Uncertain significance Last evaluated: ClinVar Relating variation to medicine. 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. It is useful for tracking sequence updates. February 6, Last modified: Help criteria provided, multiple submitters, no conflicts 2 stars out of maximum of 4 stars. Unreviewed – Annotation score:
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No significant changes were observed throughout the observation period of 2 h FCD values at the end of the observation period: Four distinct tokens exist: Conserved Domains Database More This variant’s association with FCD has not been reported in other affected individuals, fdc, taken together with the presumed autosomal dominant inheritance pattern of FCD, does not support a strong correlation between fcv variant and FCD.
EMBL nucleotide sequence database More Automatic assertion inferred from database entries i.
Do not show this banner again. However, in contrast to leukocytes the interactions were not restricted to venules, but were also observed in small arterioles.
This is version 35 of the entry and version 1 of the sequence. The aim of our present study was, therefore, to establish a model to investigate the microcirculation in the mouse small intestine.
CAP Reach 11 Dike #3 – ID # 60107
Systems used to automatically annotate proteins with high accuracy:. Kyoto Encyclopedia of Genes and Genomes More Superfamily database of structural and functional annotation More The algorithm is described in the ISO standard.
Database of comparative protein structure models More National Institutes of Health. K7RQ16 Primary citable accession number: Select the link destinations: Cutibacterium granulosum DSM Database of Orthologous Groups More Clinical assertions Summary evidence Supporting observations Help.
This variant has also been identified in the heterozygous state in one individual with late onset Fuchs corneal dystrophy FCDhowever hearing status was not reported Riazuddin In gcd, additional data is needed to determine the clinical significance of this variant. Assertion and evidence details. It is useful for tracking sequence updates.
Integrated resource of protein families, domains and functional sites More ClinVar Relating variation to medicine. February 6, Last modified: Interpretation Help Clinical significance: Pfam protein domain database More You are using a version of browser that may not display all the features of this website.
Protein Motif fingerprint database; a ccd domain database More These are stable identifiers and should be used to cite UniProtKB entries. Automatic assertion according to rules i.