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FREM2

Fraser syndrome

Recessive genetic disorder involving eye and genital abnormalities

morphogenesis during early development. It has also been associated with FREM2 and with GRIP1. By autozygosity mapping, McGregor et al. (2003) located

Fraser syndrome

Fraser_syndrome

FREM2

Protein-coding gene in the species Homo sapiens

extracellular matrix protein 2 is a protein that in humans is encoded by the FREM2 gene. This gene encodes a membrane protein that belongs to the FRAS1 family

FREM2

Microphthalmia

Birth defect of the eye

CRYBA4 CRYBB2 DHX38 DPYD ERCC1 ERCC5 FADD FAM111A FNBP4 FOXL2 FRAS1 FREM1 FREM2 FZD5 GDF3 GDF6 GJA1 GRIP1 HCCS HMGB3 HMX1 IGBP1 KAT6B KMT2D LRP2 MAB21L2

Microphthalmia

Glutamate receptor-interacting protein

found in the interaction GRIP1 has with the proteins Fras1 and Frem2. Fras1 and Frem2 are extracellular membrane proteins necessary for proper basement

Glutamate receptor-interacting protein

Glutamate_receptor-interacting_protein

Syndromic microphthalmia

Developmental disorder involving the eye

Focal dermal hypoplasia, Goltz-Gorlin syndrome FRAS1 AR Fraser syndrome 1 FREM2 AR Fraser syndrome 2 GRIP1 AR Fraser syndrome 3 ALX3 AR Frontonasal dysplasia

Syndromic microphthalmia

Syndromic_microphthalmia

List of human protein-coding genes 3

Q92837 5849 FRAT2 HGNC:16048; O75474 5850 FREM1 HGNC:23399; Q5H8C1 5851 FREM2 HGNC:25396; Q5SZK8 5852 FREM3 HGNC:25172; P0C091 5853 FREY1 HGNC:37213;

List of human protein-coding genes 3

List_of_human_protein-coding_genes_3

List of OMIM disorder codes

249420; SH3PXD2B Fraser syndrome; 219000; FRAS1 Fraser syndrome; 219000; FREM2 Frasier syndrome; 136680; WT1 Friedreich's ataxia with retained reflexes;

List of OMIM disorder codes

List_of_OMIM_disorder_codes