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Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605446 MIM: 605012 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RPGRIP1 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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RPGRIP1 - retinitis pigmentosa GTPase regulator interacting protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020366.3 | Intron | NP_065099.3 | ||||
XM_005267879.2 | Intron | XP_005267936.1 | ||||
XM_005267880.2 | Intron | XP_005267937.1 | ||||
XM_005267881.3 | Intron | XP_005267938.1 | ||||
XM_011536978.1 | Intron | XP_011535280.1 | ||||
XM_011536979.1 | Intron | XP_011535281.1 | ||||
XM_011536980.1 | Intron | XP_011535282.1 | ||||
XM_011536981.1 | Intron | XP_011535283.1 | ||||
XM_011536982.1 | Intron | XP_011535284.1 | ||||
XM_017021473.1 | Intron | XP_016876962.1 |
SUPT16H - SPT16 homolog, facilitates chromatin remodeling subunit | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |