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ATAGCCCCGTAGTAGAAATAGCCCA[C/T]GGTAGTAACTTAGGACAGGTGTCAT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 167416 MIM: 607571 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PAX9 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)
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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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PAX9 - paired box 9 | ||||||
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There are no transcripts associated with this gene. |
SLC25A21 - solute carrier family 25 member 21 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001171170.1 | 2437 | Intron | NP_001164641.1 | |||
NM_030631.3 | 2437 | UTR 3 | NP_085134.1 | |||
XM_011537287.2 | 2437 | Intron | XP_011535589.1 | |||
XM_011537288.2 | 2437 | Intron | XP_011535590.1 | |||
XM_011537289.2 | 2437 | Intron | XP_011535591.1 |
Set Membership: |
HapMap |