Incidental Mutation 'R1799:Atp10a'
ID 202935
Institutional Source Beutler Lab
Gene Symbol Atp10a
Ensembl Gene ENSMUSG00000025324
Gene Name ATPase, class V, type 10A
Synonyms pfatp, Atp10c
MMRRC Submission 039829-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.098) question?
Stock # R1799 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 58305914-58479168 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 58474182 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 1156 (D1156E)
Ref Sequence ENSEMBL: ENSMUSP00000129811 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168747]
AlphaFold O54827
Predicted Effect probably damaging
Transcript: ENSMUST00000168747
AA Change: D1156E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129811
Gene: ENSMUSG00000025324
AA Change: D1156E

DomainStartEndE-ValueType
low complexity region 15 32 N/A INTRINSIC
Pfam:PhoLip_ATPase_N 55 114 5.2e-23 PFAM
Pfam:E1-E2_ATPase 120 393 6.6e-10 PFAM
low complexity region 633 643 N/A INTRINSIC
Pfam:Cation_ATPase 685 791 1.5e-7 PFAM
Pfam:HAD 697 1054 2.1e-12 PFAM
Pfam:PhoLip_ATPase_C 1071 1316 1.1e-76 PFAM
low complexity region 1458 1477 N/A INTRINSIC
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 96.9%
  • 10x: 95.3%
  • 20x: 92.3%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. This gene is maternally expressed. It maps within the most common interval of deletion responsible for Angelman syndrome, also known as 'happy puppet syndrome'. [provided by RefSeq, Jul 2008]
PHENOTYPE: Disruption of this gene at the distal end of the p23DFiOD deletion may be responsible for the obesity phenotypes associated with that deletion. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 102 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A930011G23Rik A G 5: 99,382,435 (GRCm39) L271P probably benign Het
Adamts3 A C 5: 89,923,280 (GRCm39) D175E probably benign Het
Adcy4 T C 14: 56,008,929 (GRCm39) T833A probably benign Het
Adgrf5 A T 17: 43,750,958 (GRCm39) I508F probably damaging Het
Arhgap9 G T 10: 127,163,593 (GRCm39) V464L probably damaging Het
Atp2a1 A T 7: 126,049,314 (GRCm39) M576K probably benign Het
Atrx T C X: 104,891,235 (GRCm39) Q1536R probably damaging Het
Ccdc141 A C 2: 76,842,015 (GRCm39) V1472G possibly damaging Het
Cd84 A G 1: 171,700,317 (GRCm39) T145A possibly damaging Het
Celsr1 G T 15: 85,916,886 (GRCm39) N362K probably damaging Het
Cep290 G A 10: 100,352,058 (GRCm39) A755T probably benign Het
Cfap70 T A 14: 20,445,067 (GRCm39) E1071V probably damaging Het
Cps1 T C 1: 67,248,801 (GRCm39) V1176A probably damaging Het
Csf2rb2 A C 15: 78,181,268 (GRCm39) N41K probably damaging Het
Csn1s2a G A 5: 87,926,052 (GRCm39) V43M probably damaging Het
Cyp26b1 T C 6: 84,561,254 (GRCm39) D136G probably benign Het
Cyp7b1 A G 3: 18,151,616 (GRCm39) L199P probably benign Het
Dapk1 C T 13: 60,867,468 (GRCm39) T225I probably damaging Het
Dio2 T A 12: 90,696,680 (GRCm39) T103S probably benign Het
Dipk1a C A 5: 108,057,713 (GRCm39) V237F probably damaging Het
Dnhd1 T A 7: 105,304,974 (GRCm39) S339T probably benign Het
Drc1 A G 5: 30,523,841 (GRCm39) N737D probably damaging Het
Efhc1 C T 1: 21,049,762 (GRCm39) P541S probably benign Het
Elmo2 A T 2: 165,134,077 (GRCm39) I637N probably damaging Het
Eps15 T A 4: 109,240,034 (GRCm39) D492E probably damaging Het
Ermn G T 2: 57,938,249 (GRCm39) N121K probably benign Het
F5 A G 1: 164,021,100 (GRCm39) T1192A possibly damaging Het
