Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCATCTCTACTGCATTGCGGCTGCC[A/G]TGGTTGTAGTGACTTACCCCGTGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616234 | ||||||||||||||||||||
Literature Links: |
MFSD2B 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 |
MFSD2B - major facilitator superfamily domain containing 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080473.1 | 1877 | Missense Mutation | ATG,GTG | M,V 237 | NP_001073942.1 | |
XM_005264301.4 | 1877 | Missense Mutation | ATG,GTG | M,V 237 | XP_005264358.1 | |
XM_017004063.1 | 1877 | Missense Mutation | ATG,GTG | M,V 268 | XP_016859552.1 | |
XM_017004064.1 | 1877 | Missense Mutation | ATG,GTG | M,V 268 | XP_016859553.1 | |
XM_017004065.1 | 1877 | Missense Mutation | ATG,GTG | M,V 268 | XP_016859554.1 | |
XM_017004066.1 | 1877 | Missense Mutation | ATG,GTG | M,V 268 | XP_016859555.1 | |
XM_017004067.1 | 1877 | Missense Mutation | ATG,GTG | M,V 268 | XP_016859556.1 | |
XM_017004068.1 | 1877 | Missense Mutation | ATG,GTG | M,V 268 | XP_016859557.1 | |
XM_017004069.1 | 1877 | Intron | XP_016859558.1 | |||
XM_017004070.1 | 1877 | Intron | XP_016859559.1 |
WDCP - WD repeat and coiled coil containing | ||||||
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There are no transcripts associated with this gene. |