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GGGCTGCGTTGTGTCATCCGCCCCC[C/G]GCTCAATGGCGACTCCCTCACCGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606189 | ||||||||||||||||||||
Literature Links: |
CRIM1 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 |
CRIM1 - cysteine rich transmembrane BMP regulator 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016441.2 | 11 | Missense Mutation | CCG,CGG | P,R 95 | NP_057525.1 | |
XM_005264357.4 | 11 | Missense Mutation | CCG,CGG | P,R 95 | XP_005264414.1 | |
XM_011532898.2 | 11 | Missense Mutation | CCG,CGG | P,R 95 | XP_011531200.1 | |
XM_011532899.2 | 11 | Missense Mutation | CCG,CGG | P,R 95 | XP_011531201.1 | |
XM_011532901.2 | 11 | Missense Mutation | CCG,CGG | P,R 95 | XP_011531203.1 | |
XM_017004258.1 | 11 | Missense Mutation | CCG,CGG | P,R 95 | XP_016859747.1 | |
XM_017004259.1 | 11 | Missense Mutation | CCG,CGG | P,R 95 | XP_016859748.1 | |
XM_017004260.1 | 11 | Missense Mutation | CCG,CGG | P,R 95 | XP_016859749.1 | |
XM_017004261.1 | 11 | UTR 5 | XP_016859750.1 | |||
XM_017004262.1 | 11 | UTR 5 | XP_016859751.1 |
LOC100288911 - uncharacterized LOC100288911 | ||||||
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There are no transcripts associated with this gene. |