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Symbol
Name
ID
Sema4a
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
MGI:107560
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Attenuation of retinal blood vessels
Macular degeneration
Bone spicule pigmentation of the retina
Rod-cone dystrophy
Nyctalopia
Photophobia
Reduced visual acuity
Blindness
Peripheral visual field loss
Progressive visual loss
Epiphora
Disease(s) Associated with SEMA4A
cone-rod dystrophy 10
retinitis pigmentosa 35

Mouse Phenotypes
vision/eye phenotype
increased retina apoptosis
decreased retina photoreceptor cell number
abnormal photoreceptor outer segment morphology
absent photoreceptor outer segment
abnormal retina cone cell outer segment morphology
abnormal retina rod cell outer segment morphology
abnormal retina pigment epithelium morphology
decreased eye pigmentation
abnormal eye morphology
thin retina inner nuclear layer
thin retina inner plexiform layer
thin retina outer nuclear layer
retina degeneration
abnormal eye physiology
abnormal eye electrophysiology
Availability Mouse Genotype
Sema4aGt(OST393408)Lex/Sema4aGt(OST393408)Lex
Sema4atm1.1Akum/Sema4atm1.1Akum *
Sema4atm1Kik/Sema4atm1Kik
Sema4atm2.1Akum/Sema4atm2.1Akum *
Sema4atm3.1Akum/Sema4atm3.1Akum
Sema4atm4.1Akum/Sema4atm4.1Akum *
Sema4atm2.1Akum/Sema4atm3.1Akum *

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
05/21/2024
MGI 6.23
The Jackson Laboratory