National Institutes of Health. Help criteria provided, multiple submitters, no conflicts 2 stars out of maximum of 4 stars. Four distinct tokens exist: This variant has also been identified in the heterozygous state in one individual with late onset Fuchs corneal dystrophy FCD , however hearing status was not reported Riazuddin K7RQ16 Primary citable accession number: Although this variant has been seen in the general population, its frequency is not high enough to rule out a pathogenic role. Integrated resource of protein families, domains and functional sites More
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The algorithm is described in the ISO standard.
CAP Reach 11 Dike #3 – ID#
Select a section on the left to see content. Superfamily database of structural and functional annotation More Platelets rolled along or attached to the endothelium in a manner similar to leukocytes.
K7RQ16 Primary citable accession number: Integrated resource of protein families, domains and functional sites More National Center for Biotechnology Information 254, U.
Protein Motif fingerprint database; a protein domain database More ClinVar Relating variation to medicine.
Do not show this banner again. It lists the nodes as they appear top-down in the taxonomic tree, with the more general grouping listed first.
CAP Reach 11 Dike #3 – ID # 60107
Clinical assertions Summary evidence Supporting observations Help. These are stable identifiers and should be used to cite UniProtKB entries. Cutibacterium granulosum DSM Select item s and click on “Add to basket” to create your own collection here entries max. However, in contrast to leukocytes the interactions were not restricted to venules, but were also observed in small arterioles.
Click here to see the new Variation Report design! However, the molecular mechanisms underlying these alterations are still not fully understood. Conserved Domains Database More You are using a version of browser that may not display all the features of this website. Unreviewed – Annotation score: Pfam protein domain database More Systems used to automatically annotate proteins with high accuracy:.
Assertion and evidence details. Help criteria provided, multiple submitters, no conflicts 2 stars out of maximum of 4 stars.
This variant’s association with FCD has not been reported in other affected individuals, which, taken together with the presumed autosomal dominant inheritance pattern of FCD, does not support a strong correlation between this variant and FCD. Select the link destinations: Your basket is currently empty. Automatic assertion inferred from database entries i.