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TTGCCATCAATAATTTAAATAGTAT[A/G]GCCTTGAAAAATAAAAATTGTGAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
MIM: 604425 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LHX8 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
LHX8 - LIM homeobox 8 | ||||||
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There are no transcripts associated with this gene. |
SLC44A5 - solute carrier family 44 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130058.1 | 4681 | Intron | NP_001123530.1 | |||
NM_001320283.1 | 4681 | Intron | NP_001307212.1 | |||
NM_001320285.1 | 4681 | Intron | NP_001307214.1 | |||
NM_001320287.1 | 4681 | Intron | NP_001307216.1 | |||
NM_152697.4 | 4681 | Intron | NP_689910.2 | |||
XM_006710445.3 | 4681 | UTR 3 | XP_006710508.1 | |||
XM_011540986.2 | 4681 | UTR 3 | XP_011539288.1 | |||
XM_011540987.2 | 4681 | UTR 3 | XP_011539289.1 | |||
XM_017000607.1 | 4681 | UTR 3 | XP_016856096.1 | |||
XM_017000608.1 | 4681 | Intron | XP_016856097.1 | |||
XM_017000609.1 | 4681 | UTR 3 | XP_016856098.1 | |||
XM_017000610.1 | 4681 | UTR 3 | XP_016856099.1 | |||
XM_017000611.1 | 4681 | UTR 3 | XP_016856100.1 |