Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCTCTCTCGATCCTCTTTGTTATA[C/G]TCCATGGCTGAGGGCCCGCGGCTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 611368 | ||||||||||||||||||||
Literature Links: |
ILDR2 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 |
ILDR2 - immunoglobulin like domain containing receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_199351.2 | 1023 | Missense Mutation | GAC,GAG | D,E 392 | NP_955383.1 | |
XM_006711314.3 | 1023 | Missense Mutation | GAC,GAG | D,E 84 | XP_006711377.1 | |
XM_017001252.1 | 1023 | Missense Mutation | GAC,GAG | D,E 407 | XP_016856741.1 | |
XM_017001253.1 | 1023 | Missense Mutation | GAC,GAG | D,E 399 | XP_016856742.1 | |
XM_017001254.1 | 1023 | Missense Mutation | GAC,GAG | D,E 388 | XP_016856743.1 | |
XM_017001255.1 | 1023 | Missense Mutation | GAC,GAG | D,E 348 | XP_016856744.1 | |
XM_017001256.1 | 1023 | Missense Mutation | GAC,GAG | D,E 280 | XP_016856745.1 | |
XM_017001257.1 | 1023 | Missense Mutation | GAC,GAG | D,E 407 | XP_016856746.1 | |
XM_017001258.1 | 1023 | Intron | XP_016856747.1 |
MAEL - maelstrom spermatogenic transposon silencer | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286377.1 | 1023 | Intron | NP_001273306.1 | |||
NM_001286378.1 | 1023 | Intron | NP_001273307.1 | |||
NM_032858.2 | 1023 | Intron | NP_116247.1 | |||
XM_006711583.1 | 1023 | Intron | XP_006711646.1 | |||
XM_011510067.1 | 1023 | Intron | XP_011508369.1 | |||
XM_011510068.1 | 1023 | Intron | XP_011508370.1 | |||
XM_017002602.1 | 1023 | Intron | XP_016858091.1 | |||
XM_017002603.1 | 1023 | Intron | XP_016858092.1 |