Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614661 MIM: 610844 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PATL2 PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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PATL2 - PAT1 homolog 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145112.1 | Intron | NP_001138584.1 | ||||
XM_011521336.2 | Intron | XP_011519638.2 | ||||
XM_011521337.2 | Intron | XP_011519639.2 | ||||
XM_011521338.2 | Intron | XP_011519640.1 | ||||
XM_011521339.2 | Intron | XP_011519641.1 | ||||
XM_011521340.2 | Intron | XP_011519642.1 | ||||
XM_011521341.1 | Intron | XP_011519643.1 | ||||
XM_011521342.2 | Intron | XP_011519644.1 | ||||
XM_011521343.2 | Intron | XP_011519645.1 | ||||
XM_011521344.2 | Intron | XP_011519646.1 | ||||
XM_011521345.2 | Intron | XP_011519647.1 | ||||
XM_011521346.2 | Intron | XP_011519648.2 | ||||
XM_011521347.1 | Intron | XP_011519649.1 | ||||
XM_011521348.2 | Intron | XP_011519650.1 | ||||
XM_017022000.1 | Intron | XP_016877489.1 | ||||
XM_017022001.1 | Intron | XP_016877490.1 |
SPG11 - spastic paraplegia 11 (autosomal recessive) | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |