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Gene ENSMUSG00000026609 (Ush2a)
Chromosomal location
Chr 1: 190085914 - 190788920 (+)
Description
Usher syndrome 2A (autosomal recessive, mild) homolog (human) Gene [Source:MGI (curated);Acc:Ush2a-001]
RefSeq_dna
NM_021408 
RefSeq_peptide
NP_067383.3 
UniGene
Mm.331238 
MGI
MGI:1341292 
Uniprot/SWISSPROT
Q2QI47 
Uniprot/SPTREMBL
Q1KPK2 Q9D1Z8 
Human Ortholog
ENSG00000042781 (USH2A)
Omim 268000 - RETINITIS PIGMENTOSA  276901 - USHER SYNDROME, TYPE IIA  
UniTrap UNI31634
Vector Insertion
Chr 1: 190142973 - 190174915
Public Clones IST10219E9 (tigm) IST13719H2 (tigm)
Private Clones not available
Severity of mutation (?) Insertion after 5% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI35741
Vector Insertion
Chr 1: 190452594 - 190457459
Public Clones IST11071E2 (tigm)
Private Clones not available
Severity of mutation (?) Insertion after 42% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

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