Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 607071 MIM: 604038 MIM: 602725 MIM: 607073 | ||||||||||||||||||||
Literature Links: |
HYAL1 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 |
HYAL1 - hyaluronoglucosaminidase 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
HYAL3 - hyaluronoglucosaminidase 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001200029.1 | 862 | Missense Mutation | AGG,TGG | R,W 197 | NP_001186958.1 | |
NM_001200030.1 | 862 | Missense Mutation | AGG,TGG | R,W 197 | NP_001186959.1 | |
NM_001200031.1 | 862 | Intron | NP_001186960.1 | |||
NM_001200032.1 | 862 | Intron | NP_001186961.1 | |||
NM_003549.3 | 862 | Missense Mutation | AGG,TGG | R,W 197 | NP_003540.2 |
IFRD2 - interferon related developmental regulator 2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
LSMEM2 - leucine rich single-pass membrane protein 2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
NAT6 - N-acetyltransferase 6 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |