Incidental Mutation 'R1401:Pkd1l1'
ID 160149
Institutional Source Beutler Lab
Gene Symbol Pkd1l1
Ensembl Gene ENSMUSG00000046634
Gene Name polycystic kidney disease 1 like 1
Synonyms
MMRRC Submission 039463-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1401 (G1)
Quality Score 207
Status Validated
Chromosome 11
Chromosomal Location 8782025-8924365 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 8804487 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 1701 (Y1701*)
Ref Sequence ENSEMBL: ENSMUSP00000136518 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000178195]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000154153
AA Change: Y2151*
SMART Domains Protein: ENSMUSP00000120803
Gene: ENSMUSG00000046634
AA Change: Y2151*

DomainStartEndE-ValueType
low complexity region 172 184 N/A INTRINSIC
PKD 205 287 2.9e0 SMART
PKD 291 369 1.42e-9 SMART
Pfam:REJ 398 1001 1.7e-45 PFAM
low complexity region 1208 1218 N/A INTRINSIC
GPS 1370 1413 1.21e-1 SMART
transmembrane domain 1434 1451 N/A INTRINSIC
LH2 1479 1598 2.94e-3 SMART
transmembrane domain 1640 1659 N/A INTRINSIC
transmembrane domain 1679 1701 N/A INTRINSIC
transmembrane domain 1817 1839 N/A INTRINSIC
transmembrane domain 1854 1876 N/A INTRINSIC
Pfam:PKD_channel 2109 2339 1.5e-23 PFAM
transmembrane domain 2381 2403 N/A INTRINSIC
low complexity region 2436 2449 N/A INTRINSIC
low complexity region 2458 2469 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000155886
Predicted Effect probably null
Transcript: ENSMUST00000178195
AA Change: Y1701*
SMART Domains Protein: ENSMUSP00000136518
Gene: ENSMUSG00000046634
AA Change: Y1701*

DomainStartEndE-ValueType
Pfam:REJ 3 552 3.3e-41 PFAM
low complexity region 757 767 N/A INTRINSIC
Blast:GPS 919 965 2e-13 BLAST
transmembrane domain 983 1000 N/A INTRINSIC
Pfam:PLAT 1030 1145 7.2e-14 PFAM
transmembrane domain 1189 1208 N/A INTRINSIC
transmembrane domain 1228 1250 N/A INTRINSIC
transmembrane domain 1366 1388 N/A INTRINSIC
transmembrane domain 1403 1425 N/A INTRINSIC
Pfam:PKD_channel 1658 1889 2e-25 PFAM
transmembrane domain 1930 1952 N/A INTRINSIC
low complexity region 1985 1998 N/A INTRINSIC
low complexity region 2007 2018 N/A INTRINSIC
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.8%
  • 20x: 91.4%
Validation Efficiency 98% (87/89)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the polycystin protein family containing 11 transmembrane domains, a receptor for egg jelly (REJ) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. The encoded protein may play a role in the male reproductive system. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for an ENU induced point mutation display lethality throughout fetal growth and development with abnormalities in left right patterning and heterotaxia. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930433I11Rik A T 7: 40,642,480 (GRCm39) T141S probably benign Het
Abcg1 T A 17: 31,333,132 (GRCm39) I625N possibly damaging Het
Adam33 C A 2: 130,893,391 (GRCm39) probably benign Het
Adgrl2 A T 3: 148,528,617 (GRCm39) I1185N probably damaging Het
Afp A T 5: 90,649,486 (GRCm39) probably benign Het
Aggf1 A G 13: 95,501,356 (GRCm39) V342A probably benign Het
Ankrd11 A T 8: 123,619,789 (GRCm39) S1333R probably benign Het
Arhgef11 C A 3: 87,640,776 (GRCm39) S1311* probably null Het
Atp6v1g1 T C 4: 63,466,878 (GRCm39) Y47H probably benign Het
Atp8b4 T C 2: 126,165,013 (GRCm39) probably null Het
Barx2 A G 9: 31,770,327 (GRCm39) L67P probably damaging Het
Bbs7 G A 3: 36,627,706 (GRCm39) P694S probably benign Het
Btbd10 A T 7: 112,946,266 (GRCm39) V33E probably benign Het
C2 T C 17: 35,091,457 (GRCm39) T69A possibly damaging Het
C8b T G 4: 104,641,679 (GRCm39) L205R possibly damaging Het
Cct4 T G 11: 22,944,333 (GRCm39) N72K probably damaging Het
Cd300lg C A 11: 101,944,981 (GRCm39) P353H possibly damaging Het
Cdh20 A T 1: 104,875,222 (GRCm39) I335L possibly damaging Het
Cfhr2 T A 1: 139,738,757 (GRCm39) H268L probably benign Het
Chia1 T A 3: 106,036,255 (GRCm39) D278E probably benign Het
Cntn6 A G 6: 104,781,359 (GRCm39) T482A possibly damaging Het
Cst13 T A 2: 148,665,016 (GRCm39) F4I probably benign Het
Ctsc T A 7: 87,930,706 (GRCm39) V95E probably damaging Het
Ddhd1 A T 14: 45,842,508 (GRCm39) probably null Het
Dmxl2 A T 9: 54,322,712 (GRCm39) probably null Het
Dnah5 A C 15: 28,402,059 (GRCm39) T3407P probably damaging Het
Dock1 T A 7: 134,735,665 (GRCm39) Y1344* probably null Het
Eif4g3 T C 4: 137,933,395 (GRCm39) V1740A probably damaging Het
Epb41l5 A G 1: 119,506,634 (GRCm39) probably benign Het
Flt4 C T 11: 49,527,166 (GRCm39) probably benign Het
Fnbp1l C T 3: 122,339,955 (GRCm39) R499Q probably damaging Het
Gm10033 T C 8: 69,826,022 (GRCm39) noncoding transcript Het
Gm12790 A G 4: 101,825,396 (GRCm39) L6P probably benign Het
Gramd4 A G 15: 86,009,397 (GRCm39) D210G probably damaging Het
Hectd3 T C 4: 116,859,466 (GRCm39) S697P possibly damaging Het
Hsf4 T C 8: 106,002,235 (GRCm39) V399A probably benign Het
Hyal6 T A 6: 24,743,434 (GRCm39) C377S probably damaging Het
Myb C T 10: 21,028,844 (GRCm39) V85M probably damaging Het
Mypn A G 10: 62,988,636 (GRCm39) V463A probably damaging Het
Nav1 T A 1: 135,388,163 (GRCm39) I1144L probably benign Het
Nckap5 A G 1: 125,942,398 (GRCm39) probably benign Het
Nipbl A T 15: 8,401,657 (GRCm39) S30T probably damaging Het
Nmt1 T C 11: 102,948,307 (GRCm39) F277S probably damaging Het
Nploc4 A C 11: 120,274,115 (GRCm39) probably benign Het
Nup54 C A 5: 92,576,080 (GRCm39) R137I probably damaging Het
Or52n2b T C 7: 104,565,963 (GRCm39) Y180C probably damaging Het
Oxtr C T 6: 112,454,138 (GRCm39) R42Q probably benign Het
Plekhg6 T C 6: 125,340,072 (GRCm39) T763A probably damaging Het
Pmepa1 C T 2: 173,070,368 (GRCm39) probably null Het
Ppfia2 A G 10: 106,666,518 (GRCm39) E408G possibly damaging Het
Pramel13 G A 4: 144,121,658 (GRCm39) T122M probably benign Het
Prl8a2 G A 13: 27,537,979 (GRCm39) V218I possibly damaging Het
Ptpro T A 6: 137,420,592 (GRCm39) V1007D probably damaging Het
Rims4 C T 2: 163,705,849 (GRCm39) V262M possibly damaging Het
