Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTTACCTGGGTGTGCACCTGCTCCG[C/G]GGGGTGGAGGTGCTCCCCACAGTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609899 MIM: 614578 MIM: 602474 | ||||||||||||||||||||
Literature Links: |
KREMEN2 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 |
KREMEN2 - kringle containing transmembrane protein 2 | ||||||
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There are no transcripts associated with this gene. |
PAQR4 - progestin and adipoQ receptor family member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284511.1 | 2261 | UTR 3 | NP_001271440.1 | |||
NM_001284512.1 | 2261 | UTR 3 | NP_001271441.1 | |||
NM_001284513.1 | 2261 | UTR 3 | NP_001271442.1 | |||
NM_001324118.1 | 2261 | UTR 3 | NP_001311047.1 | |||
NM_152341.4 | 2261 | UTR 3 | NP_689554.2 |
PKMYT1 - protein kinase, membrane associated tyrosine/threonine 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258450.1 | 2261 | Silent Mutation | CCC,CCG | P,P 387 | NP_001245379.1 | |
NM_001258451.1 | 2261 | Silent Mutation | CCC,CCG | P,P 447 | NP_001245380.1 | |
NM_004203.4 | 2261 | Silent Mutation | CCC,CCG | P,P 456 | NP_004194.3 | |
NM_182687.2 | 2261 | Missense Mutation | CCC,CGC | P,R 469 | NP_872629.1 | |
XM_011522734.2 | 2261 | Silent Mutation | CCC,CCG | P,P 456 | XP_011521036.1 | |
XM_011522735.2 | 2261 | Silent Mutation | CCC,CCG | P,P 447 | XP_011521037.1 | |
XM_011522736.2 | 2261 | Silent Mutation | CCC,CCG | P,P 447 | XP_011521038.1 |