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CCACTTTCGTCGCTCTCCACAGTCA[C/G]CTGCCGGGTCCACCACTTCTTAACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611549 | ||||||||||||||||||||
Literature Links: |
NALCN 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 |
NALCN - sodium leak channel, non-selective | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_052867.2 | 4500 | Missense Mutation | CTG,GTG | L,V 1724 | NP_443099.1 | |
XM_011521067.2 | 4500 | Missense Mutation | CTG,GTG | L,V 1743 | XP_011519369.1 | |
XM_011521068.2 | 4500 | Missense Mutation | CTG,GTG | L,V 1724 | XP_011519370.1 | |
XM_011521069.2 | 4500 | Missense Mutation | CTG,GTG | L,V 1714 | XP_011519371.1 | |
XM_017020534.1 | 4500 | Missense Mutation | CTG,GTG | L,V 1695 | XP_016876023.1 | |
XM_017020535.1 | 4500 | Missense Mutation | CTG,GTG | L,V 1695 | XP_016876024.1 | |
XM_017020536.1 | 4500 | Missense Mutation | CTG,GTG | L,V 1575 | XP_016876025.1 | |
XM_017020537.1 | 4500 | Missense Mutation | CTG,GTG | L,V 1469 | XP_016876026.1 |
NALCN-AS1 - NALCN antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |