Incidental Mutation 'R4795:Atp13a4'
ID 368984
Institutional Source Beutler Lab
Gene Symbol Atp13a4
Ensembl Gene ENSMUSG00000038094
Gene Name ATPase type 13A4
Synonyms 9330174J19Rik, 4631413J11Rik
MMRRC Submission 041996-MU
Accession Numbers

Genbank: NM_001164612, NM_172613, NM_001164613

Essential gene? Non essential (E-score: 0.000) question?
Stock # R4795 (G1)
Quality Score 225
Status Validated
Chromosome 16
Chromosomal Location 29395853-29544864 bp(-) (GRCm38)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to G at 29490008 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000138479 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039090] [ENSMUST00000039090] [ENSMUST00000039090] [ENSMUST00000039090] [ENSMUST00000057018] [ENSMUST00000057018] [ENSMUST00000182013] [ENSMUST00000182013] [ENSMUST00000182627] [ENSMUST00000182627] [ENSMUST00000182627] [ENSMUST00000182627]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000039090
SMART Domains Protein: ENSMUSP00000048753
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 143 8.4e-31 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 229 476 1.7e-36 PFAM
Pfam:Hydrolase 481 769 3.9e-11 PFAM
Pfam:HAD 484 787 4.1e-14 PFAM
Pfam:Hydrolase_like2 574 637 1.2e-9 PFAM
transmembrane domain 824 846 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000039090
SMART Domains Protein: ENSMUSP00000048753
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 143 8.4e-31 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 229 476 1.7e-36 PFAM
Pfam:Hydrolase 481 769 3.9e-11 PFAM
Pfam:HAD 484 787 4.1e-14 PFAM
Pfam:Hydrolase_like2 574 637 1.2e-9 PFAM
transmembrane domain 824 846 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000039090
SMART Domains Protein: ENSMUSP00000048753
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 143 8.4e-31 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 229 476 1.7e-36 PFAM
Pfam:Hydrolase 481 769 3.9e-11 PFAM
Pfam:HAD 484 787 4.1e-14 PFAM
Pfam:Hydrolase_like2 574 637 1.2e-9 PFAM
transmembrane domain 824 846 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000039090
SMART Domains Protein: ENSMUSP00000048753
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 143 8.4e-31 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 229 476 1.7e-36 PFAM
Pfam:Hydrolase 481 769 3.9e-11 PFAM
Pfam:HAD 484 787 4.1e-14 PFAM
Pfam:Hydrolase_like2 574 637 1.2e-9 PFAM
transmembrane domain 824 846 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000057018
SMART Domains Protein: ENSMUSP00000060987
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 142 9.6e-34 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 228 476 1.6e-34 PFAM
Pfam:Hydrolase 481 767 1.1e-10 PFAM
Pfam:HAD 484 858 3.3e-23 PFAM
Pfam:Cation_ATPase 573 637 4.9e-8 PFAM
transmembrane domain 902 924 N/A INTRINSIC
transmembrane domain 934 951 N/A INTRINSIC
transmembrane domain 972 994 N/A INTRINSIC
low complexity region 1014 1023 N/A INTRINSIC
transmembrane domain 1040 1057 N/A INTRINSIC
