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Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609377 MIM: 610859 MIM: 607484 | ||||||||||||||||||||
Literature Links: |
ACD 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 |
ACD - adrenocortical dysplasia homolog | ||||||
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There are no transcripts associated with this gene. |
C16orf86 - chromosome 16 open reading frame 86 | ||||||
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There are no transcripts associated with this gene. |
CARMIL2 - capping protein regulator and myosin 1 linker 2 | ||||||
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There are no transcripts associated with this gene. |
ENKD1 - enkurin domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
PARD6A - par-6 family cell polarity regulator alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037281.1 | Intron | NP_001032358.1 | ||||
NM_016948.2 | Intron | NP_058644.1 | ||||
XM_005255977.3 | Intron | XP_005256034.1 | ||||
XM_011523095.2 | Intron | XP_011521397.1 | ||||
XM_011523096.2 | Intron | XP_011521398.1 | ||||
XM_017023261.1 | Intron | XP_016878750.1 |