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Q96GP6 Proteins EGF-like domain Repeats
Uniprot ID:Q96GP6
Protein name: Scavenger receptor class F member 2
Gene : SCARF2 SREC2 SREPCR
Protein Family:
Squence Length : 870
Sequnce
>Q96GP6 871 MEGAGPRGAGPARRRGAGGPPSPLLPSLLLLLLLWMLPDTVAPQELNPRGRNVCRAPGSQVPTCCAGWRQQGDECGIAVCEGNSTCSENEVCVRPGECRCRHGYFGANCDTKCPRQFWGPDCKELCSCHPHGQCEDVTGQCTCHARRWGARCEHACQCQHGTCHPRSGACRCEPGWWGAQCASACYCSATSRCDPQTGACLCHAGWWGRSCNNQCACNSSPCEQQSGRCQCRERTFGARCDRYCQCFRGRCHPVDGTCACEPGYRGKYCREPCPAGFYGLGCRRRCGQCKGQQPCTVAEGRCLTCEPGWNGTKCDQPCATGFYGEGCSHRCPPCRDGHACNHVTGKCTRCNAGWIGDRCETKCSNGTYGEDCAFVCADCGSGHCDFQSGRCLCSPGVHGPHCNVTCPPGLHGADCAQACSCHEDTCDPVTGACHLETNQRKGVMGAGALLVLLVCLLLSLLGCCCACRGKDPTRRPRPRRELSLGRKKAPHRLCGRFSRISMKLPRIPLRRQKLPKVVVAHHDLDNTLNCSFLEPPSGLEQPSPSWSSRASFSSFDTTDEGPVYCVPHEEAPAESRDPEVPTVPAEAPAPSPVPLTTPASAEEAIPLPASSDSERSASSVEGPGGALYARVARREARPARARGEIGGLSLSPSPERRKPPPPDPATKPKVSWIHGKHSAAAAGRAPSPPPPGSEAAPSPSKRKRTPSDKSAHTVEHGSPRTRDPTPRPPGLPEEATALAAPSPPRARARAAPRPLGAHGRRRSPAKRAEAASMLAADVRGKTRSLGRAEVALGAQGPREKPAPPQKAKRSVPPASPARAPPATETPGPEKAATDLPAPETPRKKTPIQKPPRKKSREAAGELGRAGAPTL
Domains
DOMAIN 71 110 EGF-like 1 DOMAIN 122 153 EGF-like 2 DOMAIN 148 182 EGF-like 3 DOMAIN 183 212 EGF-like 4 DOMAIN 213 241 EGF-like 5 DOMAIN 236 270 EGF-like 6 DOMAIN 372 403 EGF-like 7
EGF-like sequence regions
71 - 110 DECGIAVCEGNSTCSENEVCVRPGECRCRHGYFGANCDTK 122 - 153 ELCSCHPHGQCEDVTGQCTCHARRWGARCEHA 148 - 182 ARCEHACQCQHGTCHPRSGACRCEPGWWGAQCASA 183 - 212 CYCSATSRCDPQTGACLCHAGWWGRSCNNQ 213 - 241 CACNSSPCEQQSGRCQCRERTFGARCDRY 236 - 270 ARCDRYCQCFRGRCHPVDGTCACEPGYRGKYCREP 372 - 403 FVCADCGSGHCDFQSGRCLCSPGVHGPHCNVT
Function
"Probable adhesion protein, which mediates homophilic and heterophilic interactions. In contrast to SCARF1, it poorly mediates the binding and degradation of acetylated low density lipoprotein (Ac-LDL) (By similarity)"
Disease
"DISEASE: Van den Ende-Gupta syndrome (VDEGS) [MIM:600920]: A syndrome characterized by craniofacial and skeletal abnormalities that include blepharophimosis, a flat and wide nasal bridge, narrow and beaked nose, hypoplastic maxilla with or without cleft palate and everted lower lip, prominent ears, down-slanting eyes, arachnodactyly, and camptodactyly Patients present congenital joint contractures that improve without intervention, and normal growth and development Intelligence is normal Rarely, enlarged cerebella can be present Some patients experience respiratory problems due to laryngeal abnormalities Note=The disease is caused by mutations affecting the gene represented in this entry"