transmembrane domain 1070 1092 N/A INTRINSIC
transmembrane domain 1107 1126 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000057018
SMART Domains Protein: ENSMUSP00000060987
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 142 9.6e-34 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 228 476 1.6e-34 PFAM
Pfam:Hydrolase 481 767 1.1e-10 PFAM
Pfam:HAD 484 858 3.3e-23 PFAM
Pfam:Cation_ATPase 573 637 4.9e-8 PFAM
transmembrane domain 902 924 N/A INTRINSIC
transmembrane domain 934 951 N/A INTRINSIC
transmembrane domain 972 994 N/A INTRINSIC
low complexity region 1014 1023 N/A INTRINSIC
transmembrane domain 1040 1057 N/A INTRINSIC
transmembrane domain 1070 1092 N/A INTRINSIC
transmembrane domain 1107 1126 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000182013
SMART Domains Protein: ENSMUSP00000138583
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 84 4.2e-26 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000182013
SMART Domains Protein: ENSMUSP00000138583
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 84 4.2e-26 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000182627
SMART Domains Protein: ENSMUSP00000138479
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 143 2.1e-29 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 229 476 3.9e-35 PFAM
Pfam:Hydrolase 481 861 4.2e-16 PFAM
Pfam:HAD 484 858 1.9e-23 PFAM
Pfam:Hydrolase_like2 574 637 2.2e-8 PFAM
transmembrane domain 902 924 N/A INTRINSIC
transmembrane domain 934 951 N/A INTRINSIC
transmembrane domain 972 994 N/A INTRINSIC
low complexity region 1014 1023 N/A INTRINSIC
transmembrane domain 1040 1057 N/A INTRINSIC
transmembrane domain 1070 1092 N/A INTRINSIC
transmembrane domain 1107 1126 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000182627
SMART Domains Protein: ENSMUSP00000138479
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 143 2.1e-29 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 229 476 3.9e-35 PFAM
Pfam:Hydrolase 481 861 4.2e-16 PFAM
Pfam:HAD 484 858 1.9e-23 PFAM
Pfam:Hydrolase_like2 574 637 2.2e-8 PFAM
transmembrane domain 902 924 N/A INTRINSIC
transmembrane domain 934 951 N/A INTRINSIC
transmembrane domain 972 994 N/A INTRINSIC
low complexity region 1014 1023 N/A INTRINSIC
transmembrane domain 1040 1057 N/A INTRINSIC
transmembrane domain 1070 1092 N/A INTRINSIC
transmembrane domain 1107 1126 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000182627
SMART Domains Protein: ENSMUSP00000138479
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 143 2.1e-29 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 229 476 3.9e-35 PFAM
Pfam:Hydrolase 481 861 4.2e-16 PFAM
Pfam:HAD 484 858 1.9e-23 PFAM
Pfam:Hydrolase_like2 574 637 2.2e-8 PFAM
transmembrane domain 902 924 N/A INTRINSIC
transmembrane domain 934 951 N/A INTRINSIC
transmembrane domain 972 994 N/A INTRINSIC
low complexity region 1014 1023 N/A INTRINSIC
transmembrane domain 1040 1057 N/A INTRINSIC
transmembrane domain 1070 1092 N/A INTRINSIC
transmembrane domain 1107 1126 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000182627
