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GRHL2
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608576
MIM: 606722
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Literature Links: |
GRHL2 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
Global
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Caucasian
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CEPH (CEU)
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EAS
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African American
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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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| GRHL2 - grainyhead like transcription factor 2 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| NCALD - neurocalcin delta | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001040624.1 | 2160 | UTR 3 | NP_001035714.1 | |||
| NM_001040625.1 | 2160 | UTR 3 | NP_001035715.1 | |||
| NM_001040626.1 | 2160 | UTR 3 | NP_001035716.1 | |||
| NM_001040627.1 | 2160 | UTR 3 | NP_001035717.1 | |||
| NM_001040628.1 | 2160 | UTR 3 | NP_001035718.1 | |||
| NM_001040629.1 | 2160 | UTR 3 | NP_001035719.1 | |||
| NM_001040630.1 | 2160 | UTR 3 | NP_001035720.1 | |||
| NM_032041.2 | 2160 | UTR 3 | NP_114430.2 | |||
| XM_011517332.2 | 2160 | UTR 3 | XP_011515634.1 | |||
| XM_011517333.2 | 2160 | UTR 3 | XP_011515635.1 | |||
| XM_011517334.2 | 2160 | UTR 3 | XP_011515636.1 | |||
| XM_011517335.2 | 2160 | UTR 3 | XP_011515637.1 | |||
| XM_017013900.1 | 2160 | Intron | XP_016869389.1 | |||
| XM_017013901.1 | 2160 | UTR 3 | XP_016869390.1 | |||
| XM_017013902.1 | 2160 | UTR 3 | XP_016869391.1 | |||
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs28362495] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
HapMap
Validated
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Gene Ontology Categories:
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