Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604961 MIM: 608888 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PDE11A 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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PDE11A - phosphodiesterase 11A | ||||||
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There are no transcripts associated with this gene. |
RBM45 - RNA binding motif protein 45 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152945.3 | 485 | Intron | NP_694453.2 | |||
XM_005246287.4 | 485 | Intron | XP_005246344.1 | |||
XM_017003320.1 | 485 | Missense Mutation | TCT,TGT | S,C 116 | XP_016858809.1 | |
XM_017003321.1 | 485 | Missense Mutation | TCT,TGT | S,C 116 | XP_016858810.1 | |
XM_017003322.1 | 485 | Intron | XP_016858811.1 |
Set Membership: |
HapMap |