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Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 617003 MIM: 615798 MIM: 615799 MIM: 615403 MIM: 605914 | ||||||||||||||||||||
Literature Links: |
BICDL2 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 |
BICDL2 - BICD family like cargo adaptor 2 | ||||||
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There are no transcripts associated with this gene. |
CLDN6 - claudin 6 | ||||||
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There are no transcripts associated with this gene. |
CLDN9 - claudin 9 | ||||||
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There are no transcripts associated with this gene. |
HCFC1R1 - host cell factor C1 regulator 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002017.2 | 414 | UTR 3 | NP_001002017.1 | |||
NM_001002018.2 | 414 | UTR 3 | NP_001002018.1 | |||
NM_001288665.1 | 414 | UTR 3 | NP_001275594.1 | |||
NM_001288666.1 | 414 | UTR 3 | NP_001275595.1 | |||
NM_001288667.1 | 414 | UTR 3 | NP_001275596.1 | |||
NM_001288668.1 | 414 | UTR 3 | NP_001275597.1 | |||
NM_001308070.1 | 414 | UTR 3 | NP_001294999.1 | |||
NM_017885.3 | 414 | UTR 3 | NP_060355.1 | |||
XM_011522559.2 | 414 | UTR 3 | XP_011520861.1 | |||
XM_017023384.1 | 414 | UTR 3 | XP_016878873.1 |
LOC100128770 - uncharacterized LOC100128770 | ||||||
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There are no transcripts associated with this gene. |
THOC6 - THO complex 6 | ||||||
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There are no transcripts associated with this gene. |
TNFRSF12A - TNF receptor superfamily member 12A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016639.2 | 414 | Intron | NP_057723.1 |