Description
This panel was developed and is maintained by VCGS, and contains genes associated with isolated and syndromic anophthalmia, microphthalmia and coloboma.

This panel has been compared against the Genomics England PanelApp 'Anophthalmia or Microphthalmia' v1.31 and 'Ocular coloboma' v1.38 panels, with discrepancies reviewed and reciprocal feedback provided to Genomics England.

14 reviewers

  • Chris Richmond (Genetic Health Queensland)

  • Sue White (Victorian Clinical Genetics Services)

  • Alison Yeung (Victorian Clinical Genetics Services)

  • Teresa Zhao (Victorian Clinical Genetics Services)

  • Chirag Patel (Genetic Health Queensland)

  • Ain Roesley (Victorian Clinical Genetics Services)

  • Krithika Murali (Victorian Clinical Genetics Services)

  • Elena Savva (Victorian Clinical Genetics Services)

  • Dean Phelan (Victorian Clinical Genetics Services)

  • Crystle Lee (Victorian Clinical Genetics Services)

  • Seb Lunke (Victorian Clinical Genetics Services)

  • Michelle Torres (Victorian Clinical Genetics Services)

  • Bryony Thompson (Royal Melbourne Hospital)

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

94 Entities

94 reviewed, 76 green

List Entity Reviews Mode of inheritance Details
94 Entitiess
Green Green List (high evidence)
ACTB
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Baraitser-Winter syndrome 1, MIM#243310
Tags
Green Green List (high evidence)
ACTG1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Baraitser-Winter syndrome 2, MIM#614583
Tags
Green Green List (high evidence)
ALDH1A3
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, isolated 8, MIM# 615113
Tags
Green Green List (high evidence)
ARHGAP35
1 review
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Developmental defect of the eye (MONDO:0020145), ARHGAP35-related
Tags
Green Green List (high evidence)
ASXL1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Bohring-Opitz syndrome , MIM#605039
Tags
Green Green List (high evidence)
B3GLCT
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Peters-plus syndrome, MIM#261540
Tags
Green Green List (high evidence)
BCOR
1 review
1 green
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 2, MIM# 300166
  • Oculofaciocardiodental syndrome
  • Lenz microphthalmia
Tags
Green Green List (high evidence)
BMP4
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 6, MIM# 607932
Tags
Green Green List (high evidence)
BMPR1B
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • coloboma MONDO#0001476, BMPR1B-related
Tags
Green Green List (high evidence)
C12orf57
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Temtamy syndrome, MIM#218340
Tags
Green Green List (high evidence)
CAPN15
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Oculogastrointestinal neurodevelopmental syndrome 619318
  • microphthalmia HP:0000568
  • coloboma HP:0000589
Tags
Green Green List (high evidence)
CC2D2A
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • COACH syndrome 2, MIM# 619111
Tags
Green Green List (high evidence)
CDK5RAP2
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Microcephaly 3, primary, autosomal recessive, MIM# 604804
Tags
Green Green List (high evidence)
CHD7
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • CHARGE syndrome, MIM# 214800
Tags
Green Green List (high evidence)
CLDN19
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Hypomagnesemia 5, renal, with ocular involvement, MIM#248190
Tags
Green Green List (high evidence)
COL4A1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Brain small vessel disease with or without ocular anomalies, MIM#175780
Tags
Green Green List (high evidence)
EPHA2
1 review
1 green
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • microphthalmia, MONDO:0021129, EPHA2-related
Tags
Green Green List (high evidence)
FAM111A
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Kenny-Caffey syndrome, type 2, MIM@ 127000
Tags
Green Green List (high evidence)
FAT1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • facial dysmorphism
  • colobomatous microphthalmia
  • ptosis
  • syndactyly with or without nephropathy
Tags
Green Green List (high evidence)
FBXW11
2 reviews
2 green
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental, eye, jaw, and digital syndrome (NDEJD), MIM#618914
  • Intellectual disability
  • developmental eye anomalies
  • digital anomalies
Tags
Green Green List (high evidence)
FOXE3
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Anterior segment dysgenesis 2, multiple subtypes, MIM# 610256
Tags
Green Green List (high evidence)
FZD5
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Microphthalmia/coloboma 11, MIM# 620731
Tags
Green Green List (high evidence)
GJA1
1 review
1 green
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Oculodentodigital dysplasia, autosomal recessive, MIM# 257850
  • Oculodentodigital dysplasia, MIM# 164200
Tags
Green Green List (high evidence)
GJA8
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Cataract 1, multiple types, MIM# 116200
  • Microphthalmia
Tags
Green Green List (high evidence)
HCCS
1 review
1 green
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Linear skin defects with multiple congenital anomalies 1, MIM# 309801
