Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGGCTGCCACGCAAGAGGATCCGC[C/T]TAAGATGGGAGACCTGAGCAAGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611297 MIM: 605030 | ||||||||||||||||||||
Literature Links: |
OSR2 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 |
OSR2 - odd-skipped related transciption factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142462.2 | 1135 | Missense Mutation | CCT,CTT | P,L 131 | NP_001135934.1 | |
NM_001286841.1 | 1135 | Missense Mutation | CCT,CTT | P,L 252 | NP_001273770.1 | |
NM_053001.3 | 1135 | Missense Mutation | CCT,CTT | P,L 131 | NP_443727.2 | |
XM_005250778.4 | 1135 | Missense Mutation | CCT,CTT | P,L 252 | XP_005250835.1 | |
XM_011516825.2 | 1135 | Missense Mutation | CCT,CTT | P,L 188 | XP_011515127.1 | |
XM_011516826.2 | 1135 | Missense Mutation | CCT,CTT | P,L 184 | XP_011515128.1 | |
XM_011516827.2 | 1135 | Missense Mutation | CCT,CTT | P,L 131 | XP_011515129.1 | |
XM_017013018.1 | 1135 | Missense Mutation | CCT,CTT | P,L 131 | XP_016868507.1 |
STK3 - serine/threonine kinase 3 | ||||||
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There are no transcripts associated with this gene. |