Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTCTCCTCACCTCCAGAAGTGTGC[A/G]GATCCTCTCCAGGTCTGGGGGCTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 314690 | ||||||||||||||||||||
Literature Links: |
KDM5C 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 |
KDM5C - lysine demethylase 5C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146702.1 | 4571 | Intron | NP_001140174.1 | |||
NM_001282622.1 | 4571 | Missense Mutation | CGC,TGC | R,C 1434 | NP_001269551.1 | |
NM_004187.3 | 4571 | Missense Mutation | CGC,TGC | R,C 1435 | NP_004178.2 | |
XM_005262035.4 | 4571 | Missense Mutation | CGC,TGC | R,C 1432 | XP_005262092.1 | |
XM_011530824.2 | 4571 | Missense Mutation | CGC,TGC | R,C 1409 | XP_011529126.1 | |
XM_011530825.2 | 4571 | Missense Mutation | CGC,TGC | R,C 1394 | XP_011529127.1 | |
XM_011530826.2 | 4571 | Missense Mutation | CGC,TGC | R,C 1391 | XP_011529128.1 | |
XM_011530827.2 | 4571 | Missense Mutation | CGC,TGC | R,C 1435 | XP_011529129.1 | |
XM_011530828.1 | 4571 | Missense Mutation | CGC,TGC | R,C 1435 | XP_011529130.1 | |
XM_011530829.2 | 4571 | Missense Mutation | CGC,TGC | R,C 1270 | XP_011529131.1 | |
XM_011530830.2 | 4571 | Missense Mutation | CGC,TGC | R,C 1270 | XP_011529132.1 | |
XM_011530831.2 | 4571 | Missense Mutation | CGC,TGC | R,C 1107 | XP_011529133.1 | |
XM_017029886.1 | 4571 | Missense Mutation | CGC,TGC | R,C 1434 | XP_016885375.1 | |
XM_017029887.1 | 4571 | Missense Mutation | CGC,TGC | R,C 1432 | XP_016885376.1 | |
XM_017029888.1 | 4571 | Missense Mutation | CGC,TGC | R,C 1431 | XP_016885377.1 | |
XM_017029889.1 | 4571 | Missense Mutation | CGC,TGC | R,C 1432 | XP_016885378.1 |
MIR6894 - microRNA 6894 | ||||||
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There are no transcripts associated with this gene. |
MIR6895 - microRNA 6895 | ||||||
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There are no transcripts associated with this gene. |