Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCAGGCCAGGTTGCACCCGGGAA[A/G]CCTGCCAGAAAAAGAGAAAGTCTGA
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 - 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 |
DMKN - dermokine | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001035516.3 | 684 | Missense Mutation | GCT,GTT | A,V 76 | NP_001030593.1 | |
NM_001126056.2 | 684 | Missense Mutation | GCT,GTT | A,V 451 | NP_001119528.2 | |
NM_001126057.2 | 684 | Intron | NP_001119529.2 | |||
NM_001126058.2 | 684 | Intron | NP_001119530.2 | |||
NM_001126059.2 | 684 | Missense Mutation | GCT,GTT | A,V 175 | NP_001119531.1 | |
NM_001190347.1 | 684 | Missense Mutation | GCT,GTT | A,V 435 | NP_001177276.1 | |
NM_001190348.1 | 684 | Intron | NP_001177277.1 | |||
NM_001190349.1 | 684 | Intron | NP_001177278.1 | |||
NM_001308380.1 | 684 | Missense Mutation | GCT,GTT | A,V 189 | NP_001295309.1 | |
NM_001308383.1 | 684 | Missense Mutation | GCT,GTT | A,V 158 | NP_001295312.1 | |
NM_033317.4 | 684 | Missense Mutation | GCT,GTT | A,V 462 | NP_201574.3 | |
XM_006723477.1 | 684 | Missense Mutation | GCT,GTT | A,V 239 | XP_006723540.1 | |
XM_006723484.1 | 684 | Missense Mutation | GCT,GTT | A,V 209 | XP_006723547.1 | |
XM_006723489.1 | 684 | Missense Mutation | GCT,GTT | A,V 170 | XP_006723552.1 | |
XM_006723493.2 | 684 | Missense Mutation | GCT,GTT | A,V 138 | XP_006723556.1 | |
XM_006723494.2 | 684 | Missense Mutation | GCT,GTT | A,V 132 | XP_006723557.1 | |
XM_006723503.2 | 684 | Missense Mutation | GCT,GTT | A,V 170 | XP_006723566.1 | |
XM_011527494.2 | 684 | Missense Mutation | GCT,GTT | A,V 524 | XP_011525796.1 | |
XM_011527495.2 | 684 | Missense Mutation | GCT,GTT | A,V 524 | XP_011525797.1 | |
XM_011527496.2 | 684 | Missense Mutation | GCT,GTT | A,V 512 | XP_011525798.1 | |
XM_011527497.2 | 684 | Missense Mutation | GCT,GTT | A,V 510 | XP_011525799.1 | |
XM_011527498.2 | 684 | Missense Mutation | GCT,GTT | A,V 510 | XP_011525800.1 | |
XM_011527499.2 | 684 | Missense Mutation | GCT,GTT | A,V 509 | XP_011525801.1 | |
XM_011527500.2 | 684 | Missense Mutation | GCT,GTT | A,V 506 | XP_011525802.1 | |
XM_011527501.2 | 684 | Missense Mutation | GCT,GTT | A,V 504 | XP_011525803.1 | |
XM_011527502.2 | 684 | Missense Mutation | GCT,GTT | A,V 494 | XP_011525804.1 | |
XM_011527503.2 | 684 | Missense Mutation | GCT,GTT | A,V 492 | XP_011525805.1 | |
XM_011527504.2 | 684 | Missense Mutation | GCT,GTT | A,V 486 | XP_011525806.1 | |
XM_011527505.2 | 684 | Missense Mutation | GCT,GTT | A,V 477 | XP_011525807.1 | |
XM_011527506.2 | 684 | Missense Mutation | GCT,GTT | A,V 474 | XP_011525808.1 | |
XM_011527507.2 | 684 | Missense Mutation | GCT,GTT | A,V 462 | XP_011525809.1 | |
XM_011527508.2 | 684 | Missense Mutation | GCT,GTT | A,V 457 | XP_011525810.1 | |
XM_011527509.2 | 684 | Missense Mutation | GCT,GTT | A,V 443 | XP_011525811.1 | |
XM_011527510.2 | 684 | Missense Mutation | GCT,GTT | A,V 442 | XP_011525812.1 | |
XM_011527511.2 | 684 | Intron | XP_011525813.1 | |||
XM_011527512.2 | 684 | Intron | XP_011525814.1 | |||
XM_011527513.1 | 684 | Missense Mutation | GCT,GTT | A,V 192 | XP_011525815.1 | |
XM_011527514.1 | 684 | Missense Mutation | GCT,GTT | A,V 172 | XP_011525816.1 | |
XM_017027475.1 | 684 | Missense Mutation | GCT,GTT | A,V 207 | XP_016882964.1 | |
XM_017027476.1 | 684 | Missense Mutation | GCT,GTT | A,V 170 | XP_016882965.1 | |
XM_017027477.1 | 684 | Missense Mutation | GCT,GTT | A,V 123 | XP_016882966.1 |
KRTDAP - keratinocyte differentiation associated protein | ||||||
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There are no transcripts associated with this gene. |