Homo sapiens potassium inwardly rectifying channel subfamily J member - Nucleotide

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Kir5.1 channels: potential role in epilepsy and seizure disorders. [Am J Physiol Cell Physiol. 2022]
Kir5.1 channels: potential role in epilepsy and seizure disorders.
Staruschenko A, Hodges MR, Palygin O. Am J Physiol Cell Physiol. 2022 Sep 1; 323(3):C706-C717. Epub 2022 Jul 18.
lncRNA XIST is associated with preeclampsia and mediates trophoblast cell invasion via miR-340-5p/KCNJ16 signaling pathway. [Transpl Immunol. 2022]
lncRNA XIST is associated with preeclampsia and mediates trophoblast cell invasion via miR-340-5p/KCNJ16 signaling pathway.
Guo Y, Gao Y, Liu S. Transpl Immunol. 2022 Oct; 74:101666. Epub 2022 Jul 6.
Biallelic loss-of-function variants in KCNJ16 presenting with hypokalemic metabolic acidosis. [Eur J Hum Genet. 2021]
Biallelic loss-of-function variants in KCNJ16 presenting with hypokalemic metabolic acidosis.
Webb BD, Hotchkiss H, Prasun P, Gelb BD, Satlin L. Eur J Hum Genet. 2021 Oct; 29(10):1566-1569. Epub 2021 Apr 12.

Protein
Protein sequence from Nucleotide coding region
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Ensembl [Ensembl]
Ensembl
Kir5.1 [Guide to Pharmacology]
Kir5.1
Guide to Pharmacology
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
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Homo sapiens potassium inwardly rectifying channel subfamily J member 16 (KCNJ16...
Homo sapiens potassium inwardly rectifying channel subfamily J member 16 (KCNJ16), transcript variant 1, mRNA
gi|1825761157|ref|NM_018658.4|

Nucleotide
PREDICTED: Pyrgilauda ruficollis uncharacterized LOC121352630 (LOC121352630), mR...
PREDICTED: Pyrgilauda ruficollis uncharacterized LOC121352630 (LOC121352630), mRNA
gi|2032804016|ref|XM_041465748.1|

Nucleotide
Sweeney-Cox syndrome
Sweeney-Cox syndrome

MedGen
Abnormal hair morphology
Abnormal hair morphology

MedGen

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Nucleotide