Tags
  • SV/CNV
Green Green List (high evidence)
HMX1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Oculoauricular syndrome, MIM#612109
Tags
Green Green List (high evidence)
IKBKG
1 review
1 green
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Incontinentia pigmenti, MIM# 308300
Tags
Green Green List (high evidence)
LRP2
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Donnai-Barrow syndrome, MIM#222448
Tags
Green Green List (high evidence)
MAB21L1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Cerebellar, ocular, craniofacial, and genital syndrome OMIM#618479
Tags
Green Green List (high evidence)
MAB21L2
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia/coloboma and skeletal dysplasia syndrome, MIM# 615877
Tags
Green Green List (high evidence)
MFRP
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, isolated 5, MIM# 611040
Tags
Green Green List (high evidence)
MITF
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • COMMAD syndrome, MIM# 617306
Tags
Green Green List (high evidence)
MPDZ
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Hydrocephalus, congenital, 2, with or without brain or eye anomalies, MIM# 615219
Tags
Green Green List (high evidence)
MYRF
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Nanophthalmos
  • High hyperopia
Tags
Green Green List (high evidence)
NAA10
1 review
1 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 1, MIM# 309800
Tags
  • 5'UTR
Green Green List (high evidence)
NDP
1 review
1 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Norrie disease, MIM# 310600
Tags
Green Green List (high evidence)
NHS
1 review
1 green
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Nance-Horan syndrome, MIM# 302350
Tags
Green Green List (high evidence)
OCRL
1 review
1 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Lowe syndrome, MIM# 309000
Tags
Green Green List (high evidence)
OTX2
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 5, MIM# 610125
Tags
Green Green List (high evidence)
PACS1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Schuurs-Hoeijmakers syndrome, MIM# 615009
Tags
Green Green List (high evidence)
PAX2
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Papillorenal syndrome, MIM# 120330
  • Renal coloboma syndrome, MONDO:0007352
Tags
Green Green List (high evidence)
PAX6
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia
  • Coloboma, ocular, MIM# 120200
Tags
Green Green List (high evidence)
PIGL
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • CHIME syndrome, MIM# 280000, MONDO:0010221
Tags
  • founder
  • SV/CNV
Green Green List (high evidence)
PITX3
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Anterior segment dysgenesis 1, multiple subtypes, MIM# 107250
  • Cataract 11, multiple types, MIM# 610623
  • Microphthalmia
Tags
Green Green List (high evidence)
POMT1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1 236670
  • Walker-Walburg syndrome
Tags
Green Green List (high evidence)
PORCN
1 review
1 green
Other
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Focal dermal hypoplasia, MIM#305600
Tags
Green Green List (high evidence)
PRR12
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Neuroocular syndrome, MIM#619539
  • Complex microphthalmia
Tags
Green Green List (high evidence)
PRSS56
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, isolated 6, MIM# 613517
Tags
Green Green List (high evidence)
PUF60
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Verheij syndrome, MIM#615583
Tags
Green Green List (high evidence)
PXDN
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400
Tags
Green Green List (high evidence)
RAB18
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Warburg micro syndrome 3, MIM# 614222
Tags
  • founder
Green Green List (high evidence)
RAB3GAP1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Warburg micro syndrome 1, MIM# 600118
Tags
Green Green List (high evidence)
RAB3GAP2
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Warburg micro syndrome 2, MIM# 614225
Tags
Green Green List (high evidence)
RARB
1 review
1 green
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 12, MIM# 615524
Tags
Green Green List (high evidence)
RAX
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, isolated 3, MIM# 611038
Tags
Green Green List (high evidence)
RBP4
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Microphthalmia, isolated, with coloboma 10 MIM#616428
Tags
Green Green List (high evidence)
RERE
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart, MIM# 616975
Tags
Green Green List (high evidence)
RHOA
1 review
1 green
Other
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • normal cognition
  • leukoencephalopathy
  • micro-ophthalmia
  • strabismus
  • linear hypopigmentation
  • malar hypoplasia
  • downslanting palpebral fissures
  • microstomia
Tags
  • somatic
Green Green List (high evidence)
SALL4
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Duane-radial ray syndrome, MIM#607323
Tags
Green Green List (high evidence)
SHH
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia with coloboma 5, MIM# 611638
  • Holoprosencephaly 3, MIM# 142945
Tags
Green Green List (high evidence)
SIX3
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Holoprosencephaly 2, MIM# 157170
Tags
Green Green List (high evidence)
SIX6
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Optic disc anomalies with retinal and/or macular dystrophy, MIM# 212550
Tags
Green Green List (high evidence)
SMCHD1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Bosma arhinia microphthalmia syndrome (MIM#603457)
  • Arhinia, choanal atresia, microphthalmia MONDO:0011323
Tags
Green Green List (high evidence)
SMO
1 review
1 green
Other
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Curry-Jones syndrome, somatic mosaic, MIM#601707
Tags
  • somatic
Green Green List (high evidence)
SMOC1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia with limb anomalies, MIM# 206920
Tags
Green Green List (high evidence)
SOX2
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 3, MIM# 206900
  • Optic nerve hypoplasia and abnormalities of the central nervous system, MIM# 206900
Tags
Green Green List (high evidence)
STRA6
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, isolated, with coloboma 8, MIM# 601186
  • Microphthalmia, syndromic 9, MIM# 601186
Tags
Green Green List (high evidence)
TBC1D20
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Warburg micro syndrome 4, MIM# 615663
Tags
Green Green List (high evidence)
TENM3
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Microphthalmia, syndromic 15, MIM#615145
  • coloboma
Tags
Green Green List (high evidence)
TFAP2A
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Branchiooculofacial syndrome, MIM# 113620
Tags
Green Green List (high evidence)
TMEM98
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Nanophthalmos 4 MIM#615972
Tags
Green Green List (high evidence)
VSX2
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia with coloboma 3, MIM# 610092
  • Microphthalmia, isolated 2, MIM# 610093
Tags
Green Green List (high evidence)
WDR37
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Neurooculocardiogenitourinary syndrome, MIM# 618652
Tags
Green Green List (high evidence)
WLS
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Zaki syndrome, MIM#619648
Tags
Green Green List (high evidence)
WNT7B
2 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Pulmonary hypoplasia, Diaphragmatic anomalies, Anophthalmia/microphthalmia and Cardiac defects syndrome
  • Multiple congenital anomalies/dysmorphic features syndrome MONDO:0043005, WNT7B-related
Tags
Green Green List (high evidence)
YAP1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation, MIM#120433
Tags
Amber Amber List (moderate evidence)
ANK3
1 review
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • coloboma MONDO#0001476, ANK3-related
Tags
Amber Amber List (moderate evidence)
BMP3
1 review
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • coloboma, MONDO:0001476
  • microphthalmia, MONDO:0021129
Tags
Amber Amber List (moderate evidence)
C16orf62
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135
Tags
  • new gene name
Amber Amber List (moderate evidence)
CDON
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Coloboma
Tags
Amber Amber List (moderate evidence)
RPGRIP1L
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • COACH syndrome, MIM#216360
Tags
Amber Amber List (moderate evidence)
TOGARAM1
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Joubert syndrome 37, MIM# 619185
  • Cleft of the lip and palate
  • Microphthalmia
  • Cerebral dysgenesis
  • Hydrocephalus
Tags
Amber Amber List (moderate evidence)
ZRSR2
1 review
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Orofacialdigital syndrome MONDO:0015375, ZRSR2-related
Tags
Red Red List (low evidence)
ABCB6
1 review
1 red
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Microphthalmia, isolated, with coloboma 7 MIM#614497
Tags
Red Red List (low evidence)
CDH4
1 review
1 red
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • coloboma MONDO#0001476, CDH4-related
Tags
Red Red List (low evidence)
GDF3
2 reviews
1 green 1 red
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Red
Phenotypes
  • Microphthalmia with coloboma 6, OMIM #613703
  • Microphthalmia, isolated 7, OMIM # 613704
Tags
Red Red List (low evidence)
HESX1
1 review
1 red
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Septooptic dysplasia, MIM# 182230
Tags
Red Red List (low evidence)
KIF15
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Braddock-Carey syndrome 2 - MIM#619981
Tags
Red Red List (low evidence)
KIF17
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Microphthalmia
  • Coloboma
Tags
Red Red List (low evidence)
PDGFRA
1 review
1 red
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • coloboma MONDO#0001476, PDGFRA-related
Tags
Red Red List (low evidence)
RARA
1 review
1 red
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Syndromic chorioretinal coloboma
Tags
Red Red List (low evidence)
SALL2
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Other
Phenotypes
  • Coloboma, ocular, autosomal recessive, MIM#16820
Tags
Red Red List (low evidence)
TENM1
1 review
1 red
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Tags
Red Red List (low evidence)
VAX1
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 11, MIM# 614402
Tags

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