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Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615944 MIM: 602044 | ||||||||||||||||||||
Literature Links: |
C2CD3 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 |
C2CD3 - C2 calcium dependent domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286577.1 | Intron | NP_001273506.1 | ||||
NM_015531.5 | Intron | NP_056346.3 | ||||
XM_011544904.1 | Intron | XP_011543206.1 | ||||
XM_011544905.1 | Intron | XP_011543207.1 | ||||
XM_017017510.1 | Intron | XP_016872999.1 | ||||
XM_017017511.1 | Intron | XP_016873000.1 | ||||
XM_017017512.1 | Intron | XP_016873001.1 | ||||
XM_017017513.1 | Intron | XP_016873002.1 | ||||
XM_017017514.1 | Intron | XP_016873003.1 | ||||
XM_017017515.1 | Intron | XP_016873004.1 | ||||
XM_017017516.1 | Intron | XP_016873005.1 |
UCP3 - uncoupling protein 3 | ||||||
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There are no transcripts associated with this gene. |