Fbxo22 T C 9: 55,130,771 (GRCm39) F347L probably benign Het
Fbxw15 G A 9: 109,387,314 (GRCm39) S227F probably damaging Het
Foxj3 A G 4: 119,476,548 (GRCm39) N242S probably benign Het
Gjb3 G A 4: 127,220,224 (GRCm39) R103W probably damaging Het
Grm4 A G 17: 27,691,914 (GRCm39) V235A probably damaging Het
Gstm4 T C 3: 107,950,874 (GRCm39) N74S probably damaging Het
Gtf3c3 A G 1: 54,459,583 (GRCm39) V393A possibly damaging Het
Hltf T A 3: 20,159,855 (GRCm39) L702H probably damaging Het
Inpp4a T A 1: 37,432,059 (GRCm39) V153E possibly damaging Het
Kmt5c T C 7: 4,745,729 (GRCm39) probably null Het
Kynu A G 2: 43,494,169 (GRCm39) R201G possibly damaging Het
Lrp2 T A 2: 69,333,874 (GRCm39) T1456S probably benign Het
Lrrc40 G A 3: 157,742,441 (GRCm39) V19I probably benign Het
M1ap T A 6: 82,982,491 (GRCm39) C258* probably null Het
Man2a1 T C 17: 65,059,452 (GRCm39) L1113P probably benign Het
Man2a1 C T 17: 64,976,492 (GRCm39) R427W probably damaging Het
Meikin C A 11: 54,308,613 (GRCm39) Q404K probably benign Het
Mfsd4a T C 1: 131,981,334 (GRCm39) I222V possibly damaging Het
N4bp2 A G 5: 65,964,168 (GRCm39) N739S possibly damaging Het
Ncoa2 A T 1: 13,232,517 (GRCm39) probably null Het
Nisch G T 14: 30,899,228 (GRCm39) probably benign Het
Nmur2 A G 11: 55,920,447 (GRCm39) V266A probably damaging Het
Npcd G A 15: 79,712,987 (GRCm39) R147C probably damaging Het
Or4q3 T A 14: 50,583,537 (GRCm39) M121L probably benign Het
Or5ac25 T A 16: 59,182,243 (GRCm39) I113F probably benign Het
Pals2 T A 6: 50,173,525 (GRCm39) M463K probably damaging Het
Parp4 A T 14: 56,885,589 (GRCm39) H1556L unknown Het
Pcdh9 G T 14: 94,126,107 (GRCm39) A21E probably benign Het
Phtf1 A G 3: 103,903,958 (GRCm39) E436G probably benign Het
Piezo2 C A 18: 63,165,911 (GRCm39) probably null Het
Piezo2 T C 18: 63,241,158 (GRCm39) Y690C probably damaging Het
Pla2g4f T C 2: 120,141,549 (GRCm39) R183G possibly damaging Het
Plxnd1 T C 6: 115,971,018 (GRCm39) D250G probably damaging Het
Ppig A G 2: 69,579,744 (GRCm39) D426G unknown Het
Ppp3cb T C 14: 20,574,540 (GRCm39) E185G possibly damaging Het
Qsox1 A T 1: 155,670,364 (GRCm39) M151K probably null Het
Ralgapa2 T C 2: 146,184,648 (GRCm39) E1453G probably benign Het
Rnf167 G A 11: 70,540,838 (GRCm39) V191I probably benign Het
Rp1 T C 1: 4,419,055 (GRCm39) K686E possibly damaging Het
Ryr1 T G 7: 28,767,046 (GRCm39) Q2979P probably damaging Het
Scaf1 T A 7: 44,657,443 (GRCm39) I479F probably damaging Het
Septin8 A G 11: 53,425,310 (GRCm39) T68A probably benign Het
Sh3rf1 A T 8: 61,825,661 (GRCm39) N552I probably damaging Het
Shoc1 A T 4: 59,099,383 (GRCm39) V103D possibly damaging Het
Slc1a3 A G 15: 8,717,888 (GRCm39) L68P probably damaging Het
Slc39a6 G A 18: 24,718,524 (GRCm39) P511L probably benign Het
Slc9c1 A G 16: 45,374,652 (GRCm39) Y339C probably damaging Het
Smarcal1 G T 1: 72,625,120 (GRCm39) C89F probably damaging Het
Smu1 A T 4: 40,745,537 (GRCm39) M261K probably damaging Het
Spag8 T G 4: 43,653,087 (GRCm39) probably benign Het
Spag8 T C 4: 43,653,345 (GRCm39) probably benign Het
Spata31d1a T C 13: 59,851,216 (GRCm39) D304G probably benign Het
Spdl1 A T 11: 34,711,856 (GRCm39) L298* probably null Het
Stac2 C T 11: 97,930,444 (GRCm39) probably null Het
Stag1 A G 9: 100,835,515 (GRCm39) probably null Het
Stpg2 C T 3: 139,125,542 (GRCm39) P445L probably damaging Het
Sult2a8 A T 7: 14,157,451 (GRCm39) V128E probably damaging Het
Synm A G 7: 67,385,707 (GRCm39) F210L probably damaging Het
