Incidental Mutation 'R7237:Pcdh15'
ID 562912
Institutional Source Beutler Lab
Gene Symbol Pcdh15
Ensembl Gene ENSMUSG00000052613
Gene Name protocadherin 15
Synonyms Gm9815, nmf19, roda, Ush1f
MMRRC Submission 045344-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7237 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 72935174-74485569 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 74420023 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 1227 (D1227G)
Ref Sequence ENSEMBL: ENSMUSP00000090076 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000064562] [ENSMUST00000092420] [ENSMUST00000105424] [ENSMUST00000105426] [ENSMUST00000105429] [ENSMUST00000124046] [ENSMUST00000125055] [ENSMUST00000125517] [ENSMUST00000126920] [ENSMUST00000129404] [ENSMUST00000131321] [ENSMUST00000131724] [ENSMUST00000136096] [ENSMUST00000144302] [ENSMUST00000146682] [ENSMUST00000147189] [ENSMUST00000149977] [ENSMUST00000151116] [ENSMUST00000152655] [ENSMUST00000152819] [ENSMUST00000155701] [ENSMUST00000177107] [ENSMUST00000191709] [ENSMUST00000191854] [ENSMUST00000193174] [ENSMUST00000193361] [ENSMUST00000193739] [ENSMUST00000194315] [ENSMUST00000195531]
AlphaFold Q99PJ1
PDB Structure CRYSTAL STRUCTURE OF MOUSE CADHERIN-23 EC1-2 AND PROTOCADHERIN-15 EC1- 2 FORM I [X-RAY DIFFRACTION]
CRYSTAL STRUCTURE OF MOUSE CADHERIN-23 EC1-2 AND PROTOCADHERIN-15 EC1- 2 FORM II [X-RAY DIFFRACTION]
CRYSTAL STRUCTURE OF DEAFNESS ASSOCIATED MUTANT MOUSE CADHERIN-23 EC1- 2D124G AND PROTOCADHERIN-15 EC1-2 FORM I [X-RAY DIFFRACTION]
CRYSTAL STRUCTURE OF DEAFNESS ASSOCIATED MUTANT MOUSE CADHERIN-23 EC1- 2S70P AND PROTOCADHERIN-15 EC1-2 FORM I [X-RAY DIFFRACTION]
CRYSTAL STRUCTURE OF MOUSE CADHERIN-23 EC1-2 AND PROTOCADHERIN-15 EC1- 2, FORM I 2.2A. [X-RAY DIFFRACTION]
Predicted Effect possibly damaging
Transcript: ENSMUST00000064562
AA Change: D1156G

PolyPhen 2 Score 0.886 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000068561
Gene: ENSMUSG00000052613
AA Change: D1156G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 644 2.34e-16 SMART
CA 668 746 1.93e-26 SMART
CA 770 853 5.69e-15 SMART
CA 877 963 6.85e-9 SMART
CA 984 1071 3.09e-16 SMART
CA 1095 1179 4.49e-4 SMART
transmembrane domain 1304 1326 N/A INTRINSIC
low complexity region 1347 1374 N/A INTRINSIC
low complexity region 1583 1600 N/A INTRINSIC
low complexity region 1662 1682 N/A INTRINSIC
low complexity region 1689 1702 N/A INTRINSIC
low complexity region 1706 1756 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000092420
AA Change: D1227G

PolyPhen 2 Score 0.879 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000090076
Gene: ENSMUSG00000052613
AA Change: D1227G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 613 4.88e-14 SMART
CA 638 715 4.65e-20 SMART
CA 739 817 1.93e-26 SMART
CA 841 924 5.69e-15 SMART
CA 948 1034 6.85e-9 SMART
CA 1055 1142 3.09e-16 SMART
CA 1166 1250 4.49e-4 SMART
transmembrane domain 1377 1399 N/A INTRINSIC
low complexity region 1415 1442 N/A INTRINSIC
low complexity region 1651 1668 N/A INTRINSIC
low complexity region 1730 1750 N/A INTRINSIC
low complexity region 1757 1770 N/A INTRINSIC
low complexity region 1774 1824 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000105424
AA Change: D1227G

PolyPhen 2 Score 0.929 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000101064
Gene: ENSMUSG00000052613
AA Change: D1227G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 613 4.88e-14 SMART
CA 638 715 4.65e-20 SMART
CA 739 817 1.93e-26 SMART
CA 841 924 5.69e-15 SMART
CA 948 1034 6.85e-9 SMART
CA 1055 1142 3.09e-16 SMART
CA 1166 1250 4.49e-4 SMART
transmembrane domain 1375 1397 N/A INTRINSIC
low complexity region 1418 1445 N/A INTRINSIC
low complexity region 1656 1673 N/A INTRINSIC
low complexity region 1735 1755 N/A INTRINSIC
low complexity region 1762 1775 N/A INTRINSIC
low complexity region 1779 1829 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000105426
AA Change: D1227G

PolyPhen 2 Score 0.879 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000101066
Gene: ENSMUSG00000052613
AA Change: D1227G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 69 150 1.22e-1 SMART
CA 179 268 5.48e-8 SMART
CA 309 398 1.94e-8 SMART
CA 431 512 2.29e-10 SMART
CA 536 618 4.88e-14 SMART
CA 643 720 4.65e-20 SMART
CA 744 822 1.93e-26 SMART
CA 846 929 5.69e-15 SMART
CA 953 1039 6.85e-9 SMART
CA 1060 1147 3.09e-16 SMART
CA 1171 1255 4.49e-4 SMART
transmembrane domain 1380 1402 N/A INTRINSIC
low complexity region 1423 1450 N/A INTRINSIC
low complexity region 1661 1678 N/A INTRINSIC
low complexity region 1740 1760 N/A INTRINSIC
low complexity region 1767 1780 N/A INTRINSIC
low complexity region 1784 1834 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000105429
AA Change: D1156G

