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AAGTTTTAAATTTTATGCTAAAACT[C/T]GTATTTTATGTTTTGTAAGATGGAT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615359 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101927391 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)
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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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LOC101927391 - uncharacterized LOC101927391 | ||||||
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There are no transcripts associated with this gene. |
MIOS - meiosis regulator for oocyte development | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019005.3 | Intron | NP_061878.3 | ||||
XM_005249780.3 | Intron | XP_005249837.1 | ||||
XM_005249781.3 | Intron | XP_005249838.1 | ||||
XM_005249782.3 | Intron | XP_005249839.1 | ||||
XM_005249784.3 | Intron | XP_005249841.1 | ||||
XM_011515432.2 | Intron | XP_011513734.1 | ||||
XM_017012361.1 | Intron | XP_016867850.1 | ||||
XM_017012362.1 | Intron | XP_016867851.1 |