Incidental Mutation 'R7295:Pcdha11'
ID 566703
Institutional Source Beutler Lab
Gene Symbol Pcdha11
Ensembl Gene ENSMUSG00000102206
Gene Name protocadherin alpha 11
Synonyms A830022B16Rik, Cnr7, Crnr7
MMRRC Submission 045363-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.133) question?
Stock # R7295 (G1)
Quality Score 225.009
Status Validated
Chromosome 18
Chromosomal Location 37143911-37320710 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 37139979 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 536 (V536A)
Ref Sequence ENSEMBL: ENSMUSP00000111322 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070797] [ENSMUST00000115657] [ENSMUST00000115658] [ENSMUST00000115659] [ENSMUST00000115661] [ENSMUST00000115662] [ENSMUST00000192168] [ENSMUST00000192295] [ENSMUST00000192447] [ENSMUST00000192503] [ENSMUST00000192512] [ENSMUST00000192631] [ENSMUST00000193389] [ENSMUST00000193777] [ENSMUST00000193839] [ENSMUST00000194038] [ENSMUST00000194544] [ENSMUST00000194751] [ENSMUST00000195590]
AlphaFold Q91Y19
Predicted Effect probably benign
Transcript: ENSMUST00000070797
SMART Domains Protein: ENSMUSP00000068828
Gene: ENSMUSG00000103442

DomainStartEndE-ValueType
CA 22 132 3.09e-2 SMART
CA 156 241 6.14e-20 SMART
CA 265 349 3.92e-27 SMART
CA 373 454 4.94e-24 SMART
CA 478 564 1e-24 SMART
CA 592 672 4.55e-14 SMART
transmembrane domain 694 716 N/A INTRINSIC
Pfam:Cadherin_tail 797 931 5.3e-58 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000115657
SMART Domains Protein: ENSMUSP00000111321
Gene: ENSMUSG00000102206

DomainStartEndE-ValueType
CA 21 131 2.95e-2 SMART
CA 155 240 7.44e-19 SMART
CA 264 347 5.63e-28 SMART
CA 371 452 3.14e-26 SMART
CA 476 562 1.42e-24 SMART
CA 593 675 1.03e-12 SMART
transmembrane domain 697 719 N/A INTRINSIC
low complexity region 783 794 N/A INTRINSIC
low complexity region 918 942 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000115658
AA Change: V536A

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000111322
Gene: ENSMUSG00000007440
AA Change: V536A

DomainStartEndE-ValueType
low complexity region 15 21 N/A INTRINSIC
CA 46 132 6.34e-2 SMART
CA 156 241 4.65e-20 SMART
CA 265 349 1.25e-25 SMART
CA 373 454 9.22e-24 SMART
CA 478 564 4.3e-24 SMART
CA 595 678 5.07e-12 SMART
low complexity region 706 721 N/A INTRINSIC
Pfam:Cadherin_tail 795 929 5.3e-58 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000115659
SMART Domains Protein: ENSMUSP00000111323
Gene: ENSMUSG00000103770

DomainStartEndE-ValueType
low complexity region 44 51 N/A INTRINSIC
CA 75 161 2.46e-2 SMART
CA 185 270 8.1e-20 SMART
CA 294 378 1.69e-22 SMART
CA 402 483 1.52e-24 SMART
CA 507 593 5.68e-24 SMART
CA 624 705 6.69e-12 SMART
transmembrane domain 727 749 N/A INTRINSIC
Pfam:Cadherin_tail 828 962 5.6e-58 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000115661
SMART Domains Protein: ENSMUSP00000111325
Gene: ENSMUSG00000103458

DomainStartEndE-ValueType
CA 20 131 5.3e-2 SMART
CA 155 240 1.51e-19 SMART
CA 264 348 7.6e-25 SMART
CA 372 453 1.42e-24 SMART
CA 477 563 1.42e-24 SMART
CA 594 674 4.12e-12 SMART
low complexity region 706 721 N/A INTRINSIC
Pfam:Cadherin_tail 796 930 3.9e-58 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000115662
SMART Domains Protein: ENSMUSP00000111326
Gene: ENSMUSG00000104148

DomainStartEndE-ValueType
CA 45 131 6.34e-2 SMART
CA 155 240 2.98e-18 SMART
CA 264 348 2.17e-29 SMART
CA 372 453 2.84e-24 SMART
CA 477 563 5.02e-25 SMART
CA 594 675 8.16e-16 SMART
transmembrane domain 695 717 N/A INTRINSIC
low complexity region 916 940 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000192168
SMART Domains Protein: ENSMUSP00000142293
Gene: ENSMUSG00000103092

DomainStartEndE-ValueType
CA 21 131 2.2e-2 SMART
CA 155 240 2.05e-21 SMART
CA 264 348 8.81e-21 SMART
CA 372 453 2.01e-24 SMART
CA 477 563 1.42e-24 SMART
CA 591 673 1.63e-15 SMART
transmembrane domain 693 715 N/A INTRINSIC
low complexity region 902 926 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000192295
SMART Domains Protein: ENSMUSP00000142103
Gene: ENSMUSG00000104252

DomainStartEndE-ValueType
CA 20 131 5.3e-2 SMART
CA 155 240 1.51e-19 SMART
CA 264 348 7.6e-25 SMART
CA 372 453 1.42e-24 SMART
CA 477 568 5.38e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000192447
SMART Domains Protein: ENSMUSP00000142270
Gene: ENSMUSG00000102206

DomainStartEndE-ValueType
CA 21 131 1.5e-4 SMART
CA 155 240 3.6e-21 SMART
CA 264 347 2.8e-30 SMART
CA 371 452 1.5e-28 SMART
CA 476 562 6.8e-27 SMART
CA 593 675 4.9e-15 SMART
transmembrane domain 697 719 N/A INTRINSIC
low complexity region 783 794 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000192503
SMART Domains Protein: ENSMUSP00000141989
Gene: ENSMUSG00000102312

DomainStartEndE-ValueType
low complexity region 11 17 N/A INTRINSIC
CA 42 128 3.78e-2 SMART
CA 152 237 8.94e-22 SMART
CA 261 345 3.74e-24 SMART
CA 369 450 1.09e-25 SMART
CA 474 560 1.42e-24 SMART
CA 588 670 2.96e-13 SMART
transmembrane domain 692 714 N/A INTRINSIC
low complexity region 910 934 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000192512
SMART Domains Protein: ENSMUSP00000141408
Gene: ENSMUSG00000104252

DomainStartEndE-ValueType
CA 20 131 5.3e-2 SMART
CA 155 240 1.51e-19 SMART
CA 264 348 7.6e-25 SMART
CA 372 453 1.42e-24 SMART
CA 477 563 1.42e-24 SMART
CA 594 674 4.12e-12 SMART
low complexity region 706 721 N/A INTRINSIC
low complexity region 915 939 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000192631
SMART Domains Protein: ENSMUSP00000142156
Gene: ENSMUSG00000104318

DomainStartEndE-ValueType
CA 21 131 2.58e-2 SMART
CA 155 240 4.27e-19 SMART
CA 264 348 1.42e-24 SMART
CA 372 453 9.36e-25 SMART
CA 477 563 1.42e-24 SMART
CA 594 671 4.03e-6 SMART
transmembrane domain 696 718 N/A INTRINSIC
low complexity region 905 929 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000193389
SMART Domains Protein: ENSMUSP00000141459
Gene: ENSMUSG00000103707

DomainStartEndE-ValueType
CA 21 131 5.67e-2 SMART
CA 155 240 4.72e-21 SMART
CA 264 348 1.9e-25 SMART
CA 372 453 3.31e-25 SMART
CA 477 563 1.42e-24 SMART
CA 594 676 5.91e-13 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000193777
SMART Domains Protein: ENSMUSP00000141587
Gene: ENSMUSG00000103707

