MAMMALIAN PHENOTYPE - ANNOTATIONS
The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.
Term: abnormal retina neuronal layer morphology
Accession: MP:0006069
browse the term
Definition: any structural anomaly of any of the neuronal layers that make up the retina, including the ganglion cell, inner plexiform, inner nuclear, outer plexiform, outer nuclear layers, the inner and outer segments
Synonyms: exact_synonym: abnormal retinal neuronal layer morphology
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Cryba1
crystallin, beta A1
IAGP IMP
RGD
PMID:26303524 PMID:15721615
RGD:38676460 , RGD:126925760
NCBI chr10:62,608,373...62,614,726
Ensembl chr10:62,608,383...62,614,726
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Cryba1Hiser
crystallin, beta A1; HiSER mutant
IAGP
RGD
PMID:26303524
RGD:38676460
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Cryba1Nuc1Dbsa
crystallin, beta A1;Nuc1 mutant, Dbsa
IMP
RGD
PMID:15721615
RGD:126925760
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Cryba1
crystallin, beta A1
IMP
RGD
PMID:15721615
RGD:126925760
NCBI chr10:62,608,373...62,614,726
Ensembl chr10:62,608,383...62,614,726
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Cryba1Nuc1Dbsa
crystallin, beta A1;Nuc1 mutant, Dbsa
IMP
RGD
PMID:15721615
RGD:126925760
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Cryba1
crystallin, beta A1
IMP
RGD
PMID:15721615
RGD:126925760
NCBI chr10:62,608,373...62,614,726
Ensembl chr10:62,608,383...62,614,726
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Cryba1Nuc1Dbsa
crystallin, beta A1;Nuc1 mutant, Dbsa
IMP
RGD
PMID:15721615
RGD:126925760
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Cryba1
crystallin, beta A1
IMP
RGD
PMID:15721615
RGD:126925760
NCBI chr10:62,608,373...62,614,726
Ensembl chr10:62,608,383...62,614,726
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Cryba1Nuc1Dbsa
crystallin, beta A1;Nuc1 mutant, Dbsa
IMP
RGD
PMID:15721615
RGD:126925760
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Crb1
crumbs cell polarity complex component 1
IAGP
RGD
PMID:25878282
RGD:13451131
NCBI chr13:50,801,484...50,989,261
Ensembl chr13:50,800,959...50,989,261
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Crb1m1
crumbs 1, cell polarity complex component, mutant 1
IAGP
RGD
PMID:25878282
RGD:13451131
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Tmem67
transmembrane protein 67
IAGP
RGD
PMID:23516626
RGD:11535084
NCBI chr 5:25,536,458...25,589,378
Ensembl chr 5:25,536,458...25,589,334
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Myo15a
myosin XVA
induces
IAGP
DNA:missense mutation:cds:exon 56 T>C, p.Leu3157Pro (rat) compared to LEW/Ztm
RGD
PMID:21479269 PMID:21479269
RGD:150429616 , RGD:150429616
NCBI chr10:45,277,619...45,335,953
Ensembl chr10:45,278,737...45,335,340
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Myo15aci2
myosin XVA; ci2 mutant
induces
IAGP
compared to LEW/Ztm
RGD
PMID:21479269
RGD:150429616
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Pde6b
phosphodiesterase 6B
IMP
compared to wild-type
RGD
PMID:31009522
RGD:40924664
NCBI chr14:1,323,310...1,366,450
Ensembl chr14:1,323,310...1,366,450
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Pde6bem1Baek
phosphodiesterase 6B; Cpf1-CRISPR induced mutant1, Baek
IMP
compared to wild-type
RGD
PMID:31009522
RGD:40924664
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Myo15a
myosin XVA
induces
IAGP
DNA:missense mutation:cds:exon 56 T>C, p.Leu3157Pro (rat) compared to LEW/Ztm
RGD
PMID:21479269 PMID:21479269
RGD:150429616 , RGD:150429616
NCBI chr10:45,277,619...45,335,953
Ensembl chr10:45,278,737...45,335,340
G
Myo15aci2
myosin XVA; ci2 mutant
induces
IAGP
compared to LEW/Ztm
RGD
PMID:21479269
RGD:150429616
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Pde6b
phosphodiesterase 6B
IMP
compared to wild-type
RGD
PMID:31009522
RGD:40924664
NCBI chr14:1,323,310...1,366,450
Ensembl chr14:1,323,310...1,366,450
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Pde6bem1Baek
phosphodiesterase 6B; Cpf1-CRISPR induced mutant1, Baek
IMP
compared to wild-type
RGD
PMID:31009522
RGD:40924664
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Cd36
CD36 molecule
IAGP
RGD
PMID:18288886
RGD:2307226
NCBI chr 4:17,317,343...17,410,084
Ensembl chr 4:17,354,466...17,513,903
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Mertk
MER proto-oncogene, tyrosine kinase
IAGP
RGD
PMID:11592982
RGD:69668
NCBI chr 3:115,939,351...116,045,141
Ensembl chr 3:115,939,351...116,046,554
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Pde6b
phosphodiesterase 6B
IMP
compared to wild-type
RGD
PMID:31009522
RGD:40924664
NCBI chr14:1,323,310...1,366,450
Ensembl chr14:1,323,310...1,366,450
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Pde6bem1Baek
phosphodiesterase 6B; Cpf1-CRISPR induced mutant1, Baek
IMP
compared to wild-type
RGD
PMID:31009522
RGD:40924664
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Cacna1f
calcium voltage-gated channel subunit alpha1 F
IAGP
DNA:mutation:cds: c.2941C>T (rat)
RGD
PMID:22634626
RGD:13782386
NCBI chr X:14,868,096...14,896,413
Ensembl chr X:14,868,024...14,896,413
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Cacna1f csnb
calcium voltage-gated channel subunit alpha1 F; congenital stationary night blindness mutant
IAGP
DNA:mutation:cds: c.2941C>T (rat)
RGD
PMID:22634626
RGD:13782386
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