Incidental Mutation 'IGL01862:Pkd1l3'
ID 178402
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Pkd1l3
Ensembl Gene ENSMUSG00000048827
Gene Name polycystic kidney disease 1 like 3
Synonyms
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01862
Quality Score
Status
Chromosome 8
Chromosomal Location 110340828-110399305 bp(+) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) G to A at 110357908 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000148592 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057344] [ENSMUST00000057344] [ENSMUST00000109242] [ENSMUST00000109242] [ENSMUST00000212537] [ENSMUST00000212537]
AlphaFold Q2EG98
Predicted Effect probably null
Transcript: ENSMUST00000057344
SMART Domains Protein: ENSMUSP00000051512
Gene: ENSMUSG00000048827

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
CLECT 26 142 4.25e-1 SMART
internal_repeat_2 143 245 2.25e-8 PROSPERO
low complexity region 246 270 N/A INTRINSIC
low complexity region 272 296 N/A INTRINSIC
low complexity region 298 322 N/A INTRINSIC
low complexity region 324 348 N/A INTRINSIC
internal_repeat_1 349 431 1.22e-8 PROSPERO
internal_repeat_2 378 466 2.25e-8 PROSPERO
internal_repeat_1 518 731 1.22e-8 PROSPERO
GPS 1007 1056 3.62e-5 SMART
transmembrane domain 1075 1094 N/A INTRINSIC
LH2 1119 1238 1.01e-9 SMART
transmembrane domain 1282 1304 N/A INTRINSIC
transmembrane domain 1319 1341 N/A INTRINSIC
low complexity region 1398 1408 N/A INTRINSIC
low complexity region 1451 1460 N/A INTRINSIC
low complexity region 1484 1497 N/A INTRINSIC
transmembrane domain 1534 1556 N/A INTRINSIC
transmembrane domain 1576 1595 N/A INTRINSIC
Pfam:PKD_channel 1695 2110 2.8e-86 PFAM
Pfam:Ion_trans 1858 2114 2.9e-9 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000057344
SMART Domains Protein: ENSMUSP00000051512
Gene: ENSMUSG00000048827

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
CLECT 26 142 4.25e-1 SMART
internal_repeat_2 143 245 2.25e-8 PROSPERO
low complexity region 246 270 N/A INTRINSIC
low complexity region 272 296 N/A INTRINSIC
low complexity region 298 322 N/A INTRINSIC
low complexity region 324 348 N/A INTRINSIC
internal_repeat_1 349 431 1.22e-8 PROSPERO
internal_repeat_2 378 466 2.25e-8 PROSPERO
internal_repeat_1 518 731 1.22e-8 PROSPERO
GPS 1007 1056 3.62e-5 SMART
transmembrane domain 1075 1094 N/A INTRINSIC
LH2 1119 1238 1.01e-9 SMART
transmembrane domain 1282 1304 N/A INTRINSIC
transmembrane domain 1319 1341 N/A INTRINSIC
low complexity region 1398 1408 N/A INTRINSIC
low complexity region 1451 1460 N/A INTRINSIC
low complexity region 1484 1497 N/A INTRINSIC
transmembrane domain 1534 1556 N/A INTRINSIC
transmembrane domain 1576 1595 N/A INTRINSIC
Pfam:PKD_channel 1695 2110 2.8e-86 PFAM
Pfam:Ion_trans 1858 2114 2.9e-9 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000109242
SMART Domains Protein: ENSMUSP00000104865
Gene: ENSMUSG00000048827

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
CLECT 26 142 4.25e-1 SMART
internal_repeat_2 143 245 2.63e-8 PROSPERO
low complexity region 246 270 N/A INTRINSIC
low complexity region 272 296 N/A INTRINSIC
low complexity region 298 322 N/A INTRINSIC
low complexity region 324 348 N/A INTRINSIC
internal_repeat_1 349 440 3.96e-14 PROSPERO
internal_repeat_2 378 466 2.63e-8 PROSPERO
internal_repeat_1 518 724 3.96e-14 PROSPERO
GPS 1017 1066 3.62e-5 SMART
transmembrane domain 1085 1104 N/A INTRINSIC
LH2 1129 1248 1.01e-9 SMART
transmembrane domain 1292 1314 N/A INTRINSIC
transmembrane domain 1329 1351 N/A INTRINSIC
low complexity region 1408 1418 N/A INTRINSIC
low complexity region 1461 1470 N/A INTRINSIC
low complexity region 1494 1507 N/A INTRINSIC
transmembrane domain 1544 1566 N/A INTRINSIC
transmembrane domain 1586 1605 N/A INTRINSIC
Pfam:PKD_channel 1705 2120 1.3e-86 PFAM
Pfam:Ion_trans 1868 2124 4.3e-9 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000109242
SMART Domains Protein: ENSMUSP00000104865
Gene: ENSMUSG00000048827

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
CLECT 26 142 4.25e-1 SMART
internal_repeat_2 143 245 2.63e-8 PROSPERO
low complexity region 246 270 N/A INTRINSIC
low complexity region 272 296 N/A INTRINSIC
low complexity region 298 322 N/A INTRINSIC
low complexity region 324 348 N/A INTRINSIC
internal_repeat_1 349 440 3.96e-14 PROSPERO
internal_repeat_2 378 466 2.63e-8 PROSPERO
internal_repeat_1 518 724 3.96e-14 PROSPERO
GPS 1017 1066 3.62e-5 SMART
transmembrane domain 1085 1104 N/A INTRINSIC
LH2 1129 1248 1.01e-9 SMART
transmembrane domain 1292 1314 N/A INTRINSIC
transmembrane domain 1329 1351 N/A INTRINSIC
low complexity region 1408 1418 N/A INTRINSIC
low complexity region 1461 1470 N/A INTRINSIC
low complexity region 1494 1507 N/A INTRINSIC
transmembrane domain 1544 1566 N/A INTRINSIC
transmembrane domain 1586 1605 N/A INTRINSIC
Pfam:PKD_channel 1705 2120 1.3e-86 PFAM
Pfam:Ion_trans 1868 2124 4.3e-9 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000212537
Predicted Effect probably null
Transcript: ENSMUST00000212537
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213034
Coding Region Coverage
Validation Efficiency
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. The encoded protein contains 11 transmembrane domains, a latrophilin/CL-1-like GPCR proteolytic site (GPS) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. This protein may function as a component of cation channel pores.[provided by RefSeq, Apr 2009]
PHENOTYPE: Mice homozygous for a knock-out allele are viable, fertile and grossly normal and exhibit normal taste responsiveness in various behavioral and electrophysiological tests of taste function. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8b G T 11: 109,837,997 (GRCm39) S1085* probably null Het
Akap9 T G 5: 4,001,705 (GRCm39) S94A probably damaging Het
Akap9 T A 5: 4,115,856 (GRCm39) N3425K probably damaging Het
Anapc7 T A 5: 122,578,182 (GRCm39) I389N probably benign Het
Aqp7 G A 4: 41,045,321 (GRCm39) R20* probably null Het
Cacna1h C T 17: 25,602,457 (GRCm39) G1524R probably damaging Het
Cacng4 T C 11: 107,685,196 (GRCm39) Y32C probably damaging Het
Cep120 A C 18: 53,847,839 (GRCm39) S673R probably benign Het
Cep162 T C 9: 87,135,986 (GRCm39) E19G possibly damaging Het
Cpxm2 C T 7: 131,661,540 (GRCm39) V416I probably benign Het
Dapk1 A G 13: 60,874,424 (GRCm39) T427A probably benign Het
Ecm1 A T 3: 95,641,586 (GRCm39) D549E probably benign Het
Efemp1 T A 11: 28,871,428 (GRCm39) N342K probably damaging Het
Erc2 T C 14: 27,993,526 (GRCm39) probably benign Het
Fhip2b C T 14: 70,825,130 (GRCm39) R402H probably benign Het
Galnt13 T C 2: 54,747,926 (GRCm39) V269A probably damaging Het
