Incidental Mutation 'R6191:Zfp345'
ID 502540
Institutional Source Beutler Lab
Gene Symbol Zfp345
Ensembl Gene ENSMUSG00000074731
Gene Name zinc finger protein 345
Synonyms OTTMUSG00000015743
MMRRC Submission 044331-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.150) question?
Stock # R6191 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 150312911-150326983 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 150315010 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Aspartic acid at position 176 (Y176D)
Ref Sequence ENSEMBL: ENSMUSP00000105540 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109914]
AlphaFold A2AQA1
Predicted Effect probably benign
Transcript: ENSMUST00000109914
AA Change: Y176D

PolyPhen 2 Score 0.108 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000105540
Gene: ENSMUSG00000074731
AA Change: Y176D

DomainStartEndE-ValueType
KRAB 4 66 9.5e-20 SMART
ZnF_C2H2 103 125 2e-2 SMART
ZnF_C2H2 131 153 2.9e-6 SMART
ZnF_C2H2 159 181 4.1e-3 SMART
ZnF_C2H2 215 237 2.6e-7 SMART
ZnF_C2H2 243 265 1.6e-5 SMART
ZnF_C2H2 271 293 4e-7 SMART
ZnF_C2H2 299 321 1.1e-5 SMART
ZnF_C2H2 327 349 5.9e-7 SMART
ZnF_C2H2 365 387 4.4e-7 SMART
ZnF_C2H2 393 415 7.3e-6 SMART
ZnF_C2H2 421 443 2.7e-5 SMART
ZnF_C2H2 449 471 1.5e-4 SMART
ZnF_C2H2 477 499 1.3e-5 SMART
ZnF_C2H2 505 527 5.1e-6 SMART
ZnF_C2H2 533 555 9.2e-7 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000117906
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency 99% (84/85)
Allele List at MGI
Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930563M21Rik A C 9: 55,909,807 (GRCm39) D144E possibly damaging Het
Amigo2 T A 15: 97,143,419 (GRCm39) K334N probably benign Het
Ano6 T C 15: 95,846,380 (GRCm39) probably null Het
Ap1m2 C A 9: 21,210,601 (GRCm39) V343F probably benign Het
Apol6 T C 15: 76,940,098 (GRCm39) V307A probably benign Het
Arsi C A 18: 61,045,544 (GRCm39) A78E probably damaging Het
B2m A T 2: 121,981,396 (GRCm39) N37I possibly damaging Het
Bltp3b G T 10: 89,641,180 (GRCm39) G784C possibly damaging Het
C8a T C 4: 104,703,100 (GRCm39) K363R probably benign Het
Ccdc117 C A 11: 5,484,242 (GRCm39) probably null Het
Ccdc154 C A 17: 25,386,945 (GRCm39) Q325K probably damaging Het
Cd300e A T 11: 114,945,359 (GRCm39) V145E possibly damaging Het
Col19a1 G T 1: 24,356,474 (GRCm39) P673Q probably damaging Het
Csn2 A G 5: 87,843,885 (GRCm39) probably null Het
Ctnna1 T C 18: 35,307,408 (GRCm39) V135A probably damaging Het
Dnah11 T A 12: 118,154,632 (GRCm39) D216V probably benign Het
Dnah12 A G 14: 26,431,412 (GRCm39) H410R probably benign Het
Dock2 C T 11: 34,181,652 (GRCm39) R1637H possibly damaging Het
Dspp A G 5: 104,325,214 (GRCm39) N526D unknown Het
Frem2 T C 3: 53,562,701 (GRCm39) H602R probably benign Het
Galc A T 12: 98,218,293 (GRCm39) H186Q probably damaging Het
Grina T C 15: 76,133,218 (GRCm39) V262A probably damaging Het
Gse1 G A 8: 121,280,542 (GRCm39) probably null Het
H2-Oa C A 17: 34,312,842 (GRCm39) Q40K probably damaging Het
Hfm1 C A 5: 107,034,419 (GRCm39) D763Y possibly damaging Het
Hmcn2 T A 2: 31,348,758 (GRCm39) Y4925N probably damaging Het
Hs3st3b1 C A 11: 63,780,029 (GRCm39) R366L probably benign Het
Idh2 TCCCAGG T 7: 79,748,079 (GRCm39) probably benign Het
Iqank1 T C 15: 75,918,218 (GRCm39) probably null Het