Tbck C G 3: 132,480,263 (GRCm39) A714G probably benign Het
Tcerg1 A T 18: 42,694,012 (GRCm39) Y711F possibly damaging Het
Tnfrsf25 A G 4: 152,201,465 (GRCm39) T98A probably benign Het
Togaram2 T C 17: 71,998,450 (GRCm39) S218P probably damaging Het
Tpp1 A T 7: 105,399,515 (GRCm39) D84E probably benign Het
Trim30d G T 7: 104,132,682 (GRCm39) Q202K probably damaging Het
Trim37 T A 11: 87,068,845 (GRCm39) V397E probably damaging Het
Triml1 A T 8: 43,583,512 (GRCm39) I363N probably damaging Het
Trpm6 T A 19: 18,869,363 (GRCm39) probably null Het
Tsc2 T C 17: 24,823,382 (GRCm39) S1055G probably benign Het
Ubr5 T C 15: 37,989,621 (GRCm39) D2065G probably damaging Het
Uggt2 G T 14: 119,269,688 (GRCm39) P948Q probably benign Het
Vps13c A T 9: 67,851,399 (GRCm39) S2345C probably damaging Het
Wtap G T 17: 13,199,771 (GRCm39) R48S possibly damaging Het
Zbtb38 A G 9: 96,570,934 (GRCm39) V50A probably damaging Het
Zcchc2 T A 1: 105,958,017 (GRCm39) S829R probably benign Het
Zfp385b T C 2: 77,246,316 (GRCm39) D237G probably benign Het
Other mutations in Atp10a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00649:Atp10a APN 7 58,444,230 (GRCm39) missense probably benign 0.06
IGL00973:Atp10a APN 7 58,457,218 (GRCm39) missense probably damaging 1.00
IGL00984:Atp10a APN 7 58,308,489 (GRCm39) missense probably damaging 1.00
IGL01086:Atp10a APN 7 58,474,066 (GRCm39) missense probably damaging 0.96
IGL01296:Atp10a APN 7 58,463,373 (GRCm39) missense probably benign 0.02
IGL01731:Atp10a APN 7 58,447,310 (GRCm39) missense probably benign 0.16
IGL02081:Atp10a APN 7 58,477,604 (GRCm39) missense possibly damaging 0.62
IGL02095:Atp10a APN 7 58,457,141 (GRCm39) missense probably damaging 1.00
IGL02549:Atp10a APN 7 58,469,481 (GRCm39) missense probably benign 0.00
IGL02558:Atp10a APN 7 58,469,390 (GRCm39) missense probably damaging 0.98
IGL02659:Atp10a APN 7 58,463,379 (GRCm39) missense probably benign
IGL02986:Atp10a APN 7 58,478,469 (GRCm39) missense probably benign
IGL03218:Atp10a APN 7 58,438,196 (GRCm39) critical splice donor site probably null
PIT4260001:Atp10a UTSW 7 58,440,866 (GRCm39) nonsense probably null
PIT4445001:Atp10a UTSW 7 58,453,215 (GRCm39) missense probably damaging 0.98
PIT4810001:Atp10a UTSW 7 58,463,596 (GRCm39) missense probably damaging 0.99
R0091:Atp10a UTSW 7 58,423,794 (GRCm39) splice site probably benign
R0349:Atp10a UTSW 7 58,453,215 (GRCm39) missense probably damaging 0.98
R0426:Atp10a UTSW 7 58,434,482 (GRCm39) missense probably benign 0.00
R0609:Atp10a UTSW 7 58,469,488 (GRCm39) splice site probably null
R0722:Atp10a UTSW 7 58,465,931 (GRCm39) missense possibly damaging 0.75
R0741:Atp10a UTSW 7 58,478,337 (GRCm39) missense possibly damaging 0.90
R1172:Atp10a UTSW 7 58,453,514 (GRCm39) missense probably benign 0.05
R1342:Atp10a UTSW 7 58,465,894 (GRCm39) splice site probably benign
R1648:Atp10a UTSW 7 58,434,575 (GRCm39) missense probably damaging 1.00
R1715:Atp10a UTSW 7 58,436,253 (GRCm39) missense probably damaging 0.98
R1737:Atp10a UTSW 7 58,476,986 (GRCm39) splice site probably benign
R1909:Atp10a UTSW 7 58,478,460 (GRCm39) missense probably benign 0.12
R1918:Atp10a UTSW 7 58,477,683 (GRCm39) missense possibly damaging 0.82
R2031:Atp10a UTSW 7 58,477,678 (GRCm39) nonsense probably null
R2080:Atp10a UTSW 7 58,474,075 (GRCm39) missense probably damaging 0.97
R2424:Atp10a UTSW 7 58,444,303 (GRCm39) missense probably benign 0.16
R2696:Atp10a UTSW 7 58,463,366 (GRCm39) missense probably benign 0.00
