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CCTAGGAGGCAGCCGGGCGTCGCCG[A/G]CCCCGGCGCCGTCACGCTCGCCCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615624 MIM: 606195 | ||||||||||||||||||||
Literature Links: |
CRNDE 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 |
CRNDE - colorectal neoplasia differentially expressed (non-protein coding) | ||||||
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There are no transcripts associated with this gene. |
IRX5 - iroquois homeobox 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252197.1 | 1578 | Missense Mutation | ACC,GCC | T,A 378 | NP_001239126.1 | |
NM_005853.5 | 1578 | Missense Mutation | ACC,GCC | T,A 379 | NP_005844.4 | |
XM_011522809.1 | 1578 | Missense Mutation | ACC,GCC | T,A 309 | XP_011521111.1 |