Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGATGGGGACCTGCCAGTCCTCTTG[A/C]TTGGAGATCTCAAACACGATCTGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 613539 MIM: 604789 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FEM1B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
FEM1B - fem-1 homolog B | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
ITGA11 - integrin subunit alpha 11 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001004439.1 | 3489 | Missense Mutation | AAG,AAT | K,N 1134 | NP_001004439.1 | |
XM_005254228.3 | 3489 | Missense Mutation | AAG,AAT | K,N 1032 | XP_005254285.1 | |
XM_011521363.2 | 3489 | Missense Mutation | AAG,AAT | K,N 1065 | XP_011519665.1 |