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Search Thermo Fisher Scientific
TCGCGGGATGATCACATCGGCATAC[C/T]TCTTTGTCTGTAAGGCACAAGGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607423 MIM: 609328 | ||||||||||||||||||||
Literature Links: |
POMT1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
POMT1 - protein O-mannosyltransferase 1 | ||||||
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There are no transcripts associated with this gene. |
UCK1 - uridine-cytidine kinase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135954.2 | 676 | Silent Mutation | GAA,GAG | E,E 172 | NP_001129426.1 | |
NM_001261450.2 | 676 | Missense Mutation | AAG,AGG | K,R 195 | NP_001248379.1 | |
NM_001261451.2 | 676 | Missense Mutation | AAG,AGG | K,R 209 | NP_001248380.1 | |
NM_001318519.1 | 676 | Missense Mutation | AAG,AGG | K,R 181 | NP_001305448.1 | |
NM_031432.3 | 676 | Missense Mutation | AAG,AGG | K,R 204 | NP_113620.1 | |
XM_005272224.2 | 676 | Missense Mutation | AAG,AGG | K,R 218 | XP_005272281.1 |