Itpr2 A G 6: 146,229,833 (GRCm39) V1221A probably benign Het
Kdm6b T C 11: 69,297,584 (GRCm39) N285S probably benign Het
Klk1b1 T A 7: 43,620,081 (GRCm39) N181K probably damaging Het
Kmt2a C A 9: 44,738,125 (GRCm39) probably benign Het
Lama5 T C 2: 179,827,752 (GRCm39) D2170G probably damaging Het
Lama5 T A 2: 179,822,404 (GRCm39) T2890S probably damaging Het
Lsm2 T A 17: 35,201,131 (GRCm39) probably benign Het
Map3k5 G T 10: 19,899,415 (GRCm39) C232F probably damaging Het
Mapk9 T G 11: 49,754,383 (GRCm39) D45E probably damaging Het
Mpnd T C 17: 56,319,482 (GRCm39) V315A possibly damaging Het
Msh2 A G 17: 88,030,900 (GRCm39) I926V probably benign Het
Mtcl1 C T 17: 66,650,521 (GRCm39) R1345H probably damaging Het
Nbeal2 A G 9: 110,457,058 (GRCm39) probably null Het
Neo1 T C 9: 58,796,312 (GRCm39) D1205G probably damaging Het
Nhlrc2 A G 19: 56,559,291 (GRCm39) S259G probably benign Het
Nkain4 G A 2: 180,577,796 (GRCm39) P186L probably damaging Het
Nkain4 G A 2: 180,577,797 (GRCm39) P186S probably damaging Het
Nlrp1b T A 11: 71,109,283 (GRCm39) R73* probably null Het
Nr5a2 T C 1: 136,818,536 (GRCm39) D330G probably damaging Het
Nup54 A G 5: 92,572,153 (GRCm39) L299P probably damaging Het
Or2v1 T C 11: 49,025,877 (GRCm39) L286P probably damaging Het
Or5aq7 A G 2: 86,938,296 (GRCm39) V145A probably damaging Het
Pcdhb8 T A 18: 37,489,279 (GRCm39) V319E probably benign Het
Pcsk6 T A 7: 65,578,875 (GRCm39) D129E probably benign Het
Pld5 G A 1: 175,798,100 (GRCm39) T433I probably benign Het
Plin1 A T 7: 79,371,347 (GRCm39) L459H probably benign Het
Psd4 T C 2: 24,284,499 (GRCm39) V121A probably damaging Het
Pxdn A T 12: 30,032,716 (GRCm39) I167F possibly damaging Het
R3hdm2 T C 10: 127,320,384 (GRCm39) S569P probably damaging Het
Rfng T A 11: 120,673,516 (GRCm39) T202S probably damaging Het
Robo1 T C 16: 72,730,696 (GRCm39) S266P probably benign Het
Sema3c G T 5: 17,858,804 (GRCm39) V68L probably damaging Het
Slco6c1 C T 1: 96,993,808 (GRCm39) R645H possibly damaging Het
Slfn8 A G 11: 82,907,626 (GRCm39) Y306H possibly damaging Het
Snap91 T C 9: 86,720,105 (GRCm39) D144G probably damaging Het
St7l T G 3: 104,775,349 (GRCm39) F75C probably damaging Het
Stard10 A G 7: 100,992,468 (GRCm39) I145V probably damaging Het
Tekt3 C T 11: 62,968,999 (GRCm39) A242V probably damaging Het
Tex44 A G 1: 86,354,306 (GRCm39) probably benign Het
Thg1l T C 11: 45,844,988 (GRCm39) Q88R probably benign Het
Trav8n-2 T A 14: 53,583,744 (GRCm39) I67N probably damaging Het
Ttn G A 2: 76,677,770 (GRCm39) probably benign Het
Ube4a A T 9: 44,861,051 (GRCm39) L253* probably null Het
Uggt1 A T 1: 36,201,289 (GRCm39) N1150K probably damaging Het
Ush2a T A 1: 187,995,298 (GRCm39) L23* probably null Het
Usp22 T A 11: 61,065,602 (GRCm39) N37I probably benign Het
Usp53 T A 3: 122,743,390 (GRCm39) K515N probably damaging Het
Vmn2r4 T C 3: 64,322,702 (GRCm39) K6E probably benign Het
Vps13d C T 4: 144,875,918 (GRCm39) V1530M probably damaging Het
Vwa3b A G 1: 37,153,612 (GRCm39) I485V possibly damaging Het
Wnk4 T C 11: 101,155,156 (GRCm39) Y356H probably damaging Het
Zcchc2 A G 1: 105,917,900 (GRCm39) probably benign Het
Zfp598 T C 17: 24,896,850 (GRCm39) F238S possibly damaging Het
Zkscan17 T C 11: 59,393,820 (GRCm39) D10G probably damaging Het
Zmat4 T G 8: 24,392,083 (GRCm39) M13R probably damaging Het