PolyPhen 2 Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000101069
Gene: ENSMUSG00000052613
AA Change: D1156G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 644 2.34e-16 SMART
CA 668 746 1.93e-26 SMART
CA 770 853 5.69e-15 SMART
CA 877 963 6.85e-9 SMART
CA 984 1071 3.09e-16 SMART
CA 1095 1179 4.49e-4 SMART
transmembrane domain 1304 1326 N/A INTRINSIC
low complexity region 1347 1374 N/A INTRINSIC
low complexity region 1585 1602 N/A INTRINSIC
low complexity region 1664 1684 N/A INTRINSIC
low complexity region 1691 1704 N/A INTRINSIC
low complexity region 1708 1758 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000124046
AA Change: D838G

PolyPhen 2 Score 0.607 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000121130
Gene: ENSMUSG00000052613
AA Change: D838G

DomainStartEndE-ValueType
CA 30 118 7.87e-9 SMART
CA 142 224 4.88e-14 SMART
CA 249 326 4.65e-20 SMART
CA 350 428 1.93e-26 SMART
CA 452 535 5.69e-15 SMART
CA 559 645 6.85e-9 SMART
CA 666 753 3.09e-16 SMART
CA 777 861 4.49e-4 SMART
transmembrane domain 986 1008 N/A INTRINSIC
low complexity region 1029 1056 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000125055
SMART Domains Protein: ENSMUSP00000114326
Gene: ENSMUSG00000052613

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 613 4.88e-14 SMART
low complexity region 649 665 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000125517
SMART Domains Protein: ENSMUSP00000115399
Gene: ENSMUSG00000052613

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
low complexity region 430 468 N/A INTRINSIC
low complexity region 521 584 N/A INTRINSIC
low complexity region 610 641 N/A INTRINSIC
low complexity region 657 685 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000126920
AA Change: D1205G

PolyPhen 2 Score 0.879 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000121939
Gene: ENSMUSG00000052613
AA Change: D1205G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 42 123 1.22e-1 SMART
CA 152 241 5.48e-8 SMART
CA 282 371 1.94e-8 SMART
CA 404 485 2.29e-10 SMART
CA 509 591 4.88e-14 SMART
CA 616 693 4.65e-20 SMART
CA 717 795 1.93e-26 SMART
CA 819 902 5.69e-15 SMART
CA 926 1012 6.85e-9 SMART
CA 1033 1120 3.09e-16 SMART
CA 1144 1228 4.49e-4 SMART
transmembrane domain 1353 1375 N/A INTRINSIC
low complexity region 1396 1423 N/A INTRINSIC
low complexity region 1634 1651 N/A INTRINSIC
low complexity region 1713 1733 N/A INTRINSIC
low complexity region 1740 1753 N/A INTRINSIC
low complexity region 1757 1807 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000129404
AA Change: D1205G

PolyPhen 2 Score 0.929 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000117731
Gene: ENSMUSG00000052613
AA Change: D1205G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 42 123 1.22e-1 SMART
CA 152 241 5.48e-8 SMART
CA 282 371 1.94e-8 SMART
CA 404 485 2.29e-10 SMART
CA 509 591 4.88e-14 SMART
CA 616 693 4.65e-20 SMART
CA 717 795 1.93e-26 SMART
CA 819 902 5.69e-15 SMART
CA 926 1012 6.85e-9 SMART
CA 1033 1120 3.09e-16 SMART
CA 1144 1228 4.49e-4 SMART
transmembrane domain 1355 1377 N/A INTRINSIC
low complexity region 1393 1420 N/A INTRINSIC
low complexity region 1631 1648 N/A INTRINSIC
low complexity region 1710 1730 N/A INTRINSIC
low complexity region 1737 1750 N/A INTRINSIC
low complexity region 1754 1804 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000131321
AA Change: D1227G

PolyPhen 2 Score 0.879 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000122911
Gene: ENSMUSG00000052613
AA Change: D1227G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 613 4.88e-14 SMART
CA 638 715 4.65e-20 SMART
CA 739 817 1.93e-26 SMART
CA 841 924 5.69e-15 SMART
CA 948 1034 6.85e-9 SMART
CA 1055 1142 3.09e-16 SMART
CA 1166 1250 4.49e-4 SMART
transmembrane domain 1375 1397 N/A INTRINSIC
low complexity region 1418 1445 N/A INTRINSIC
low complexity region 1654 1671 N/A INTRINSIC
low complexity region 1733 1753 N/A INTRINSIC
low complexity region 1760 1773 N/A INTRINSIC
low complexity region 1777 1827 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000131724
AA Change: D1227G

PolyPhen 2 Score 0.299 (Sensitivity: 0.91; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000122466
Gene: ENSMUSG00000052613
AA Change: D1227G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 613 4.88e-14 SMART
CA 638 715 4.65e-20 SMART
CA 739 817 1.93e-26 SMART
CA 841 924 5.69e-15 SMART
CA 948 1034 6.85e-9 SMART
CA 1055 1142 3.09e-16 SMART
CA 1166 1250 4.49e-4 SMART
transmembrane domain 1375 1397 N/A INTRINSIC
low complexity region 1418 1445 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000136096
SMART Domains Protein: ENSMUSP00000121534
Gene: ENSMUSG00000052613

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 613 4.88e-14 SMART
low complexity region 649 665 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000144302
SMART Domains Protein: ENSMUSP00000122606
Gene: ENSMUSG00000052613

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
low complexity region 313 326 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000146682
SMART Domains Protein: ENSMUSP00000134863
Gene: ENSMUSG00000052613

DomainStartEndE-ValueType
transmembrane domain 128 150 N/A INTRINSIC
low complexity region 215 232 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000147189
AA Change: D1190G

