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Search Thermo Fisher Scientific
TCCTGCAGTCTGTCCAGTCTCAGGA[A/G]CTAGAAATACAGCAAGGAAGAATAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 126110 MIM: 601105 | ||||||||||||||||||||
Literature Links: |
ARNT 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 |
ARNT - aryl hydrocarbon receptor nuclear translocator | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001197325.1 | 2145 | Missense Mutation | GCT,GTT | A,V 689 | NP_001184254.1 | |
NM_001286035.1 | 2145 | Missense Mutation | GCT,GTT | A,V 691 | NP_001272964.1 | |
NM_001286036.1 | 2145 | Missense Mutation | GCT,GTT | A,V 703 | NP_001272965.1 | |
NM_001668.3 | 2145 | Missense Mutation | GCT,GTT | A,V 705 | NP_001659.1 | |
NM_178427.2 | 2145 | Missense Mutation | GCT,GTT | A,V 690 | NP_848514.1 | |
XM_005245151.1 | 2145 | Missense Mutation | GCT,GTT | A,V 704 | XP_005245208.1 | |
XM_005245153.1 | 2145 | Missense Mutation | GCT,GTT | A,V 700 | XP_005245210.1 | |
XM_005245154.3 | 2145 | Missense Mutation | GCT,GTT | A,V 696 | XP_005245211.1 | |
XM_005245157.1 | 2145 | Missense Mutation | GCT,GTT | A,V 668 | XP_005245214.1 | |
XM_011509542.2 | 2145 | Missense Mutation | GCT,GTT | A,V 704 | XP_011507844.1 | |
XM_011509543.2 | 2145 | Missense Mutation | GCT,GTT | A,V 704 | XP_011507845.1 | |
XM_011509544.2 | 2145 | Missense Mutation | GCT,GTT | A,V 703 | XP_011507846.1 | |
XM_011509545.2 | 2145 | Missense Mutation | GCT,GTT | A,V 689 | XP_011507847.1 | |
XM_011509546.1 | 2145 | Missense Mutation | GCT,GTT | A,V 673 | XP_011507848.1 | |
XM_011509547.2 | 2145 | Missense Mutation | GCT,GTT | A,V 688 | XP_011507849.1 | |
XM_017001288.1 | 2145 | Missense Mutation | GCT,GTT | A,V 695 | XP_016856777.1 | |
XM_017001289.1 | 2145 | Missense Mutation | GCT,GTT | A,V 691 | XP_016856778.1 | |
XM_017001290.1 | 2145 | Missense Mutation | GCT,GTT | A,V 681 | XP_016856779.1 | |
XM_017001291.1 | 2145 | Missense Mutation | GCT,GTT | A,V 680 | XP_016856780.1 | |
XM_017001292.1 | 2145 | Missense Mutation | GCT,GTT | A,V 659 | XP_016856781.1 | |
XM_017001293.1 | 2145 | Missense Mutation | GCT,GTT | A,V 643 | XP_016856782.1 | |
XM_017001294.1 | 2145 | Missense Mutation | GCT,GTT | A,V 667 | XP_016856783.1 | |
XM_017001295.1 | 2145 | Missense Mutation | GCT,GTT | A,V 663 | XP_016856784.1 | |
XM_017001296.1 | 2145 | Missense Mutation | GCT,GTT | A,V 653 | XP_016856785.1 |
CTSK - cathepsin K | ||||||
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There are no transcripts associated with this gene. |