Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604914 MIM: 615262 MIM: 600813 | ||||||||||||||||||||
Literature Links: |
JMJD6 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 |
JMJD6 - arginine demethylase and lysine hydroxylase | ||||||
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There are no transcripts associated with this gene. |
METTL23 - methyltransferase like 23 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080510.4 | 850 | Missense Mutation | AGT,GGT | S,G 136 | NP_001073979.3 | |
NM_001206983.2 | 850 | Missense Mutation | AGT,GGT | S,G 136 | NP_001193912.1 | |
NM_001206984.2 | 850 | Missense Mutation | AGT,GGT | S,G 136 | NP_001193913.1 | |
NM_001206985.2 | 850 | Missense Mutation | AGT,GGT | S,G 69 | NP_001193914.1 | |
NM_001206986.2 | 850 | Missense Mutation | AGT,GGT | S,G 69 | NP_001193915.1 | |
NM_001206987.2 | 850 | Missense Mutation | AGT,GGT | S,G 69 | NP_001193916.1 | |
NM_001302703.1 | 850 | Missense Mutation | AGT,GGT | S,G 136 | NP_001289632.1 | |
NM_001302704.1 | 850 | Missense Mutation | AGT,GGT | S,G 69 | NP_001289633.1 | |
NM_001302705.1 | 850 | Missense Mutation | AGT,GGT | S,G 132 | NP_001289634.1 | |
XM_006721674.3 | 850 | Missense Mutation | AGT,GGT | S,G 136 | XP_006721737.1 | |
XM_006721675.1 | 850 | Missense Mutation | AGT,GGT | S,G 132 | XP_006721738.1 | |
XM_006721676.3 | 850 | Missense Mutation | AGT,GGT | S,G 132 | XP_006721739.1 | |
XM_006721678.3 | 850 | Missense Mutation | AGT,GGT | S,G 132 | XP_006721741.1 | |
XM_006721679.3 | 850 | Missense Mutation | AGT,GGT | S,G 125 | XP_006721742.1 | |
XM_006721680.2 | 850 | Missense Mutation | AGT,GGT | S,G 69 | XP_006721743.1 | |
XM_011524282.1 | 850 | Missense Mutation | AGT,GGT | S,G 132 | XP_011522584.1 | |
XM_017024145.1 | 850 | Missense Mutation | AGG,GGG | R,G 132 | XP_016879634.1 | |
XM_017024146.1 | 850 | Missense Mutation | AGT,GGT | S,G 160 | XP_016879635.1 |
MFSD11 - major facilitator superfamily domain containing 11 | ||||||
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There are no transcripts associated with this gene. |
MIR636 - microRNA 636 | ||||||
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There are no transcripts associated with this gene. |
SRSF2 - serine and arginine rich splicing factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195427.1 | 850 | Intron | NP_001182356.1 | |||
NM_003016.4 | 850 | Intron | NP_003007.2 | |||
XM_017024942.1 | 850 | Intron | XP_016880431.1 |