DomainStartEndE-ValueType
CA 21 131 5.67e-2 SMART
CA 155 240 4.72e-21 SMART
CA 264 348 1.9e-25 SMART
CA 372 453 3.31e-25 SMART
CA 477 563 1.42e-24 SMART
CA 594 676 5.91e-13 SMART
low complexity region 914 938 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000193839
SMART Domains Protein: ENSMUSP00000142308
Gene: ENSMUSG00000103442

DomainStartEndE-ValueType
CA 22 132 3.09e-2 SMART
CA 156 241 6.14e-20 SMART
CA 265 349 3.92e-27 SMART
CA 373 454 4.94e-24 SMART
CA 478 564 1e-24 SMART
CA 592 672 4.55e-14 SMART
transmembrane domain 694 716 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000193984
Predicted Effect probably benign
Transcript: ENSMUST00000194038
SMART Domains Protein: ENSMUSP00000142159
Gene: ENSMUSG00000103800

DomainStartEndE-ValueType
CA 20 131 6.34e-2 SMART
CA 155 240 4.27e-19 SMART
CA 264 348 2.04e-25 SMART
CA 372 453 2.84e-24 SMART
CA 477 563 9.88e-24 SMART
CA 594 676 8.62e-15 SMART
transmembrane domain 699 721 N/A INTRINSIC
low complexity region 914 938 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000194544
SMART Domains Protein: ENSMUSP00000141847
Gene: ENSMUSG00000102836

DomainStartEndE-ValueType
Blast:CA 18 66 5e-20 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000194751
SMART Domains Protein: ENSMUSP00000142285
Gene: ENSMUSG00000103707

DomainStartEndE-ValueType
low complexity region 15 21 N/A INTRINSIC
Pfam:Cadherin_2 29 112 4.5e-32 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000195590
SMART Domains Protein: ENSMUSP00000141355
Gene: ENSMUSG00000104148

