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GGTCAGCAGGAGATCCTGCCAAGGT[A/C]TCTTTTCTGATGGGGCTCACAACAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606421 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ELMO2 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) - Not Available | |||
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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ELMO2 - engulfment and cell motility 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318253.1 | Intron | NP_001305182.1 | ||||
NM_133171.4 | Intron | NP_573403.1 | ||||
NM_182764.2 | Intron | NP_877496.1 | ||||
XM_005260496.3 | Intron | XP_005260553.1 | ||||
XM_005260498.3 | Intron | XP_005260555.1 | ||||
XM_005260499.3 | Intron | XP_005260556.1 | ||||
XM_005260500.3 | Intron | XP_005260557.1 | ||||
XM_005260501.4 | Intron | XP_005260558.1 | ||||
XM_006723854.3 | Intron | XP_006723917.1 | ||||
XM_017028009.1 | Intron | XP_016883498.1 | ||||
XM_017028010.1 | Intron | XP_016883499.1 | ||||
XM_017028011.1 | Intron | XP_016883500.1 |
SLC35C2 - solute carrier family 35 member C2 | ||||||
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There are no transcripts associated with this gene. |