosomal Recessive Irf8 Deficiency

Chronic Epstein-Barr Virus Infection Syndrome

Caebv Syndrome

Chronic Ebv Infection Syndrome

Autosomal Recessive Monocyte And Dendritic Cell Deficiency

Immunodeficiency, Type 32b

Monocyte And Dendritic Cell Deficiency, Autosomal Recessive

Dendritic Cell Deficiency
Coffin-Siris Syndrome 1

Coffin-Siris Syndrome

Fifth Digit Syndrome

Css

CSS1

Mrd12

Mental Retardation, Autosomal Dominant 12

Hhid

Dwarfism-Onychodysplasia

Hypertrichosis, Hyperkeratosis, Mental Retardation, And Distinctive Facial Features

Autosomal Dominant Mental Retardation 12

Short Stature-Onychodysplasia.

Intellectual Disability With Absent Fifth Fingernail And Terminal Phalanx

Mental Retardation With Hypoplastic Fifth Fingernails And Toenails

Short Stature-Onychodysplasia

Coffin-Siris Syndrome, Type 1

Mental Retardation, Autosomal Dominant, Type 12

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