Table 2.
Gene | Localization | Introns | Transcript information | Protein size | Molecular weight | Pi |
CLDN1 | 3q28 | 3 | One form | 211 | 22,744 | 8.41 |
CLDN2 | Xq22 | 1 | One form | 230 | 24,549 | 8.47 |
CLDN3 | 7q11 | 0 | One form | 220 | 23,319 | 8.37 |
CLDN4 | 7q11 | 0 | One form | 209 | 22,077 | 8.38 |
CLDN5 | 22q11 | 1 | Two variants: alternative splicing, coding unaffected | 218 | 23,147 | 8.25 |
CLDN6 | 16p13 | 1 | One form | 220 | 23,292 | 8.32 |
CLDN7 | 17p13 | 3 | One form | 211 | 22,390 | 8.91 |
CLDN8 | 21q22 | 0 | One form | 225 | 24,845 | 9 |
CLDN9 | 16p13 | 1 | One form | 217 | 22,848 | 6.54 |
CLDN10 | 13q31 | 1 | Two variants: alternative transcription start site, different amino termini | a: 226 | 24,251 | 9.24 |
b: 228 | 24,488 | 8.32 | ||||
CLDN11 | 3q26 | 2 | One form | 207 | 21,993 | 8.22 |
CLDN12 | 7q21 | 2 | One form | 244 | 27,110 | 8.8 |
CLDN14 | 21q22 | 2 | Two variants: alternative splicing, coding unaffected | 239 | 25,699 | 8.94 |
CLDN15 | 7q11 | 4 | One form | 228 | 24,356 | 5.61 |
CLDN16 | 3q28 | 4 | One form | 305 | 33,836 | 8.26 |
CLDN17 | 21q22 | 0 | One form | 224 | 24,603 | 9.8 |
CLDN18 | 3q34 | 4 | Two variants: alternative transcription start site, different amino termini | a: 261 | 27,856 | 8.39 |
b: 261 | 27,720 | 8.39 | ||||
CLDN19 | 1p34 | 4 | Two variants: alternative splicing, different carboxyl termini | a: 224 | 23,229 | 8.48 |
b: 211 | 22,076 | 7.52 | ||||
CLDN20 | 6q25 | 1 | One form | 219 | 23,515 | 6.98 |
CLDN21 | 11q23 | 0 | One form | 229 | 25,393 | 5.37 |
CLDN22 | 4q35 | 0 | One form | 220 | 25,509 | 5.37 |
CLDN23 | 8p23 | 0 | One form | 292 | 31,915 | 7.51 |
CLDN24 | 4q35 | 0 | One form | 205 | 22,802 | 4.87 |
The chromosomal localization, intron number, and transcript details are indicated for each of the claudin genes, together with the size (in amino acids), molecular weight (in Da), and isoelectric point (Pi) of their encoded proteins. CLDN10, CLDN18, and CLDN19 have two variants giving rise to slightly different proteins. Only the variants documented in GenBank are indicated and other variants may exist.