Incidental Mutation 'R7778:Zfp936'
ID 598995
Institutional Source Beutler Lab
Gene Symbol Zfp936
Ensembl Gene ENSMUSG00000064194
Gene Name zinc finger protein 936
Synonyms EG435970, Gm9272, I1C0022H11Rik
MMRRC Submission 045834-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.686) question?
Stock # R7778 (G1)
Quality Score 147.008
Status Validated
Chromosome 7
Chromosomal Location 42763653-42841533 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 42839720 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 396 (T396A)
Ref Sequence ENSEMBL: ENSMUSP00000143800 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072829] [ENSMUST00000200973] [ENSMUST00000202535] [ENSMUST00000205912]
AlphaFold Q3ULA8
Predicted Effect possibly damaging
Transcript: ENSMUST00000072829
AA Change: T395A

PolyPhen 2 Score 0.704 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000072608
Gene: ENSMUSG00000064194
AA Change: T395A

DomainStartEndE-ValueType
KRAB 3 65 5.32e-19 SMART
ZnF_C2H2 148 170 5.9e-3 SMART
ZnF_C2H2 176 198 5.9e-3 SMART
ZnF_C2H2 204 226 1.4e-4 SMART
ZnF_C2H2 232 254 1.2e-3 SMART
ZnF_C2H2 260 282 7.37e-4 SMART
ZnF_C2H2 288 310 2.27e-4 SMART
ZnF_C2H2 316 338 2.09e-3 SMART
ZnF_C2H2 344 366 1.45e-2 SMART
ZnF_C2H2 372 394 1.82e-3 SMART
ZnF_C2H2 400 422 2.53e-2 SMART
ZnF_C2H2 428 450 4.54e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000200973
SMART Domains Protein: ENSMUSP00000144191
Gene: ENSMUSG00000064194

DomainStartEndE-ValueType
KRAB 4 66 1.4e-21 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000202535
AA Change: T396A

PolyPhen 2 Score 0.704 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000143800
Gene: ENSMUSG00000064194
AA Change: T396A

DomainStartEndE-ValueType
KRAB 4 66 2.3e-21 SMART
ZnF_C2H2 149 171 2.6e-5 SMART
ZnF_C2H2 177 199 2.5e-5 SMART
ZnF_C2H2 205 227 5.9e-7 SMART
ZnF_C2H2 233 255 5.1e-6 SMART
ZnF_C2H2 261 283 3.1e-6 SMART
ZnF_C2H2 289 311 9.4e-7 SMART
ZnF_C2H2 317 339 8.7e-6 SMART
ZnF_C2H2 345 367 6.3e-5 SMART
ZnF_C2H2 373 395 7.7e-6 SMART
ZnF_C2H2 401 423 1.1e-4 SMART
ZnF_C2H2 429 451 2e-6 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000205912
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 100% (60/60)
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932414N04Rik T C 2: 68,569,855 (GRCm39) S524P possibly damaging Het
Aplf A C 6: 87,635,184 (GRCm39) probably null Het
Asb5 A C 8: 55,037,827 (GRCm39) H173P Het
Atp6v0a2 A G 5: 124,779,443 (GRCm39) E186G probably damaging Het
Bbs2 A T 8: 94,816,388 (GRCm39) probably null Het
Chrm5 A G 2: 112,310,301 (GRCm39) S272P probably benign Het
Chrna6 T C 8: 27,897,392 (GRCm39) I162V probably damaging Het
Cldn6 T A 17: 23,900,581 (GRCm39) C182S probably damaging Het
Cysltr2 A G 14: 73,267,203 (GRCm39) I169T probably benign Het
Ddx11 T C 17: 66,437,543 (GRCm39) probably null Het
Efhc1 A T 1: 21,049,685 (GRCm39) Y515F probably damaging Het
Elmo1 A G 13: 20,773,812 (GRCm39) probably null Het
Ep300 T C 15: 81,470,887 (GRCm39) S20P unknown Het
Gfpt2 T G 11: 49,715,268 (GRCm39) I421R probably damaging Het
Gm14226 T A 2: 154,866,630 (GRCm39) C196S possibly damaging Het
Grm8 T C 6: 27,363,671 (GRCm39) R615G possibly damaging Het
Hic1 C T 11: 75,057,042 (GRCm39) V616M possibly damaging Het
Ing1 A G 8: 11,611,814 (GRCm39) E178G probably benign Het
Kansl3 A T 1: 36,387,758 (GRCm39) L530H probably damaging Het
Kcna5 A T 6: 126,511,768 (GRCm39) L120* probably null Het
Kcnt1 T G 2: 25,791,901 (GRCm39) I617S probably benign Het
Lama1 T A 17: 68,111,468 (GRCm39) S2240T Het
Lcn2 T C 2: 32,277,927 (GRCm39) D55G probably benign Het
Ldlrad4 G T 18: 68,368,740 (GRCm39) A66S possibly damaging Het
Matn2 A T 15: 34,399,223 (GRCm39) H370L possibly damaging Het
Mettl23 T G 11: 116,740,096 (GRCm39) V189G probably benign Het
Mpp4 G A 1: 59,162,672 (GRCm39) T543M not run Het
Odf4 A T 11: 68,812,898 (GRCm39) S253R probably benign Het
Or10d4 C A 9: 39,580,534 (GRCm39) F60L possibly damaging Het
Or11h23 G T 14: 50,947,928 (GRCm39) C47F possibly damaging Het
Or7d9 A G 9: 20,193,708 (GRCm39) probably benign Het
Or8b36 T A 9: 37,937,963 (GRCm39) I287N probably damaging Het
Or8g21 T A 9: 38,906,203 (GRCm39) H176L probably damaging Het
Pcdha11 A T 18: 37,145,733 (GRCm39) Y608F possibly damaging Het
Pcdhga5 A G 18: 37,828,578 (GRCm39) D342G probably damaging Het
Pde6d A G 1: 86,471,250 (GRCm39) S143P probably damaging Het
Plec A T 15: 76,061,135 (GRCm39) I2934N probably damaging Het
Primpol G T 8: 47,039,459 (GRCm39) P387Q probably damaging Het
Prkcd C T 14: 30,327,772 (GRCm39) probably null Het
Prph2 T C 17: 47,221,732 (GRCm39) L37S possibly damaging Het
Prrt4 A G 6: 29,177,718 (GRCm39) L17P probably damaging Het
Pycr3 T C 15: 75,790,138 (GRCm39) D171G probably damaging Het
Rapsn A G 2: 90,875,293 (GRCm39) T359A probably benign Het
Setd6 A T 8: 96,442,866 (GRCm39) H101L probably benign Het
Sez6 T C 11: 77,865,375 (GRCm39) S671P probably damaging Het
Son T C 16: 91,453,416 (GRCm39) L721S probably damaging Het
Spata31d1b A T 13: 59,865,047 (GRCm39) R732W possibly damaging Het
Srd5a3 T A 5: 76,302,618 (GRCm39) F328I probably damaging Het
Tfap2b G A 1: 19,304,531 (GRCm39) G447D probably damaging Het
Thoc3 A C 13: 54,611,591 (GRCm39) F232C probably damaging Het
Tmem69 A G 4: 116,410,595 (GRCm39) L125P probably damaging Het
Tnfsf13 C T 11: 69,575,989 (GRCm39) V33M probably damaging Het
Togaram2 T A 17: 72,011,746 (GRCm39) M476K probably benign Het
Tube1 A G 10: 39,018,294 (GRCm39) I124V probably benign Het
Uevld A T 7: 46,576,100 (GRCm39) I462N probably damaging Het
Utrn G A 10: 12,362,354 (GRCm39) R2660C probably damaging Het
Vcan T C 13: 89,836,773 (GRCm39) T2924A probably damaging Het
Vmn2r120 T C 17: 57,832,942 (GRCm39) Y79C probably damaging Het
Vwa8 T C 14: 79,275,587 (GRCm39) V790A probably benign Het
Zfp874b A G 13: 67,622,093 (GRCm39) F402L probably benign Het
Zfp978 T C 4: 147,469,760 (GRCm39) probably null Het
Other mutations in Zfp936
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02231:Zfp936 APN 7 42,836,909 (GRCm39) splice site probably null
IGL02245:Zfp936 APN 7 42,836,722 (GRCm39) critical splice donor site probably null
IGL02335:Zfp936 APN 7 42,836,691 (GRCm39) missense probably damaging 1.00
FR4340:Zfp936 UTSW 7 42,838,913 (GRCm39) missense possibly damaging 0.63
R0437:Zfp936 UTSW 7 42,838,734 (GRCm39) missense probably benign 0.00
R3899:Zfp936 UTSW 7 42,839,158 (GRCm39) missense possibly damaging 0.93
R4120:Zfp936 UTSW 7 42,839,630 (GRCm39) missense probably benign 0.10
R4406:Zfp936 UTSW 7 42,839,748 (GRCm39) missense possibly damaging 0.82
R4959:Zfp936 UTSW 7 42,839,034 (GRCm39) missense probably damaging 1.00
R5023:Zfp936 UTSW 7 42,836,681 (GRCm39) missense probably damaging 1.00
R5163:Zfp936 UTSW 7 42,839,664 (GRCm39) missense probably damaging 1.00
R5182:Zfp936 UTSW 7 42,839,331 (GRCm39) missense probably damaging 1.00
R5292:Zfp936 UTSW 7 42,838,759 (GRCm39) nonsense probably null
R5668:Zfp936 UTSW 7 42,839,858 (GRCm39) missense possibly damaging 0.93
R6057:Zfp936 UTSW 7 42,839,787 (GRCm39) missense probably benign 0.00
R6901:Zfp936 UTSW 7 42,839,467 (GRCm39) missense probably damaging 1.00
R7139:Zfp936 UTSW 7 42,839,715 (GRCm39) missense possibly damaging 0.54
R7258:Zfp936 UTSW 7 42,839,803 (GRCm39) missense probably damaging 1.00
R7440:Zfp936 UTSW 7 42,836,685 (GRCm39) missense probably damaging 1.00
R7537:Zfp936 UTSW 7 42,839,239 (GRCm39) nonsense probably null
R7561:Zfp936 UTSW 7 42,839,339 (GRCm39) missense probably damaging 0.98
R7662:Zfp936 UTSW 7 42,839,336 (GRCm39) nonsense probably null
R7775:Zfp936 UTSW 7 42,839,720 (GRCm39) missense possibly damaging 0.70
R8016:Zfp936 UTSW 7 42,838,848 (GRCm39) missense possibly damaging 0.61
R8121:Zfp936 UTSW 7 42,839,547 (GRCm39) missense possibly damaging 0.55
R9012:Zfp936 UTSW 7 42,839,416 (GRCm39) nonsense probably null
R9058:Zfp936 UTSW 7 42,839,196 (GRCm39) missense probably benign 0.32
R9188:Zfp936 UTSW 7 42,839,768 (GRCm39) missense probably benign 0.00
R9236:Zfp936 UTSW 7 42,836,922 (GRCm39) missense probably benign 0.00
R9596:Zfp936 UTSW 7 42,839,834 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CACACCAGAGTAATCTCCGAATA -3'
(R):5'- GACTCCAGTGTGAATAGGCTTCA -3'

Sequencing Primer
(F):5'- GTGTGATAAAGCCTTTGCACACC -3'
(R):5'- GTGAATAGGCTTCATCACATTGG -3'
Posted On 2019-11-26