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Symbol
Name
ID
Lztfl1
leucine zipper transcription factor-like 1
MGI:1934860
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Macular atrophy
Bone spicule pigmentation of the retina
Retinal degeneration
Cone/cone-rod dystrophy
Rod-cone dystrophy
Visual impairment
Disease(s) Associated with LZTFL1
Bardet-Biedl syndrome 17

Mouse Phenotypes
abnormal photoreceptor outer segment morphology
short photoreceptor outer segment
disorganized photoreceptor outer segment
photoreceptor outer segment degeneration
retina cone cell degeneration
retina rod cell degeneration
retina photoreceptor degeneration
increased susceptibility to age-related retinal degeneration
retina degeneration
decreased a-wave amplitude
decreased b-wave amplitude
Availability Mouse Genotype
Lztfl1tm1.1Zpl/Lztfl1tm1.1Zpl
Lztfl1tm1.3Zpl/Lztfl1tm1.3Zpl
Lztfl1tm1e(KOMP)Wtsi/Lztfl1tm1e(KOMP)Wtsi
Lztfl1tm1Zpl/Lztfl1tm1Zpl

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory