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Gene ENSMUSG00000056569 (Mpz)
Chromosomal location
Chr 1: 173080844 - 173091254 (+)
Description
myelin protein zero Gene [Source:MGI (curated);Acc:Mpz-001]
RefSeq_dna
NM_008623 
RefSeq_peptide
NP_032649.2 
UniGene
Mm.9986 Mm.392404 
MGI
MGI:103177 
Uniprot/SWISSPROT
P27573 
Uniprot/SPTREMBL
Q542C9 
Human Ortholog
ENSG00000158887 (MPZ)
Omim 103100 - ADIE PUPIL  118200 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B  145900 - HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS  180800 - ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA  605253 - NEUROPATHY, CONGENITAL HYPOMYELINATING  607677 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I  607736 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J  607791 - CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D  
UniTrap UNI33756
Vector Insertion
Chr 1: 173080866 - 173081952
Public Clones IST14616G5 (tigm)
Private Clones not available
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI25654
Vector Insertion
Chr 1: 173082068 - 173085645
Public Clones not available
Private Clones OST171440 (lexicon)
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

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