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CCTCACCTTGCTGCTACAGTGGCTA[A/C]AGCTCCGCCTTTTGCTCTTCTTCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
10 submissions
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Phenotype: |
MIM: 610393 | ||||||||||||||||||||
Literature Links: |
GON4L 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 |
GON4L - gon-4 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282856.1 | 5751 | Missense Mutation | NP_001269785.1 | |||
NM_001282858.1 | 5751 | Missense Mutation | NP_001269787.1 | |||
NM_001282860.1 | 5751 | Missense Mutation | NP_001269789.1 | |||
NM_001282861.1 | 5751 | Intron | NP_001269790.1 | |||
NM_032292.5 | 5751 | Intron | NP_115668.4 | |||
XM_005245284.3 | 5751 | Missense Mutation | XP_005245341.1 | |||
XM_005245286.3 | 5751 | Missense Mutation | XP_005245343.1 | |||
XM_006711393.3 | 5751 | Missense Mutation | XP_006711456.1 | |||
XM_006711394.3 | 5751 | Missense Mutation | XP_006711457.1 | |||
XM_011509658.2 | 5751 | Missense Mutation | XP_011507960.1 | |||
XM_011509659.2 | 5751 | Missense Mutation | XP_011507961.1 |
LOC100505728 - uncharacterized LOC100505728 | ||||||
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There are no transcripts associated with this gene. |
MSTO2P - misato family member 2, pseudogene | ||||||
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There are no transcripts associated with this gene. |