Shisal2b A T 13: 105,000,113 (GRCm39) C37S probably damaging Het
Slc13a1 A T 6: 24,118,082 (GRCm39) probably null Het
Slc17a8 T A 10: 89,427,076 (GRCm39) T342S probably damaging Het
Slc30a9 A G 5: 67,510,005 (GRCm39) E519G probably benign Het
Slc35e1 T C 8: 73,246,415 (GRCm39) probably benign Het
Slc39a5 G A 10: 128,233,610 (GRCm39) L296F probably damaging Het
Slco6b1 A C 1: 96,857,610 (GRCm39) noncoding transcript Het
Slco6d1 G A 1: 98,418,341 (GRCm39) G509D probably damaging Het
Spen A G 4: 141,199,132 (GRCm39) V3142A probably damaging Het
Spta1 T A 1: 174,050,250 (GRCm39) H1763Q probably damaging Het
Srcap T C 7: 127,159,124 (GRCm39) probably benign Het
Stard9 T C 2: 120,543,328 (GRCm39) probably benign Het
Stat4 A G 1: 52,111,106 (GRCm39) probably benign Het
Svbp T A 4: 119,053,225 (GRCm39) probably benign Het
Tm2d1 A T 4: 98,258,833 (GRCm39) probably benign Het
Trpv1 C A 11: 73,130,952 (GRCm39) probably null Het
Trrap A G 5: 144,794,232 (GRCm39) D3713G possibly damaging Het
Ubr1 T A 2: 120,786,125 (GRCm39) D165V probably benign Het
Utrn C A 10: 12,524,897 (GRCm39) M2195I probably benign Het
Vmn1r229 G A 17: 21,034,904 (GRCm39) V50I possibly damaging Het
Vmn1r44 A T 6: 89,870,632 (GRCm39) H126L probably benign Het
Vmn2r116 T C 17: 23,605,570 (GRCm39) probably benign Het
Vmn2r27 A C 6: 124,168,591 (GRCm39) Y846* probably null Het
Vmn2r84 T A 10: 130,227,859 (GRCm39) S126C possibly damaging Het
Xylb T A 9: 119,197,133 (GRCm39) probably benign Het
Zfp282 A T 6: 47,867,108 (GRCm39) K232* probably null Het
Zfp39 C A 11: 58,781,149 (GRCm39) V538L probably benign Het
Zfp560 T C 9: 20,263,149 (GRCm39) N76D possibly damaging Het
Zmym4 C T 4: 126,804,962 (GRCm39) V433I probably benign Het
Zscan5b A G 7: 6,233,425 (GRCm39) E83G probably damaging Het
Other mutations in Pkd1l1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00093:Pkd1l1 APN 11 8,911,971 (GRCm39) missense unknown
IGL00156:Pkd1l1 APN 11 8,900,515 (GRCm39) missense probably damaging 1.00
IGL00161:Pkd1l1 APN 11 8,879,353 (GRCm39) critical splice donor site probably null
IGL00489:Pkd1l1 APN 11 8,784,773 (GRCm39) critical splice donor site probably null
IGL00495:Pkd1l1 APN 11 8,818,493 (GRCm39) missense probably benign 0.34
IGL00983:Pkd1l1 APN 11 8,794,585 (GRCm39) missense probably benign
IGL01071:Pkd1l1 APN 11 8,798,921 (GRCm39) missense probably benign 0.00
IGL01093:Pkd1l1 APN 11 8,851,345 (GRCm39) missense probably benign 0.06
IGL01295:Pkd1l1 APN 11 8,883,685 (GRCm39) missense possibly damaging 0.93
IGL01311:Pkd1l1 APN 11 8,851,174 (GRCm39) missense possibly damaging 0.53
IGL01412:Pkd1l1 APN 11 8,900,409 (GRCm39) missense possibly damaging 0.73
IGL01978:Pkd1l1 APN 11 8,911,336 (GRCm39) missense unknown
IGL01999:Pkd1l1 APN 11 8,786,291 (GRCm39) missense probably benign
IGL02080:Pkd1l1 APN 11 8,911,345 (GRCm39) missense unknown
IGL02106:Pkd1l1 APN 11 8,783,800 (GRCm39) missense probably damaging 1.00
IGL02216:Pkd1l1 APN 11 8,784,897 (GRCm39) missense probably damaging 0.96