SMART Domains Protein: ENSMUSP00000138479
Gene: ENSMUSG00000038094

DomainStartEndE-ValueType
Pfam:P5-ATPase 17 143 2.1e-29 PFAM
Cation_ATPase_N 147 223 1.09e-1 SMART
Pfam:E1-E2_ATPase 229 476 3.9e-35 PFAM
Pfam:Hydrolase 481 861 4.2e-16 PFAM
Pfam:HAD 484 858 1.9e-23 PFAM
Pfam:Hydrolase_like2 574 637 2.2e-8 PFAM
transmembrane domain 902 924 N/A INTRINSIC
transmembrane domain 934 951 N/A INTRINSIC
transmembrane domain 972 994 N/A INTRINSIC
low complexity region 1014 1023 N/A INTRINSIC
transmembrane domain 1040 1057 N/A INTRINSIC
transmembrane domain 1070 1092 N/A INTRINSIC
transmembrane domain 1107 1126 N/A INTRINSIC
Meta Mutation Damage Score 0.9492 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 93.7%
Validation Efficiency 98% (123/125)
Allele List at MGI
Other mutations in this stock
Total: 105 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 T G 3: 122,176,123 (GRCm38) L2259R probably damaging Het
Acd A G 8: 105,701,015 (GRCm38) S2P possibly damaging Het
Acsf3 A G 8: 122,780,157 (GRCm38) Y63C possibly damaging Het
Adam21 T C 12: 81,560,974 (GRCm38) I5V probably benign Het
Adamts6 C A 13: 104,444,128 (GRCm38) S783* probably null Het
Adamtsl1 T C 4: 86,243,769 (GRCm38) probably null Het
Adck2 T A 6: 39,576,393 (GRCm38) S313T probably benign Het
Adgb A G 10: 10,357,872 (GRCm38) I1285T probably benign Het
Angptl1 T A 1: 156,860,583 (GRCm38) M485K possibly damaging Het
Ank3 G A 10: 69,858,265 (GRCm38) V289I probably benign Het
Atp1a1 A G 3: 101,583,775 (GRCm38) L648P probably benign Het
Atp2a3 A G 11: 72,973,029 (GRCm38) I194V probably benign Het
Bglap A C 3: 88,384,405 (GRCm38) I4S unknown Het
Cacna1b T A 2: 24,637,487 (GRCm38) T1621S possibly damaging Het
Ccdc112 T A 18: 46,287,672 (GRCm38) Q337L probably benign Het
Cd34 T G 1: 194,951,011 (GRCm38) S194A probably damaging Het
Cdh20 A G 1: 104,941,264 (GRCm38) D160G probably damaging Het
Clock T C 5: 76,265,916 (GRCm38) K44R probably damaging Het
Commd9 A G 2: 101,898,896 (GRCm38) N116D probably benign Het
Dab2 C A 15: 6,429,611 (GRCm38) P335T probably benign Het
Epb41l3 T A 17: 69,248,719 (GRCm38) probably null Het
Epha2 A G 4: 141,322,416 (GRCm38) probably null Het
Fam78b T C 1: 167,078,647 (GRCm38) V125A probably benign Het
Fars2 A T 13: 36,537,426 (GRCm38) E448V probably damaging Het
Fkbpl G A 17: 34,645,329 (GRCm38) A24T probably benign Het
Glyr1 A C 16: 5,047,758 (GRCm38) V44G probably benign Het
Gm1527 A G 3: 28,920,663 (GRCm38) I542V possibly damaging Het
Gm18856 C A 13: 13,965,208 (GRCm38) probably benign Het
Gm44501 A G 17: 40,578,714 (GRCm38) K40E probably benign Het
Gm6583 A G 5: 112,355,299 (GRCm38) S180P possibly damaging Het
Hdhd5 T C 6: 120,523,446 (GRCm38) H97R probably benign Het
Hmcn1 A G 1: 150,753,611 (GRCm38) V965A probably benign Het
Hsf5 A G 11: 87,635,620 (GRCm38) M373V probably benign Het
Igbp1b C T 6: 138,657,805 (GRCm38) E214K probably benign Het
Iigp1 T A 18: 60,389,892 (GRCm38) F27L probably benign Het
