AXDND1 - axonemal dynein light chain domain containing 1 Gene

Also Known as C1orf125

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 126859

About AXDND1

This gene has 14 transcripts (splice variants) and 182 orthologues. Biased expression in testis (RPKM 7.6), duodenum (RPKM 0.7) and 3 other tissues.

AXDND1 Products (1)

mRNA Protein Name
NM_144696.6 NP_653297.3 axonemal dynein light chain domain-containing protein 1

Gene Ontology

  • Cellular Component
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
34759295 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

AXDND1 Protein Structure

Ax_dynein_light

Ax_dynein_light: Axonemal dynein light chain (210 - 305)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1012 a.a.
Protein Preferred Names Protein Names

axonemal dynein light chain domain-containing protein 1

Related Diseases

Diseases Alias
Genetic Nephrotic Syndrome

  • Hereditary Nephrotic Syndrome
Nephrotic Syndrome, Type 24

  • NPHS24

  • Idiopathic Steroid-Resistant Nephrotic Syndrome

  • Idiopathic Srns

  • Nephrotic Syndrome 24

  • Nephrotic Syndrome, Idiopathic, Steroid-Resistant

  • Nephrotic Syndrome, Steroid-Resistant, Autosomal Recessive
Idiopathic Nephrotic Syndrome
Nephrotic Syndrome, Type 2

  • NPHS2

  • Nephrotic Syndrome, Steroid-Resistant, Autosomal Recessive

  • Srn1

  • Nephrotic Syndrome Type 2

  • Steroid-Resistant Autosomal Recessive Nephrotic Syndrome

  • Nephrotic Syndrome 2

  • Autosomal Recessive Steroid-Resistant Nephrotic Syndrome

  • Srn

  • Nephrotic Syndrome, Type 2, Susceptibility To

  • Idiopathic Nephrotic Syndrome
Focal Segmental Glomerulosclerosis

  • Familial Idiopathic Steroid-Resistant Nephrotic Syndrome

  • Focal Glomerulosclerosis

  • Fsgs

  • Segmental Glomerulosclerosis

  • Glomerulosclerosis, Focal Segmental

  • Fgs

  • Focal Glomerular Sclerosis

  • Familial Idiopathic Nephrotic Syndrome

  • Focal Sclerosis With Hyalinosis

  • Glomerulosclerosis, Focal

  • Glomerulosclerosis Focal

  • Glomerulosclerosis, Segmental, Focal

  • Focal Segmental Glomerulosclerosis, Not Otherwise Specified
Chronic Kidney Disease

  • Chronic Renal Disease

  • Chronic Kidney Failure

  • Ckd

  • Chronic Renal Failure

  • Kidney Failure, Chronic

  • Chronic Renal Failure Syndrome

  • Crf

  • Renal Failure - Chronic

  • Renal Failure Chronic

  • Chronic Kidney Diseases

  • Chronic Kidney Disease Stage 5

  • Ckd - [Chronic Kidney Disease]

  • Crf - [Chronic Renal Failure]

  • Chronic Kidney Impairment

  • Chronic Renal Impairment

  • Chronic Kidney Shutdown

  • Chronic Hypoxic Kidney Failure

  • Chronic Kidney Collapse

  • Chronic Renal Insufficiency

  • Chronic Kidney Toxaemia

  • Chronic Kidney Hypofunction

  • Chronic Renal Suppression

  • Chronic Renal Failure, Stage 5

  • Ckd - [Chronic Kidney Disease] Stage 5

  • End Stage Kidney Failure

  • End Stage Renal Failure

  • End Stage Kidney Disease

  • End Stage Renal Disease

  • End Stage Chronic Renal Failure

  • Esrf - [End Stage Renal Failure]

  • Esrd - [End Stage Renal Diseases]

  • Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
Nephrotic Syndrome

  • Finnish Congenital Nephrotic Syndrome

  • Ns - [Nephrotic Syndrome]

  • Nephrosis Syndrome

  • Nephrosis Nos

  • Glomerular Lesion Nephrosis
Diamond-Blackfan Anemia 10

  • DBA10

  • Rps26-Related Diamond-Blackfan Anemia

  • Anemia, Diamond-Blackfan, Type 10
Spondylocarpotarsal Synostosis Syndrome

  • SCT

  • Spondylocarpotarsal Syndrome

  • Vertebral Fusion With Carpal Coalition

  • Congenital Scoliosis With Unilateral Unsegmented Bar

  • Congenital Synspondylism

  • Spondylocarpotarsal Synostosis

  • Synspondylism, Congenital

  • Scoliosis, Congenital, With Unilateral Unsegmented Bar

  • Scoliosis, Congenital With Unilateral Unsegmented Bar

  • Synspondylism Congenital

  • Sct Syndrome

  • Synspondylism
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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS01290 AXDND1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris AXDND1 VGNC VGNC:38323
Mus musculus AXDND1 MGD MGI:1924602
Felis catus AXDND1 VGNC VGNC:82458
Macaca mulatta AXDND1 VGNC VGNC:70135
Rattus norvegicus AXDND1 RGD RGD:1566124
Bos taurus AXDND1 VGNC VGNC:26363
Others AXDND1 NCBI