Incidental Mutation 'IGL02487:Podxl'
ID 295494
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Podxl
Ensembl Gene ENSMUSG00000025608
Gene Name podocalyxin-like
Synonyms podocalyxin, PC, Pclp1, Podxl1, Ly102
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL02487
Quality Score
Status
Chromosome 6
Chromosomal Location 31496428-31540872 bp(-) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) T to C at 31499957 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Tryptophan at position 504 (*504W)
Ref Sequence ENSEMBL: ENSMUSP00000026698 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026698]
AlphaFold Q9R0M4
Predicted Effect probably null
Transcript: ENSMUST00000026698
AA Change: *504W
SMART Domains Protein: ENSMUSP00000026698
Gene: ENSMUSG00000025608
AA Change: *504W

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 61 91 N/A INTRINSIC
low complexity region 104 130 N/A INTRINSIC
low complexity region 196 208 N/A INTRINSIC
low complexity region 265 278 N/A INTRINSIC
Pfam:CD34_antigen 301 503 6e-76 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136877
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit neonatal lethality and severe kidney defects including absence of the podocyte slit diaphragm and foot processes and anuria. While a subset display edema and/or omphalocele, most mice appear normal at birth. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl6 T A 11: 54,227,769 (GRCm39) I308N possibly damaging Het
Adal C T 2: 120,985,877 (GRCm39) T204I probably benign Het
Akirin1 A G 4: 123,637,357 (GRCm39) F76S probably benign Het
Arhgef5 A T 6: 43,260,916 (GRCm39) N1447I probably damaging Het
Atp2a3 C A 11: 72,866,165 (GRCm39) H262N probably benign Het
B230217C12Rik A G 11: 97,733,054 (GRCm39) N125S probably benign Het
Dcaf11 G T 14: 55,806,571 (GRCm39) K457N probably benign Het
Dnah10 G A 5: 124,870,916 (GRCm39) V2348M possibly damaging Het
Eif4g3 T C 4: 137,930,689 (GRCm39) V1665A possibly damaging Het
Fat4 A T 3: 38,941,394 (GRCm39) I96F probably damaging Het
Gm29253 T C 1: 75,149,321 (GRCm39) probably null Het
Gvin-ps6 A G 7: 106,022,471 (GRCm39) noncoding transcript Het
Hnrnpm C A 17: 33,867,787 (GRCm39) G676C probably damaging Het
Iah1 T C 12: 21,371,440 (GRCm39) M185T probably damaging Het
Klc1 A T 12: 111,738,886 (GRCm39) I45F probably damaging Het
Lce1h G A 3: 92,671,048 (GRCm39) P35S unknown Het
Lrrc37a T C 11: 103,386,863 (GRCm39) E2419G unknown Het
Lrrc8c T A 5: 105,754,457 (GRCm39) S77R probably benign Het
Mcm3ap T A 10: 76,343,389 (GRCm39) probably benign Het
Mon1b G T 8: 114,365,455 (GRCm39) R261L possibly damaging Het
Ntng1 A T 3: 109,842,363 (GRCm39) S137T probably damaging Het
Odf2 C A 2: 29,810,851 (GRCm39) A578E possibly damaging Het
Pecam1 G A 11: 106,562,606 (GRCm39) T698I probably damaging Het
Pex10 A T 4: 155,155,190 (GRCm39) H288L probably damaging Het
Pkhd1l1 T C 15: 44,322,822 (GRCm39) V36A possibly damaging Het
Rab42 A G 4: 132,029,614 (GRCm39) S203P probably benign Het
Rsf1 T C 7: 97,288,698 (GRCm39) S192P probably damaging Het
Scap C T 9: 110,207,758 (GRCm39) T489I probably benign Het
Sost C A 11: 101,857,633 (GRCm39) R56L possibly damaging Het
Speer4a3 T A 5: 26,156,605 (GRCm39) I125F probably benign Het
Spmip10 T A 18: 56,727,571 (GRCm39) W90R possibly damaging Het
Sptbn4 A G 7: 27,118,522 (GRCm39) V264A probably damaging Het
Stx3 A G 19: 11,760,469 (GRCm39) V236A probably damaging Het
Syt2 T C 1: 134,668,603 (GRCm39) F5S probably damaging Het
Thrap3 T C 4: 126,060,794 (GRCm39) D855G possibly damaging Het
Ticrr T C 7: 79,332,769 (GRCm39) V874A possibly damaging Het
Tmem26 A G 10: 68,614,563 (GRCm39) E326G probably benign Het
Tsga13 A T 6: 30,884,362 (GRCm39) Y119N probably damaging Het
Tspoap1 C T 11: 87,653,342 (GRCm39) T136I possibly damaging Het
Ttc21b T C 2: 66,065,500 (GRCm39) T425A probably benign Het
Ttc27 A G 17: 75,163,549 (GRCm39) Y719C probably damaging Het
Usp10 C A 8: 120,675,514 (GRCm39) S511Y probably damaging Het
Vmn1r197 A G 13: 22,512,792 (GRCm39) M238V probably damaging Het
Other mutations in Podxl
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01081:Podxl APN 6 31,505,639 (GRCm39) missense possibly damaging 0.53
IGL01576:Podxl APN 6 31,501,319 (GRCm39) missense probably damaging 1.00
IGL02151:Podxl APN 6 31,501,394 (GRCm39) missense possibly damaging 0.65
IGL02240:Podxl APN 6 31,501,933 (GRCm39) missense probably damaging 1.00
IGL02598:Podxl APN 6 31,501,355 (GRCm39) missense probably damaging 1.00
IGL02957:Podxl APN 6 31,505,384 (GRCm39) splice site probably benign
R2042:Podxl UTSW 6 31,500,051 (GRCm39) missense possibly damaging 0.75
R3840:Podxl UTSW 6 31,500,016 (GRCm39) missense probably damaging 1.00
R4675:Podxl UTSW 6 31,503,579 (GRCm39) missense possibly damaging 0.95
R5509:Podxl UTSW 6 31,503,548 (GRCm39) missense probably benign 0.00
R5754:Podxl UTSW 6 31,501,329 (GRCm39) missense probably damaging 1.00
R5876:Podxl UTSW 6 31,505,391 (GRCm39) critical splice donor site probably null
R6242:Podxl UTSW 6 31,503,180 (GRCm39) missense probably benign 0.30
R6376:Podxl UTSW 6 31,505,432 (GRCm39) missense probably benign 0.00
R6493:Podxl UTSW 6 31,501,981 (GRCm39) missense probably damaging 1.00
R7113:Podxl UTSW 6 31,501,668 (GRCm39) critical splice acceptor site probably null
R7299:Podxl UTSW 6 31,501,371 (GRCm39) missense probably damaging 1.00
R7301:Podxl UTSW 6 31,501,371 (GRCm39) missense probably damaging 1.00
R7338:Podxl UTSW 6 31,505,941 (GRCm39) missense unknown
R7358:Podxl UTSW 6 31,501,929 (GRCm39) missense probably benign 0.03
R8799:Podxl UTSW 6 31,501,400 (GRCm39) missense probably damaging 1.00
Z1176:Podxl UTSW 6 31,505,569 (GRCm39) missense probably damaging 0.98
Z1177:Podxl UTSW 6 31,505,459 (GRCm39) missense possibly damaging 0.65
Posted On 2015-04-16