PolyPhen 2 Score 0.929 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000122940
Gene: ENSMUSG00000052613
AA Change: D1190G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
low complexity region 209 225 N/A INTRINSIC
CA 267 356 1.94e-8 SMART
CA 389 470 2.29e-10 SMART
CA 494 576 4.88e-14 SMART
CA 601 678 4.65e-20 SMART
CA 702 780 1.93e-26 SMART
CA 804 887 5.69e-15 SMART
CA 911 997 6.85e-9 SMART
CA 1018 1105 3.09e-16 SMART
CA 1129 1213 4.49e-4 SMART
transmembrane domain 1340 1362 N/A INTRINSIC
low complexity region 1378 1405 N/A INTRINSIC
low complexity region 1614 1631 N/A INTRINSIC
low complexity region 1693 1713 N/A INTRINSIC
low complexity region 1720 1733 N/A INTRINSIC
low complexity region 1737 1787 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000149977
AA Change: D1227G

PolyPhen 2 Score 0.520 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000118833
Gene: ENSMUSG00000052613
AA Change: D1227G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 613 4.88e-14 SMART
CA 638 715 4.65e-20 SMART
CA 739 817 1.93e-26 SMART
CA 841 924 5.69e-15 SMART
CA 948 1034 6.85e-9 SMART
CA 1055 1142 3.09e-16 SMART
CA 1166 1250 4.49e-4 SMART
transmembrane domain 1375 1397 N/A INTRINSIC
low complexity region 1418 1445 N/A INTRINSIC
low complexity region 1477 1494 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000151116
AA Change: D1239G

PolyPhen 2 Score 0.797 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000119662
Gene: ENSMUSG00000052613
AA Change: D1239G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 69 150 1.22e-1 SMART
CA 179 268 5.48e-8 SMART
CA 309 398 1.94e-8 SMART
CA 431 519 7.87e-9 SMART
CA 543 625 4.88e-14 SMART
CA 650 727 4.65e-20 SMART
CA 751 829 1.93e-26 SMART
CA 853 936 5.69e-15 SMART
CA 960 1046 6.85e-9 SMART
CA 1067 1154 3.09e-16 SMART
CA 1178 1262 4.49e-4 SMART
transmembrane domain 1387 1409 N/A INTRINSIC
low complexity region 1430 1457 N/A INTRINSIC
low complexity region 1489 1519 N/A INTRINSIC
low complexity region 1521 1539 N/A INTRINSIC
low complexity region 1592 1655 N/A INTRINSIC
low complexity region 1681 1712 N/A INTRINSIC
low complexity region 1728 1756 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000152655
SMART Domains Protein: ENSMUSP00000118201
Gene: ENSMUSG00000052613

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 6e-4 SMART
CA 174 263 2.8e-10 SMART
CA 304 393 9.4e-11 SMART
CA 426 507 1.2e-12 SMART
CA 531 613 2.3e-16 SMART
CA 638 726 3.4e-6 SMART
low complexity region 783 846 N/A INTRINSIC
low complexity region 872 903 N/A INTRINSIC
low complexity region 919 947 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000152819
SMART Domains Protein: ENSMUSP00000123647
Gene: ENSMUSG00000052613

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
Blast:CA 304 363 1e-33 BLAST
low complexity region 364 399 N/A INTRINSIC
low complexity region 452 515 N/A INTRINSIC
low complexity region 541 572 N/A INTRINSIC
low complexity region 588 616 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000155701
SMART Domains Protein: ENSMUSP00000135495
Gene: ENSMUSG00000052613

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
Blast:CA 304 330 2e-8 BLAST
Predicted Effect possibly damaging
Transcript: ENSMUST00000177107
AA Change: D1232G

PolyPhen 2 Score 0.464 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000135501
Gene: ENSMUSG00000052613
AA Change: D1232G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 69 150 1.22e-1 SMART
CA 179 268 5.48e-8 SMART
CA 309 398 1.94e-8 SMART
CA 431 512 2.29e-10 SMART
CA 536 618 4.88e-14 SMART
CA 643 720 4.65e-20 SMART
CA 744 822 1.93e-26 SMART
CA 846 929 5.69e-15 SMART
CA 953 1039 6.85e-9 SMART
CA 1060 1147 3.09e-16 SMART
CA 1171 1255 4.49e-4 SMART
transmembrane domain 1380 1402 N/A INTRINSIC
low complexity region 1423 1450 N/A INTRINSIC
low complexity region 1482 1499 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000191709
AA Change: D1232G

PolyPhen 2 Score 0.797 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000142313
Gene: ENSMUSG00000052613
AA Change: D1232G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 69 150 1.22e-1 SMART
CA 179 268 5.48e-8 SMART
CA 309 398 1.94e-8 SMART
CA 431 512 2.29e-10 SMART
CA 536 618 4.88e-14 SMART
CA 643 720 4.65e-20 SMART
CA 744 822 1.93e-26 SMART
CA 846 929 5.69e-15 SMART
CA 953 1039 6.85e-9 SMART
CA 1060 1147 3.09e-16 SMART
CA 1171 1255 4.49e-4 SMART
transmembrane domain 1380 1402 N/A INTRINSIC
low complexity region 1423 1450 N/A INTRINSIC
low complexity region 1480 1510 N/A INTRINSIC
low complexity region 1512 1530 N/A INTRINSIC
low complexity region 1583 1646 N/A INTRINSIC
low complexity region 1672 1703 N/A INTRINSIC
low complexity region 1719 1747 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000191854
AA Change: D1227G

PolyPhen 2 Score 0.607 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000141973
Gene: ENSMUSG00000052613
AA Change: D1227G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 1.22e-1 SMART
CA 174 263 5.48e-8 SMART
CA 304 393 1.94e-8 SMART
CA 426 507 2.29e-10 SMART
CA 531 613 4.88e-14 SMART
CA 638 715 4.65e-20 SMART
CA 739 817 1.93e-26 SMART
CA 841 924 5.69e-15 SMART
CA 948 1034 6.85e-9 SMART
CA 1055 1142 3.09e-16 SMART
CA 1166 1250 4.49e-4 SMART
transmembrane domain 1375 1397 N/A INTRINSIC
low complexity region 1418 1445 N/A INTRINSIC
low complexity region 1477 1494 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000193174
AA Change: D1234G

PolyPhen 2 Score 0.942 (Sensitivity: 0.80; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000142238
Gene: ENSMUSG00000052613
AA Change: D1234G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 6e-4 SMART
CA 174 263 2.8e-10 SMART
CA 304 393 9.4e-11 SMART
CA 426 514 3.8e-11 SMART
CA 538 620 2.3e-16 SMART
CA 645 722 2.3e-22 SMART
CA 746 824 9.3e-29 SMART
CA 848 931 2.8e-17 SMART
CA 955 1041 3.3e-11 SMART
CA 1062 1149 1.5e-18 SMART
CA 1173 1257 2.3e-6 SMART
transmembrane domain 1382 1404 N/A INTRINSIC
low complexity region 1425 1452 N/A INTRINSIC
low complexity region 1482 1512 N/A INTRINSIC
low complexity region 1514 1532 N/A INTRINSIC
low complexity region 1585 1648 N/A INTRINSIC
low complexity region 1674 1705 N/A INTRINSIC
low complexity region 1721 1749 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000193361
AA Change: D1232G

PolyPhen 2 Score 0.942 (Sensitivity: 0.80; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000141792
Gene: ENSMUSG00000052613
AA Change: D1232G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 69 150 1.22e-1 SMART
CA 179 268 5.48e-8 SMART
CA 309 398 1.94e-8 SMART
CA 431 512 2.29e-10 SMART
CA 536 618 4.88e-14 SMART
CA 643 720 4.65e-20 SMART
CA 744 822 1.93e-26 SMART
CA 846 929 5.69e-15 SMART
CA 953 1039 6.85e-9 SMART
CA 1060 1147 3.09e-16 SMART
CA 1171 1255 4.49e-4 SMART
transmembrane domain 1380 1402 N/A INTRINSIC
low complexity region 1423 1450 N/A INTRINSIC
low complexity region 1661 1678 N/A INTRINSIC
low complexity region 1740 1760 N/A INTRINSIC
low complexity region 1767 1780 N/A INTRINSIC
low complexity region 1784 1834 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000193739
AA Change: D1232G

PolyPhen 2 Score 0.607 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000142173
Gene: ENSMUSG00000052613
AA Change: D1232G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 69 150 1.22e-1 SMART
CA 179 268 5.48e-8 SMART
CA 309 398 1.94e-8 SMART
CA 431 512 2.29e-10 SMART
CA 536 618 4.88e-14 SMART
CA 643 720 4.65e-20 SMART
CA 744 822 1.93e-26 SMART
CA 846 929 5.69e-15 SMART
CA 953 1039 6.85e-9 SMART
CA 1060 1147 3.09e-16 SMART
CA 1171 1255 4.49e-4 SMART
transmembrane domain 1382 1404 N/A INTRINSIC
low complexity region 1420 1447 N/A INTRINSIC
low complexity region 1477 1494 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000194315
AA Change: D632G

PolyPhen 2 Score 0.901 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000141594
Gene: ENSMUSG00000052613
AA Change: D632G

DomainStartEndE-ValueType
CA 43 120 2.3e-22 SMART
CA 144 222 9.3e-29 SMART
CA 246 329 2.8e-17 SMART
CA 353 439 3.3e-11 SMART
CA 460 547 1.5e-18 SMART
CA 571 655 2.3e-6 SMART
transmembrane domain 780 802 N/A INTRINSIC
low complexity region 823 850 N/A INTRINSIC
low complexity region 1051 1068 N/A INTRINSIC
low complexity region 1130 1150 N/A INTRINSIC
low complexity region 1157 1170 N/A INTRINSIC
low complexity region 1174 1224 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000195531
AA Change: D1227G

PolyPhen 2 Score 0.659 (Sensitivity: 0.86; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000141920
Gene: ENSMUSG00000052613
AA Change: D1227G

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
CA 64 145 6e-4 SMART
CA 174 263 2.8e-10 SMART
CA 304 393 9.4e-11 SMART
CA 426 507 1.2e-12 SMART
CA 531 613 2.3e-16 SMART
CA 638 715 2.3e-22 SMART
CA 739 817 9.3e-29 SMART
CA 841 924 2.8e-17 SMART
CA 948 1034 3.3e-11 SMART
CA 1055 1142 1.5e-18 SMART
CA 1166 1250 2.3e-6 SMART
transmembrane domain 1377 1399 N/A INTRINSIC
low complexity region 1415 1442 N/A INTRINSIC
low complexity region 1514 1531 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.6%
Validation Efficiency 98% (83/85)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F). Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur. [provided by RefSeq, Dec 2008]
PHENOTYPE: Homozygotes for severe mutations exhibit circling, head-tossing, hyperactivity, impaired swimming and profound deafness. Mice have defects in cochlea and degeneration of hair cells, spiral ganglion cells and saccular macula. Females are poor mothers. [provided by MGI curators]
Allele List at MGI

All alleles(11) : Gene trapped(2) Transgenic(1) Spontaneous(6) Chemically induced(2)

Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap21 A T 2: 20,854,783 (GRCm39) C1536* probably null Het
Armc9 C A 1: 86,092,571 (GRCm39) Q169K possibly damaging Het
Aspm T A 1: 139,405,667 (GRCm39) M1518K possibly damaging Het
AU018091 A G 7: 3,209,006 (GRCm39) I360T probably benign Het
BB014433 C A 8: 15,091,765 (GRCm39) V363L probably benign Het
Bcam T C 7: 19,503,232 (GRCm39) probably null Het
Cacna1g T C 11: 94,328,705 (GRCm39) S1071G probably benign Het
Card9 A T 2: 26,246,787 (GRCm39) S354T probably benign Het
Ccdc87 A G 19: 4,889,790 (GRCm39) N94S probably benign Het
Cdc27 A G 11: 104,408,245 (GRCm39) V555A probably benign Het
Coro1a T A 7: 126,299,478 (GRCm39) D411V probably benign Het
Cybrd1 GGTCCTGCAC G 2: 70,948,553 (GRCm39) probably benign Het
Cyth1 A T 11: 118,076,321 (GRCm39) I95N probably damaging Het
Dnah7b A T 1: 46,179,126 (GRCm39) E933V probably damaging Het
Dync2h1 A T 9: 6,993,966 (GRCm39) I3968N probably benign Het
Fam184a T C 10: 53,510,489 (GRCm39) probably benign Het
Fat3 G A 9: 16,288,510 (GRCm39) L338F probably damaging Het
Fcgr3 A G 1: 170,886,870 (GRCm39) L18P probably damaging Het
Gbp5 T C 3: 142,213,461 (GRCm39) V459A probably benign Het
Gja4 A T 4: 127,205,956 (GRCm39) M269K probably benign Het
Gm4787 A G 12: 81,424,442 (GRCm39) V572A probably damaging Het
Grin2d G T 7: 45,515,600 (GRCm39) S131* probably null Het
Gys1 A G 7: 45,104,586 (GRCm39) D671G probably benign Het
Haspin T C 11: 73,027,712 (GRCm39) N459S probably benign Het
Hdac10 G T 15: 89,009,580 (GRCm39) Q451K probably benign Het
Hdac9 T C 12: 34,424,139 (GRCm39) probably null Het
Hmcn1 A G 1: 150,598,394 (GRCm39) V1636A probably damaging Het
Hpca A G 4: 129,012,407 (GRCm39) L43P probably damaging Het
Hycc2 G A 1: 58,569,107 (GRCm39) Q491* probably null Het
Insm1 C A 2: 146,064,448 (GRCm39) A88E possibly damaging Het
Itga9 A G 9: 118,465,670 (GRCm39) K175E probably benign Het
Kif13a A G 13: 46,962,632 (GRCm39) probably null Het
Kif20b T A 19: 34,928,005 (GRCm39) L1089H probably damaging Het
Lamp5 A T 2: 135,901,755 (GRCm39) H152L probably benign Het
Lrp4 T C 2: 91,303,528 (GRCm39) F76L probably benign Het
Magi3 T C 3: 103,935,227 (GRCm39) D902G probably damaging Het
Map10 C T 8: 126,397,963 (GRCm39) P452L probably benign Het
Mapk6 A G 9: 75,304,895 (GRCm39) L174P probably damaging Het
Meak7 C T 8: 120,489,054 (GRCm39) G410S probably damaging Het
Ndufa4 C T 6: 11,906,018 (GRCm39) probably null Het
Nedd4 A T 9: 72,632,346 (GRCm39) E393D probably benign Het
Nlrp4b G A 7: 10,449,143 (GRCm39) V449I probably benign Het
Nufip2 T A 11: 77,583,596 (GRCm39) N503K probably benign Het
Or10ac1 T C 6: 42,515,581 (GRCm39) D125G probably damaging Het
Or6y1 C T 1: 174,276,905 (GRCm39) R239C probably benign Het
P4ha1 A G 10: 59,184,065 (GRCm39) T176A probably benign Het
Palm3 A G 8: 84,756,117 (GRCm39) K543R probably benign Het
Parvg G A 15: 84,225,557 (GRCm39) A302T probably benign Het
Pdzd8 C T 19: 59,333,571 (GRCm39) G150D probably damaging Het
Pitpnm2 A G 5: 124,263,360 (GRCm39) probably null Het
Pld5 T C 1: 176,102,301 (GRCm39) Q47R possibly damaging Het
Ppp2r5d T C 17: 46,997,206 (GRCm39) S329G possibly damaging Het
Prss56 T C 1: 87,112,637 (GRCm39) V144A probably damaging Het
Psg28 A T 7: 18,161,769 (GRCm39) Y245N possibly damaging Het
Ptpn3 C T 4: 57,239,625 (GRCm39) V302I probably damaging Het
Ptprn2 A G 12: 117,125,347 (GRCm39) H627R probably benign Het
Rasgrp2 A T 19: 6,454,838 (GRCm39) H226L possibly damaging Het
Rbm20 C T 19: 53,839,930 (GRCm39) T973M probably benign Het
Rigi T A 4: 40,205,938 (GRCm39) I885F probably benign Het
Riok2 T A 17: 17,598,045 (GRCm39) L44Q probably damaging Het
Rusc1 G T 3: 88,998,805 (GRCm39) Q326K possibly damaging Het
Rxylt1 A T 10: 121,917,523 (GRCm39) L330* probably null Het
Sart3 A T 5: 113,892,307 (GRCm39) H397Q possibly damaging Het
Sec31b T A 19: 44,506,147 (GRCm39) T920S probably damaging Het
Serpinb13 A G 1: 106,926,679 (GRCm39) E225G probably damaging Het
Slc25a47 T C 12: 108,821,386 (GRCm39) L165P probably damaging Het
Slc2a10 G A 2: 165,357,197 (GRCm39) V286I probably benign Het
Slc39a13 G T 2: 90,895,979 (GRCm39) T174N probably benign Het
