Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610886 MIM: 605431 MIM: 611994 MIM: 601817 MIM: 611659 | ||||||||||||||||||||
Literature Links: |
EME2 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 |
EME2 - essential meiotic structure-specific endonuclease subunit 2 | ||||||
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There are no transcripts associated with this gene. |
MAPK8IP3 - mitogen-activated protein kinase 8 interacting protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040439.1 | 653 | Intron | NP_001035529.1 | |||
NM_001318852.1 | 653 | Intron | NP_001305781.1 | |||
NM_015133.4 | 653 | Intron | NP_055948.2 | |||
XM_005255190.2 | 653 | Intron | XP_005255247.1 | |||
XM_006720869.2 | 653 | Intron | XP_006720932.1 | |||
XM_011522429.2 | 653 | Intron | XP_011520731.1 | |||
XM_011522430.2 | 653 | Intron | XP_011520732.1 | |||
XM_011522431.2 | 653 | Intron | XP_011520733.1 | |||
XM_011522432.2 | 653 | Intron | XP_011520734.1 | |||
XM_011522433.2 | 653 | Intron | XP_011520735.1 | |||
XM_017023079.1 | 653 | Intron | XP_016878568.1 | |||
XM_017023080.1 | 653 | Intron | XP_016878569.1 | |||
XM_017023081.1 | 653 | Intron | XP_016878570.1 |
MRPS34 - mitochondrial ribosomal protein S34 | ||||||
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There are no transcripts associated with this gene. |
NME3 - NME/NM23 nucleoside diphosphate kinase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002513.2 | 653 | Missense Mutation | CAC,CGC | H,R 144 | NP_002504.2 | |
XM_005255332.4 | 653 | Silent Mutation | CCA,CCG | P,P 141 | XP_005255389.1 | |
XM_011522503.2 | 653 | Missense Mutation | CAC,CGC | H,R 145 | XP_011520805.1 | |
XM_011522504.2 | 653 | UTR 3 | XP_011520806.1 |
SPSB3 - splA/ryanodine receptor domain and SOCS box containing 3 | ||||||
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There are no transcripts associated with this gene. |