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GTCTCATATACAACAAGACTGACAA[C/T]CTTTGAAACTGCAAGAAAAGACTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605722 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNJ16 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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KCNJ16 - potassium voltage-gated channel subfamily J member 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270422.1 | Intron | NP_001257351.1 | ||||
NM_001291622.1 | Intron | NP_001278551.1 | ||||
NM_001291623.1 | Intron | NP_001278552.1 | ||||
NM_001291624.1 | Intron | NP_001278553.1 | ||||
NM_001291625.1 | Intron | NP_001278554.1 | ||||
NM_018658.2 | Intron | NP_061128.2 | ||||
NM_170741.2 | Intron | NP_733937.2 | ||||
NM_170742.2 | Intron | NP_733938.2 | ||||
XM_005257337.4 | Intron | XP_005257394.1 | ||||
XM_006721885.3 | Intron | XP_006721948.1 | ||||
XM_006721886.3 | Intron | XP_006721949.1 | ||||
XM_006721887.3 | Intron | XP_006721950.1 | ||||
XM_011524781.2 | Intron | XP_011523083.1 | ||||
XM_017024609.1 | Intron | XP_016880098.1 | ||||
XM_017024610.1 | Intron | XP_016880099.1 | ||||
XM_017024611.1 | Intron | XP_016880100.1 | ||||
XM_017024612.1 | Intron | XP_016880101.1 | ||||
XM_017024613.1 | Intron | XP_016880102.1 |
LINC01028 - long intergenic non-protein coding RNA 1028 | ||||||
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There are no transcripts associated with this gene. |