|Institutional Source||Beutler Lab|
|Gene Name||serine peptidase inhibitor, Kazal type 5|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||R7726 (G1)|
|Chromosomal Location||43963235-44022501 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to C at 43963352 bp|
|Amino Acid Change||Leucine to Proline at position 16 (L16P)|
|Ref Sequence||ENSEMBL: ENSMUSP00000066214 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000069245]|
|Predicted Effect||probably damaging
AA Change: L16P
PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
AA Change: L16P
|Coding Region Coverage||
|Validation Efficiency||100% (65/65)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a multidomain serine protease inhibitor that contains 15 potential inhibitory domains. The encoded preproprotein is proteolytically processed to generate multiple protein products, which may exhibit unique activities and specificities. These proteins may play a role in skin and hair morphogenesis, as well as anti-inflammatory and antimicrobial protection of mucous epithelia. Mutations in this gene may result in Netherton syndrome, a disorder characterized by ichthyosis, defective cornification, and atopy. This gene is present in a gene cluster on chromosome 5. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]
PHENOTYPE: Homozygous mutant mice display neonatal lethality, exfoliative erythroderma, and severe dehydration. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Spink5||
(F):5'- CTAACATGAGCCTGAACAACTG -3'
(R):5'- TTGTTAGGAGGGCCTCTCAG -3'
(F):5'- AACAACTGGTTCTGTGTGTGTCAC -3'
(R):5'- TTAGGAGGGCCTCTCAGAGATAAAAG -3'