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ACACACGGGCTTCATGTCGAACTCC[A/T]CAAACTTGTTCCTGAGGAGGAAGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603071 MIM: 607908 MIM: 606541 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GPR17 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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GPR17 - G protein-coupled receptor 17 | ||||||
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There are no transcripts associated with this gene. |
LIMS2 - LIM zinc finger domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136037.2 | 1167 | Missense Mutation | GAG,GTG | E,V 319 | NP_001129509.2 | |
NM_001161403.1 | 1167 | Missense Mutation | GAG,GTG | E,V 297 | NP_001154875.1 | |
NM_001161404.1 | 1167 | Missense Mutation | GAG,GTG | E,V 292 | NP_001154876.1 | |
NM_001256542.1 | 1167 | Missense Mutation | GAG,GTG | E,V 145 | NP_001243471.1 | |
NM_017980.4 | 1167 | Missense Mutation | GAG,GTG | E,V 321 | NP_060450.2 | |
XM_005263710.2 | 1167 | Missense Mutation | GAG,GTG | E,V 228 | XP_005263767.1 | |
XM_006712627.3 | 1167 | Missense Mutation | GAG,GTG | E,V 181 | XP_006712690.1 | |
XM_006712628.3 | 1167 | Intron | XP_006712691.1 | |||
XM_011511453.1 | 1167 | Missense Mutation | GAG,GTG | E,V 280 | XP_011509755.1 | |
XM_017004469.1 | 1167 | Missense Mutation | GAG,GTG | E,V 194 | XP_016859958.1 |
MYO7B - myosin VIIB | ||||||
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There are no transcripts associated with this gene. |