Go Annotations as Summary Text (Tabular View) (GO Graph)

GO curators for mouse genes have assigned the following annotations to the gene product of Kcns2. (This text reflects annotations as of Wednesday, January 23, 2013.)

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Summary text based on GO annotations supported by experimental evidence in other organisms

• From comparative sequence analysis (see table for details), MGI curators have determined that the gene product of Kcns2:
  • performs the following molecular functions:
    • delayed rectifier potassium channel activity

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Summary text based on GO annotations supported by structural data

• Kcns2 encodes a protein or proteins that contain the following InterPro domains: BTB/POZ fold, BTB/POZ-like, Ion transport 2, Ion transport domain, Potassium channel tetramerisation-type BTB domain, Potassium channel, voltage dependent, Kv, Potassium channel, voltage dependent, Kv9, Voltage-dependent potassium channel, indicating that the gene product:
  • participates in the following biological processes:
    • ion transport
    • potassium ion transport
    • protein homooligomerization
    • transmembrane transport
  • performs the following molecular functions:
    • ion channel activity
    • voltage-gated potassium channel activity
  • is located in the following cellular components:
    • membrane
    • voltage-gated potassium channel complex

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Summary text for additional MGI annotations

• Automated translation to GO terms of SwissProt keywords that describe Kcns2 indicates that it:
  • participates in the following biological processes:
    • ion transport
    • potassium ion transmembrane transport
    • potassium ion transport
    • regulation of ion transmembrane transport
    • transport
  • performs the following molecular functions:
    • ion channel activity
    • potassium channel activity
    • voltage-gated ion channel activity
  • is located in the following cellular components:
    • integral to membrane
    • membrane
    • plasma membrane

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Gene Ontology Evidence Code Abbreviations:

EXP Inferred from experiment

IC Inferred by curator

IDA Inferred from direct assay

IEA Inferred from electronic annotation

IGI Inferred from genetic interaction

IMP Inferred from mutant phenotype

IPI Inferred from physical interaction

ISS Inferred from sequence or structural similarity

ISO Inferred from sequence orthology

ISA Inferred from sequence alignment

ISM Inferred from sequence model

NAS Non-traceable author statement

ND No biological data available

RCA Reviewed computational analysis

TAS Traceable author statement

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