DomainStartEndE-ValueType
CA 45 131 6.34e-2 SMART
CA 155 240 2.98e-18 SMART
CA 264 348 2.17e-29 SMART
CA 372 453 2.84e-24 SMART
CA 477 563 5.02e-25 SMART
CA 594 675 8.16e-16 SMART
transmembrane domain 695 717 N/A INTRINSIC
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 98% (59/60)
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 protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
a A T 2: 154,887,678 (GRCm39) D46V probably damaging Het
Acp7 A T 7: 28,328,955 (GRCm39) F75Y possibly damaging Het
Adamts19 T A 18: 58,970,955 (GRCm39) Y180N probably damaging Het
Adck1 G T 12: 88,397,815 (GRCm39) D150Y probably damaging Het
Alb T A 5: 90,610,693 (GRCm39) probably null Het
Baat A T 4: 49,490,275 (GRCm39) Y270N probably damaging Het
Bmp7 A T 2: 172,781,690 (GRCm39) I58N probably damaging Het
Bpifb9a C T 2: 154,109,616 (GRCm39) T504M probably damaging Het
Cbfa2t3 T G 8: 123,364,768 (GRCm39) D338A probably benign Het
Ccnd2 A T 6: 127,125,725 (GRCm39) C104S possibly damaging Het
Clip1 G T 5: 123,765,419 (GRCm39) Q713K probably benign Het
Ddx28 G A 8: 106,737,476 (GRCm39) S194L probably benign Het
Dync1h1 T C 12: 110,631,183 (GRCm39) probably null Het
Edil3 T A 13: 89,279,902 (GRCm39) Y193* probably null Het
Eprs1 A G 1: 185,150,407 (GRCm39) probably null Het
Ercc6l2 T G 13: 63,967,589 (GRCm39) I63R probably damaging Het
Fam171a2 T C 11: 102,329,064 (GRCm39) E565G possibly damaging Het
Fbn1 T A 2: 125,177,407 (GRCm39) D1810V probably damaging Het
Foxj2 T C 6: 122,817,190 (GRCm39) S506P probably benign Het
Frmpd1 A G 4: 45,285,700 (GRCm39) E1507G probably damaging Het
Gfm1 G A 3: 67,347,514 (GRCm39) V258I probably benign Het
Gphn T C 12: 78,538,876 (GRCm39) V174A probably benign Het
Gtpbp3 C A 8: 71,942,139 (GRCm39) S123R possibly damaging Het
H2bc8 T C 13: 23,755,943 (GRCm39) S113P probably benign Het
Hbs1l T C 10: 21,186,051 (GRCm39) V491A probably benign Het
Hoxc12 A G 15: 102,846,810 (GRCm39) N234S probably damaging Het
Il22b A T 10: 118,130,848 (GRCm39) L16* probably null Het
Kcnj5 T C 9: 32,234,087 (GRCm39) D76G probably damaging Het
Klhl11 A G 11: 100,363,068 (GRCm39) Y163H probably damaging Het
Lonp1 G T 17: 56,929,495 (GRCm39) Q181K possibly damaging Het
Mgst1 A T 6: 138,124,754 (GRCm39) I23F probably benign Het
Muc21 G A 17: 35,929,761 (GRCm39) A1475V unknown Het
Myocos T C 1: 162,484,687 (GRCm39) R41G unknown Het
Myod1 A G 7: 46,027,643 (GRCm39) D261G probably benign Het
Nop14 C T 5: 34,796,376 (GRCm39) R781Q probably damaging Het
Nsmaf A G 4: 6,438,083 (GRCm39) V63A probably benign Het
Ntsr1 A T 2: 180,142,725 (GRCm39) H172L probably damaging Het
Or4k6 T C 14: 50,476,073 (GRCm39) K90E probably damaging Het
Or8b1c A T 9: 38,384,739 (GRCm39) E232V probably benign Het
Pcdha6 T A 18: 37,101,189 (GRCm39) N127K probably damaging Het
Prps1l1 T A 12: 35,035,679 (GRCm39) C265S probably benign Het
Prune2 A G 19: 17,097,261 (GRCm39) S922G probably benign Het
Qpctl A T 7: 18,883,055 (GRCm39) M19K probably benign Het
Rad51 C T 2: 118,964,599 (GRCm39) T230I possibly damaging Het
Rad9b A G 5: 122,472,341 (GRCm39) F246L possibly damaging Het
Rarb A T 14: 16,508,932 (GRCm38) probably null Het
Sdcbp2 T C 2: 151,429,321 (GRCm39) S214P possibly damaging Het
