OXLD1 - oxidoreductase like domain containing 1 Gene

Also Known as C17orf90

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 339229

About OXLD1

This gene has 7 transcripts (splice variants) and 181 orthologues. Ubiquitous expression in spleen (RPKM 8.6), lymph node (RPKM 6.4) and 25 other tissues.

OXLD1 Products (4)

mRNA Protein Name
NM_001039842.3 NP_001034931.1 oxidoreductase-like domain-containing protein 1 isoform a
NM_001304994.2 NP_001291923.1 oxidoreductase-like domain-containing protein 1 isoform b
NM_001304995.2 NP_001291924.1 oxidoreductase-like domain-containing protein 1 isoform c
NM_001304999.2 NP_001291928.1 oxidoreductase-like domain-containing protein 1 isoform c

OXLD1 Protein Structure

Oxidored-like

Oxidored-like: Oxidoreductase-like protein, N-terminal (81 - 108)

  • 0
  • 100
  • 147 a.a.
Protein Preferred Names Protein Names

oxidoreductase-like domain-containing protein 1

Related Diseases

Diseases Alias
Mixed Receptive-Expressive Language Disorder
Baraitser-Winter Syndrome
  • Fryns-Aftimos Syndrome

  • Brws

  • Cerebro-Frontofacial Syndrome, Type 3

  • Iris Coloboma With Ptosis, Hypertelorism, And Mental Retardation

  • Iris Coloboma With Ptosis Hypertelorism And Intellectual Disability

  • Trigonocephaly Ptosis Coloboma

  • Trigonocephaly Ptosis Intellectual Disability

  • Cerebrofrontofacial Syndrome Type 3

Total Anomalous Pulmonary Venous Return 1
  • Scimitar Syndrome

  • Total Anomalous Pulmonary Venous Return

  • Anomalous Pulmonary Venous Return

  • Scimitar Anomaly

  • TAPVR1

  • Apvr

  • Halasz Syndrome

  • Hypogenetic Lung Syndrome

  • Pulmonary Venolobar Syndrome

  • TAPVR

  • Congenital Total Pulmonary Venous Return Anomaly

  • Congenital Venolobar Syndrome

  • Mirror-Image Lung Syndrome

  • Vena Cava Bronchovascular Syndrome

  • Pulmonary Venous Return Anomaly

  • Congenital Pulmonary Venolobar Syndrome

  • Epibronchial Right Pulmonary Vein Syndrome

Laryngomalacia
  • Congenital Laryngomalacia

  • Congenital Laryngeal Stridor

  • Laryngomalacia Congenital

  • Floppy Epiglottis

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
Bos taurus OXLD1 VGNC VGNC:32511
Felis catus OXLD1 VGNC VGNC:99316
Macaca mulatta OXLD1 VGNC VGNC:75687
Canis familiaris OXLD1 VGNC VGNC:44201
Mus musculus OXLD1 MGD MGI:1913681
Rattus norvegicus OXLD1 RGD RGD:1590060
Others OXLD1 NCBI