Isl1 T C 13: 116,305,430 (GRCm38) N89S probably benign Het
Itga1 C A 13: 115,035,385 (GRCm38) W61C probably damaging Het
Itga5 T C 15: 103,347,760 (GRCm38) R922G probably benign Het
Kbtbd3 G A 9: 4,331,073 (GRCm38) W482* probably null Het
Kcnq1 A G 7: 143,182,757 (GRCm38) T168A probably benign Het
Lrch3 A G 16: 33,005,704 (GRCm38) N631S probably damaging Het
Lrrk1 T A 7: 66,262,665 (GRCm38) I1716F possibly damaging Het
Ly75 T C 2: 60,349,940 (GRCm38) E631G probably benign Het
Map4 T C 9: 110,035,263 (GRCm38) S519P probably benign Het
Mkl1 C T 15: 81,017,033 (GRCm38) S419N probably damaging Het
Mroh2a A G 1: 88,258,664 (GRCm38) S64G probably benign Het
Muc5b A G 7: 141,849,567 (GRCm38) E755G unknown Het
Ncaph2 T G 15: 89,370,807 (GRCm38) V478G probably damaging Het
Ncbp1 A G 4: 46,152,967 (GRCm38) R247G possibly damaging Het
Necab1 G T 4: 15,111,208 (GRCm38) D73E possibly damaging Het
Nedd9 T C 13: 41,317,900 (GRCm38) K208E probably benign Het
Nfyb A T 10: 82,752,368 (GRCm38) probably benign Het
Nol4 T C 18: 22,921,887 (GRCm38) Q162R probably damaging Het
Nwd2 G A 5: 63,805,433 (GRCm38) D787N probably benign Het
Olfr2 C T 7: 107,001,335 (GRCm38) G175D probably damaging Het
Olfr205 C T 16: 59,328,850 (GRCm38) V220I probably benign Het
Olfr49 A G 14: 54,282,547 (GRCm38) M116T probably damaging Het
Olfr535 A G 7: 140,493,007 (GRCm38) D123G probably damaging Het
Olfr713 A T 7: 107,036,914 (GRCm38) Y253F probably benign Het
Olfr740 A C 14: 50,453,417 (GRCm38) M122L probably damaging Het
Olfr908 T A 9: 38,516,503 (GRCm38) M157K probably damaging Het
Orai3 T C 7: 127,773,888 (GRCm38) V187A probably benign Het
Parn T C 16: 13,606,202 (GRCm38) T444A probably benign Het
Pcdh11x A C X: 120,400,240 (GRCm38) N460T probably damaging Het
Pcnt C T 10: 76,370,024 (GRCm38) R2516H probably benign Het
Pde4d T A 13: 109,938,171 (GRCm38) probably benign Het
Pdgfra A G 5: 75,189,311 (GRCm38) N952S probably benign Het
Pgm1 A G 5: 64,103,874 (GRCm38) Y237C probably damaging Het
Plcb2 A G 2: 118,711,124 (GRCm38) V975A probably benign Het
Polk T C 13: 96,489,256 (GRCm38) T347A probably benign Het
Ppp6r1 C T 7: 4,641,054 (GRCm38) V430M possibly damaging Het
Ptges2 C A 2: 32,396,322 (GRCm38) C16* probably null Het
Relb A T 7: 19,619,839 (GRCm38) I38N probably damaging Het
Runx1t1 T A 4: 13,837,767 (GRCm38) N51K probably damaging Het
Samsn1 A G 16: 75,883,845 (GRCm38) probably benign Het
Scrn1 A G 6: 54,520,769 (GRCm38) V279A possibly damaging Het
Sec31b A G 19: 44,531,746 (GRCm38) S200P probably benign Het
Selp A G 1: 164,144,906 (GRCm38) T705A probably benign Het
Slc2a1 G A 4: 119,132,445 (GRCm38) R61Q probably damaging Het
Slit3 G A 11: 35,651,820 (GRCm38) probably null Het
Smo T A 6: 29,755,574 (GRCm38) V415E probably damaging Het
Spag8 C A 4: 43,652,035 (GRCm38) V350L possibly damaging Het
Tbck T G 3: 132,707,798 (GRCm38) L132R possibly damaging Het
Thnsl1 T A 2: 21,212,045 (GRCm38) C203* probably null Het
Tm9sf2 T A 14: 122,149,840 (GRCm38) probably null Het
Tmem131 A G 1: 36,841,676 (GRCm38) V171A probably damaging Het
