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AGCGACGCGAAGTGAAGAGGATTCT[A/G]GGGGAGGCGGCGGTGGACCTGAGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
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Phenotype: |
MIM: 604013 MIM: 601019 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
B4GALT2 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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B4GALT2 - beta-1,4-galactosyltransferase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001005417.2 | 226 | Intron | NP_001005417.1 | |||
NM_003780.4 | 226 | Intron | NP_003771.1 | |||
NM_030587.2 | 226 | Intron | NP_085076.2 | |||
XM_017002716.1 | 226 | Intron | XP_016858205.1 | |||
XM_017002717.1 | 226 | Intron | XP_016858206.1 |
CCDC24 - coiled-coil domain containing 24 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152499.2 | 226 | Silent Mutation | CTA,CTG | L,L 28 | NP_689712.1 | |
XM_017000423.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855912.1 | |
XM_017000424.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855913.1 | |
XM_017000425.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855914.1 | |
XM_017000426.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855915.1 | |
XM_017000427.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855916.1 | |
XM_017000428.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855917.1 | |
XM_017000429.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855918.1 | |
XM_017000430.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855919.1 | |
XM_017000431.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855920.1 | |
XM_017000432.1 | 226 | UTR 5 | XP_016855921.1 | |||
XM_017000433.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855922.1 | |
XM_017000434.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855923.1 | |
XM_017000435.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855924.1 | |
XM_017000436.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855925.1 | |
XM_017000437.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855926.1 | |
XM_017000438.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855927.1 | |
XM_017000439.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855928.1 | |
XM_017000440.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855929.1 | |
XM_017000441.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855930.1 | |
XM_017000442.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855931.1 | |
XM_017000443.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855932.1 | |
XM_017000444.1 | 226 | Silent Mutation | CTA,CTG | L,L 28 | XP_016855933.1 | |
XM_017000445.1 | 226 | UTR 5 | XP_016855934.1 | |||
XM_017000446.1 | 226 | UTR 5 | XP_016855935.1 |
SLC6A9 - solute carrier family 6 member 9 | ||||||
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There are no transcripts associated with this gene. |