Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611203 MIM: 610866 | ||||||||||||||||||||
Literature Links: |
DNAJC5 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 |
DNAJC5 - DnaJ heat shock protein family (Hsp40) member C5 | ||||||
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There are no transcripts associated with this gene. |
MIR1914 - microRNA 1914 | ||||||
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There are no transcripts associated with this gene. |
MIR647 - microRNA 647 | ||||||
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There are no transcripts associated with this gene. |
UCKL1 - uridine-cytidine kinase 1 like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193379.1 | 1548 | Missense Mutation | CTC,TTC | L,F 408 | NP_001180308.1 | |
NM_017859.3 | 1548 | Missense Mutation | CTC,TTC | L,F 423 | NP_060329.2 | |
XM_005260216.2 | 1548 | Missense Mutation | CTC,TTC | L,F 431 | XP_005260273.1 | |
XM_006723806.2 | 1548 | Missense Mutation | CTC,TTC | L,F 433 | XP_006723869.1 | |
XM_006723807.2 | 1548 | Missense Mutation | CTC,TTC | L,F 432 | XP_006723870.1 | |
XM_006723808.1 | 1548 | Missense Mutation | CTC,TTC | L,F 432 | XP_006723871.1 | |
XM_006723809.1 | 1548 | Missense Mutation | CTC,TTC | L,F 425 | XP_006723872.1 | |
XM_006723810.1 | 1548 | Missense Mutation | CTC,TTC | L,F 424 | XP_006723873.1 | |
XM_006723811.3 | 1548 | Missense Mutation | CTC,TTC | L,F 417 | XP_006723874.1 | |
XM_011528868.2 | 1548 | Missense Mutation | CTC,TTC | L,F 418 | XP_011527170.1 | |
XM_011528869.1 | 1548 | Missense Mutation | CTC,TTC | L,F 317 | XP_011527171.1 | |
XM_011528870.1 | 1548 | Missense Mutation | CTC,TTC | L,F 307 | XP_011527172.1 | |
XM_011528871.1 | 1548 | Missense Mutation | CTC,TTC | L,F 307 | XP_011527173.1 | |
XM_011528872.1 | 1548 | Missense Mutation | CTC,TTC | L,F 307 | XP_011527174.1 | |
XM_011528873.2 | 1548 | Intron | XP_011527175.1 | |||
XM_017027894.1 | 1548 | Intron | XP_016883383.1 | |||
XM_017027895.1 | 1548 | Intron | XP_016883384.1 | |||
XM_017027896.1 | 1548 | Missense Mutation | CTC,TTC | L,F 424 | XP_016883385.1 | |
XM_017027897.1 | 1548 | Intron | XP_016883386.1 | |||
XM_017027898.1 | 1548 | Missense Mutation | CTC,TTC | L,F 423 | XP_016883387.1 | |
XM_017027899.1 | 1548 | Missense Mutation | CTC,TTC | L,F 422 | XP_016883388.1 | |
XM_017027900.1 | 1548 | Missense Mutation | CTC,TTC | L,F 408 | XP_016883389.1 | |
XM_017027901.1 | 1548 | Missense Mutation | CTC,TTC | L,F 407 | XP_016883390.1 | |
XM_017027902.1 | 1548 | Missense Mutation | CTC,TTC | L,F 309 | XP_016883391.1 | |
XM_017027903.1 | 1548 | Missense Mutation | CTC,TTC | L,F 305 | XP_016883392.1 | |
XM_017027904.1 | 1548 | Missense Mutation | CTC,TTC | L,F 217 | XP_016883393.1 | |
XM_017027905.1 | 1548 | Missense Mutation | CTC,TTC | L,F 215 | XP_016883394.1 | |
XM_017027906.1 | 1548 | Missense Mutation | CTC,TTC | L,F 215 | XP_016883395.1 | |
XM_017027907.1 | 1548 | Missense Mutation | CTC,TTC | L,F 204 | XP_016883396.1 | |
XM_017027908.1 | 1548 | Missense Mutation | CTC,TTC | L,F 204 | XP_016883397.1 |