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GCCATAGTGATAGACAAAGTCATAG[C/T]TGCTGGGCTCCTTGGGGATGGGGGG
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 |
---|---|---|
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 |
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 | 2764 | Missense Mutation | AAC,AGC | N,S 624 | NP_001305182.1 | |
NM_133171.4 | 2764 | Missense Mutation | AAC,AGC | N,S 712 | NP_573403.1 | |
NM_182764.2 | 2764 | Missense Mutation | AAC,AGC | N,S 712 | NP_877496.1 | |
XM_005260496.3 | 2764 | Missense Mutation | AAC,AGC | N,S 712 | XP_005260553.1 | |
XM_005260498.3 | 2764 | Missense Mutation | AAC,AGC | N,S 624 | XP_005260555.1 | |
XM_005260499.3 | 2764 | Missense Mutation | AAC,AGC | N,S 624 | XP_005260556.1 | |
XM_005260500.3 | 2764 | Missense Mutation | AAC,AGC | N,S 624 | XP_005260557.1 | |
XM_005260501.4 | 2764 | Missense Mutation | AAC,AGC | N,S 529 | XP_005260558.1 | |
XM_006723854.3 | 2764 | Missense Mutation | AAC,AGC | N,S 712 | XP_006723917.1 | |
XM_017028009.1 | 2764 | Missense Mutation | AAC,AGC | N,S 529 | XP_016883498.1 | |
XM_017028010.1 | 2764 | Missense Mutation | AAC,AGC | N,S 529 | XP_016883499.1 | |
XM_017028011.1 | 2764 | Missense Mutation | AAC,AGC | N,S 529 | XP_016883500.1 |
SLC35C2 - solute carrier family 35 member C2 | ||||||
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There are no transcripts associated with this gene. |