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EF-Hand Domain (C-terminal) Containing 1 Proteins (EFHC1)

EFHC1 encodes an EF-hand-containing calcium binding protein. Additionally we are shipping EFHC1 Antibodies (35) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
Rat EFHC1 EFHC1 301295  
EFHC1 114327 Q5JVL4
EFHC1 71877 Q9D9T8
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Top EFHC1 Proteins at antibodies-online.com

Showing 4 out of 5 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details
HOST_Human Human Un-conjugated   20 μg Log in to see 9 to 11 Days
$785.40
Details

EFHC1 Proteins by Origin and Source

Origin Expressed in Conjugate
Human , ,
,
Mouse (Murine)

More Proteins for EF-Hand Domain (C-terminal) Containing 1 (EFHC1) Interaction Partners

Xenopus laevis EF-Hand Domain (C-terminal) Containing 1 (EFHC1) interaction partners

  1. EFHC1 domains are involved in ciliary localization, ciliogenesis, and the regulation of Wnt8a (show WNT8A Proteins) signaling

Human EF-Hand Domain (C-terminal) Containing 1 (EFHC1) interaction partners

  1. some EFHC1 mutations may be pathogenic only when introduced into specific genetic backgrounds to juvenile myoclonic epilepsy

  2. Myoclonin1/EFHC1 mutation was suggested releated to juvenile myoclonic epilepsy.

  3. Three SNP alleles in BRD2 (show BRD2 Proteins), Cx-36 (show GJD2 Proteins), and ME2 and microdeletions in 15q13.3, 15q11.2, and 16p13.11 also contribute risk to juvenile myclonic epilepsy.

  4. These results show how Myoclonin1/EFHC1 mutations disrupt brain development and potentially produce structural brain abnormalities on which epileptogenesis is established.

  5. we conclude that mutations in the Myoclonin1/EFHC1 gene are an important cause of juvenile myoclonic epilepsy in Mexican patients.

  6. The juvenile myoclonic epilepsy-related protein EFHC1 interacts with the redox-sensitive TRPM2 (show CLU Proteins) channel linked to cell death.

  7. Mutation analyses identified five missense mutations in EFHC1 that cosegregated with epilepsy or EEG polyspike wave in affected members of six unrelated families with JME and did not occur in 382 control individuals

  8. Deletion analyses revealed that the N-terminal region of EFHC1 is crucial for the association with the mitotic spindle and the midbody. Our results suggest that EFHC1 could play an important role during cell division.

  9. We found no evidence that EFHC1 is a major genetic risk factor for JME susceptibility in Dutch patients.

  10. Mutations in the EFHC1 gene may underlie different types of epilepsy syndromes.

Mouse (Murine) EF-Hand Domain (C-terminal) Containing 1 (EFHC1) interaction partners

  1. Efhc1 (-/-) mouse did not show any abnormalities such as disruption of mitotic spindle structure, impaired M-phase progression, and an increase of apoptosis. Further investigations are required to clarify these discrepancies.

  2. The juvenile myoclonic epilepsy-related protein EFHC1 interacts with the redox-sensitive TRPM2 (show TRPM2 Proteins) channel linked to cell death.

  3. In the adult, low mRNA expression was detected in several brain structures such as cortex, striatum, hippocampus and cerebellum. At E16, EFHC1 mRNA was shown to be expressed in all layers of cortex and not only in cells lining ventricles.

  4. Data report the expression profile and distribution of Efhc1 messenger RNA during mouse and rat brain development, and suggest that Efhc1 expression is more important during initial phases of brain development.

  5. Decrease or loss of function of myoclonin1 may be the molecular basis for epilepsies caused by EFHC1 mutations.

  6. Efhc1 is most abundantly expressed in tissues rich in highly ciliated cells, such as olfactory sensory neurons, and is predicted to be important to cilia.

EFHC1 Protein Profile

Protein Summary

This gene encodes an EF-hand-containing calcium binding protein. The encoded protein likely plays a role in calcium homeostasis. Mutations in this gene have been associated with susceptibility to juvenile myoclonic epilepsy and juvenile absence epilepsy. Alternatively spliced transcript variants have been described.

Gene names and symbols associated with EFHC1

  • EF-hand domain (C-terminal) containing 1 (Efhc1)
  • EF-hand domain (C-terminal) containing 1 (EFHC1)
  • EF-hand domain (C-terminal) containing 1 (efhc1)
  • EF-hand domain (C-terminal) containing 1 (LOC100222292)
  • 1700029F22Rik protein
  • dJ304B14.2 protein
  • MGC63931 protein
  • MGC84469 protein
  • MGC89313 protein
  • mRib72-1 protein
  • myoclonin1 protein
  • zgc:63931 protein

Protein level used designations for EFHC1

EF-hand domain-containing protein 1 , EF-hand domain (C-terminal) containing 1 , EF-hand domain-containing protein 1-like , myoclonin-1

GENE ID SPECIES
301295 Rattus norvegicus
422041 Gallus gallus
474935 Canis lupus familiaris
510124 Bos taurus
100069174 Equus caballus
100152550 Sus scrofa
393942 Danio rerio
444838 Xenopus laevis
462765 Pan troglodytes
493468 Xenopus (Silurana) tropicalis
708517 Macaca mulatta
100016656 Monodelphis domestica
100222292 Taeniopygia guttata
100352671 Oryctolagus cuniculus
100399650 Callithrix jacchus
100443991 Pongo abelii
100482736 Ailuropoda melanoleuca
100557931 Anolis carolinensis
100586187 Nomascus leucogenys
100079150 Ornithorhynchus anatinus
100547670 Meleagris gallopavo
114327 Homo sapiens
71877 Mus musculus
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