Product Details

SNP ID
rs2377029
Assay Type
Functionally Tested
NCBI dbSNP Submissions
39
Location
Chr.1:226231465 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATTTGAAAAAAATTTATATTTTGA[C/G]TTTATAATATTCTATTAAAACGAAG
Phenotype
MIM: 609375 MIM: 609852
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
LIN9 PubMed Links

Gene Details

Gene
LIN9
Gene Name
lin-9 DREAM MuvB core complex component
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001270409.1 2684 UTR 3 NP_001257338.1
NM_001270410.1 2684 UTR 3 NP_001257339.1
NM_173083.3 2684 UTR 3 NP_775106.2
XM_005273102.3 2684 UTR 3 XP_005273159.1
XM_006711766.2 2684 UTR 3 XP_006711829.2
XM_006711767.3 2684 UTR 3 XP_006711830.1
XM_011544173.2 2684 Intron XP_011542475.1
XM_017001084.1 2684 UTR 3 XP_016856573.1
Gene
MIXL1
Gene Name
Mix paired-like homeobox
There are no transcripts associated with this gene.

View Full Product Details