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Search Thermo Fisher Scientific
ACCGAGGAAGAAGGTGAGACTCCCC[C/G]CTGCAAAAAGATCAAAGGAAAGTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DMKN PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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DMKN - dermokine | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001035516.3 | 659 | Missense Mutation | CGG,GGG | R,G 68 | NP_001030593.1 | |
NM_001126056.2 | 659 | Missense Mutation | CGG,GGG | R,G 443 | NP_001119528.2 | |
NM_001126057.2 | 659 | Intron | NP_001119529.2 | |||
NM_001126058.2 | 659 | Intron | NP_001119530.2 | |||
NM_001126059.2 | 659 | Missense Mutation | CGG,GGG | R,G 167 | NP_001119531.1 | |
NM_001190347.1 | 659 | Missense Mutation | CGG,GGG | R,G 427 | NP_001177276.1 | |
NM_001190348.1 | 659 | Intron | NP_001177277.1 | |||
NM_001190349.1 | 659 | Intron | NP_001177278.1 | |||
NM_001308380.1 | 659 | Missense Mutation | CGG,GGG | R,G 181 | NP_001295309.1 | |
NM_001308383.1 | 659 | Missense Mutation | CGG,GGG | R,G 150 | NP_001295312.1 | |
NM_033317.4 | 659 | Missense Mutation | CGG,GGG | R,G 454 | NP_201574.3 | |
XM_006723477.1 | 659 | Missense Mutation | CGG,GGG | R,G 231 | XP_006723540.1 | |
XM_006723484.1 | 659 | Missense Mutation | CGG,GGG | R,G 201 | XP_006723547.1 | |
XM_006723489.1 | 659 | Missense Mutation | CGG,GGG | R,G 162 | XP_006723552.1 | |
XM_006723493.2 | 659 | Missense Mutation | CGG,GGG | R,G 130 | XP_006723556.1 | |
XM_006723494.2 | 659 | Missense Mutation | CGG,GGG | R,G 124 | XP_006723557.1 | |
XM_006723503.2 | 659 | Missense Mutation | CGG,GGG | R,G 162 | XP_006723566.1 | |
XM_011527494.2 | 659 | Missense Mutation | CGG,GGG | R,G 516 | XP_011525796.1 | |
XM_011527495.2 | 659 | Missense Mutation | CGG,GGG | R,G 516 | XP_011525797.1 | |
XM_011527496.2 | 659 | Missense Mutation | CGG,GGG | R,G 504 | XP_011525798.1 | |
XM_011527497.2 | 659 | Missense Mutation | CGG,GGG | R,G 502 | XP_011525799.1 | |
XM_011527498.2 | 659 | Missense Mutation | CGG,GGG | R,G 502 | XP_011525800.1 | |
XM_011527499.2 | 659 | Missense Mutation | CGG,GGG | R,G 501 | XP_011525801.1 | |
XM_011527500.2 | 659 | Missense Mutation | CGG,GGG | R,G 498 | XP_011525802.1 | |
XM_011527501.2 | 659 | Missense Mutation | CGG,GGG | R,G 496 | XP_011525803.1 | |
XM_011527502.2 | 659 | Missense Mutation | CGG,GGG | R,G 486 | XP_011525804.1 | |
XM_011527503.2 | 659 | Missense Mutation | CGG,GGG | R,G 484 | XP_011525805.1 | |
XM_011527504.2 | 659 | Missense Mutation | CGG,GGG | R,G 478 | XP_011525806.1 | |
XM_011527505.2 | 659 | Missense Mutation | CGG,GGG | R,G 469 | XP_011525807.1 | |
XM_011527506.2 | 659 | Missense Mutation | CGG,GGG | R,G 466 | XP_011525808.1 | |
XM_011527507.2 | 659 | Missense Mutation | CGG,GGG | R,G 454 | XP_011525809.1 | |
XM_011527508.2 | 659 | Missense Mutation | CGG,GGG | R,G 449 | XP_011525810.1 | |
XM_011527509.2 | 659 | Missense Mutation | CGG,GGG | R,G 435 | XP_011525811.1 | |
XM_011527510.2 | 659 | Missense Mutation | CGG,GGG | R,G 434 | XP_011525812.1 | |
XM_011527511.2 | 659 | Intron | XP_011525813.1 | |||
XM_011527512.2 | 659 | Intron | XP_011525814.1 | |||
XM_011527513.1 | 659 | Missense Mutation | CGG,GGG | R,G 184 | XP_011525815.1 | |
XM_011527514.1 | 659 | Missense Mutation | CGG,GGG | R,G 164 | XP_011525816.1 | |
XM_017027475.1 | 659 | Missense Mutation | CGG,GGG | R,G 199 | XP_016882964.1 | |
XM_017027476.1 | 659 | Missense Mutation | CGG,GGG | R,G 162 | XP_016882965.1 | |
XM_017027477.1 | 659 | Missense Mutation | CGG,GGG | R,G 115 | XP_016882966.1 |
KRTDAP - keratinocyte differentiation associated protein | ||||||
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There are no transcripts associated with this gene. |