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AGAACCTGGAGCTGCCGGAGGAAGC[C/T]TGAGTTAGGGCAGATATTGCGGTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613191 MIM: 611575 | ||||||||||||||||||||
Literature Links: |
DUSP13 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 |
DUSP13 - dual specificity phosphatase 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007271.1 | 1039 | UTR 3 | NP_001007272.1 | |||
NM_001007272.1 | 1039 | Missense Mutation | AGC,GGC | S,G 229 | NP_001007273.1 | |
NM_001007273.1 | 1039 | Missense Mutation | AGC,GGC | S,G 272 | NP_001007274.1 | |
NM_001320842.1 | 1039 | Missense Mutation | AGC,GGC | S,G 272 | NP_001307771.1 | |
NM_001320843.1 | 1039 | Missense Mutation | AGC,GGC | S,G 179 | NP_001307772.1 | |
NM_016364.3 | 1039 | Missense Mutation | AGC,GGC | S,G 179 | NP_057448.3 | |
XM_005269883.3 | 1039 | Missense Mutation | AGC,GGC | S,G 398 | XP_005269940.1 | |
XM_005269884.4 | 1039 | Missense Mutation | AGC,GGC | S,G 315 | XP_005269941.3 | |
XM_005269887.1 | 1039 | Missense Mutation | AGC,GGC | S,G 272 | XP_005269944.1 | |
XM_005269890.1 | 1039 | Missense Mutation | AGC,GGC | S,G 179 | XP_005269947.1 | |
XM_011539853.1 | 1039 | Missense Mutation | AGC,GGC | S,G 308 | XP_011538155.1 | |
XM_011539854.2 | 1039 | Missense Mutation | AGC,GGC | S,G 179 | XP_011538156.1 | |
XM_011539855.1 | 1039 | Missense Mutation | AGC,GGC | S,G 179 | XP_011538157.1 | |
XM_011539856.2 | 1039 | Missense Mutation | AGC,GGC | S,G 179 | XP_011538158.1 | |
XM_017016313.1 | 1039 | Missense Mutation | AGC,GGC | S,G 227 | XP_016871802.1 | |
XM_017016314.1 | 1039 | Intron | XP_016871803.1 |
SAMD8 - sterile alpha motif domain containing 8 | ||||||
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There are no transcripts associated with this gene. |