Incidental Mutation 'R8978:Pate7'
ID 716017
Institutional Source Beutler Lab
Gene Symbol Pate7
Ensembl Gene ENSMUSG00000090738
Gene Name prostate and testis expressed 7
Synonyms Gm17727
MMRRC Submission 068811-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R8978 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 35687820-35689405 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 35688069 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000139380 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171898] [ENSMUST00000184431]
AlphaFold E9Q4V7
Predicted Effect probably benign
Transcript: ENSMUST00000171898
SMART Domains Protein: ENSMUSP00000129553
Gene: ENSMUSG00000090738

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000184431
SMART Domains Protein: ENSMUSP00000139380
Gene: ENSMUSG00000098847

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 32 43 N/A INTRINSIC
low complexity region 64 81 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 97.8%
Validation Efficiency 99% (66/67)
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg4 A G 9: 44,192,395 (GRCm39) F224L probably benign Het
Adam39 A G 8: 41,278,707 (GRCm39) D366G probably damaging Het
Adamts14 T A 10: 61,038,795 (GRCm39) E902V probably damaging Het
Adamts6 T C 13: 104,512,247 (GRCm39) C490R probably damaging Het
Btbd3 T C 2: 138,126,055 (GRCm39) V413A possibly damaging Het
Card6 TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG 15: 5,128,173 (GRCm39) probably benign Het
Cdadc1 G T 14: 59,813,197 (GRCm39) N403K probably damaging Het
Cdc27 C T 11: 104,399,211 (GRCm39) V734I possibly damaging Het
Celf3 A G 3: 94,392,667 (GRCm39) D122G probably benign Het
Chgb T C 2: 132,634,498 (GRCm39) S147P probably benign Het
Col9a1 G A 1: 24,278,396 (GRCm39) G808D probably damaging Het
Cpne7 A G 8: 123,861,177 (GRCm39) probably null Het
Crhr1 T C 11: 104,064,480 (GRCm39) F330S possibly damaging Het
Csmd1 A C 8: 15,971,056 (GRCm39) N3086K probably benign Het
Ctnnb1 A G 9: 120,786,650 (GRCm39) D624G probably damaging Het
Dcaf8 G A 1: 172,022,124 (GRCm39) R554H probably benign Het
Dmbt1 T C 7: 130,639,611 (GRCm39) Y50H possibly damaging Het
Dmxl1 T C 18: 50,055,679 (GRCm39) L2573P probably benign Het
Ebf2 G A 14: 67,661,548 (GRCm39) G559S probably benign Het
Fancd2 A G 6: 113,562,507 (GRCm39) probably benign Het
Fkbp10 A T 11: 100,313,936 (GRCm39) I427F probably benign Het
Gipc1 T C 8: 84,389,046 (GRCm39) probably null Het
Gm1110 A T 9: 26,807,095 (GRCm39) probably benign Het
Gsdmc3 A G 15: 63,731,455 (GRCm39) L359P probably damaging Het
Hspg2 A G 4: 137,291,341 (GRCm39) D3897G probably benign Het
Ift122 T A 6: 115,902,769 (GRCm39) M1117K possibly damaging Het
Itgbl1 A T 14: 124,209,617 (GRCm39) D456V probably damaging Het
Itprid2 T A 2: 79,491,257 (GRCm39) L1014Q probably damaging Het
Kctd1 G T 18: 15,119,491 (GRCm39) L675I Het
Kyat3 C T 3: 142,443,596 (GRCm39) T403M probably benign Het
Ltbp2 T C 12: 84,834,164 (GRCm39) T1442A probably benign Het
Mier2 A C 10: 79,376,790 (GRCm39) S45R unknown Het
Mon2 T A 10: 122,871,469 (GRCm39) K383* probably null Het
Mroh4 G T 15: 74,499,473 (GRCm39) T136K probably benign Het
Mtif3 A T 5: 146,895,846 (GRCm39) S80R probably benign Het