Tmem209 T C 6: 30,501,955 (GRCm38) T83A probably benign Het
Tmem63a T C 1: 180,954,851 (GRCm38) Y138H probably damaging Het
Trim80 A G 11: 115,447,943 (GRCm38) Y533C probably damaging Het
Trpv2 A G 11: 62,581,180 (GRCm38) D66G possibly damaging Het
Trrap T A 5: 144,832,488 (GRCm38) I2620N probably benign Het
Ttyh3 A T 5: 140,634,786 (GRCm38) I232N probably damaging Het
Ube2dnl1 G A X: 114,905,785 (GRCm38) C119Y possibly damaging Het
Unc13c T A 9: 73,932,187 (GRCm38) S461C probably damaging Het
Unc80 T G 1: 66,527,941 (GRCm38) I902S probably damaging Het
Usp42 C A 5: 143,723,937 (GRCm38) G170W probably damaging Het
Vldlr T C 19: 27,238,852 (GRCm38) probably null Het
Ywhab A G 2: 164,015,345 (GRCm38) Y180C probably damaging Het
Zan A T 5: 137,380,850 (GRCm38) C5329* probably null Het
Zbtb40 C T 4: 136,998,642 (GRCm38) M535I probably benign Het
Zdhhc1 CGGGGG CGGGGGG 8: 105,483,744 (GRCm38) probably null Het
Zfp318 A G 17: 46,412,062 (GRCm38) T1664A probably benign Het
Zfp7 T A 15: 76,891,346 (GRCm38) C529* probably null Het
Zfp768 T C 7: 127,343,375 (GRCm38) Q527R possibly damaging Het
Zfp975 T A 7: 42,665,146 (GRCm38) probably null Het
Other mutations in Atp13a4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00563:Atp13a4 APN 16 29,403,778 (GRCm38) splice site probably benign
IGL01577:Atp13a4 APN 16 29,441,284 (GRCm38) missense possibly damaging 0.77
IGL01834:Atp13a4 APN 16 29,415,777 (GRCm38) splice site probably benign
IGL02165:Atp13a4 APN 16 29,434,010 (GRCm38) missense probably damaging 1.00
IGL02194:Atp13a4 APN 16 29,456,629 (GRCm38) missense probably damaging 1.00
IGL02322:Atp13a4 APN 16 29,440,102 (GRCm38) missense probably benign 0.00
IGL02553:Atp13a4 APN 16 29,422,703 (GRCm38) missense probably benign 0.03
IGL02821:Atp13a4 APN 16 29,441,307 (GRCm38) missense probably benign 0.01
IGL03349:Atp13a4 APN 16 29,456,671 (GRCm38) missense probably benign 0.01
G5030:Atp13a4 UTSW 16 29,455,488 (GRCm38) missense probably damaging 1.00
R0091:Atp13a4 UTSW 16 29,455,395 (GRCm38) missense probably damaging 1.00
R0100:Atp13a4 UTSW 16 29,421,724 (GRCm38) missense probably damaging 1.00
R0278:Atp13a4 UTSW 16 29,454,834 (GRCm38) missense probably damaging 1.00
R1263:Atp13a4 UTSW 16 29,471,953 (GRCm38) missense possibly damaging 0.60
R1378:Atp13a4 UTSW 16 29,420,428 (GRCm38) missense probably damaging 1.00
R1575:Atp13a4 UTSW 16 29,409,710 (GRCm38) missense probably benign 0.01
R1720:Atp13a4 UTSW 16 29,408,928 (GRCm38) missense probably damaging 0.99
R1759:Atp13a4 UTSW 16 29,456,611 (GRCm38) missense probably damaging 0.99
R1967:Atp13a4 UTSW 16 29,479,854 (GRCm38) missense probably damaging 0.99
R2030:Atp13a4 UTSW 16 29,422,684 (GRCm38) missense probably damaging 1.00
R2113:Atp13a4 UTSW 16 29,441,284 (GRCm38) missense possibly damaging 0.77
R3409:Atp13a4 UTSW 16 29,413,749 (GRCm38) missense probably damaging 1.00
R3410:Atp13a4 UTSW 16 29,413,749 (GRCm38) missense probably damaging 1.00
R4032:Atp13a4 UTSW 16 29,418,571 (GRCm38) missense probably damaging 1.00
