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Gene ENSMUSG00000028943 (Espn)
Chromosomal location
Chr 4: 151494977 - 151526331 (-)
Description
espin Gene [Source:MGI (curated);Acc:Espn-008]
RefSeq_dna
NM_207687 NM_207688 NM_207691 NM_207689 NM_207690 NM_019585 
RefSeq_peptide
NP_997570.1 NP_997571.1 NP_997574.2 NP_997572.1 NP_997573.1 NP_062531.2 
UniGene
Mm.264215 
MGI
MGI:1861630 
Uniprot/SWISSPROT
Q9ET47 
Uniprot/SPTREMBL
B1AWQ4 Q9WUH6 B1AWQ1 B1AWQ3 Q3UM31 Q9QY28 B1AWP7 B1AWP8 B1AWP9 B1AWQ0 Q9DD12 
Human Ortholog
ENSG00000116219 (ESPNP)
Omim 609006 - DEAFNESS, AUTOSOMAL RECESSIVE 36  
UniTrap UNI23276
Vector Insertion
Chr 4: 151502663 - 151502878
Public Clones not available
Private Clones OST267646 (lexicon)
Severity of mutation (?) Insertion after 60% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI36868
Vector Insertion
Chr 4: 151495229 - 151497738
Public Clones IST12638A6 (tigm)
Private Clones not available
Severity of mutation (?) Insertion after 95% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI36377
Vector Insertion
Chr 4: 151494990 - 151495375
Public Clones IST12293G11 (tigm)
Private Clones not available
Severity of mutation (?) Insertion after 95% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

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