Slc22a1 T A 17: 12,875,892 (GRCm39) M441L probably benign Het
Slc35f1 G A 10: 52,938,637 (GRCm39) V190I probably benign Het
Spon1 A T 7: 113,629,475 (GRCm39) Q373L possibly damaging Het
Ssbp2 T A 13: 91,842,122 (GRCm39) probably null Het
Sult1e1 T A 5: 87,726,512 (GRCm39) R201* probably null Het
Traj32 T A 14: 54,423,606 (GRCm39) L16Q Het
Ttc16 T C 2: 32,664,437 (GRCm39) I67V probably null Het
Ttn T A 2: 76,556,899 (GRCm39) K30035N probably damaging Het
Ttn T A 2: 76,776,473 (GRCm39) Y1607F unknown Het
Usp16 G A 16: 87,268,977 (GRCm39) R290H probably benign Het
Utp3 G C 5: 88,702,376 (GRCm39) probably benign Het
Xpnpep3 A G 15: 81,298,735 (GRCm39) H56R probably damaging Het
Zfp592 G T 7: 80,674,070 (GRCm39) D345Y probably damaging Het
Zfp931 A T 2: 177,709,824 (GRCm39) Y187* probably null Het
Other mutations in Pcdha11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01522:Pcdha11 APN 18 37,318,061 (GRCm39) missense probably damaging 1.00
IGL01843:Pcdha11 APN 18 37,145,886 (GRCm39) missense probably benign 0.28
R1165:Pcdha11 UTSW 18 37,140,757 (GRCm39) intron probably benign
R2422:Pcdha11 UTSW 18 37,140,325 (GRCm39) missense probably damaging 0.99
R2423:Pcdha11 UTSW 18 37,140,477 (GRCm39) missense possibly damaging 0.89
R2508:Pcdha11 UTSW 18 37,145,907 (GRCm39) missense possibly damaging 0.86
R3114:Pcdha11 UTSW 18 37,144,860 (GRCm39) missense probably damaging 1.00
R4173:Pcdha11 UTSW 18 37,145,676 (GRCm39) missense probably damaging 0.99
R4255:Pcdha11 UTSW 18 37,145,843 (GRCm39) missense probably benign 0.23
R4369:Pcdha11 UTSW 18 37,139,796 (GRCm39) missense possibly damaging 0.70
R4454:Pcdha11 UTSW 18 37,140,426 (GRCm39) missense probably benign 0.13
R4489:Pcdha11 UTSW 18 37,139,969 (GRCm39) missense possibly damaging 0.78
R4626:Pcdha11 UTSW 18 37,140,051 (GRCm39) missense probably damaging 1.00
R4751:Pcdha11 UTSW 18 37,139,997 (GRCm39) missense probably damaging 1.00
R4801:Pcdha11 UTSW 18 37,138,518 (GRCm39) missense probably damaging 1.00
R4802:Pcdha11 UTSW 18 37,138,518 (GRCm39) missense probably damaging 1.00
R4857:Pcdha11 UTSW 18 37,144,505 (GRCm39) missense probably benign 0.02
R4995:Pcdha11 UTSW 18 37,144,080 (GRCm39) missense probably benign 0.24
R5042:Pcdha11 UTSW 18 37,144,649 (GRCm39) missense probably damaging 1.00
R5480:Pcdha11 UTSW 18 37,138,935 (GRCm39) missense probably benign 0.04
R5495:Pcdha11 UTSW 18 37,144,079 (GRCm39) missense probably benign
R5523:Pcdha11 UTSW 18 37,145,439 (GRCm39) missense probably damaging 1.00
R5584:Pcdha11 UTSW 18 37,139,818 (GRCm39) missense probably damaging 1.00
R5682:Pcdha11 UTSW 18 37,144,502 (GRCm39) missense probably damaging 1.00
R5834:Pcdha11 UTSW 18 37,145,676 (GRCm39) missense probably damaging 0.99
R5842:Pcdha11 UTSW 18 37,144,337 (GRCm39) missense possibly damaging 0.85
R5859:Pcdha11 UTSW 18 37,140,336 (GRCm39) missense probably damaging 1.00
R6110:Pcdha11 UTSW 18 37,144,509 (GRCm39) missense probably damaging 1.00
R6135:Pcdha11 UTSW 18 37,138,870 (GRCm39) missense probably damaging 1.00
R6248:Pcdha11 UTSW 18 37,138,950 (GRCm39) missense probably benign 0.26
R6416:Pcdha11 UTSW 18 37,145,222 (GRCm39) splice site probably null
R6450:Pcdha11 UTSW 18 37,146,215 (GRCm39) missense probably damaging 1.00
R6594:Pcdha11 UTSW 18 37,144,235 (GRCm39) missense probably benign 0.04
R6631:Pcdha11 UTSW 18 37,138,844 (GRCm39) missense probably damaging 1.00
R6883:Pcdha11 UTSW 18 37,144,242 (GRCm39) missense probably damaging 1.00
R7088:Pcdha11 UTSW 18 37,138,470 (GRCm39) missense probably benign 0.00
R7129:Pcdha11 UTSW 18 37,140,291 (GRCm39) missense probably benign 0.45
R7153:Pcdha11 UTSW 18 37,144,278 (GRCm39) missense probably damaging 1.00
R7244:Pcdha11 UTSW 18 37,144,421 (GRCm39) nonsense probably null
R7319:Pcdha11 UTSW 18 37,146,245 (GRCm39) missense probably benign 0.10
R7352:Pcdha11 UTSW 18 37,139,898 (GRCm39) missense probably damaging 1.00
R7516:Pcdha11 UTSW 18 37,144,671 (GRCm39) missense probably damaging 1.00
R7519:Pcdha11 UTSW 18 37,139,319 (GRCm39) nonsense probably null
R7660:Pcdha11 UTSW 18 37,138,904 (GRCm39) missense probably benign 0.17
R7677:Pcdha11 UTSW 18 37,144,605 (GRCm39) missense probably damaging 1.00
R7707:Pcdha11 UTSW 18 37,144,845 (GRCm39) missense probably benign 0.00
R7775:Pcdha11 UTSW 18 37,145,733 (GRCm39) missense possibly damaging 0.64
R7778:Pcdha11 UTSW 18 37,145,733 (GRCm39) missense possibly damaging 0.64
R7780:Pcdha11 UTSW 18 37,145,849 (GRCm39) missense probably damaging 0.97
R7916:Pcdha11 UTSW 18 37,140,441 (GRCm39) missense probably benign 0.01
R7991:Pcdha11 UTSW 18 37,145,909 (GRCm39) missense probably damaging 0.99
R8068:Pcdha11 UTSW 18 37,138,618 (GRCm39) missense probably damaging 1.00
R8220:Pcdha11 UTSW 18 37,139,624 (GRCm39) missense probably benign 0.01
R8252:Pcdha11 UTSW 18 37,140,590 (GRCm39) missense possibly damaging 0.65
R8392:Pcdha11 UTSW 18 37,139,212 (GRCm39) nonsense probably null
R8398:Pcdha11 UTSW 18 37,146,116 (GRCm39) missense possibly damaging 0.65
R8470:Pcdha11 UTSW 18 37,145,937 (GRCm39) missense probably benign 0.07
R8812:Pcdha11 UTSW 18 37,140,716 (GRCm39) missense probably benign 0.00
R8900:Pcdha11 UTSW 18 37,145,799 (GRCm39) missense probably damaging 1.00
R8968:Pcdha11 UTSW 18 37,145,307 (GRCm39) missense probably damaging 1.00
R9065:Pcdha11 UTSW 18 37,139,877 (GRCm39) missense possibly damaging 0.93
R9192:Pcdha11 UTSW 18 37,140,527 (GRCm39) missense probably benign 0.42
R9224:Pcdha11 UTSW 18 37,139,073 (GRCm39) missense probably damaging 0.99
R9228:Pcdha11 UTSW 18 37,144,512 (GRCm39) missense probably damaging 1.00
R9237:Pcdha11 UTSW 18 37,145,260 (GRCm39) missense probably damaging 1.00
R9336:Pcdha11 UTSW 18 37,144,514 (GRCm39) missense probably damaging 1.00
R9449:Pcdha11 UTSW 18 37,145,484 (GRCm39) missense probably damaging 1.00
R9475:Pcdha11 UTSW 18 37,140,591 (GRCm39) missense probably damaging 1.00
R9476:Pcdha11 UTSW 18 37,139,532 (GRCm39) missense probably benign 0.26
R9510:Pcdha11 UTSW 18 37,139,532 (GRCm39) missense probably benign 0.26
R9578:Pcdha11 UTSW 18 37,140,176 (GRCm39) missense probably damaging 1.00
R9654:Pcdha11 UTSW 18 37,145,333 (GRCm39) missense probably damaging 1.00
RF017:Pcdha11 UTSW 18 37,138,577 (GRCm39) missense possibly damaging 0.92
Z1177:Pcdha11 UTSW 18 37,145,976 (GRCm39) missense probably benign 0.43
Predicted Primers PCR Primer
(F):5'- ACGTCTTCACAGTATTGGCG -3'
(R):5'- CAAGCATTGTAACCAGAGTCCG -3'

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