Gm6465 T G 5: 11,899,020 (GRCm39) L171R probably damaging Het
Gpatch1 A G 7: 34,994,703 (GRCm39) V521A probably benign Het
Heatr5b A T 17: 79,103,914 (GRCm39) V1087E possibly damaging Het
Ikzf2 A T 1: 69,578,057 (GRCm39) V484D probably damaging Het
Ints4 T A 7: 97,190,360 (GRCm39) V953E probably damaging Het
Iqce T C 5: 140,685,480 (GRCm39) D15G possibly damaging Het
Kif3a T A 11: 53,461,368 (GRCm39) N4K possibly damaging Het
Lrch4 A T 5: 137,635,271 (GRCm39) I254F probably damaging Het
Ly75 A T 2: 60,129,516 (GRCm39) V1623D probably damaging Het
Mapt T A 11: 104,180,828 (GRCm39) probably benign Het
Mast1 A T 8: 85,639,875 (GRCm39) probably null Het
Mcc G T 18: 44,892,363 (GRCm39) Q84K probably benign Het
Mgat4f G A 1: 134,318,349 (GRCm39) V374I probably benign Het
Mtfr2 G A 10: 20,224,149 (GRCm39) V28M probably benign Het
Myh8 T A 11: 67,180,520 (GRCm39) Y585* probably null Het
Napsa T C 7: 44,231,917 (GRCm39) V202A probably damaging Het
Nsd2 A G 5: 34,001,080 (GRCm39) K199R probably null Het
Ntpcr C T 8: 126,462,837 (GRCm39) A18V probably benign Het
Or2aj4 A T 16: 19,385,426 (GRCm39) M69K probably damaging Het
Or2g25 G T 17: 37,970,368 (GRCm39) N285K probably damaging Het
Or56b35 T A 7: 104,963,439 (GRCm39) I76N probably damaging Het
Or5g9 G T 2: 85,552,472 (GRCm39) C241F probably damaging Het
Or8b9 A G 9: 37,766,477 (GRCm39) D121G probably damaging Het
Os9 A G 10: 126,935,573 (GRCm39) V299A probably benign Het
Pcdhb7 T C 18: 37,476,915 (GRCm39) S684P possibly damaging Het
Phf19 A C 2: 34,787,067 (GRCm39) probably null Het
Pkhd1 A G 1: 20,429,134 (GRCm39) I2422T probably damaging Het
Plxna2 T A 1: 194,326,258 (GRCm39) V64E possibly damaging Het
Psme4 T A 11: 30,762,038 (GRCm39) C459* probably null Het
Ptk6 T C 2: 180,841,433 (GRCm39) S159G probably benign Het
Rhd T C 4: 134,617,650 (GRCm39) I329T possibly damaging Het
Scfd1 A G 12: 51,492,494 (GRCm39) Y601C probably damaging Het
Shroom3 T C 5: 93,110,148 (GRCm39) S1753P probably damaging Het
Slc8a1 A C 17: 81,749,630 (GRCm39) probably null Het
Spg7 T A 8: 123,803,669 (GRCm39) L233Q probably damaging Het
Strip1 C A 3: 107,529,198 (GRCm39) R353L probably damaging Het
Ubr1 T C 2: 120,764,823 (GRCm39) N544D possibly damaging Het
Ubr4 A G 4: 139,204,469 (GRCm39) T4794A possibly damaging Het
Usp24 A G 4: 106,266,095 (GRCm39) probably benign Het
Vmn1r193 A T 13: 22,403,984 (GRCm39) C3S probably benign Het
Yju2b G T 8: 84,987,163 (GRCm39) probably benign Het
Zdhhc5 C T 2: 84,520,836 (GRCm39) R447H probably benign Het
Zfp202 A G 9: 40,123,124 (GRCm39) I629V probably benign Het
Zfp462 T A 4: 55,023,441 (GRCm39) C990S probably damaging Het
Other mutations in Pkd1l3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00336:Pkd1l3 APN 8 110,356,869 (GRCm39) missense possibly damaging 0.53
IGL00562:Pkd1l3 APN 8 110,382,779 (GRCm39) missense possibly damaging 0.53
IGL00563:Pkd1l3 APN 8 110,382,779 (GRCm39) missense possibly damaging 0.53
IGL01061:Pkd1l3 APN 8 110,365,338 (GRCm39) missense probably damaging 1.00
IGL01105:Pkd1l3 APN 8 110,388,873 (GRCm39) missense possibly damaging 0.81
IGL01574:Pkd1l3 APN 8 110,350,403 (GRCm39) missense probably benign 0.01
IGL01597:Pkd1l3 APN 8 110,350,153 (GRCm39) missense probably benign 0.33
IGL01634:Pkd1l3 APN 8 110,394,157 (GRCm39) critical splice acceptor site probably null
