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CAGCAGTAGGAGGCCCCCCAGGGTG[A/C]TGCCTACAATGATCCAGATGGGGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613539 MIM: 604789 | ||||||||||||||||||||
Literature Links: |
FEM1B 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 |
FEM1B - fem-1 homolog B | ||||||
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There are no transcripts associated with this gene. |
ITGA11 - integrin subunit alpha 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001004439.1 | 3530 | Missense Mutation | AGC,ATC | S,I 1148 | NP_001004439.1 | |
XM_005254228.3 | 3530 | Missense Mutation | AGC,ATC | S,I 1046 | XP_005254285.1 | |
XM_011521363.2 | 3530 | Missense Mutation | AGC,ATC | S,I 1079 | XP_011519665.1 |