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See other HLCS GT Assays ›
SNP ID:
rs151042283
Gene
HLCS SIM2
Gene Name
Set Membership:
-
Chromosome Location:
Chr.21: 36752390 - 36752390 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

CAAAACATAGCATGTTTTTCATTAA[A/G]TAACCCCCAAAGAAATTCAAAAAGT

Assay ID C_167601312_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 609018 MIM: 600892

Literature Links:

 HLCS PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.00)
(1.00)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
G (0.00)
(1.00)
African American - Not Available YRI (Yoruba) - Not Available
SAS
G (0.00)
(1.00)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
G (0.00)
(1.00)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
G (0.00)
(1.00)
AMR
G (0.00)
(1.00)
HLCS - holocarboxylase synthetase
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_000411.6 4353 UTR 3 NP_000402.3
NM_001242784.1 4353 UTR 3 NP_001229713.1
NM_001242785.1 4353 UTR 3 NP_001229714.1
XM_005260953.3 4353 UTR 3 XP_005261010.1
XM_005260955.3 4353 UTR 3 XP_005261012.1
XM_005260956.3 4353 UTR 3 XP_005261013.1
XM_006723994.2 4353 UTR 3 XP_006724057.1
XM_006723995.1 4353 UTR 3 XP_006724058.1
XM_011529538.1 4353 UTR 3 XP_011527840.1
XM_011529539.2 4353 UTR 3 XP_011527841.1
XM_011529540.2 4353 Intron XP_011527842.1
XM_011529541.2 4353 UTR 3 XP_011527843.1
XM_017028330.1 4353 UTR 3 XP_016883819.1
SIM2 - single-minded family bHLH transcription factor 2
There are no transcripts associated with this gene.

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