CPED1 - cadherin like and PC-esterase domain containing 1 Gene

Also Known as C7orf58

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79974

About CPED1

This gene has 10 transcripts (splice variants) and 187 orthologues. Broad expression in fat (RPKM 27.4), ovary (RPKM 24.4) and 19 other tissues.

Summary

Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

CPED1 Products (2)

mRNA Protein Name
NM_001105533.1 NP_001099003.1 cadherin-like and PC-esterase domain-containing protein 1 isoform 2 precursor
NM_024913.5 NP_079189.4 cadherin-like and PC-esterase domain-containing protein 1 isoform 1 precursor

CPED1 Protein Structure

Cadherin-like

Cadherin-like: Cadherin-like beta sandwich domain (583 - 667)

PC-Esterase

PC-Esterase: GDSL/SGNH-like Acyl-Esterase family found in Pmr5 and Cas1p (757 - 1021)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1026 a.a.
Protein Preferred Names Protein Names

cadherin-like and PC-esterase domain-containing protein 1

Related Diseases

Diseases Alias
Calvarial Doughnut Lesions With Bone Fragility
  • Calvarial Doughnut Lesions With Bone Fragility With Or Without Spondylometaphyseal Dysplasia

  • Calvarial Doughnut Lesions-Bone Fragility Syndrome

  • CDL

  • Doughnut Lesions Of Skull, Familial

  • Calvarial Doughnut Lesions With Bone Fragility And Spondylometaphyseal Dysplasia

  • Familial Doughnut Lesions Of Skull

  • CDLSMD

Omodysplasia 1
  • OMOD1

  • Autosomal Recessive Omodysplasia

  • Omodysplasia Autosomal Recessive

  • Omodysplasia Generalized Form

  • Omodysplasia Type 1

  • Omodysplasia, Generalized Form

  • Omodysplasia, Autosomal Recessive

  • Micromelic Dysplasia, Congenital, With Dislocation Of Radius

  • Micromelic Dysplasia Congenita With Dislocation Of Radius

  • Micromelic Dysplasia-Dislocation Of Radius Syndrome

  • Micromelic Dysplasia Congenital With Dislocation Of Radius

  • Omodysplasia, Type 1

Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, And Seizures Syndrome
  • Door Syndrome

  • Doors Syndrome

  • Digitorenocerebral Syndrome

  • Autosomal Recessive Deafness-Onychodystrophy Syndrome

  • Deafness-Onychoosteodystrophy-Intellectual Disability Syndrome

  • DOORS

  • Drc Syndrome

  • Eronen Syndrome

  • Deafness-Onychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

  • Brachydactyly Due To Absence Of Distal Phalanges

  • Deafness-Onychodystrophy-Osteodystrophy-Intellectual Disability-Seizures Syndrome

  • Deafness, Onychodystrophy, Osteodystrophy, And Mental Retardation Syndrome

  • Deafness-Oncychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

  • Autosomal Recessive Hearing Loss-Onychodystrophy Syndrome

  • Hearing Loss-Onychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

  • Hearing Loss-Onychodystrophy-Osteodystrophy-Intellectual Disability-Seizures Syndrome

  • Hearing Loss-Onychoosteodystrophy-Intellectual Disability Syndrome

  • Deafness, Onychodystrophy, Osteodystrophy, Intellectual Disability, And Seizures Syndrome

  • Deafness, Congenital Onychodystrophy, Recessive Form

  • Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation Syndrome

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
Rattus norvegicus CPED1 RGD RGD:1563491
Canis familiaris CPED1 VGNC VGNC:54757
Mus musculus CPED1 MGD MGI:2444814
Felis catus CPED1 VGNC VGNC:61122
Macaca mulatta CPED1 VGNC VGNC:71585
Bos taurus CPED1 VGNC VGNC:27651
Others CPED1 NCBI