Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 605908 MIM: 605794 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MLC1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | JPT (Japanese)
|
||||||
AFR
|
Japanese - Not Available | CHB (Han Chinese)
|
||||||
EUR
|
||||||||
AMR
|
MLC1 - megalencephalic leukoencephalopathy with subcortical cysts 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
MOV10L1 - Mov10 RISC complex RNA helicase like 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164104.1 | 252 | Missense Mutation | ATG,TTG | M,L 57 | NP_001157576.1 | |
NM_001164105.1 | 252 | Missense Mutation | ATG,TTG | M,L 37 | NP_001157577.1 | |
NM_001164106.1 | 252 | Intron | NP_001157578.1 | |||
NM_018995.2 | 252 | Missense Mutation | ATG,TTG | M,L 57 | NP_061868.1 | |
XM_005261923.3 | 252 | Missense Mutation | ATG,TTG | M,L 37 | XP_005261980.1 | |
XM_011530696.1 | 252 | Missense Mutation | ATG,TTG | M,L 57 | XP_011528998.1 | |
XM_011530697.1 | 252 | Missense Mutation | ATG,TTG | M,L 37 | XP_011528999.1 | |
XM_011530698.1 | 252 | Missense Mutation | ATG,TTG | M,L 57 | XP_011529000.1 | |
XM_011530699.1 | 252 | Missense Mutation | ATG,TTG | M,L 5 | XP_011529001.1 | |
XM_011530700.2 | 252 | Missense Mutation | ATG,TTG | M,L 5 | XP_011529002.1 | |
XM_011530701.1 | 252 | Missense Mutation | ATG,TTG | M,L 57 | XP_011529003.1 | |
XM_011530702.1 | 252 | UTR 5 | XP_011529004.1 | |||
XM_011530703.1 | 252 | Intron | XP_011529005.1 | |||
XM_011530704.1 | 252 | Missense Mutation | ATG,TTG | M,L 57 | XP_011529006.1 | |
XM_017028833.1 | 252 | Missense Mutation | ATG,TTG | M,L 57 | XP_016884322.1 | |
XM_017028834.1 | 252 | Missense Mutation | ATG,TTG | M,L 57 | XP_016884323.1 | |
XM_017028835.1 | 252 | Intron | XP_016884324.1 | |||
XM_017028836.1 | 252 | Intron | XP_016884325.1 | |||
XM_017028837.1 | 252 | Missense Mutation | ATG,TTG | M,L 57 | XP_016884326.1 |