Knowledge (XXG)

Peroxin-7

Source 📝

222: 40: 263: 282: 168: 64: 52: 45: 287: 256: 206: 160: 192: 197: 57: 249: 110: 164: 202: 233: 221: 105: 134: 114: 276: 229: 81: 144: 88: 198:
GeneReviews/NIH/NCBI/UW entry on Rhizomelic Chondrodysplasia Punctata Type 1
93: 180: 76: 69: 237: 140: 130: 125: 104: 99: 87: 75: 63: 51: 39: 31: 26: 21: 193:GeneReviews/NCBI/NIH/UW entry on Refsum Disease 257: 8: 264: 250: 122: 205:at the U.S. National Library of Medicine 18: 7: 218: 216: 169:rhizomelic chondrodysplasia punctata 236:. You can help Knowledge (XXG) by 14: 220: 22:peroxisomal biogenesis factor 7 1: 16:Family of transport proteins 283:Genes on human chromosome 6 304: 215: 121: 207:Medical Subject Headings 203:PEX7+protein,+human 288:Biochemistry stubs 245: 244: 154: 153: 150: 149: 295: 266: 259: 252: 224: 217: 165:Refsum's disease 163:associated with 123: 19: 303: 302: 298: 297: 296: 294: 293: 292: 273: 272: 271: 270: 213: 189: 177: 17: 12: 11: 5: 301: 299: 291: 290: 285: 275: 274: 269: 268: 261: 254: 246: 243: 242: 225: 211: 210: 200: 195: 188: 187:External links 185: 184: 183: 176: 173: 152: 151: 148: 147: 142: 138: 137: 132: 128: 127: 119: 118: 108: 102: 101: 97: 96: 91: 85: 84: 79: 73: 72: 67: 61: 60: 55: 49: 48: 43: 37: 36: 33: 29: 28: 24: 23: 15: 13: 10: 9: 6: 4: 3: 2: 300: 289: 286: 284: 281: 280: 278: 267: 262: 260: 255: 253: 248: 247: 241: 239: 235: 232:article is a 231: 226: 223: 219: 214: 208: 204: 201: 199: 196: 194: 191: 190: 186: 182: 179: 178: 174: 172: 170: 166: 162: 158: 146: 143: 139: 136: 133: 129: 124: 120: 117: 116: 112: 109: 107: 103: 98: 95: 92: 90: 86: 83: 80: 78: 74: 71: 68: 66: 62: 59: 56: 54: 50: 47: 44: 42: 38: 34: 30: 25: 20: 238:expanding it 230:biochemistry 227: 212: 156: 155: 113: 135:Swiss-model 27:Identifiers 277:Categories 131:Structures 126:Search for 100:Other data 157:Peroxin-7 115:q21-q22.2 82:NM_000288 41:NCBI gene 175:See also 171:type 1. 161:receptor 145:InterPro 181:Peroxin 141:Domains 89:UniProt 209:(MeSH) 111:Chr. 6 94:O00628 77:RefSeq 70:601757 32:Symbol 228:This 159:is a 106:Locus 234:stub 167:and 65:OMIM 58:8860 53:HGNC 46:5191 35:PEX7 279:: 265:e 258:t 251:v 240:.

Index

NCBI gene
5191
HGNC
8860
OMIM
601757
RefSeq
NM_000288
UniProt
O00628
Locus
Chr. 6
q21-q22.2
Swiss-model
InterPro
receptor
Refsum's disease
rhizomelic chondrodysplasia punctata
Peroxin
GeneReviews/NCBI/NIH/UW entry on Refsum Disease
GeneReviews/NIH/NCBI/UW entry on Rhizomelic Chondrodysplasia Punctata Type 1
PEX7+protein,+human
Medical Subject Headings
Stub icon
biochemistry
stub
expanding it
v
t
e

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