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Gene ENSMUSG00000079194 (AC133103.5-209)
Chromosomal location
Chr NT_166281: 30465 - 185012 (-)
Description
Putative uncharacterized protein  [Source:UniProtKB/TrEMBL;Acc:Q3UT50]
Uniprot/SPTREMBL
Q3UT50 
Human Ortholog
ENSG00000135899 (SP110)
Omim 235550 - HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY  
UniTrap UNI15268
Vector Insertion
Chr NT_166281: 34958 - 185013
Public Clones (sanger) PST10473-NR (escells) IST12673G7 (tigm) IST12277G8 (tigm)
IST14980G1 (tigm) IST13746F8 (tigm) IST10793F7 (tigm) IST14484A9 (tigm)
IST13656G7 (tigm) IST14502A3 (tigm) IST12586B9 (tigm) IST11686H1 (tigm)
IST13145F6 (tigm) IST14941G6 (tigm) IST12702A2BBF1 (tigm) IST14267B5 (tigm)
IST11354B12 (tigm) IST13519F5 (tigm)
Private Clones not available
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

Show all transcripts and translations:

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