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Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 Proteins (KCNJ13)

KCNJ13 encodes a member of the inwardly rectifying potassium channel family of proteins. Additionally we are shipping KCNJ13 Antibodies (33) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
KCNJ13 3769 O60928
KCNJ13 100040591 P86046
Rat KCNJ13 KCNJ13 94341 O70617
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Top KCNJ13 Proteins at antibodies-online.com

Showing 4 out of 4 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
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 49 to 54 Days
$6,041.49
Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 49 to 54 Days
$4,244.78
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

KCNJ13 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
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Mouse (Murine) ,
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More Proteins for Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 (KCNJ13) Interaction Partners

Cow (Bovine) Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 (KCNJ13) interaction partners

  1. the activity of Kir channels in the RPE is critically dependent on the regeneration of membrane PIP2 by PI4 kinases and that this may explain the dependence of these channels on hydrolyzable ATP.

Zebrafish Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 (KCNJ13) interaction partners

  1. These results suggest that the cellular defect of the Kir7.1 mutation is directly responsible for the pattern change in the jaguar/obelix mutant.

Human Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 (KCNJ13) interaction partners

  1. Kir7.1 mutations are associated with vision disorders to include novel insights into the molecular mechanism of disease pathobiology in Leber Congenital Amaurosis.

  2. Juvenile or early-adult-onset cataract in the setting of a congenital vitreo-retinal dystrophy (show MERTK Proteins) notable for fibrosis over the disc and clumped pigmentation in the posterior pole is a unique phenotype that suggests recessive KCNJ13 mutations.

  3. Kir7.1 regulates the transition from quiescence to contractions in the pregnant uterus.

  4. Kir7.1, R162W mutant showed a reduction of IKir7.1 and positive shift in '0' current potential.

  5. Kir7.1 expression was found in 100% of choroid plexus tumors and was absent in endolymphatic sac (show ADCY10 Proteins) tumors.

  6. A homozygous nonsense mutation was found in the potassium channel subunit (show KCNT1 Proteins) gene KCNJ13 that caused leber congenital amaurosis.

  7. This study confirms the expression of Kir7.1 in human RPE (show RPE Proteins), identifies a Kir7.1 splice variant resulting in predicted changes in protein sequence, and indicates that there is no functional interaction between this splice variant and full-length Kir7.1.

  8. Kir7.1 channels are modulated by intracellular protons by diverse mechanisms; H26 is important for channel activation at physiological pH(i) and it influences an unidentified proton-induced inhibitory mechanism.

  9. These results indicate that the KCNJ13 R162W mutation can cause Snowflake vitreoretinal degeneration and further show that vitreoretinal degeneration can arise through mutations in genes whose products are not structural components of the vitreous.

  10. This study demonstrates the dual regulation of Kir7.1 channel function by PKA and PKC.

Mouse (Murine) Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 (KCNJ13) interaction partners

  1. These results suggest that KCNJ13 expression is required for RPE (show RPE Proteins) cells to maintain photoreceptor survival.

  2. Kir7.1 regulates the transition from quiescence to contractions in the pregnant uterus.

  3. Coupling of MC4R (show MC4R Proteins) to Kir7.1 may explain unusual aspects of the control of energy homeostasis by melanocortin signalling, including the gene dosage effect of MC4R (show MC4R Proteins) and the sustained effects of AgRP (show AGRP Proteins) on food intake.

KCNJ13 Protein Profile

Protein Summary

This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.

Gene names and symbols associated with KCNJ13

  • potassium inwardly-rectifying channel, subfamily J, member 13 (KCNJ13)
  • potassium inwardly-rectifying channel, subfamily J, member 13 (kcnj13)
  • potassium inwardly-rectifying channel, subfamily J, member 13 (Kcnj13)
  • KIR1.4 protein
  • Kir7.1 protein
  • LCA16 protein
  • SVD protein

Protein level used designations for KCNJ13

potassium inwardly-rectifying channel, subfamily J, member 13 , inward rectifier potassium channel 13 , jag , obe , jaguar , obelix , inwardly rectifying potassium channel 7.1 , inward rectifier potassium channel 13-like , inward rectifier K(+) channel Kir7.1 , potassium channel, inwardly rectifying subfamily J member 13 , inwardly rectifying potassium channel Kir7.1

GENE ID SPECIES
477411 Canis lupus familiaris
512288 Bos taurus
555691 Danio rerio
100125048 Xenopus (Silurana) tropicalis
100402605 Callithrix jacchus
100595442 Nomascus leucogenys
100615579 Pan troglodytes
3769 Homo sapiens
100040591 Mus musculus
94341 Rattus norvegicus
100379277 Cavia porcellus
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