Slc7a13 T A 4: 19,839,364 (GRCm39) N322K probably benign Het
Stk38 T C 17: 29,193,620 (GRCm39) T326A possibly damaging Het
Sult1a1 T C 7: 126,272,622 (GRCm39) M244V probably benign Het
Tas2r144 C T 6: 42,192,800 (GRCm39) T180I probably damaging Het
Tbc1d12 T A 19: 38,887,346 (GRCm39) M366K probably benign Het
Terb1 T C 8: 105,221,959 (GRCm39) I147V possibly damaging Het
Tnik T C 3: 28,692,568 (GRCm39) Y820H probably damaging Het
Tnxb C A 17: 34,901,170 (GRCm39) L995I possibly damaging Het
Trim34b A G 7: 103,978,794 (GRCm39) T14A possibly damaging Het
Urb1 T C 16: 90,588,054 (GRCm39) E418G probably damaging Het
Vmn1r12 T A 6: 57,136,550 (GRCm39) C216S possibly damaging Het
Vmn2r90 T A 17: 17,924,249 (GRCm39) V16E possibly damaging Het
Vps11 A T 9: 44,265,803 (GRCm39) V492D probably damaging Het
Wdr62 A C 7: 29,969,869 (GRCm39) probably null Het
Zc3h14 T A 12: 98,746,408 (GRCm39) M539K probably benign Het
Zfp871 A T 17: 32,994,289 (GRCm39) H295Q probably damaging Het
Other mutations in Pcdh15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00421:Pcdh15 APN 10 74,021,177 (GRCm39) nonsense probably null
IGL00432:Pcdh15 APN 10 74,126,914 (GRCm39) splice site probably benign
IGL00533:Pcdh15 APN 10 74,338,552 (GRCm39) missense probably damaging 1.00
IGL00596:Pcdh15 APN 10 74,466,576 (GRCm39) missense probably benign 0.00
IGL00930:Pcdh15 APN 10 74,466,530 (GRCm39) missense probably benign 0.08
IGL00970:Pcdh15 APN 10 74,215,172 (GRCm39) missense probably damaging 1.00
IGL01087:Pcdh15 APN 10 74,178,464 (GRCm39) missense possibly damaging 0.90
IGL01763:Pcdh15 APN 10 74,046,293 (GRCm39) missense probably benign 0.09
IGL01787:Pcdh15 APN 10 74,286,115 (GRCm39) missense probably benign 0.25
IGL02070:Pcdh15 APN 10 74,466,700 (GRCm39) missense probably benign 0.00
IGL02234:Pcdh15 APN 10 74,467,694 (GRCm39) missense probably benign 0.02
IGL02268:Pcdh15 APN 10 74,178,504 (GRCm39) missense probably damaging 1.00
IGL02280:Pcdh15 APN 10 74,058,295 (GRCm39) missense probably damaging 1.00
IGL02363:Pcdh15 APN 10 74,152,918 (GRCm39) missense probably damaging 0.98
IGL02420:Pcdh15 APN 10 74,138,938 (GRCm39) missense probably damaging 0.98
IGL02749:Pcdh15 APN 10 74,466,900 (GRCm39) missense probably benign 0.00
IGL02939:Pcdh15 APN 10 74,340,648 (GRCm39) splice site probably benign
IGL02970:Pcdh15 APN 10 74,126,794 (GRCm39) splice site probably benign
IGL03010:Pcdh15 APN 10 74,221,777 (GRCm39) missense probably damaging 1.00
IGL03061:Pcdh15 APN 10 74,152,843 (GRCm39) missense probably damaging 0.97
IGL03095:Pcdh15 APN 10 74,191,706 (GRCm39) missense probably damaging 1.00
IGL03149:Pcdh15 APN 10 74,466,527 (GRCm39) missense probably damaging 1.00
IGL03187:Pcdh15 APN 10 74,191,706 (GRCm39) missense probably damaging 1.00
IGL03279:Pcdh15 APN 10 74,152,904 (GRCm39) missense probably damaging 1.00
IGL03392:Pcdh15 APN 10 74,460,104 (GRCm39) missense probably damaging 1.00
loop UTSW 10 74,021,210 (GRCm39) missense probably damaging 1.00
mcduck UTSW 10 74,462,676 (GRCm39) critical splice donor site probably null
spaz UTSW 10 74,046,257 (GRCm39) missense probably damaging 1.00
sphere UTSW 10 74,460,116 (GRCm39) missense probably damaging 1.00
squirm UTSW 10 0 () large deletion
Tortilla UTSW 10 74,215,249 (GRCm39) splice site probably null
1mM(1):Pcdh15 UTSW 10 74,461,969 (GRCm39) intron probably benign
BB009:Pcdh15 UTSW 10 74,481,359 (GRCm39) missense probably benign 0.18
BB019:Pcdh15 UTSW 10 74,481,359 (GRCm39) missense probably benign 0.18
R0038:Pcdh15 UTSW 10 74,479,272 (GRCm39) missense possibly damaging 0.95
R0103:Pcdh15 UTSW 10 74,046,257 (GRCm39) missense probably damaging 1.00
R0110:Pcdh15 UTSW 10 74,126,808 (GRCm39) missense probably damaging 1.00
R0111:Pcdh15 UTSW 10 74,462,651 (GRCm39) nonsense probably null
R0119:Pcdh15 UTSW 10 74,006,407 (GRCm39) missense probably damaging 1.00
R0131:Pcdh15 UTSW 10 74,006,440 (GRCm39) missense probably null 1.00
R0445:Pcdh15 UTSW 10 74,178,381 (GRCm39) missense probably damaging 1.00
R0464:Pcdh15 UTSW 10 74,462,676 (GRCm39) critical splice donor site probably null
R0503:Pcdh15 UTSW 10 74,046,217 (GRCm39) missense probably damaging 1.00
