Incidental Mutation 'R6652:Yipf7'
ID528087
Institutional Source Beutler Lab
Gene Symbol Yipf7
Ensembl Gene ENSMUSG00000029158
Gene NameYip1 domain family, member 7
Synonyms2310016N21Rik, Yip1b
MMRRC Submission
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R6652 (G1)
Quality Score225.009
Status Validated
Chromosome5
Chromosomal Location69516671-69542648 bp(-) (GRCm38)
Type of Mutationstart codon destroyed
DNA Base Change (assembly) A to G at 69541161 bp
ZygosityHeterozygous
Amino Acid Change Methionine to Threonine at position 1 (M1T)
Ref Sequence ENSEMBL: ENSMUSP00000031045 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031045] [ENSMUST00000202423]
Predicted Effect probably null
Transcript: ENSMUST00000031045
AA Change: M1T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000031045
Gene: ENSMUSG00000029158
AA Change: M1T

DomainStartEndE-ValueType
Pfam:Yip1 93 253 4.2e-13 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000202423
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.7%
Validation Efficiency 100% (42/42)
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca14 A G 7: 120,246,941 D605G probably damaging Het
Cfh A T 1: 140,144,068 I294N probably benign Het
Clk3 A G 9: 57,761,795 S49P probably damaging Het
Cmya5 T C 13: 93,093,039 D1847G probably damaging Het
Cmya5 A G 13: 93,092,895 V1895A probably benign Het
Cwf19l1 T C 19: 44,114,699 D359G probably benign Het
Dag1 A T 9: 108,209,090 M284K probably damaging Het
Ergic2 T C 6: 148,189,581 Y211C probably damaging Het
Espnl A C 1: 91,344,699 I594L probably benign Het
Fam193b A G 13: 55,542,790 S226P probably damaging Het
Fat2 T A 11: 55,252,262 I4254L probably benign Het
Fhdc1 T C 3: 84,464,324 Y108C probably damaging Het
Fut9 G C 4: 25,620,619 T65S probably benign Het
Gm9507 A T 10: 77,811,659 probably benign Het
Gpt2 G A 8: 85,518,052 E325K probably benign Het
Grap2 A T 15: 80,648,522 N297Y probably damaging Het
Igfn1 A G 1: 135,963,871 F2302S probably damaging Het
Ighv1-81 T A 12: 115,920,431 I67F probably damaging Het
Kidins220 T A 12: 25,010,060 probably null Het
Kti12 T A 4: 108,848,533 S215T probably benign Het
Mc1r G A 8: 123,407,631 G41D probably damaging Het
Mov10l1 A G 15: 88,993,902 Y129C probably damaging Het
Mthfsd A T 8: 121,098,821 L337Q probably damaging Het
Musk C T 4: 58,368,977 A629V probably damaging Het
Nadsyn1 A T 7: 143,811,218 M250K probably benign Het
Ncapd2 G A 6: 125,186,270 H92Y probably benign Het
Olfr1507 C T 14: 52,490,793 R57Q probably benign Het
Olfr220 G A 1: 174,449,061 C146Y probably damaging Het
Plec A T 15: 76,179,774 V2100E probably damaging Het
Prss37 C A 6: 40,519,156 probably benign Het
Sebox A T 11: 78,503,805 E32V probably damaging Het
Senp7 C A 16: 56,123,894 Q194K probably benign Het
Sfxn3 G A 19: 45,049,915 probably null Het
Spg20 G A 3: 55,124,827 E361K probably benign Het
Stn1 T C 19: 47,507,578 T334A probably benign Het
Stoml1 A G 9: 58,256,734 D112G probably damaging Het
Thap2 T A 10: 115,376,536 D28V probably damaging Het
Ubap2 A T 4: 41,196,743 N872K possibly damaging Het
Vezt A G 10: 93,970,279 F757L probably damaging Het
Vmn1r204 T C 13: 22,556,403 I68T probably damaging Het
Wnt10a A G 1: 74,803,454 probably null Het
Zdhhc19 T C 16: 32,497,229 F48S probably damaging Het
Zfp317 C T 9: 19,647,039 T183I probably damaging Het
Other mutations in Yipf7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01160:Yipf7 APN 5 69519317 missense probably benign 0.13
IGL02829:Yipf7 APN 5 69541091 missense probably benign 0.22
R0581:Yipf7 UTSW 5 69521063 missense probably benign 0.37
R2104:Yipf7 UTSW 5 69521119 missense possibly damaging 0.92
R2697:Yipf7 UTSW 5 69541140 missense possibly damaging 0.79
R4329:Yipf7 UTSW 5 69521122 missense probably damaging 1.00
R4621:Yipf7 UTSW 5 69519361 missense possibly damaging 0.79
R6103:Yipf7 UTSW 5 69541062 missense probably benign
R6823:Yipf7 UTSW 5 69517070 missense probably damaging 1.00
R7674:Yipf7 UTSW 5 69519229 missense probably damaging 0.99
R7796:Yipf7 UTSW 5 69527253 missense possibly damaging 0.85
R8115:Yipf7 UTSW 5 69527227 missense probably benign
R8284:Yipf7 UTSW 5 69517196 missense probably benign 0.25
R8512:Yipf7 UTSW 5 69517044 missense probably benign 0.03
Predicted Primers PCR Primer
(F):5'- ACTAACTGGCAGAACACTGG -3'
(R):5'- CTCTAAATTGCTATGAGGAGGGG -3'

Sequencing Primer
(F):5'- CTGGCACTTCTAAAAATGAGAGC -3'
(R):5'- AGGGGAAGTACATTGGTGATTTC -3'
Posted On2018-07-24