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Allele Nt change(s) AA change(s) Phenotype: Type Phenotype: Description Reference Availability Comments

public

ΔmntH (Keio:JW2388)

deletion

deletion

PMID:16738554

Shigen
CGSC9908[1]

public

mntHN37D

N37D

Loss of function

seeded from UniProt:P0A769

public

mntHE102D,Q

E102D,Q

Loss of function

seeded from UniProt:P0A769

public

mntHG36P

G36P

Loss of function

seeded from UniProt:P0A769

public

mntHD109E,N

D109E,N

Transports manganese to a very low level

seeded from UniProt:P0A769

public

mntHE112D,Q

E112D,Q

Transports manganese to a very low level

seeded from UniProt:P0A769

public

mntHP35N,Q

P35N,Q

Loss of function

seeded from UniProt:P0A769

public

mntHD34E,N

D34E,N

Loss of function

seeded from UniProt:P0A769

public

mntHG115A,P

G115A,P

Loss of function

seeded from UniProt:P0A769

public

mntHE154Q

E154Q

Transports manganese to a level half of that of wild-type

seeded from UniProt:P0A769

public

mntHD238N

D238N

Transports manganese to a very low level

seeded from UniProt:P0A769

public

ΔmntH729::kan

PMID:16738554

CGSC:101894


  1. CGSC: The Coli Genetics Stock Center



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