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Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611712 MIM: 605725 | ||||||||||||||||||||||||||||||||
Literature Links: |
HIPK4 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
HIPK4 - homeodomain interacting protein kinase 4 | ||||||
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There are no transcripts associated with this gene. |
PRX - periaxin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020956.2 | 4166 | UTR 3 | NP_066007.1 | |||
NM_181882.2 | 4166 | Missense Mutation | CCG,CGG | P,R 1083 | NP_870998.2 | |
XM_011527171.2 | 4166 | Missense Mutation | CCG,CGG | P,R 1083 | XP_011525473.1 | |
XM_017027046.1 | 4166 | Missense Mutation | CCG,CGG | P,R 1049 | XP_016882535.1 | |
XM_017027047.1 | 4166 | Missense Mutation | CCG,CGG | P,R 1049 | XP_016882536.1 |