IGL02305:Pkd1l1 APN 11 8,852,467 (GRCm39) missense probably benign
IGL02337:Pkd1l1 APN 11 8,892,079 (GRCm39) missense probably damaging 1.00
IGL02576:Pkd1l1 APN 11 8,794,560 (GRCm39) missense possibly damaging 0.61
IGL02704:Pkd1l1 APN 11 8,784,910 (GRCm39) missense probably benign 0.00
IGL02814:Pkd1l1 APN 11 8,852,582 (GRCm39) missense probably benign 0.01
IGL02904:Pkd1l1 APN 11 8,818,450 (GRCm39) splice site probably benign
IGL02972:Pkd1l1 APN 11 8,813,908 (GRCm39) missense probably damaging 0.99
IGL03091:Pkd1l1 APN 11 8,805,564 (GRCm39) missense probably damaging 1.00
IGL03113:Pkd1l1 APN 11 8,784,793 (GRCm39) missense probably benign 0.20
IGL03210:Pkd1l1 APN 11 8,915,127 (GRCm39) missense unknown
PIT4581001:Pkd1l1 UTSW 11 8,866,298 (GRCm39) frame shift probably null
R0020:Pkd1l1 UTSW 11 8,825,765 (GRCm39) splice site probably benign
R0020:Pkd1l1 UTSW 11 8,825,765 (GRCm39) splice site probably benign
R0496:Pkd1l1 UTSW 11 8,879,430 (GRCm39) missense probably damaging 0.96
R0547:Pkd1l1 UTSW 11 8,786,448 (GRCm39) splice site probably benign
R0582:Pkd1l1 UTSW 11 8,881,699 (GRCm39) splice site probably benign
R0761:Pkd1l1 UTSW 11 8,804,375 (GRCm39) missense probably damaging 1.00
R0969:Pkd1l1 UTSW 11 8,886,898 (GRCm39) missense probably damaging 1.00
R1348:Pkd1l1 UTSW 11 8,784,806 (GRCm39) missense probably benign 0.18
R1366:Pkd1l1 UTSW 11 8,891,038 (GRCm39) splice site probably benign
R1444:Pkd1l1 UTSW 11 8,804,386 (GRCm39) missense probably damaging 1.00
R1445:Pkd1l1 UTSW 11 8,820,313 (GRCm39) missense probably benign 0.00
R1463:Pkd1l1 UTSW 11 8,866,302 (GRCm39) missense probably damaging 1.00
R1496:Pkd1l1 UTSW 11 8,891,077 (GRCm39) missense possibly damaging 0.95
R1542:Pkd1l1 UTSW 11 8,824,179 (GRCm39) missense possibly damaging 0.82
R1543:Pkd1l1 UTSW 11 8,851,200 (GRCm39) missense probably damaging 1.00
R1619:Pkd1l1 UTSW 11 8,900,413 (GRCm39) missense probably damaging 0.98
R1875:Pkd1l1 UTSW 11 8,794,670 (GRCm39) splice site probably benign
R1929:Pkd1l1 UTSW 11 8,786,197 (GRCm39) splice site probably benign
R1958:Pkd1l1 UTSW 11 8,824,161 (GRCm39) missense probably benign 0.01
R2223:Pkd1l1 UTSW 11 8,900,422 (GRCm39) missense probably benign
R2223:Pkd1l1 UTSW 11 8,839,063 (GRCm39) missense probably benign 0.18
R2264:Pkd1l1 UTSW 11 8,829,112 (GRCm39) missense probably damaging 0.97
R2349:Pkd1l1 UTSW 11 8,776,819 (GRCm39) splice site probably null
R2431:Pkd1l1 UTSW 11 8,897,197 (GRCm39) missense probably damaging 0.99
R2483:Pkd1l1 UTSW 11 8,912,701 (GRCm39) missense probably damaging 1.00
R2517:Pkd1l1 UTSW 11 8,908,900 (GRCm39) missense unknown
R2888:Pkd1l1 UTSW 11 8,897,251 (GRCm39) missense probably damaging 1.00
R2965:Pkd1l1 UTSW 11 8,824,236 (GRCm39) missense probably damaging 1.00
R3123:Pkd1l1 UTSW 11 8,923,021 (GRCm39) missense unknown
R3153:Pkd1l1 UTSW 11 8,817,207 (GRCm39) missense probably benign 0.01
R3840:Pkd1l1 UTSW 11 8,839,050 (GRCm39) missense probably damaging 1.00
R3855:Pkd1l1 UTSW 11 8,915,047 (GRCm39) critical splice donor site probably null
R3880:Pkd1l1 UTSW 11 8,911,983 (GRCm39) missense unknown
