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CTTGTCATCACCCCGCTGCCTTCCG[C/G]GGACGTAGCCGCCACATTCCAGTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611453 MIM: 610272 | ||||||||||||||||||||
Literature Links: |
DBNDD2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
DBNDD2 - dysbindin domain containing 2 | ||||||
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There are no transcripts associated with this gene. |
MIR6812 - microRNA 6812 | ||||||
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There are no transcripts associated with this gene. |
PIGT - phosphatidylinositol glycan anchor biosynthesis class T | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184728.2 | 137 | Missense Mutation | GCG,GGG | A,G 42 | NP_001171657.1 | |
NM_001184729.2 | 137 | Missense Mutation | GCG,GGG | A,G 42 | NP_001171658.1 | |
NM_001184730.2 | 137 | Missense Mutation | GCG,GGG | A,G 42 | NP_001171659.1 | |
NM_015937.5 | 137 | Missense Mutation | GCG,GGG | A,G 42 | NP_057021.2 | |
XM_005260430.2 | 137 | Missense Mutation | GCG,GGG | A,G 42 | XP_005260487.1 | |
XM_005260432.2 | 137 | UTR 5 | XP_005260489.1 |
SYS1-DBNDD2 - SYS1-DBNDD2 readthrough (NMD candidate) | ||||||
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There are no transcripts associated with this gene. |