Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGTCCTGCAGGATGGAGCCAGCAC[C/G]CTCAGAGGTTCGACTCGCCGTCCGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613442 MIM: 611140 | ||||||||||||||||||||
Literature Links: |
PTX4 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 |
PTX4 - pentraxin 4 | ||||||
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There are no transcripts associated with this gene. |
TELO2 - telomere maintenance 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016111.3 | 364 | Missense Mutation | CCC,CGC | P,R 5 | NP_057195.2 | |
XM_011522773.2 | 364 | Missense Mutation | CCC,CGC | P,R 5 | XP_011521075.1 | |
XM_011522774.2 | 364 | Missense Mutation | CCC,CGC | P,R 5 | XP_011521076.1 | |
XM_011522775.2 | 364 | Missense Mutation | CCC,CGC | P,R 5 | XP_011521077.1 | |
XM_011522776.2 | 364 | Missense Mutation | CCC,CGC | P,R 5 | XP_011521078.1 | |
XM_011522777.2 | 364 | Missense Mutation | CCC,CGC | P,R 5 | XP_011521079.1 | |
XM_011522778.2 | 364 | Missense Mutation | CCC,CGC | P,R 5 | XP_011521080.1 | |
XM_017023914.1 | 364 | Missense Mutation | CCC,CGC | P,R 5 | XP_016879403.1 |