IGL01645:Pkd1l3 APN 8 110,361,934 (GRCm39) missense possibly damaging 0.59
IGL01770:Pkd1l3 APN 8 110,375,134 (GRCm39) critical splice acceptor site probably null
IGL01837:Pkd1l3 APN 8 110,356,798 (GRCm39) missense possibly damaging 0.85
IGL01938:Pkd1l3 APN 8 110,361,933 (GRCm39) missense probably benign 0.00
IGL01990:Pkd1l3 APN 8 110,387,438 (GRCm39) missense probably damaging 1.00
IGL02056:Pkd1l3 APN 8 110,358,010 (GRCm39) missense probably benign 0.14
IGL02069:Pkd1l3 APN 8 110,362,012 (GRCm39) missense probably damaging 1.00
IGL02086:Pkd1l3 APN 8 110,392,217 (GRCm39) missense probably damaging 1.00
IGL02152:Pkd1l3 APN 8 110,395,924 (GRCm39) missense probably damaging 1.00
IGL02209:Pkd1l3 APN 8 110,365,296 (GRCm39) missense probably damaging 1.00
IGL02213:Pkd1l3 APN 8 110,357,977 (GRCm39) missense probably damaging 1.00
IGL02218:Pkd1l3 APN 8 110,387,434 (GRCm39) missense possibly damaging 0.92
IGL02225:Pkd1l3 APN 8 110,365,310 (GRCm39) missense probably damaging 1.00
IGL02252:Pkd1l3 APN 8 110,357,708 (GRCm39) missense possibly damaging 0.92
IGL02351:Pkd1l3 APN 8 110,373,129 (GRCm39) unclassified probably benign
IGL02358:Pkd1l3 APN 8 110,373,129 (GRCm39) unclassified probably benign
IGL02369:Pkd1l3 APN 8 110,342,977 (GRCm39) missense unknown
IGL02481:Pkd1l3 APN 8 110,341,414 (GRCm39) missense unknown
IGL02505:Pkd1l3 APN 8 110,359,848 (GRCm39) missense probably damaging 1.00
IGL02506:Pkd1l3 APN 8 110,374,132 (GRCm39) missense probably damaging 1.00
IGL02535:Pkd1l3 APN 8 110,367,522 (GRCm39) nonsense probably null
IGL02715:Pkd1l3 APN 8 110,353,458 (GRCm39) missense probably damaging 0.96
IGL02979:Pkd1l3 APN 8 110,388,736 (GRCm39) splice site probably benign
IGL03059:Pkd1l3 APN 8 110,374,999 (GRCm39) missense probably damaging 1.00
IGL03090:Pkd1l3 APN 8 110,382,165 (GRCm39) nonsense probably null
IGL03206:Pkd1l3 APN 8 110,350,345 (GRCm39) missense probably benign 0.18
IGL03328:Pkd1l3 APN 8 110,388,738 (GRCm39) splice site probably benign
BB006:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
PIT4453001:Pkd1l3 UTSW 8 110,387,433 (GRCm39) missense probably damaging 0.99
PIT4468001:Pkd1l3 UTSW 8 110,391,131 (GRCm39) missense possibly damaging 0.85
R0001:Pkd1l3 UTSW 8 110,355,265 (GRCm39) splice site probably benign
R0066:Pkd1l3 UTSW 8 110,347,103 (GRCm39) missense unknown
R0066:Pkd1l3 UTSW 8 110,347,103 (GRCm39) missense unknown
R0233:Pkd1l3 UTSW 8 110,377,412 (GRCm39) nonsense probably null
R0233:Pkd1l3 UTSW 8 110,377,412 (GRCm39) nonsense probably null
R0255:Pkd1l3 UTSW 8 110,365,386 (GRCm39) missense probably damaging 1.00
R0288:Pkd1l3 UTSW 8 110,373,131 (GRCm39) splice site probably null
R0311:Pkd1l3 UTSW 8 110,350,295 (GRCm39) missense probably benign 0.33
R0311:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0403:Pkd1l3 UTSW 8 110,350,295 (GRCm39) missense probably benign 0.33
R0403:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0441:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0446:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0465:Pkd1l3 UTSW 8 110,350,295 (GRCm39) missense probably benign 0.33
R0465:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0466:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0467:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0468:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0488:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0488:Pkd1l3 UTSW 8 110,350,295 (GRCm39) missense probably benign 0.33