R3932:Atp10a UTSW 7 58,476,852 (GRCm39) missense possibly damaging 0.69
R4198:Atp10a UTSW 7 58,463,434 (GRCm39) missense probably damaging 1.00
R4453:Atp10a UTSW 7 58,308,248 (GRCm39) small deletion probably benign
R4632:Atp10a UTSW 7 58,457,186 (GRCm39) missense possibly damaging 0.48
R4661:Atp10a UTSW 7 58,308,248 (GRCm39) small deletion probably benign
R4782:Atp10a UTSW 7 58,440,843 (GRCm39) missense probably benign
R4888:Atp10a UTSW 7 58,435,055 (GRCm39) missense probably damaging 1.00
R4935:Atp10a UTSW 7 58,463,512 (GRCm39) missense probably damaging 1.00
R5051:Atp10a UTSW 7 58,389,994 (GRCm39) frame shift probably null
R5213:Atp10a UTSW 7 58,423,731 (GRCm39) missense probably damaging 0.99
R5617:Atp10a UTSW 7 58,453,423 (GRCm39) missense probably benign 0.06
R5834:Atp10a UTSW 7 58,308,366 (GRCm39) missense probably benign 0.01
R5885:Atp10a UTSW 7 58,463,548 (GRCm39) missense possibly damaging 0.92
R6013:Atp10a UTSW 7 58,447,538 (GRCm39) missense probably benign 0.05
R6136:Atp10a UTSW 7 58,478,088 (GRCm39) missense probably benign
R6269:Atp10a UTSW 7 58,453,487 (GRCm39) missense possibly damaging 0.51
R6380:Atp10a UTSW 7 58,469,432 (GRCm39) nonsense probably null
R6743:Atp10a UTSW 7 58,447,562 (GRCm39) missense possibly damaging 0.89
R6875:Atp10a UTSW 7 58,447,100 (GRCm39) missense probably benign 0.01
R6975:Atp10a UTSW 7 58,423,733 (GRCm39) missense probably damaging 1.00
R7082:Atp10a UTSW 7 58,308,567 (GRCm39) missense probably damaging 1.00
R7203:Atp10a UTSW 7 58,436,221 (GRCm39) missense probably benign
R7224:Atp10a UTSW 7 58,447,219 (GRCm39) missense probably benign 0.00
R7287:Atp10a UTSW 7 58,477,017 (GRCm39) missense probably damaging 1.00
R7437:Atp10a UTSW 7 58,308,288 (GRCm39) missense unknown
R7474:Atp10a UTSW 7 58,308,275 (GRCm39) missense unknown
R7530:Atp10a UTSW 7 58,423,724 (GRCm39) missense probably benign 0.02
R7561:Atp10a UTSW 7 58,476,881 (GRCm39) missense probably damaging 0.98
R7743:Atp10a UTSW 7 58,453,457 (GRCm39) missense probably damaging 1.00
R7767:Atp10a UTSW 7 58,308,597 (GRCm39) missense probably damaging 1.00
R7861:Atp10a UTSW 7 58,438,107 (GRCm39) missense probably damaging 1.00
R7903:Atp10a UTSW 7 58,308,570 (GRCm39) missense probably damaging 1.00
R8015:Atp10a UTSW 7 58,453,245 (GRCm39) missense probably benign 0.00
R8166:Atp10a UTSW 7 58,457,270 (GRCm39) missense possibly damaging 0.46
R8201:Atp10a UTSW 7 58,469,424 (GRCm39) nonsense probably null
R8465:Atp10a UTSW 7 58,478,058 (GRCm39) missense probably benign 0.32
R8858:Atp10a UTSW 7 58,465,971 (GRCm39) missense probably damaging 1.00
R8985:Atp10a UTSW 7 58,438,092 (GRCm39) missense probably benign 0.03
R9003:Atp10a UTSW 7 58,457,203 (GRCm39) missense probably damaging 1.00
R9274:Atp10a UTSW 7 58,478,369 (GRCm39) missense probably benign 0.22
R9385:Atp10a UTSW 7 58,477,887 (GRCm39) missense probably benign 0.00
R9432:Atp10a UTSW 7 58,469,418 (GRCm39) missense possibly damaging 0.95
R9454:Atp10a UTSW 7 58,308,339 (GRCm39) missense probably benign
R9596:Atp10a UTSW 7 58,477,553 (GRCm39) missense probably damaging 1.00
R9736:Atp10a UTSW 7 58,474,078 (GRCm39) missense probably damaging 1.00
Z1176:Atp10a UTSW 7 58,438,195 (GRCm39) critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- TAGATGAGTCTCAGTAGTGACAGC -3'
(R):5'- GCAGACAGCATCCCTTCTAC -3'

Sequencing Primer
(F):5'- GTCTCAGTAGTGACAGCAAAAAC -3'
(R):5'- GACAGCATCCCTTCTACAACTTC -3'
Posted On 2014-06-23