CAPSL - calcyphosine like Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 133690

About CAPSL

Cytogenetic location: 5p13.2 Genomic coordinates (GRCh38): 5:35,904,288-35,938,779 (from NCBI)

This gene has 5 transcripts (splice variants), 205 orthologues and 5 paralogues. Biased expression in testis (RPKM 4.0), lung (RPKM 3.4) and 3 other tissues.

Summary

Predicted to enable calcium ion binding activity. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

CAPSL Products (2)

mRNA Protein Name
NM_001042625.2 NP_001036090.1 calcyphosin-like protein
NM_144647.4 NP_653248.3 calcyphosin-like protein

CAPSL Protein Structure

EF-hand_7

EF-hand_7: EF-hand domain pair (44 - 101)

EF-hand_7

EF-hand_7: EF-hand domain pair (116 - 185)

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

calcyphosin-like protein

Related Diseases

Diseases Alias
Lipomatosis

  • Benign Symmetrical Lipomatosis
Lipomatosis, Multiple Symmetric

  • Multiple Symmetric Lipomatosis

  • Lipomatosis, Familial Benign Cervical

  • Lipomatosis, Multiple Symmetrical

  • Lipodystrophy, Cephalothoracic

  • Benign Symmetrical Lipomatosis

  • Madelung Disease

  • Madelung'S Disease

  • MSL

  • Cervical Symmetrical Lipomatosis

  • Launois-Bensaude'S Lipomatosis

  • Madelung'S Neck

  • Multiple Symmetrical Lipomatosis

  • Familial Symmetric Lipomatosis

  • Launois-Bensaude Syndrome

  • Cephalothoracic Lipodystrophy

  • Familial Benign Cervical Lipomatosis

  • Launois-Bensaude Lipomatosis
Developmental And Epileptic Encephalopathy 28

  • DEE28

  • Epileptic Encephalopathy, Early Infantile, 28

  • Eiee28

  • Developmental And Epileptic Encephalopathy, 28

  • Early Infantile Epileptic Encephalopathy 28

  • Encephalopathy, Epileptic, Early Infantile, Type 28
Spinocerebellar Ataxia, Autosomal Recessive 12

  • Autosomal Recessive Spinocerebellar Ataxia 12

  • SCAR12

  • Spinocerebellar Ataxia With Mental Retardation And Epilepsy

  • Autosomal Recessive Cerebellar Ataxia-Epilepsy-Intellectual Disability Syndrome Due To Wwox Deficiency

  • Autosomal Recessive Spinocerebellar Ataxia Type 12

  • Spinocerebellar Ataxia, Autosomal Recessive, 12

  • Ataxia, Spinocerebellar, Autosomal Recessive, Type 12
Type 1 Diabetes Mellitus 5

  • Diabetes Mellitus, Insulin-Dependent, 5

  • Latent Autoimmune Diabetes In Adults

  • IDDM5

  • Insulin-Dependent Diabetes Mellitus 5

  • T1D5

  • Lada

  • Type 1.5 Diabetes

  • Diabetes Mellitus, Insulin-Dependent, Type 5
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-RS01901 CAPSL Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris CAPSL VGNC VGNC:49856
Macaca mulatta CAPSL VGNC VGNC:70653
Mus musculus CAPSL MGD MGI:1922818
Felis catus CAPSL VGNC VGNC:60360
Rattus norvegicus CAPSL RGD RGD:1308776
Bos taurus CAPSL VGNC VGNC:26755
Others CAPSL NCBI