R0515:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0534:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0650:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R0689:Pkd1l3 UTSW 8 110,350,281 (GRCm39) missense possibly damaging 0.70
R1422:Pkd1l3 UTSW 8 110,348,340 (GRCm39) missense unknown
R1464:Pkd1l3 UTSW 8 110,363,059 (GRCm39) splice site probably benign
R1467:Pkd1l3 UTSW 8 110,343,000 (GRCm39) missense unknown
R1467:Pkd1l3 UTSW 8 110,343,000 (GRCm39) missense unknown
R1469:Pkd1l3 UTSW 8 110,373,585 (GRCm39) missense possibly damaging 0.72
R1469:Pkd1l3 UTSW 8 110,373,585 (GRCm39) missense possibly damaging 0.72
R1509:Pkd1l3 UTSW 8 110,367,402 (GRCm39) missense probably damaging 0.99
R1561:Pkd1l3 UTSW 8 110,341,445 (GRCm39) missense unknown
R1574:Pkd1l3 UTSW 8 110,341,445 (GRCm39) missense unknown
R1599:Pkd1l3 UTSW 8 110,363,016 (GRCm39) missense probably benign 0.01
R1688:Pkd1l3 UTSW 8 110,350,450 (GRCm39) missense probably benign 0.18
R1792:Pkd1l3 UTSW 8 110,359,237 (GRCm39) missense probably damaging 1.00
R1818:Pkd1l3 UTSW 8 110,375,038 (GRCm39) missense probably benign 0.03
R1896:Pkd1l3 UTSW 8 110,350,831 (GRCm39) missense possibly damaging 0.92
R2105:Pkd1l3 UTSW 8 110,374,205 (GRCm39) nonsense probably null
R2185:Pkd1l3 UTSW 8 110,359,827 (GRCm39) missense possibly damaging 0.95
R2192:Pkd1l3 UTSW 8 110,347,156 (GRCm39) missense unknown
R2260:Pkd1l3 UTSW 8 110,350,268 (GRCm39) missense probably benign 0.18
R2363:Pkd1l3 UTSW 8 110,355,341 (GRCm39) missense probably benign 0.01
R2418:Pkd1l3 UTSW 8 110,397,353 (GRCm39) makesense probably null
R2435:Pkd1l3 UTSW 8 110,377,334 (GRCm39) missense probably benign 0.07
R2443:Pkd1l3 UTSW 8 110,350,447 (GRCm39) missense probably benign 0.18
R2850:Pkd1l3 UTSW 8 110,350,622 (GRCm39) missense possibly damaging 0.92
R2910:Pkd1l3 UTSW 8 110,394,268 (GRCm39) splice site probably benign
R3755:Pkd1l3 UTSW 8 110,359,171 (GRCm39) missense probably damaging 1.00
R3791:Pkd1l3 UTSW 8 110,362,949 (GRCm39) missense probably damaging 0.99
R3905:Pkd1l3 UTSW 8 110,373,511 (GRCm39) missense probably benign 0.02
R4027:Pkd1l3 UTSW 8 110,350,603 (GRCm39) missense possibly damaging 0.68
R4028:Pkd1l3 UTSW 8 110,350,603 (GRCm39) missense possibly damaging 0.68
R4029:Pkd1l3 UTSW 8 110,350,603 (GRCm39) missense possibly damaging 0.68
R4274:Pkd1l3 UTSW 8 110,350,751 (GRCm39) missense possibly damaging 0.92
R4461:Pkd1l3 UTSW 8 110,359,345 (GRCm39) splice site probably null
R4893:Pkd1l3 UTSW 8 110,365,026 (GRCm39) missense probably benign 0.15
R4907:Pkd1l3 UTSW 8 110,367,475 (GRCm39) missense probably damaging 0.99
R5037:Pkd1l3 UTSW 8 110,392,268 (GRCm39) missense probably damaging 1.00
R5045:Pkd1l3 UTSW 8 110,349,787 (GRCm39) missense unknown
R5207:Pkd1l3 UTSW 8 110,359,823 (GRCm39) missense probably damaging 1.00
R5307:Pkd1l3 UTSW 8 110,367,424 (GRCm39) missense probably damaging 1.00
R5408:Pkd1l3 UTSW 8 110,393,684 (GRCm39) missense probably damaging 1.00
R5595:Pkd1l3 UTSW 8 110,382,152 (GRCm39) missense probably damaging 1.00
R5615:Pkd1l3 UTSW 8 110,356,842 (GRCm39) missense probably benign
R5623:Pkd1l3 UTSW 8 110,350,351 (GRCm39) missense possibly damaging 0.53
