Incidental Mutation 'R5918:Zscan29'
ID 461448
Institutional Source Beutler Lab
Gene Symbol Zscan29
Ensembl Gene ENSMUSG00000050619
Gene Name zinc finger SCAN domains 29
Synonyms Zfp690
MMRRC Submission 044115-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.159) question?
Stock # R5918 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 120988754-121001606 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 120994518 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Asparagine at position 489 (T489N)
Ref Sequence ENSEMBL: ENSMUSP00000125987 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079024] [ENSMUST00000110661] [ENSMUST00000146243] [ENSMUST00000163766]
AlphaFold E9Q5B4
Predicted Effect possibly damaging
Transcript: ENSMUST00000079024
AA Change: T454N

PolyPhen 2 Score 0.770 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000078033
Gene: ENSMUSG00000050619
AA Change: T454N

DomainStartEndE-ValueType
SCAN 13 125 5.83e-70 SMART
Pfam:Myb_DNA-bind_4 238 323 3e-21 PFAM
Pfam:Myb_DNA-bind_4 399 484 4.1e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000110661
AA Change: T454N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000106289
Gene: ENSMUSG00000050619
AA Change: T454N

DomainStartEndE-ValueType
SCAN 13 125 5.83e-70 SMART
Pfam:Myb_DNA-bind_4 238 323 5.4e-21 PFAM
Pfam:Myb_DNA-bind_4 399 484 7.4e-22 PFAM
low complexity region 518 532 N/A INTRINSIC
ZnF_C2H2 665 687 2.99e-4 SMART
ZnF_C2H2 693 715 2.75e-3 SMART
ZnF_C2H2 721 743 8.02e-5 SMART
ZnF_C2H2 749 771 1.13e-4 SMART
ZnF_C2H2 777 799 1.18e-2 SMART
ZnF_C2H2 805 827 1.33e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000146243
SMART Domains Protein: ENSMUSP00000120997
Gene: ENSMUSG00000050619

DomainStartEndE-ValueType
SCAN 13 118 4.23e-58 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000156370
Predicted Effect probably damaging
Transcript: ENSMUST00000163766
AA Change: T489N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000125987
Gene: ENSMUSG00000050619
AA Change: T489N

DomainStartEndE-ValueType
SCAN 13 125 5.83e-70 SMART
Pfam:Myb_DNA-bind_4 238 323 5.9e-21 PFAM
Pfam:Myb_DNA-bind_4 434 519 1.3e-21 PFAM
low complexity region 553 567 N/A INTRINSIC
ZnF_C2H2 700 722 2.99e-4 SMART
ZnF_C2H2 728 750 2.75e-3 SMART
ZnF_C2H2 756 778 8.02e-5 SMART
ZnF_C2H2 784 806 1.13e-4 SMART
ZnF_C2H2 812 834 1.18e-2 SMART
ZnF_C2H2 840 862 1.33e-1 SMART
Meta Mutation Damage Score 0.1673 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.8%
  • 20x: 93.6%
Validation Efficiency 93% (66/71)
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afap1 A T 5: 36,131,869 (GRCm39) I399F possibly damaging Het
Aknad1 C T 3: 108,659,703 (GRCm39) P239L probably benign Het
Ankrd9 A G 12: 110,943,200 (GRCm39) V245A probably benign Het
Anxa1 T C 19: 20,355,857 (GRCm39) probably benign Het
Arhgef2 A G 3: 88,543,387 (GRCm39) K454R probably damaging Het
AU040320 A G 4: 126,708,064 (GRCm39) T227A probably benign Het
Bbs2 C T 8: 94,824,931 (GRCm39) R17H probably damaging Het
Bcl2l12 A G 7: 44,640,888 (GRCm39) probably benign Het
C1qtnf9 G T 14: 61,009,737 (GRCm39) probably benign Het
Ccdc38 C G 10: 93,406,748 (GRCm39) Y219* probably null Het
Ceacam3 G T 7: 16,893,670 (GRCm39) D394Y probably damaging Het
Crip1 A C 12: 113,117,287 (GRCm39) probably null Het
Dnah7b T C 1: 46,260,803 (GRCm39) V1987A probably benign Het
Dnah9 C A 11: 65,725,025 (GRCm39) C4376F probably damaging Het
Galnt9 T C 5: 110,763,332 (GRCm39) F446L probably damaging Het
Garin1a A G 6: 29,285,942 (GRCm39) R76G probably null Het
Gm14322 A G 2: 177,411,499 (GRCm39) D103G probably benign Het
Gpa33 T C 1: 165,958,107 (GRCm39) probably null Het
Lactb2 T A 1: 13,720,954 (GRCm39) I93F probably benign Het
Lifr A T 15: 7,188,897 (GRCm39) T93S probably benign Het
Lmbr1l A T 15: 98,810,308 (GRCm39) I101N probably damaging Het
Lrrc8c G A 5: 105,756,117 (GRCm39) V631M possibly damaging Het
Mctp2 A C 7: 71,878,288 (GRCm39) D263E probably damaging Het
Nbeal1 T A 1: 60,307,051 (GRCm39) I1627N possibly damaging Het
Neb T C 2: 52,087,906 (GRCm39) Y5188C probably damaging Het
Nf1 T C 11: 79,460,048 (GRCm39) probably benign Het
Nr6a1 T C 2: 38,629,103 (GRCm39) D250G probably damaging Het
Ola1 T C 2: 72,987,128 (GRCm39) E168G probably benign Het
Or1a1 T C 11: 74,086,944 (GRCm39) V205A probably damaging Het
Or2d2b T A 7: 106,705,828 (GRCm39) Q80L probably damaging Het
Or4k2 A G 14: 50,424,425 (GRCm39) I83T probably benign Het
Or7g22 T C 9: 19,048,684 (GRCm39) Y132H probably damaging Het
Or9i1b T A 19: 13,897,139 (GRCm39) F252I probably damaging Het
Pik3r6 C T 11: 68,416,497 (GRCm39) Q29* probably null Het
Ppargc1a C T 5: 51,620,579 (GRCm39) probably benign Het
Ppl C T 16: 4,922,765 (GRCm39) R242H probably benign Het
Ppp1r37 G T 7: 19,266,036 (GRCm39) Q577K probably benign Het
Prcd A G 11: 116,548,366 (GRCm39) E25G probably damaging Het
Prpsap2 C T 11: 61,627,870 (GRCm39) R202H probably damaging Het
Ptgs1 A C 2: 36,141,089 (GRCm39) E512A probably damaging Het
Radil T G 5: 142,473,357 (GRCm39) I535L probably benign Het
Rbl2 G T 8: 91,816,758 (GRCm39) V373F probably benign Het
Ryr1 T C 7: 28,708,577 (GRCm39) Y4802C probably benign Het
Sdc2 A G 15: 33,028,313 (GRCm39) T144A probably benign Het
Senp6 T C 9: 80,021,398 (GRCm39) probably null Het
Sipa1l3 T C 7: 29,096,631 (GRCm39) D531G probably damaging Het
Slc22a27 C A 19: 7,887,411 (GRCm39) C189F possibly damaging Het
Srcin1 T C 11: 97,424,323 (GRCm39) probably null Het
Svep1 C T 4: 58,069,345 (GRCm39) E2814K possibly damaging Het
Tjp3 T G 10: 81,113,746 (GRCm39) H504P probably benign Het
Tmprss4 T A 9: 45,086,414 (GRCm39) K378* probably null Het
Tns4 C T 11: 98,964,497 (GRCm39) probably null Het
Ttn T C 2: 76,580,298 (GRCm39) T15205A possibly damaging Het
Ush2a G T 1: 188,089,011 (GRCm39) G322V probably benign Het
Vac14 A T 8: 111,363,104 (GRCm39) probably null Het
Vmn1r175 T G 7: 23,508,372 (GRCm39) D85A probably damaging Het
Vmn2r93 T C 17: 18,546,030 (GRCm39) L634P probably damaging Het
Zeb2 A T 2: 45,001,271 (GRCm39) probably benign Het
Zfp616 T A 11: 73,974,086 (GRCm39) H118Q possibly damaging Het
Zfp945 T A 17: 23,069,955 (GRCm39) H648L probably damaging Het
Other mutations in Zscan29
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01935:Zscan29 APN 2 121,000,538 (GRCm39) missense probably damaging 1.00
IGL01938:Zscan29 APN 2 120,996,690 (GRCm39) missense probably benign 0.16
IGL02220:Zscan29 APN 2 120,997,170 (GRCm39) missense probably damaging 0.99
IGL02370:Zscan29 APN 2 120,994,314 (GRCm39) missense probably benign 0.00
IGL02585:Zscan29 APN 2 120,994,357 (GRCm39) nonsense probably null
R0284:Zscan29 UTSW 2 120,997,214 (GRCm39) unclassified probably benign
R0842:Zscan29 UTSW 2 120,991,960 (GRCm39) missense possibly damaging 0.84
R1245:Zscan29 UTSW 2 120,996,984 (GRCm39) missense probably damaging 1.00
R1586:Zscan29 UTSW 2 120,991,641 (GRCm39) missense probably damaging 1.00
R1654:Zscan29 UTSW 2 120,995,260 (GRCm39) missense probably benign 0.06
R1958:Zscan29 UTSW 2 121,000,289 (GRCm39) critical splice donor site probably null
R2073:Zscan29 UTSW 2 120,991,336 (GRCm39) nonsense probably null
R2085:Zscan29 UTSW 2 121,000,427 (GRCm39) nonsense probably null
R2145:Zscan29 UTSW 2 121,000,587 (GRCm39) missense probably damaging 1.00
R2201:Zscan29 UTSW 2 120,999,883 (GRCm39) missense probably damaging 1.00
R2875:Zscan29 UTSW 2 120,994,581 (GRCm39) missense probably damaging 1.00
R2876:Zscan29 UTSW 2 120,994,581 (GRCm39) missense probably damaging 1.00
R3861:Zscan29 UTSW 2 120,991,212 (GRCm39) missense probably benign 0.01
R4244:Zscan29 UTSW 2 120,995,275 (GRCm39) splice site probably null
R4245:Zscan29 UTSW 2 120,995,275 (GRCm39) splice site probably null
R4447:Zscan29 UTSW 2 121,000,367 (GRCm39) splice site probably null
R4662:Zscan29 UTSW 2 120,997,096 (GRCm39) missense probably benign 0.26
R4757:Zscan29 UTSW 2 120,991,392 (GRCm39) missense possibly damaging 0.92
R4777:Zscan29 UTSW 2 120,999,805 (GRCm39) missense probably damaging 0.96
R4905:Zscan29 UTSW 2 120,991,864 (GRCm39) missense possibly damaging 0.53
R4970:Zscan29 UTSW 2 120,999,676 (GRCm39) splice site probably null
R5860:Zscan29 UTSW 2 120,994,518 (GRCm39) missense probably damaging 1.00
R5861:Zscan29 UTSW 2 120,994,518 (GRCm39) missense probably damaging 1.00
R5862:Zscan29 UTSW 2 120,994,518 (GRCm39) missense probably damaging 1.00
R5916:Zscan29 UTSW 2 120,994,518 (GRCm39) missense probably damaging 1.00
R5917:Zscan29 UTSW 2 120,994,518 (GRCm39) missense probably damaging 1.00
R6335:Zscan29 UTSW 2 120,991,917 (GRCm39) missense possibly damaging 0.49
R7214:Zscan29 UTSW 2 120,999,761 (GRCm39) nonsense probably null
R7326:Zscan29 UTSW 2 120,991,469 (GRCm39) missense probably damaging 1.00
R7997:Zscan29 UTSW 2 120,991,221 (GRCm39) missense probably benign 0.01
R8787:Zscan29 UTSW 2 120,996,876 (GRCm39) missense probably damaging 1.00
RF001:Zscan29 UTSW 2 120,994,477 (GRCm39) missense possibly damaging 0.95
Predicted Primers PCR Primer
(F):5'- GGTTCTCTGGAGGCAACAAG -3'
(R):5'- TTTCCTAGAAGCCGGCAGTAAAAC -3'

Sequencing Primer
(F):5'- CTCTGGAGGCAACAAGAAACTGTTTC -3'
(R):5'- AGGTGATGCTGAAATCTCTCTTC -3'
Posted On 2017-02-28