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ATGGCATGCACTTACCAGGCACTCA[A/G]CGCAACGGACACAAAGCCTCGCCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609770 MIM: 611707 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
JAML PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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JAML - junction adhesion molecule like | ||||||
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There are no transcripts associated with this gene. |
MPZL3 - myelin protein zero like 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286152.1 | 709 | Missense Mutation | GCT,GTT | A,V 212 | NP_001273081.1 | |
NM_198275.2 | 709 | Missense Mutation | GCT,GTT | A,V 224 | NP_938016.1 | |
XM_006718775.2 | 709 | Missense Mutation | GCT,GTT | A,V 206 | XP_006718838.1 | |
XM_017017304.1 | 709 | Missense Mutation | GCT,GTT | A,V 208 | XP_016872793.1 |