R5896:Pkd1l3 UTSW 8 110,353,468 (GRCm39) missense probably damaging 1.00
R6101:Pkd1l3 UTSW 8 110,367,478 (GRCm39) missense probably damaging 1.00
R6105:Pkd1l3 UTSW 8 110,367,478 (GRCm39) missense probably damaging 1.00
R6170:Pkd1l3 UTSW 8 110,349,811 (GRCm39) missense unknown
R6330:Pkd1l3 UTSW 8 110,373,541 (GRCm39) missense probably benign 0.00
R6346:Pkd1l3 UTSW 8 110,358,016 (GRCm39) missense probably damaging 0.98
R6395:Pkd1l3 UTSW 8 110,350,595 (GRCm39) missense probably benign 0.20
R6475:Pkd1l3 UTSW 8 110,349,844 (GRCm39) missense unknown
R6480:Pkd1l3 UTSW 8 110,365,019 (GRCm39) nonsense probably null
R6519:Pkd1l3 UTSW 8 110,355,404 (GRCm39) missense probably benign
R6654:Pkd1l3 UTSW 8 110,350,915 (GRCm39) missense probably benign 0.23
R6717:Pkd1l3 UTSW 8 110,341,401 (GRCm39) missense unknown
R6733:Pkd1l3 UTSW 8 110,375,126 (GRCm39) splice site probably null
R6753:Pkd1l3 UTSW 8 110,351,081 (GRCm39) missense probably damaging 1.00
R6777:Pkd1l3 UTSW 8 110,353,446 (GRCm39) missense probably benign 0.00
R6901:Pkd1l3 UTSW 8 110,341,246 (GRCm39) missense unknown
R6975:Pkd1l3 UTSW 8 110,387,539 (GRCm39) missense possibly damaging 0.73
R6991:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7018:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7083:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7139:Pkd1l3 UTSW 8 110,362,972 (GRCm39) missense probably damaging 0.96
R7153:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7235:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7238:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7252:Pkd1l3 UTSW 8 110,387,330 (GRCm39) missense probably benign 0.01
R7296:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7309:Pkd1l3 UTSW 8 110,374,893 (GRCm39) splice site probably null
R7362:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7462:Pkd1l3 UTSW 8 110,355,409 (GRCm39) missense probably benign 0.00
R7470:Pkd1l3 UTSW 8 110,365,008 (GRCm39) missense probably benign 0.09
R7478:Pkd1l3 UTSW 8 110,359,947 (GRCm39) missense probably damaging 1.00
R7483:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7516:Pkd1l3 UTSW 8 110,361,861 (GRCm39) missense probably damaging 1.00
R7553:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7559:Pkd1l3 UTSW 8 110,351,072 (GRCm39) missense probably benign 0.03
R7650:Pkd1l3 UTSW 8 110,399,217 (GRCm39) missense probably benign 0.23
R7654:Pkd1l3 UTSW 8 110,365,049 (GRCm39) missense probably damaging 1.00
R7742:Pkd1l3 UTSW 8 110,341,204 (GRCm39) missense unknown
R7749:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7751:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7755:Pkd1l3 UTSW 8 110,356,798 (GRCm39) missense possibly damaging 0.85
R7816:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7831:Pkd1l3 UTSW 8 110,357,990 (GRCm39) missense possibly damaging 0.47
R7835:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7849:Pkd1l3 UTSW 8 110,350,420 (GRCm39) small deletion probably benign
R7917:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7929:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R7952:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8054:Pkd1l3 UTSW 8 110,373,008 (GRCm39) missense probably damaging 1.00
