Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTTTCCAAAGACCCGTCAAGCCTT[C/T]GGTTGTTGCTATTATTCTGTACGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 610196 MIM: 113730 | ||||||||||||||||||||
Literature Links: |
ELMOD2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
ELMOD2 - ELMO domain containing 2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
UCP1 - uncoupling protein 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021833.4 | 578 | Missense Mutation | AAA,GAA | K,E 168 | NP_068605.1 | |
XM_005263206.3 | 578 | Missense Mutation | AAA,GAA | K,E 167 | XP_005263263.1 | |
XM_011532228.2 | 578 | Missense Mutation | AAA,GAA | K,E 168 | XP_011530530.1 |