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GGAGATAAATAATCCAGAGAAGTCT[C/T]ATTGGAGGTTGTTGTAGGCACAGCC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607280 | |||||||||||||||||||||||
Literature Links: |
CNTN4 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
CNTN4 - contactin 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206955.1 | Intron | NP_001193884.1 | ||||
NM_001206956.1 | Intron | NP_001193885.1 | ||||
NM_175607.2 | Intron | NP_783200.1 | ||||
NM_175613.2 | Intron | NP_783302.1 | ||||
XM_006713004.3 | Intron | XP_006713067.1 | ||||
XM_011533425.2 | Intron | XP_011531727.1 | ||||
XM_011533426.2 | Intron | XP_011531728.1 | ||||
XM_011533427.2 | Intron | XP_011531729.1 | ||||
XM_011533428.2 | Intron | XP_011531730.1 | ||||
XM_011533429.2 | Intron | XP_011531731.1 | ||||
XM_011533430.2 | Intron | XP_011531732.1 | ||||
XM_011533431.2 | Intron | XP_011531733.1 | ||||
XM_017005782.1 | Intron | XP_016861271.1 | ||||
XM_017005783.1 | Intron | XP_016861272.1 | ||||
XM_017005784.1 | Intron | XP_016861273.1 | ||||
XM_017005785.1 | Intron | XP_016861274.1 | ||||
XM_017005786.1 | Intron | XP_016861275.1 | ||||
XM_017005787.1 | Intron | XP_016861276.1 | ||||
XM_017005788.1 | Intron | XP_016861277.1 |
CNTN4-AS2 - CNTN4 antisense RNA 2 | ||||||
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There are no transcripts associated with this gene. |