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Gene ENSMUSG00000062115 (Rai1)
Chromosomal location
Chr 11: 59918515 - 60012699 (+)
Description
retinoic acid induced 1 Gene [Source:MGI (curated);Acc:Rai1-001]
RefSeq_dna
NM_001037764 NM_009021 
RefSeq_peptide
NP_033047.2 NP_001032853.1 
UniGene
Mm.419978 Mm.296366 
MGI
MGI:103291 
Uniprot/SWISSPROT
Q61818 
Uniprot/SPTREMBL
B1AU85 B1AU87 Q5QGZ6 A6H6H9 B1AU86 Q810L5 
Human Ortholog
ENSG00000108557 (RAI1)
Omim 182290 - SMITH-MAGENIS SYNDROME  
UniTrap UNI26372
Vector Insertion
Chr 11: 59953742 - 59953873
Public Clones not available
Private Clones OST122802 (lexicon)
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI12067
Vector Insertion
Chr 11: 59953873 - 59989380
Public Clones M073F06 (ggtc) IST15073E4 (tigm) IST14856E10 (tigm) IST13608F4 (tigm)
IST12251E8 (tigm)
Private Clones not available
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI29836
Vector Insertion
Chr 11: 59989464 - 59998597
Public Clones (sanger) E052H01 (ggtc) D150H01 (ggtc) IST12482C9 (tigm) IST14874G2 (tigm)
IST14951H4 (tigm) IST14393G1 (tigm) IST13241C9 (tigm)
Private Clones not available
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

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