R0507:Pcdh15 UTSW 10 74,457,129 (GRCm39) missense probably damaging 1.00
R0510:Pcdh15 UTSW 10 74,126,808 (GRCm39) missense probably damaging 1.00
R0742:Pcdh15 UTSW 10 74,457,129 (GRCm39) missense probably damaging 1.00
R0790:Pcdh15 UTSW 10 74,466,885 (GRCm39) missense probably benign 0.01
R0829:Pcdh15 UTSW 10 74,338,598 (GRCm39) missense probably damaging 1.00
R0839:Pcdh15 UTSW 10 74,462,614 (GRCm39) missense probably null 1.00
R0882:Pcdh15 UTSW 10 74,178,488 (GRCm39) missense probably damaging 1.00
R0894:Pcdh15 UTSW 10 74,460,087 (GRCm39) missense probably damaging 1.00
R0944:Pcdh15 UTSW 10 74,046,302 (GRCm39) missense probably damaging 0.99
R1081:Pcdh15 UTSW 10 74,286,145 (GRCm39) missense probably damaging 1.00
R1148:Pcdh15 UTSW 10 74,006,392 (GRCm39) missense probably damaging 1.00
R1148:Pcdh15 UTSW 10 74,006,392 (GRCm39) missense probably damaging 1.00
R1484:Pcdh15 UTSW 10 74,126,833 (GRCm39) missense probably damaging 1.00
R1521:Pcdh15 UTSW 10 74,430,023 (GRCm39) missense probably damaging 1.00
R1694:Pcdh15 UTSW 10 74,429,995 (GRCm39) missense probably damaging 1.00
R1795:Pcdh15 UTSW 10 74,460,087 (GRCm39) missense probably damaging 1.00
R2021:Pcdh15 UTSW 10 74,467,025 (GRCm39) missense possibly damaging 0.93
R2022:Pcdh15 UTSW 10 74,467,025 (GRCm39) missense possibly damaging 0.93
R2023:Pcdh15 UTSW 10 74,467,025 (GRCm39) missense possibly damaging 0.93
R2076:Pcdh15 UTSW 10 74,178,479 (GRCm39) missense probably damaging 1.00
R2199:Pcdh15 UTSW 10 74,006,341 (GRCm39) missense probably damaging 1.00
R2510:Pcdh15 UTSW 10 74,467,331 (GRCm39) missense probably benign 0.39
R2511:Pcdh15 UTSW 10 74,481,828 (GRCm39) missense possibly damaging 0.94
R3418:Pcdh15 UTSW 10 74,420,054 (GRCm39) missense probably benign 0.12
R3419:Pcdh15 UTSW 10 74,420,054 (GRCm39) missense probably benign 0.12
R3433:Pcdh15 UTSW 10 74,467,331 (GRCm39) missense probably benign 0.39
R3619:Pcdh15 UTSW 10 74,479,227 (GRCm39) missense probably benign 0.19
R3723:Pcdh15 UTSW 10 74,481,680 (GRCm39) missense probably benign 0.05
R3724:Pcdh15 UTSW 10 74,481,680 (GRCm39) missense probably benign 0.05
R3778:Pcdh15 UTSW 10 73,782,983 (GRCm39) splice site probably null
R3851:Pcdh15 UTSW 10 74,467,518 (GRCm39) missense probably damaging 0.97
R4175:Pcdh15 UTSW 10 74,467,829 (GRCm39) intron probably benign
R4261:Pcdh15 UTSW 10 74,481,512 (GRCm39) missense probably damaging 1.00
R4385:Pcdh15 UTSW 10 74,386,322 (GRCm39) missense probably damaging 1.00
R4585:Pcdh15 UTSW 10 74,460,116 (GRCm39) missense probably damaging 1.00
R4602:Pcdh15 UTSW 10 74,430,046 (GRCm39) missense probably damaging 1.00
R4639:Pcdh15 UTSW 10 74,479,439 (GRCm39) missense probably benign 0.00
R4703:Pcdh15 UTSW 10 74,285,995 (GRCm39) missense probably damaging 1.00
R4819:Pcdh15 UTSW 10 74,160,221 (GRCm39) missense probably damaging 1.00
R4906:Pcdh15 UTSW 10 74,340,625 (GRCm39) nonsense probably null
R4961:Pcdh15 UTSW 10 74,215,249 (GRCm39) splice site probably null
R5018:Pcdh15 UTSW 10 74,479,607 (GRCm39) missense possibly damaging 0.68
R5125:Pcdh15 UTSW 10 74,419,912 (GRCm39) missense probably damaging 0.98
R5225:Pcdh15 UTSW 10 74,138,986 (GRCm39) missense probably damaging 1.00
R5259:Pcdh15 UTSW 10 74,232,204 (GRCm39) missense possibly damaging 0.67
R5279:Pcdh15 UTSW 10 74,430,015 (GRCm39) missense probably damaging 1.00
R5395:Pcdh15 UTSW 10 74,021,119 (GRCm39) missense probably damaging 1.00
R5458:Pcdh15 UTSW 10 74,340,611 (GRCm39) missense probably damaging 1.00
R5617:Pcdh15 UTSW 10 74,471,504 (GRCm39) intron probably benign
R5665:Pcdh15 UTSW 10 74,462,620 (GRCm39) missense probably damaging 1.00
R5770:Pcdh15 UTSW 10 74,021,177 (GRCm39) nonsense probably null
R5805:Pcdh15 UTSW 10 74,066,091 (GRCm39) missense probably damaging 1.00
R5914:Pcdh15 UTSW 10 74,466,768 (GRCm39) missense probably benign 0.42
R5988:Pcdh15 UTSW 10 74,215,189 (GRCm39) missense probably benign 0.05
R6133:Pcdh15 UTSW 10 74,481,805 (GRCm39) splice site probably null
R6189:Pcdh15 UTSW 10 74,178,483 (GRCm39) missense probably null 1.00
R6414:Pcdh15 UTSW 10 74,021,258 (GRCm39) missense probably damaging 1.00
R6536:Pcdh15 UTSW 10 74,467,221 (GRCm39) missense probably damaging 1.00
