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GTGAGGAGCTGGATATGCGGGGCAA[A/G]AAGAGGAGCTGGGGCTTGTAAAAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300522 MIM: 314690 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
IQSEC2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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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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IQSEC2 - IQ motif and Sec7 domain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001111125.2 | 5762 | UTR 3 | NP_001104595.1 | |||
NM_001243197.1 | 5762 | Intron | NP_001230126.1 | |||
NM_015075.1 | 5762 | UTR 3 | NP_055890.1 | |||
XM_006724579.2 | 5762 | UTR 3 | XP_006724642.1 | |||
XM_006724580.3 | 5762 | UTR 3 | XP_006724643.1 | |||
XM_006724581.3 | 5762 | Intron | XP_006724644.1 | |||
XM_006724582.3 | 5762 | Intron | XP_006724645.1 | |||
XM_006724583.3 | 5762 | Intron | XP_006724646.1 | |||
XM_006724584.2 | 5762 | Intron | XP_006724647.1 | |||
XM_011530773.2 | 5762 | UTR 3 | XP_011529075.1 | |||
XM_011530774.2 | 5762 | Intron | XP_011529076.1 | |||
XM_011530776.1 | 5762 | Intron | XP_011529078.1 | |||
XM_011530777.1 | 5762 | Intron | XP_011529079.1 | |||
XM_017029359.1 | 5762 | UTR 3 | XP_016884848.1 | |||
XM_017029360.1 | 5762 | UTR 3 | XP_016884849.1 |
KDM5C - lysine demethylase 5C | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |