Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300427 | ||||||||||||||||||||
Literature Links: |
NLGN4X 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 |
NLGN4X - neuroligin 4, X-linked | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282145.1 | 3072 | Intron | NP_001269074.1 | |||
NM_001282146.1 | 3072 | Missense Mutation | AAA,AAC | K,N 796 | NP_001269075.1 | |
NM_020742.3 | 3072 | Intron | NP_065793.1 | |||
NM_181332.2 | 3072 | Intron | NP_851849.1 | |||
XM_005274564.2 | 3072 | Intron | XP_005274621.1 | |||
XM_005274565.2 | 3072 | Missense Mutation | AAA,AAC | K,N 816 | XP_005274622.1 | |
XM_005274566.4 | 3072 | Intron | XP_005274623.1 | |||
XM_006724504.3 | 3072 | Missense Mutation | AAA,AAC | K,N 816 | XP_006724567.1 | |
XM_011545547.2 | 3072 | Missense Mutation | AAA,AAC | K,N 816 | XP_011543849.1 | |
XM_011545548.2 | 3072 | Intron | XP_011543850.1 | |||
XM_017029690.1 | 3072 | Missense Mutation | AAA,AAC | K,N 816 | XP_016885179.1 | |
XM_017029691.1 | 3072 | Missense Mutation | AAA,AAC | K,N 796 | XP_016885180.1 | |
XM_017029692.1 | 3072 | Intron | XP_016885181.1 | |||
XM_017029693.1 | 3072 | Missense Mutation | AAA,AAC | K,N 796 | XP_016885182.1 |