R6612:Pcdh15 UTSW 10 74,021,210 (GRCm39) missense probably damaging 1.00
R6711:Pcdh15 UTSW 10 74,478,219 (GRCm39) missense possibly damaging 0.83
R6793:Pcdh15 UTSW 10 74,466,971 (GRCm39) missense probably damaging 1.00
R6841:Pcdh15 UTSW 10 74,286,052 (GRCm39) missense probably damaging 1.00
R6845:Pcdh15 UTSW 10 74,466,465 (GRCm39) missense probably benign
R6915:Pcdh15 UTSW 10 74,479,641 (GRCm39) missense probably benign 0.16
R6954:Pcdh15 UTSW 10 74,481,821 (GRCm39) missense possibly damaging 0.92
R6970:Pcdh15 UTSW 10 74,338,519 (GRCm39) missense probably damaging 0.98
R7018:Pcdh15 UTSW 10 74,302,186 (GRCm39) missense probably damaging 1.00
R7064:Pcdh15 UTSW 10 74,466,446 (GRCm39) missense possibly damaging 0.67
R7079:Pcdh15 UTSW 10 74,152,957 (GRCm39) missense probably benign 0.21
R7172:Pcdh15 UTSW 10 74,338,597 (GRCm39) missense probably damaging 1.00
R7220:Pcdh15 UTSW 10 74,178,441 (GRCm39) missense possibly damaging 0.64
R7266:Pcdh15 UTSW 10 74,215,222 (GRCm39) nonsense probably null
R7276:Pcdh15 UTSW 10 74,160,224 (GRCm39) missense probably benign 0.25
R7359:Pcdh15 UTSW 10 74,420,048 (GRCm39) missense probably damaging 0.99
R7396:Pcdh15 UTSW 10 74,466,522 (GRCm39) missense probably benign 0.17
R7421:Pcdh15 UTSW 10 74,289,897 (GRCm39) missense possibly damaging 0.90
R7424:Pcdh15 UTSW 10 74,342,317 (GRCm39) missense probably benign 0.09
R7463:Pcdh15 UTSW 10 74,467,602 (GRCm39) missense possibly damaging 0.66
R7469:Pcdh15 UTSW 10 74,481,812 (GRCm39) missense probably benign
R7512:Pcdh15 UTSW 10 74,477,214 (GRCm39) missense possibly damaging 0.81
R7767:Pcdh15 UTSW 10 74,322,088 (GRCm39) missense probably benign 0.07
R7830:Pcdh15 UTSW 10 74,221,733 (GRCm39) missense probably damaging 1.00
R7890:Pcdh15 UTSW 10 74,478,146 (GRCm39) missense probably damaging 1.00
R7897:Pcdh15 UTSW 10 74,289,827 (GRCm39) missense probably damaging 1.00
R7908:Pcdh15 UTSW 10 74,479,414 (GRCm39) missense probably benign 0.04
R7932:Pcdh15 UTSW 10 74,481,359 (GRCm39) missense probably benign 0.18
R7940:Pcdh15 UTSW 10 74,430,022 (GRCm39) missense probably damaging 1.00
R8230:Pcdh15 UTSW 10 74,191,707 (GRCm39) missense probably damaging 1.00
R8307:Pcdh15 UTSW 10 74,342,307 (GRCm39) nonsense probably null
R8382:Pcdh15 UTSW 10 74,479,227 (GRCm39) missense probably benign 0.19
R8397:Pcdh15 UTSW 10 74,126,865 (GRCm39) missense probably damaging 1.00
R8498:Pcdh15 UTSW 10 74,317,974 (GRCm39) missense probably damaging 1.00
R8692:Pcdh15 UTSW 10 74,289,805 (GRCm39) missense possibly damaging 0.63
R8797:Pcdh15 UTSW 10 74,419,978 (GRCm39) missense probably damaging 1.00
R9020:Pcdh15 UTSW 10 74,481,443 (GRCm39) missense probably benign 0.01
R9033:Pcdh15 UTSW 10 74,302,138 (GRCm39) missense probably damaging 1.00
R9056:Pcdh15 UTSW 10 74,221,731 (GRCm39) missense probably damaging 1.00
R9177:Pcdh15 UTSW 10 74,479,455 (GRCm39) missense probably benign 0.13
R9191:Pcdh15 UTSW 10 74,161,981 (GRCm39) missense probably benign 0.38
R9268:Pcdh15 UTSW 10 74,479,455 (GRCm39) missense probably benign 0.13
R9279:Pcdh15 UTSW 10 74,461,756 (GRCm39) intron probably benign
R9294:Pcdh15 UTSW 10 74,479,560 (GRCm39) missense unknown
R9387:Pcdh15 UTSW 10 74,066,192 (GRCm39) missense probably damaging 0.98
R9409:Pcdh15 UTSW 10 74,160,190 (GRCm39) missense probably damaging 0.98
R9410:Pcdh15 UTSW 10 74,481,663 (GRCm39) frame shift probably null
R9412:Pcdh15 UTSW 10 74,481,663 (GRCm39) frame shift probably null
R9432:Pcdh15 UTSW 10 74,460,170 (GRCm39) missense probably damaging 1.00
R9444:Pcdh15 UTSW 10 74,478,176 (GRCm39) missense probably damaging 1.00
R9579:Pcdh15 UTSW 10 74,457,117 (GRCm39) missense possibly damaging 0.89
R9643:Pcdh15 UTSW 10 74,479,335 (GRCm39) missense probably benign 0.18
R9784:Pcdh15 UTSW 10 74,467,212 (GRCm39) missense probably benign 0.00
RF020:Pcdh15 UTSW 10 74,021,242 (GRCm39) missense probably damaging 1.00
Z1176:Pcdh15 UTSW 10 74,466,533 (GRCm39) missense probably benign 0.00
Z1177:Pcdh15 UTSW 10 74,340,632 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGACACGGGTAATTACAGTGC -3'
(R):5'- GGAGACCCTGCCTAACAAAG -3'

Sequencing Primer
(F):5'- GGTAATTACAGTGCCATGGCCTAC -3'
(R):5'- TTAACTAGAAAGGCCATATACCCTG -3'
Posted On 2019-06-26