Myh2 A C 11: 67,068,188 (GRCm39) E272A probably damaging Het
Myh2 A G 11: 67,080,323 (GRCm39) Q1179R probably damaging Het
Nfatc3 G A 8: 106,835,402 (GRCm39) C916Y probably benign Het
Or13a17 A T 7: 140,271,642 (GRCm39) T275S probably benign Het
Or2w2 T A 13: 21,758,279 (GRCm39) T116S probably benign Het
Or7g21 T A 9: 19,032,582 (GRCm39) C107* probably null Het
Orc2 T C 1: 58,511,499 (GRCm39) D370G possibly damaging Het
Pcdhga6 T A 18: 37,840,716 (GRCm39) N145K probably benign Het
Pih1d2 A G 9: 50,536,232 (GRCm39) M296V probably benign Het
Prickle4 A T 17: 47,999,772 (GRCm39) probably benign Het
Rabl6 G A 2: 25,477,541 (GRCm39) P303L probably damaging Het
Rara T G 11: 98,862,595 (GRCm39) I332S probably damaging Het
Reln A G 5: 22,090,512 (GRCm39) F3449L possibly damaging Het
Rhoq T C 17: 87,271,767 (GRCm39) L61P Het
Rigi A G 4: 40,239,650 (GRCm39) I16T probably damaging Het
Slc6a15 G A 10: 103,230,953 (GRCm39) W226* probably null Het
Spef2 A T 15: 9,725,263 (GRCm39) S165T possibly damaging Het
Stab2 T C 10: 86,785,782 (GRCm39) N620S possibly damaging Het
Suds3 A G 5: 117,232,973 (GRCm39) probably null Het
Sult1b1 A G 5: 87,682,900 (GRCm39) I15T possibly damaging Het
Synm C A 7: 67,384,672 (GRCm39) V997L probably damaging Het
Tgfbi C A 13: 56,778,391 (GRCm39) D387E probably benign Het
Thrb T C 14: 17,981,886 (GRCm38) C4R possibly damaging Het
Tk2 A G 8: 104,957,809 (GRCm39) V179A possibly damaging Het
Trim25 T C 11: 88,907,027 (GRCm39) V462A probably benign Het
Tub T C 7: 108,629,393 (GRCm39) Y483H probably damaging Het
Vav1 A G 17: 57,603,710 (GRCm39) T131A probably benign Het
Vav1 A G 17: 57,631,650 (GRCm39) T781A probably benign Het
Zbtb34 A G 2: 33,301,048 (GRCm39) S498P possibly damaging Het
Zfp568 T A 7: 29,716,683 (GRCm39) H194Q probably benign Het
Zfp683 A T 4: 133,781,239 (GRCm39) Q18L probably benign Het
Other mutations in Pate7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01285:Pate7 APN 9 35,688,044 (GRCm39) missense possibly damaging 0.73
IGL02044:Pate7 APN 9 35,687,959 (GRCm39) missense probably benign 0.19
IGL02352:Pate7 APN 9 35,689,180 (GRCm39) start codon destroyed probably null 0.04
IGL02359:Pate7 APN 9 35,689,180 (GRCm39) start codon destroyed probably null 0.04
R0827:Pate7 UTSW 9 35,689,147 (GRCm39) missense probably damaging 0.97
R1382:Pate7 UTSW 9 35,689,390 (GRCm39) start gained probably benign
R1591:Pate7 UTSW 9 35,687,952 (GRCm39) missense probably damaging 0.99
R1794:Pate7 UTSW 9 35,688,418 (GRCm39) missense probably benign 0.01
R5419:Pate7 UTSW 9 35,689,407 (GRCm39) splice site probably null
R6110:Pate7 UTSW 9 35,688,442 (GRCm39) missense possibly damaging 0.90
R6379:Pate7 UTSW 9 35,689,381 (GRCm39) start gained probably benign
R6614:Pate7 UTSW 9 35,688,421 (GRCm39) missense probably damaging 0.99
R7698:Pate7 UTSW 9 35,688,472 (GRCm39) missense probably benign 0.27
R7833:Pate7 UTSW 9 35,688,406 (GRCm39) missense probably damaging 1.00
R8110:Pate7 UTSW 9 35,689,329 (GRCm39) makesense probably null
R8881:Pate7 UTSW 9 35,689,384 (GRCm39) utr 5 prime probably benign
Predicted Primers PCR Primer
(F):5'- CTGGACGAAGCCATAAGATAATCTG -3'
(R):5'- TCAGGATCTCCACAAAGCCTAG -3'

Sequencing Primer
(F):5'- GGACCATTCATCACTTGG -3'
(R):5'- ATGTTTACCAAGTACTTTGTGCC -3'
Posted On 2022-06-24