Other mutations in Zfp345
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00833:Zfp345 APN 2 150,314,649 (GRCm39) missense probably damaging 1.00
IGL00846:Zfp345 APN 2 150,314,538 (GRCm39) missense possibly damaging 0.76
IGL01020:Zfp345 APN 2 150,314,967 (GRCm39) missense possibly damaging 0.68
IGL01931:Zfp345 APN 2 150,315,270 (GRCm39) missense probably benign 0.38
IGL02237:Zfp345 APN 2 150,316,805 (GRCm39) splice site probably benign
IGL02335:Zfp345 APN 2 150,316,463 (GRCm39) missense possibly damaging 0.92
IGL02592:Zfp345 APN 2 150,315,229 (GRCm39) missense probably benign 0.36
IGL02736:Zfp345 APN 2 150,316,474 (GRCm39) missense probably damaging 0.99
R0095:Zfp345 UTSW 2 150,314,220 (GRCm39) missense probably damaging 1.00
R0096:Zfp345 UTSW 2 150,314,220 (GRCm39) missense probably damaging 1.00
R0143:Zfp345 UTSW 2 150,314,475 (GRCm39) missense probably benign
R0371:Zfp345 UTSW 2 150,313,983 (GRCm39) missense possibly damaging 0.81
R0412:Zfp345 UTSW 2 150,315,323 (GRCm39) missense probably benign 0.00
R0415:Zfp345 UTSW 2 150,316,479 (GRCm39) splice site probably benign
R0420:Zfp345 UTSW 2 150,315,163 (GRCm39) missense possibly damaging 0.74
R0697:Zfp345 UTSW 2 150,314,829 (GRCm39) missense probably benign 0.13
R0799:Zfp345 UTSW 2 150,314,271 (GRCm39) missense probably benign 0.27
R1881:Zfp345 UTSW 2 150,314,275 (GRCm39) missense probably damaging 1.00
R1954:Zfp345 UTSW 2 150,316,741 (GRCm39) missense probably damaging 1.00
R2004:Zfp345 UTSW 2 150,314,038 (GRCm39) missense possibly damaging 0.90
R2152:Zfp345 UTSW 2 150,314,578 (GRCm39) missense probably benign 0.00
R2153:Zfp345 UTSW 2 150,314,578 (GRCm39) missense probably benign 0.00
R3051:Zfp345 UTSW 2 150,316,772 (GRCm39) missense probably benign 0.07
R3880:Zfp345 UTSW 2 150,314,075 (GRCm39) missense possibly damaging 0.91
R3939:Zfp345 UTSW 2 150,314,473 (GRCm39) missense probably damaging 1.00
R4801:Zfp345 UTSW 2 150,315,228 (GRCm39) missense possibly damaging 0.91
R4802:Zfp345 UTSW 2 150,315,228 (GRCm39) missense possibly damaging 0.91
R4897:Zfp345 UTSW 2 150,314,608 (GRCm39) missense probably benign 0.05
R5606:Zfp345 UTSW 2 150,316,788 (GRCm39) nonsense probably null
R6009:Zfp345 UTSW 2 150,314,437 (GRCm39) missense probably damaging 1.00
R6194:Zfp345 UTSW 2 150,314,551 (GRCm39) missense probably damaging 1.00
R6782:Zfp345 UTSW 2 150,315,274 (GRCm39) missense probably damaging 0.97
R6932:Zfp345 UTSW 2 150,315,331 (GRCm39) missense probably damaging 0.99
R7356:Zfp345 UTSW 2 150,314,209 (GRCm39) missense probably damaging 1.00
R7980:Zfp345 UTSW 2 150,314,723 (GRCm39) nonsense probably null
R8387:Zfp345 UTSW 2 150,314,740 (GRCm39) missense probably damaging 0.96
R8515:Zfp345 UTSW 2 150,314,348 (GRCm39) missense probably benign 0.01
R8940:Zfp345 UTSW 2 150,314,277 (GRCm39) missense probably benign 0.40
R9038:Zfp345 UTSW 2 150,313,864 (GRCm39) missense probably benign 0.02
R9383:Zfp345 UTSW 2 150,314,503 (GRCm39) missense possibly damaging 0.89
R9480:Zfp345 UTSW 2 150,315,212 (GRCm39) nonsense probably null
R9723:Zfp345 UTSW 2 150,314,189 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- GGCTTTACCACACTGTATACATTC -3'
(R):5'- TGTGGTAAATCCTTTGCGAGAAA -3'

Sequencing Primer
(F):5'- CTGGGACTTGCAAAATCTTTACCAC -3'
(R):5'- CCTTTGCGAGAAAGAGTCATCTC -3'
Posted On 2018-02-27