R4163:Atp13a4 UTSW 16 29,541,250 (GRCm38) missense possibly damaging 0.87
R4652:Atp13a4 UTSW 16 29,452,603 (GRCm38) missense probably damaging 1.00
R4772:Atp13a4 UTSW 16 29,420,835 (GRCm38) intron probably benign
R4898:Atp13a4 UTSW 16 29,408,961 (GRCm38) nonsense probably null
R4996:Atp13a4 UTSW 16 29,472,004 (GRCm38) missense probably damaging 1.00
R5112:Atp13a4 UTSW 16 29,409,868 (GRCm38) missense possibly damaging 0.87
R5259:Atp13a4 UTSW 16 29,456,610 (GRCm38) missense probably damaging 1.00
R5395:Atp13a4 UTSW 16 29,456,604 (GRCm38) missense possibly damaging 0.94
R5395:Atp13a4 UTSW 16 29,420,888 (GRCm38) nonsense probably null
R5640:Atp13a4 UTSW 16 29,415,831 (GRCm38) missense probably damaging 0.98
R5809:Atp13a4 UTSW 16 29,433,987 (GRCm38) missense possibly damaging 0.56
R5856:Atp13a4 UTSW 16 29,433,987 (GRCm38) missense possibly damaging 0.94
R5912:Atp13a4 UTSW 16 29,456,571 (GRCm38) missense probably benign 0.33
R6282:Atp13a4 UTSW 16 29,434,004 (GRCm38) missense probably benign 0.00
R6404:Atp13a4 UTSW 16 29,471,901 (GRCm38) nonsense probably null
R6497:Atp13a4 UTSW 16 29,479,901 (GRCm38) missense probably damaging 1.00
R6577:Atp13a4 UTSW 16 29,479,841 (GRCm38) missense probably benign 0.03
R6806:Atp13a4 UTSW 16 29,469,280 (GRCm38) missense probably damaging 1.00
R7229:Atp13a4 UTSW 16 29,420,905 (GRCm38) missense probably benign 0.05
R7438:Atp13a4 UTSW 16 29,441,196 (GRCm38) missense
R7493:Atp13a4 UTSW 16 29,471,956 (GRCm38) missense
R7712:Atp13a4 UTSW 16 29,459,487 (GRCm38) missense
R7739:Atp13a4 UTSW 16 29,456,601 (GRCm38) missense
R7897:Atp13a4 UTSW 16 29,396,466 (GRCm38) missense
R7950:Atp13a4 UTSW 16 29,449,917 (GRCm38) missense
R8217:Atp13a4 UTSW 16 29,403,801 (GRCm38) missense
R8227:Atp13a4 UTSW 16 29,403,845 (GRCm38) missense
R8273:Atp13a4 UTSW 16 29,471,902 (GRCm38) missense
R8488:Atp13a4 UTSW 16 29,417,836 (GRCm38) missense possibly damaging 0.63
R8508:Atp13a4 UTSW 16 29,454,769 (GRCm38) nonsense probably null
R8773:Atp13a4 UTSW 16 29,441,580 (GRCm38) missense
R8921:Atp13a4 UTSW 16 29,454,774 (GRCm38) missense
R8940:Atp13a4 UTSW 16 29,454,690 (GRCm38) critical splice donor site probably null
R9056:Atp13a4 UTSW 16 29,471,888 (GRCm38) critical splice donor site probably null
R9272:Atp13a4 UTSW 16 29,449,979 (GRCm38) missense
R9292:Atp13a4 UTSW 16 29,422,682 (GRCm38) missense
R9415:Atp13a4 UTSW 16 29,409,003 (GRCm38) missense
R9453:Atp13a4 UTSW 16 29,420,841 (GRCm38) missense unknown
R9497:Atp13a4 UTSW 16 29,469,312 (GRCm38) critical splice acceptor site probably null
R9541:Atp13a4 UTSW 16 29,422,726 (GRCm38) missense
R9614:Atp13a4 UTSW 16 29,441,580 (GRCm38) missense
R9622:Atp13a4 UTSW 16 29,420,459 (GRCm38) missense
R9727:Atp13a4 UTSW 16 29,409,771 (GRCm38) missense
Z1176:Atp13a4 UTSW 16 29,422,587 (GRCm38) missense probably null
Predicted Primers PCR Primer
(F):5'- ACACGTTCACATTCGCTCTAAC -3'
(R):5'- TTGCAGGAAATATTTGGCTATCGG -3'

Sequencing Primer
(F):5'- TTCGCTCTAACACTTGCAAAAGTAGC -3'
(R):5'- ATATTTGGCTATCGGACTCAAGGC -3'
Posted On 2016-02-04