Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGATGTTGCCCTACACAGTGAACTT[C/G]AAGGTGTCGGCGCGCACCCTCACGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 606417 | ||||||||||||||||||||
Literature Links: |
WDR11 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
WDR11 - WD repeat domain 11 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018117.11 | 41 | Missense Mutation | TTC,TTG | F,L 8 | NP_060587.8 | |
XM_005269962.2 | 41 | Intron | XP_005270019.1 | |||
XM_005269963.2 | 41 | UTR 5 | XP_005270020.1 | |||
XM_005269964.2 | 41 | Intron | XP_005270021.1 | |||
XM_017016397.1 | 41 | Missense Mutation | TTC,TTG | F,L 8 | XP_016871886.1 | |
XM_017016398.1 | 41 | UTR 5 | XP_016871887.1 | |||
XM_017016399.1 | 41 | UTR 5 | XP_016871888.1 | |||
XM_017016400.1 | 41 | Missense Mutation | TTC,TTG | F,L 8 | XP_016871889.1 |
WDR11-AS1 - WDR11 antisense RNA 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |