HCG25 - HLA complex group 25 Gene

Also Known as dJ1033B10.16

Species: Homo sapiens

Gene Type: ncRNA
Gene ID: 414765

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