|
3321
|
|
|
CD93 molecule |
C1QR1, C1qR(P), C1qRP, CDw93, ECSM3, MXRA4, dJ737E23.1 |
|
|
3322
|
|
|
Microtubule associated protein RP/EB family member 1 |
EB1 |
|
|
3323
|
|
|
Kinesin associated protein 3 |
FLA3, KAP-1, KAP-3, KAP3, SMAP, Smg-GDS, dJ190I16.1 |
|
|
3324
|
|
|
Microtubule associated protein RP/EB family member 3 |
EB3, EBF3, EBF3-S, RP3 |
|
|
3325
|
|
|
Activating transcription factor 6 |
ACHM7, ATF6A, ATP6alpha |
Achromatopsia, Anetoderma, Asbestosis, Color blindness, Cone monochromatism, Cone-rod dystrophy, Congenital nystagmus, Creutzfeldt-jakob disease, Diabetes mellitus, Dyschromatopsia, Exotropia, Hyperopia, Macular dystrophy, Narcolepsy, Nyctalopia, Nystagmus, Pendular nystagmus, Retinitis pigmentosaView all (3 more) |
|
3326
|
|
|
RAB3 GTPase activating protein catalytic subunit 1 |
MARTS2, P130, RAB3GAP, RAB3GAP130, WARBM1 |
Abnormal dermatoglyphic pattern, Acquired kyphoscoliosis, Agenesis of corpus callosum, Brachycephaly, Cataract, Cataract-intellectual disability-hypogonadism syndrome, Central visual impairment, Cerebellar hypoplasia, Cerebral atrophy, Cerebral cortical atrophy, Congenital cataract, Congenital hypoplasia of penis, Congenital kyphoscoliosis, Cryptorchidism, Developmental delay, Diabetes mellitus, Dwarfism, Dysmorphic features, Fundus coloboma, High palate, Hydronephrosis, Hypogonadotropic hypogonadism, Hypoplasia of corpus callosum, Mental retardation, Leukemia, Spastic diplegia, Macrotia, Martsolf syndrome, Micro syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multiple congenital anomalies, Nervous system diseases, Optic atrophy, Osteoporosis, Pachygyria, Ptosis, Retinal coloboma, Scoliosis, Warburg micro syndromeView all (27 more) |
|
3327
|
|
|
RAB18, member RAS oncogene family |
RAB18LI1, WARBM3 |
Acquired kyphoscoliosis, Blepharophimosis, Brachycephaly, Camptodactyly of fingers, Cataract, Central visual impairment, Cerebral cortical atrophy, Congenital hypoplasia of penis, Congenital kyphoscoliosis, Cryptorchidism, Developmental delay, Dwarfism, Fundus coloboma, High palate, Hydronephrosis, Hypertrichosis, Hypoplasia of corpus callosum, Mental retardation, Macrotia, Micro syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Nervous system diseases, Nystagmus, Optic atrophy, Pachygyria, Penis agenesis, Polymicrogyria, Retinal coloboma, Scoliosis, Spastic quadriplegia, Warburg micro syndromeView all (19 more) |
|
3328
|
|
|
POM121 and ZP3 fusion |
POM-ZP3 |
|
|
3329
|
|
|
Sirtuin 2 |
SIR2, SIR2L, SIR2L2 |
|
|
3330
|
|
|
Ribose 5-phosphate isomerase A |
RPI, RPIAD |
|
