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AGCTCAGGGCAGGGTATAAGGGTAT[C/T]GGAGGCCACGTAAAGCCATCCAGGC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
14 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 - Not Available | Caucasian - Not Available | CEPH (CEU)
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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 |
B4GALT2 - beta-1,4-galactosyltransferase 2 | ||||||
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There are no transcripts associated with this gene. |
SLC6A9 - solute carrier family 6 member 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001024845.2 | 2633 | UTR 3 | NP_001020016.1 | |||
NM_001261380.1 | 2633 | UTR 3 | NP_001248309.1 | |||
NM_006934.3 | 2633 | UTR 3 | NP_008865.2 | |||
NM_201649.3 | 2633 | UTR 3 | NP_964012.2 | |||
XM_011542017.2 | 2633 | Intron | XP_011540319.1 | |||
XM_017002151.1 | 2633 | UTR 3 | XP_016857640.1 | |||
XM_017002152.1 | 2633 | UTR 3 | XP_016857641.1 | |||
XM_017002153.1 | 2633 | UTR 3 | XP_016857642.1 |
Set Membership: |
HapMap |