##gff-version 3 P29371 UniProtKB Chain 1 465 . . . ID=PRO_0000069899;Note=Neuromedin-K receptor P29371 UniProtKB Topological domain 1 84 . . . Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Transmembrane 85 107 . . . Note=Helical%3B Name%3D1;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Topological domain 108 117 . . . Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Transmembrane 118 139 . . . Note=Helical%3B Name%3D2;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Topological domain 140 159 . . . Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Transmembrane 160 181 . . . Note=Helical%3B Name%3D3;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Topological domain 182 201 . . . Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Transmembrane 202 222 . . . Note=Helical%3B Name%3D4;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Topological domain 223 245 . . . Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Transmembrane 246 270 . . . Note=Helical%3B Name%3D5;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Topological domain 271 299 . . . Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Transmembrane 300 321 . . . Note=Helical%3B Name%3D6;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Topological domain 322 334 . . . Note=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Transmembrane 335 359 . . . Note=Helical%3B Name%3D7;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Topological domain 360 465 . . . Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Region 415 465 . . . Note=Disordered;Ontology_term=ECO:0000256;evidence=ECO:0000256|SAM:MobiDB-lite P29371 UniProtKB Compositional bias 436 465 . . . Note=Polar residues;Ontology_term=ECO:0000256;evidence=ECO:0000256|SAM:MobiDB-lite P29371 UniProtKB Lipidation 374 374 . . . Note=S-palmitoyl cysteine;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Glycosylation 23 23 . . . Note=N-linked (GlcNAc...) asparagine;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Glycosylation 50 50 . . . Note=N-linked (GlcNAc...) asparagine;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Glycosylation 73 73 . . . Note=N-linked (GlcNAc...) asparagine;Ontology_term=ECO:0000255;evidence=ECO:0000255 P29371 UniProtKB Disulfide bond 158 233 . . . Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00521 P29371 UniProtKB Natural variant 93 93 . . . ID=VAR_069177;Note=In HH11%3B unequivocal evidence of impaired receptor signaling. G->D;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:19079066;Dbxref=dbSNP:rs121918124,PMID:19079066 P29371 UniProtKB Natural variant 137 137 . . . ID=VAR_072976;Note=In HH11. F->V;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25077900;Dbxref=PMID:25077900 P29371 UniProtKB Natural variant 286 286 . . . ID=VAR_049422;Note=May contribute to hypogonadotropic hypogonadism in patients carrying disease-causing mutations in FGFR1. K->R;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23643382;Dbxref=dbSNP:rs2276973,PMID:23643382 P29371 UniProtKB Natural variant 346 346 . . . ID=VAR_072977;Note=In HH11. M->V;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25077900;Dbxref=dbSNP:rs200148989,PMID:25077900 P29371 UniProtKB Natural variant 353 353 . . . ID=VAR_069178;Note=In HH11%3B unequivocal evidence of impaired receptor signaling. P->S;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:19079066;Dbxref=dbSNP:rs121918125,PMID:19079066 P29371 UniProtKB Natural variant 364 364 . . . ID=VAR_069963;Note=In HH11%3B the patient also carries a mutation in FGFR1. R->Q;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23643382;Dbxref=dbSNP:rs150288991,PMID:23643382 P29371 UniProtKB Natural variant 449 449 . . . ID=VAR_049423;Note=May contribute to hypogonadotropic hypogonadism in patients carrying disease-causing mutations in SPRY4 or KAL1. A->T;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23643382;Dbxref=dbSNP:rs17033889,PMID:23643382 P29371 UniProtKB Sequence conflict 3 3 . . . Note=T->I;Ontology_term=ECO:0000305;evidence=ECO:0000305 P29371 UniProtKB Sequence conflict 63 63 . . . Note=A->R;Ontology_term=ECO:0000305;evidence=ECO:0000305 P29371 UniProtKB Sequence conflict 439 439 . . . Note=C->F;Ontology_term=ECO:0000305;evidence=ECO:0000305