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

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

Homo sapiens

Also known as C7orf58

Gene ID: 79974 | Gene type: protein coding

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
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  • 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