R3970:Pkd1l1 UTSW 11 8,824,218 (GRCm39) missense probably damaging 1.00
R4195:Pkd1l1 UTSW 11 8,859,929 (GRCm39) missense probably damaging 1.00
R4196:Pkd1l1 UTSW 11 8,859,929 (GRCm39) missense probably damaging 1.00
R4246:Pkd1l1 UTSW 11 8,815,543 (GRCm39) missense possibly damaging 0.51
R4247:Pkd1l1 UTSW 11 8,815,543 (GRCm39) missense possibly damaging 0.51
R4249:Pkd1l1 UTSW 11 8,815,543 (GRCm39) missense possibly damaging 0.51
R4250:Pkd1l1 UTSW 11 8,815,543 (GRCm39) missense possibly damaging 0.51
R4593:Pkd1l1 UTSW 11 8,851,253 (GRCm39) missense probably damaging 0.97
R4609:Pkd1l1 UTSW 11 8,908,964 (GRCm39) missense unknown
R4797:Pkd1l1 UTSW 11 8,911,340 (GRCm39) missense unknown
R4910:Pkd1l1 UTSW 11 8,879,360 (GRCm39) missense possibly damaging 0.50
R4940:Pkd1l1 UTSW 11 8,794,585 (GRCm39) missense probably benign
R5084:Pkd1l1 UTSW 11 8,892,004 (GRCm39) missense probably benign 0.05
R5147:Pkd1l1 UTSW 11 8,799,003 (GRCm39) missense possibly damaging 0.71
R5360:Pkd1l1 UTSW 11 8,829,204 (GRCm39) missense probably benign
R5483:Pkd1l1 UTSW 11 8,851,141 (GRCm39) critical splice donor site probably null
R5604:Pkd1l1 UTSW 11 8,783,877 (GRCm39) missense probably damaging 0.98
R5642:Pkd1l1 UTSW 11 8,829,202 (GRCm39) missense probably damaging 1.00
R5652:Pkd1l1 UTSW 11 8,859,889 (GRCm39) missense probably benign 0.03
R5751:Pkd1l1 UTSW 11 8,817,204 (GRCm39) missense possibly damaging 0.45
R5761:Pkd1l1 UTSW 11 8,866,301 (GRCm39) missense probably damaging 1.00
R5800:Pkd1l1 UTSW 11 8,811,302 (GRCm39) missense probably benign
R5874:Pkd1l1 UTSW 11 8,858,688 (GRCm39) missense probably damaging 1.00
R5897:Pkd1l1 UTSW 11 8,829,176 (GRCm39) missense probably benign 0.03
R5913:Pkd1l1 UTSW 11 8,813,849 (GRCm39) missense probably benign 0.00
R5930:Pkd1l1 UTSW 11 8,908,969 (GRCm39) missense unknown
R6000:Pkd1l1 UTSW 11 8,900,427 (GRCm39) missense probably benign 0.00
R6005:Pkd1l1 UTSW 11 8,807,113 (GRCm39) missense probably damaging 1.00
R6013:Pkd1l1 UTSW 11 8,819,452 (GRCm39) splice site probably null
R6027:Pkd1l1 UTSW 11 8,866,272 (GRCm39) nonsense probably null
R6028:Pkd1l1 UTSW 11 8,786,267 (GRCm39) missense probably benign 0.06
R6129:Pkd1l1 UTSW 11 8,818,543 (GRCm39) missense probably benign 0.00
R6182:Pkd1l1 UTSW 11 8,815,555 (GRCm39) missense probably benign 0.36
R6226:Pkd1l1 UTSW 11 8,851,287 (GRCm39) missense probably benign 0.00
R6257:Pkd1l1 UTSW 11 8,892,195 (GRCm39) missense probably benign 0.22
R6340:Pkd1l1 UTSW 11 8,794,649 (GRCm39) missense probably benign 0.09
R6478:Pkd1l1 UTSW 11 8,813,911 (GRCm39) missense probably benign 0.00
R6558:Pkd1l1 UTSW 11 8,839,052 (GRCm39) missense probably benign 0.00
R6750:Pkd1l1 UTSW 11 8,923,217 (GRCm39) missense unknown
R6987:Pkd1l1 UTSW 11 8,852,575 (GRCm39) missense probably benign 0.01
R6996:Pkd1l1 UTSW 11 8,799,046 (GRCm39) missense probably damaging 1.00
R7139:Pkd1l1 UTSW 11 8,840,737 (GRCm39) missense
R7224:Pkd1l1 UTSW 11 8,895,241 (GRCm39) missense
R7244:Pkd1l1 UTSW 11 8,821,771 (GRCm39) missense
R7265:Pkd1l1 UTSW 11 8,879,402 (GRCm39) missense
R7358:Pkd1l1 UTSW 11 8,895,202 (GRCm39) missense
R7387:Pkd1l1 UTSW 11 8,851,203 (GRCm39) missense
R7414:Pkd1l1 UTSW 11 8,866,267 (GRCm39) missense
R7459:Pkd1l1 UTSW 11 8,852,428 (GRCm39) missense
R7478:Pkd1l1 UTSW 11 8,879,441 (GRCm39) missense
R7485:Pkd1l1 UTSW 11 8,915,148 (GRCm39) missense
R7490:Pkd1l1 UTSW 11 8,866,265 (GRCm39) missense
R7644:Pkd1l1 UTSW 11 8,825,758 (GRCm39) missense
R7647:Pkd1l1 UTSW 11 8,897,296 (GRCm39) missense
R7676:Pkd1l1 UTSW 11 8,912,708 (GRCm39) missense
R7687:Pkd1l1 UTSW 11 8,804,390 (GRCm39) missense
R7699:Pkd1l1 UTSW 11 8,915,142 (GRCm39) missense
R7922:Pkd1l1 UTSW 11 8,859,857 (GRCm39) missense
R7922:Pkd1l1 UTSW 11 8,799,013 (GRCm39) missense
R7980:Pkd1l1 UTSW 11 8,804,375 (GRCm39) missense probably damaging 1.00
R7993:Pkd1l1 UTSW 11 8,895,262 (GRCm39) missense
R8052:Pkd1l1 UTSW 11 8,897,315 (GRCm39) missense
R8125:Pkd1l1 UTSW 11 8,897,241 (GRCm39) missense probably damaging 1.00
R8420:Pkd1l1 UTSW 11 8,820,277 (GRCm39) nonsense probably null
R8675:Pkd1l1 UTSW 11 8,798,916 (GRCm39) critical splice donor site probably null
R8683:Pkd1l1 UTSW 11 8,821,805 (GRCm39) missense
R8709:Pkd1l1 UTSW 11 8,805,567 (GRCm39) missense
R8711:Pkd1l1 UTSW 11 8,815,550 (GRCm39) missense
R8725:Pkd1l1 UTSW 11 8,911,482 (GRCm39) missense
R8733:Pkd1l1 UTSW 11 8,883,657 (GRCm39) missense
R8822:Pkd1l1 UTSW 11 8,806,312 (GRCm39) missense
R8871:Pkd1l1 UTSW 11 8,900,503 (GRCm39) missense
R9009:Pkd1l1 UTSW 11 8,881,552 (GRCm39) missense
R9099:Pkd1l1 UTSW 11 8,922,986 (GRCm39) missense
R9119:Pkd1l1 UTSW 11 8,829,107 (GRCm39) missense
R9150:Pkd1l1 UTSW 11 8,786,256 (GRCm39) missense
R9314:Pkd1l1 UTSW 11 8,829,153 (GRCm39) missense
R9341:Pkd1l1 UTSW 11 8,911,305 (GRCm39) missense
R9341:Pkd1l1 UTSW 11 8,786,399 (GRCm39) missense
R9343:Pkd1l1 UTSW 11 8,911,305 (GRCm39) missense
R9343:Pkd1l1 UTSW 11 8,786,399 (GRCm39) missense
R9392:Pkd1l1 UTSW 11 8,794,567 (GRCm39) missense
R9424:Pkd1l1 UTSW 11 8,820,091 (GRCm39) missense
R9496:Pkd1l1 UTSW 11 8,783,773 (GRCm39) critical splice donor site probably null
R9504:Pkd1l1 UTSW 11 8,815,631 (GRCm39) missense
R9563:Pkd1l1 UTSW 11 8,815,502 (GRCm39) missense
R9570:Pkd1l1 UTSW 11 8,840,697 (GRCm39) missense
R9585:Pkd1l1 UTSW 11 8,804,390 (GRCm39) missense
R9618:Pkd1l1 UTSW 11 8,911,420 (GRCm39) missense
R9709:Pkd1l1 UTSW 11 8,799,016 (GRCm39) missense probably damaging 0.98
R9741:Pkd1l1 UTSW 11 8,897,224 (GRCm39) missense
R9801:Pkd1l1 UTSW 11 8,908,964 (GRCm39) nonsense probably null
X0024:Pkd1l1 UTSW 11 8,900,413 (GRCm39) missense probably benign 0.01
X0063:Pkd1l1 UTSW 11 8,879,430 (GRCm39) missense probably damaging 0.96
X0065:Pkd1l1 UTSW 11 8,859,921 (GRCm39) missense probably benign 0.10
Z1176:Pkd1l1 UTSW 11 8,776,801 (GRCm39) missense
Z1177:Pkd1l1 UTSW 11 8,895,208 (GRCm39) missense
Predicted Primers PCR Primer
(F):5'- GGCTGAGGCTAAGACTCCACAATG -3'
(R):5'- CATCTGTCCCCATGAAGGCTAATCG -3'

Sequencing Primer
(F):5'- AGACCCTAGTCTCATAGTGTGGAG -3'
(R):5'- GTGTTTTGGACATGGTGACACAG -3'
Posted On 2014-03-14