R8098:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8099:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8276:Pkd1l3 UTSW 8 110,397,353 (GRCm39) makesense probably null
R8352:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8376:Pkd1l3 UTSW 8 110,350,420 (GRCm39) small deletion probably benign
R8377:Pkd1l3 UTSW 8 110,361,982 (GRCm39) missense probably benign 0.08
R8398:Pkd1l3 UTSW 8 110,350,520 (GRCm39) missense possibly damaging 0.93
R8399:Pkd1l3 UTSW 8 110,350,520 (GRCm39) missense possibly damaging 0.93
R8400:Pkd1l3 UTSW 8 110,350,520 (GRCm39) missense possibly damaging 0.93
R8412:Pkd1l3 UTSW 8 110,360,022 (GRCm39) missense possibly damaging 0.85
R8530:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8539:Pkd1l3 UTSW 8 110,362,919 (GRCm39) missense probably damaging 1.00
R8546:Pkd1l3 UTSW 8 110,393,615 (GRCm39) missense possibly damaging 0.52
R8558:Pkd1l3 UTSW 8 110,362,012 (GRCm39) missense probably damaging 1.00
R8719:Pkd1l3 UTSW 8 110,341,255 (GRCm39) missense unknown
R8769:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8797:Pkd1l3 UTSW 8 110,374,946 (GRCm39) missense probably benign 0.15
R8840:Pkd1l3 UTSW 8 110,349,842 (GRCm39) missense unknown
R8846:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8874:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8893:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8956:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8963:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R8968:Pkd1l3 UTSW 8 110,350,420 (GRCm39) small deletion probably benign
R9035:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9054:Pkd1l3 UTSW 8 110,392,304 (GRCm39) missense probably benign 0.08
R9058:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9119:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9134:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9138:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9158:Pkd1l3 UTSW 8 110,394,207 (GRCm39) nonsense probably null
R9180:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9181:Pkd1l3 UTSW 8 110,375,318 (GRCm39) missense probably damaging 0.98
R9218:Pkd1l3 UTSW 8 110,382,128 (GRCm39) nonsense probably null
R9249:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9269:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9338:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9383:Pkd1l3 UTSW 8 110,350,601 (GRCm39) small deletion probably benign
R9396:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9423:Pkd1l3 UTSW 8 110,350,312 (GRCm39) missense possibly damaging 0.53
R9514:Pkd1l3 UTSW 8 110,395,849 (GRCm39) missense probably damaging 1.00
R9515:Pkd1l3 UTSW 8 110,395,849 (GRCm39) missense probably damaging 1.00
R9567:Pkd1l3 UTSW 8 110,394,173 (GRCm39) missense probably damaging 0.99
R9668:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9684:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
R9748:Pkd1l3 UTSW 8 110,373,555 (GRCm39) missense probably benign 0.00
R9778:Pkd1l3 UTSW 8 110,357,937 (GRCm39) missense probably benign 0.00
RF016:Pkd1l3 UTSW 8 110,350,174 (GRCm39) missense probably benign 0.18
RF029:Pkd1l3 UTSW 8 110,350,827 (GRCm39) small deletion probably benign
X0026:Pkd1l3 UTSW 8 110,341,185 (GRCm39) missense probably null
Z1176:Pkd1l3 UTSW 8 110,349,874 (GRCm39) missense unknown
Z31818:Pkd1l3 UTSW 8 110,395,924 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07