kallikrein-11 isoform 2 [Mus musculus]

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Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorder. [Br J Dermatol. 2023]
Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorder.
Gong Z, Dai S, Jiang X, Lee M, Zhu X, Wang H, Lin Z. Br J Dermatol. 2023 Jan 23; 188(1):100-111.
KLK11 promotes the activation of mTOR and protein synthesis to facilitate cardiac hypertrophy. [BMC Cardiovasc Disord. 2021]
KLK11 promotes the activation of mTOR and protein synthesis to facilitate cardiac hypertrophy.
Wang Y, Liao H, Wang Y, Zhou J, Wang F, Xie Y, Zhao K, Gao W. BMC Cardiovasc Disord. 2021 May 31; 21(1):266. Epub 2021 May 31.
Deficiency of KLF4 compromises the lung function in an acute mouse model of allergic asthma. [Biochem Biophys Res Commun. 2017]
Deficiency of KLF4 compromises the lung function in an acute mouse model of allergic asthma.
Nimpong JA, Gebregziabher W, Singh UP, Nagarkatti P, Nagarkatti M, Hodge J, Liu C, Fan D, Ai W. Biochem Biophys Res Commun. 2017 Nov 4; 493(1):598-603. Epub 2017 Sep 1.

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Ensembl [Ensembl]
Ensembl
Ensembl [Ensembl]
Ensembl
Ensembl [Ensembl]
Ensembl
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

References and Bibliography - Management of Neonatal Hyperbilirubinemia
References and Bibliography - Management of Neonatal Hyperbilirubinemia
PREDICTED: Homo sapiens golgin B1 (GOLGB1), transcript variant X13, mRNA
PREDICTED: Homo sapiens golgin B1 (GOLGB1), transcript variant X13, mRNA
gi|2217343419|ref|XM_017006191.2|

Nucleotide
PREDICTED: Homo sapiens golgin B1 (GOLGB1), transcript variant X12, mRNA
PREDICTED: Homo sapiens golgin B1 (GOLGB1), transcript variant X12, mRNA
gi|2217343418|ref|XM_005247373.3|

Nucleotide
golgin subfamily B member 1 isoform X2 [Homo sapiens]
golgin subfamily B member 1 isoform X2 [Homo sapiens]
gi|2217343409|ref|XP_047303944.1|

Protein
PREDICTED: Homo sapiens golgin B1 (GOLGB1), transcript variant X4, mRNA
PREDICTED: Homo sapiens golgin B1 (GOLGB1), transcript variant X4, mRNA
gi|2462589187|ref|XM_054346224.1|

Nucleotide

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Protein