Incidental Mutation 'R5659:Zfp637'
ID 443970
Institutional Source Beutler Lab
Gene Symbol Zfp637
Ensembl Gene ENSMUSG00000059689
Gene Name zinc finger protein 637
Synonyms
MMRRC Submission 043303-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.243) question?
Stock # R5659 (G1)
Quality Score 225
Status Not validated
Chromosome 6
Chromosomal Location 117818165-117822917 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 117820291 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Glutamic Acid at position 3 (G3E)
Ref Sequence ENSEMBL: ENSMUSP00000152569 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000112858] [ENSMUST00000112859] [ENSMUST00000112860] [ENSMUST00000112861] [ENSMUST00000134526] [ENSMUST00000136889] [ENSMUST00000137224] [ENSMUST00000164472] [ENSMUST00000223041]
AlphaFold Q80V23
Predicted Effect unknown
Transcript: ENSMUST00000112858
AA Change: G3E
Predicted Effect unknown
Transcript: ENSMUST00000112859
AA Change: G3E
Predicted Effect probably damaging
Transcript: ENSMUST00000112860
AA Change: G3E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000108481
Gene: ENSMUSG00000059689
AA Change: G3E

DomainStartEndE-ValueType
ZnF_C2H2 90 112 3.69e-4 SMART
ZnF_C2H2 118 140 1.84e-4 SMART
ZnF_C2H2 146 168 9.22e-5 SMART
ZnF_C2H2 174 196 8.47e-4 SMART
ZnF_C2H2 202 224 2.84e-5 SMART
ZnF_C2H2 230 252 5.34e0 SMART
ZnF_C2H2 258 278 1.08e1 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000112861
AA Change: G3E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000108482
Gene: ENSMUSG00000059689
AA Change: G3E

DomainStartEndE-ValueType
ZnF_C2H2 76 98 3.69e-4 SMART
ZnF_C2H2 104 126 1.84e-4 SMART
ZnF_C2H2 132 154 9.22e-5 SMART
ZnF_C2H2 160 182 8.47e-4 SMART
ZnF_C2H2 188 210 2.84e-5 SMART
ZnF_C2H2 216 238 5.34e0 SMART
ZnF_C2H2 244 264 1.08e1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127593
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132644
Predicted Effect probably damaging
Transcript: ENSMUST00000134526
AA Change: G3E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000115733
Gene: ENSMUSG00000059689
AA Change: G3E

DomainStartEndE-ValueType
ZnF_C2H2 76 98 3.69e-4 SMART
ZnF_C2H2 104 126 1.84e-4 SMART
ZnF_C2H2 132 152 2.45e0 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000136889
AA Change: G3E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000123106
Gene: ENSMUSG00000059689
AA Change: G3E

DomainStartEndE-ValueType
ZnF_C2H2 76 98 3.69e-4 SMART
ZnF_C2H2 104 126 1.84e-4 SMART
ZnF_C2H2 132 152 2.45e0 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000137224
AA Change: G3E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000120884
Gene: ENSMUSG00000059689
AA Change: G3E

DomainStartEndE-ValueType
ZnF_C2H2 90 112 3.69e-4 SMART
ZnF_C2H2 118 140 1.84e-4 SMART
ZnF_C2H2 146 168 9.22e-5 SMART
ZnF_C2H2 174 196 8.47e-4 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000164472
AA Change: G3E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000130144
Gene: ENSMUSG00000059689
AA Change: G3E

DomainStartEndE-ValueType
ZnF_C2H2 76 98 3.69e-4 SMART
ZnF_C2H2 104 126 1.84e-4 SMART
ZnF_C2H2 132 154 9.22e-5 SMART
ZnF_C2H2 160 182 8.47e-4 SMART
ZnF_C2H2 188 210 2.84e-5 SMART
ZnF_C2H2 216 238 5.34e0 SMART
ZnF_C2H2 244 264 1.08e1 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000223041
AA Change: G3E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 95.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ankhd1 T C 18: 36,694,103 (GRCm39) S105P probably damaging Het
Ano5 G A 7: 51,233,562 (GRCm39) R658H possibly damaging Het
Ap3b2 T A 7: 81,126,500 (GRCm39) I367F probably damaging Het
Apaf1 A T 10: 90,898,015 (GRCm39) C247* probably null Het
Aqp8 G A 7: 123,065,889 (GRCm39) W228* probably null Het
Arhgap32 T A 9: 32,093,256 (GRCm39) V178D probably damaging Het
Atp10b T A 11: 43,136,252 (GRCm39) W1127R probably damaging Het
Bcl6 A T 16: 23,787,159 (GRCm39) C580* probably null Het
Brd1 T C 15: 88,597,584 (GRCm39) T568A probably benign Het
Brsk1 C T 7: 4,718,371 (GRCm39) P665L possibly damaging Het
Cblc A G 7: 19,526,857 (GRCm39) L125P probably damaging Het
Ccdc87 T C 19: 4,890,878 (GRCm39) S457P probably damaging Het
Cxcr5 C T 9: 44,424,690 (GRCm39) M322I probably benign Het
Cyb5r4 T A 9: 86,937,881 (GRCm39) F300Y probably benign Het
Cyp3a25 T C 5: 145,928,356 (GRCm39) T230A possibly damaging Het
Dhx9 A G 1: 153,347,481 (GRCm39) V409A probably damaging Het
Dnah7b A G 1: 46,392,009 (GRCm39) D3790G probably damaging Het
Gin1 A G 1: 97,703,257 (GRCm39) T27A possibly damaging Het
Gipc1 A T 8: 84,390,755 (GRCm39) M287L probably benign Het
Kat6a T A 8: 23,428,176 (GRCm39) L1177* probably null Het
Klhl20 A G 1: 160,918,040 (GRCm39) V82A probably damaging Het
Kmt2e T C 5: 23,702,805 (GRCm39) I995T probably damaging Het
Lpin1 A T 12: 16,590,990 (GRCm39) V814E probably damaging Het
Luzp1 T A 4: 136,269,787 (GRCm39) V670D probably damaging Het
Lyst C A 13: 13,809,212 (GRCm39) A294E possibly damaging Het
Olr1 T A 6: 129,476,992 (GRCm39) E91V probably damaging Het
Or1j1 A T 2: 36,702,966 (GRCm39) I46N probably damaging Het
Or2k2 A T 4: 58,785,672 (GRCm39) F17I probably damaging Het
Or8b55 C T 9: 38,727,072 (GRCm39) T91I probably benign Het
Pam T C 1: 97,770,024 (GRCm39) Y476C probably damaging Het
Pcdhac1 T C 18: 37,225,470 (GRCm39) L761P probably damaging Het
Phf21b C T 15: 84,678,101 (GRCm39) W300* probably null Het
Pld2 T C 11: 70,448,387 (GRCm39) *945Q probably null Het
Ppp1r37 C T 7: 19,269,448 (GRCm39) V145M probably damaging Het
Rasgrf1 T A 9: 89,866,342 (GRCm39) N593K probably damaging Het
Rhot1 T G 11: 80,141,181 (GRCm39) probably null Het
Rmnd1 A T 10: 4,377,382 (GRCm39) M99K probably benign Het
Ros1 G A 10: 52,019,482 (GRCm39) T697I possibly damaging Het
Scgb1b10 G T 7: 31,800,303 (GRCm39) A4S probably benign Het
Shc3 T C 13: 51,670,630 (GRCm39) Y39C probably damaging Het
Slc25a23 A G 17: 57,352,500 (GRCm39) probably benign Het
Slc5a8 C T 10: 88,755,290 (GRCm39) L466F possibly damaging Het
Sqor G A 2: 122,629,523 (GRCm39) C127Y probably benign Het
Sv2a G C 3: 96,097,619 (GRCm39) W467S possibly damaging Het
Togaram2 G T 17: 71,994,667 (GRCm39) D39Y probably damaging Het
Tspan11 T A 6: 127,915,240 (GRCm39) probably null Het
Usp32 A G 11: 84,968,240 (GRCm39) V141A possibly damaging Het
Zbtb38 T C 9: 96,569,473 (GRCm39) H537R probably damaging Het
Zfat T C 15: 67,990,862 (GRCm39) Y1008C probably damaging Het
Zfp788 T A 7: 41,299,540 (GRCm39) Y673* probably null Het
Zhx2 T C 15: 57,685,704 (GRCm39) S358P probably benign Het
Other mutations in Zfp637
AlleleSourceChrCoordTypePredicted EffectPPH Score
curds UTSW 6 117,822,285 (GRCm39) missense probably damaging 1.00
R0009:Zfp637 UTSW 6 117,822,629 (GRCm39) missense probably damaging 0.97
R0594:Zfp637 UTSW 6 117,822,647 (GRCm39) nonsense probably null
R0827:Zfp637 UTSW 6 117,822,405 (GRCm39) missense possibly damaging 0.71
R1772:Zfp637 UTSW 6 117,822,373 (GRCm39) missense probably damaging 1.00
R1920:Zfp637 UTSW 6 117,822,681 (GRCm39) missense probably damaging 1.00
R5383:Zfp637 UTSW 6 117,820,270 (GRCm39) utr 5 prime probably benign
R5890:Zfp637 UTSW 6 117,822,047 (GRCm39) missense possibly damaging 0.92
R6375:Zfp637 UTSW 6 117,822,285 (GRCm39) missense probably damaging 1.00
R8169:Zfp637 UTSW 6 117,822,252 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTGCAGTGACATTACCTCAGAAAG -3'
(R):5'- CATTTCCAATCCCAGCTTGCAG -3'

Sequencing Primer
(F):5'- CAGTGACATTACCTCAGAAAGTCTGG -3'
(R):5'- AGGCTTTCCCTGCAACCTGTAG -3'
Posted On 2016-11-09