Incidental Mutation 'R1884:Coro7'
ID 209392
Institutional Source Beutler Lab
Gene Symbol Coro7
Ensembl Gene ENSMUSG00000039637
Gene Name coronin 7
Synonyms 0610011B16Rik
MMRRC Submission 039905-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.089) question?
Stock # R1884 (G1)
Quality Score 223
Status Validated
Chromosome 16
Chromosomal Location 4444748-4497584 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to T at 4446683 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000119723 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000014445] [ENSMUST00000038552] [ENSMUST00000135823] [ENSMUST00000156889]
AlphaFold Q9D2V7
Predicted Effect probably benign
Transcript: ENSMUST00000014445
SMART Domains Protein: ENSMUSP00000014445
Gene: ENSMUSG00000014301

DomainStartEndE-ValueType
Pfam:Pam16 1 125 4.9e-63 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000038552
SMART Domains Protein: ENSMUSP00000048489
Gene: ENSMUSG00000039637

DomainStartEndE-ValueType
DUF1899 3 64 6.41e-15 SMART
WD40 66 106 1.83e-7 SMART
WD40 115 154 4.13e0 SMART
WD40 157 196 1.78e-5 SMART
DUF1900 251 385 4.49e-60 SMART
low complexity region 427 456 N/A INTRINSIC
DUF1899 463 528 1.2e-19 SMART
WD40 531 570 3.64e-2 SMART
WD40 580 620 8.55e-8 SMART
WD40 623 662 1.16e-9 SMART
low complexity region 667 679 N/A INTRINSIC
DUF1900 718 854 6.69e-68 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127120
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127125
Predicted Effect probably benign
Transcript: ENSMUST00000135823
SMART Domains Protein: ENSMUSP00000118310
Gene: ENSMUSG00000039637

DomainStartEndE-ValueType
DUF1899 3 64 6.41e-15 SMART
WD40 66 106 1.83e-7 SMART
WD40 115 154 4.13e0 SMART
WD40 157 196 1.78e-5 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139072
Predicted Effect noncoding transcript
Transcript: ENSMUST00000150724
Predicted Effect noncoding transcript
Transcript: ENSMUST00000150028
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143723
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151156
Predicted Effect probably benign
Transcript: ENSMUST00000156889
Predicted Effect noncoding transcript
Transcript: ENSMUST00000229767
Coding Region Coverage
  • 1x: 97.3%
  • 3x: 96.7%
  • 10x: 95.1%
  • 20x: 92.3%
Validation Efficiency 99% (94/95)
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele are viable and overtly normal but exhibit disruption of the Golgi apparatus. Mutant fibroblasts show increased cell spreading and cellular F-actin content, increased cell polarization and migration, and enhanced wound healing in a scratch-wound assay. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acad11 T C 9: 103,991,684 (GRCm39) M573T probably benign Het
Ank3 A G 10: 69,851,422 (GRCm39) T1162A possibly damaging Het
Anxa2 TCCC TCC 9: 69,397,036 (GRCm39) probably null Het
Arpp21 T A 9: 111,972,595 (GRCm39) D232V probably damaging Het
Atg2a T C 19: 6,304,414 (GRCm39) Y1144H probably damaging Het
Auh G A 13: 52,989,532 (GRCm39) P308L probably benign Het
Brs3 T C X: 56,092,449 (GRCm39) I311T probably benign Het
Cenpf C T 1: 189,379,046 (GRCm39) V2915I probably benign Het
Cep170 G T 1: 176,602,245 (GRCm39) T287K probably benign Het
Chst2 G A 9: 95,287,611 (GRCm39) T245I probably damaging Het
Cnot4 C T 6: 35,055,092 (GRCm39) V66I probably damaging Het
Cntn4 A G 6: 106,656,353 (GRCm39) T885A probably benign Het
Col20a1 C T 2: 180,634,703 (GRCm39) T131I possibly damaging Het
Cpne8 C A 15: 90,532,831 (GRCm39) probably benign Het
Dbnl G A 11: 5,749,247 (GRCm39) G356E probably benign Het
Ddx31 T A 2: 28,749,002 (GRCm39) I266N probably damaging Het
Dnah7a A T 1: 53,580,159 (GRCm39) I1592N probably damaging Het
Dok6 A T 18: 89,492,130 (GRCm39) L149Q probably damaging Het
Eri2 G A 7: 119,390,346 (GRCm39) T94I probably benign Het
Ermp1 A G 19: 29,594,079 (GRCm39) V697A probably benign Het
Foxc1 C T 13: 31,991,648 (GRCm39) T153M probably damaging Het
Fry A G 5: 150,326,985 (GRCm39) I1224V probably benign Het
Fzd5 G A 1: 64,774,813 (GRCm39) T316M probably damaging Het
Gcm1 G T 9: 77,966,861 (GRCm39) V27L probably benign Het
Gm5773 A T 3: 93,681,348 (GRCm39) D340V probably benign Het
Gucy2d T A 7: 98,100,815 (GRCm39) H379Q probably benign Het
Hectd1 T A 12: 51,847,738 (GRCm39) M392L probably benign Het
Itpr2 A C 6: 146,287,469 (GRCm39) D452E probably benign Het
Krtap2-4 G C 11: 99,505,505 (GRCm39) probably benign Het
Lrit1 T C 14: 36,783,710 (GRCm39) V346A possibly damaging Het
Lrrk1 A G 7: 65,912,185 (GRCm39) S1792P probably benign Het
Marveld2 A T 13: 100,737,129 (GRCm39) V168E probably benign Het
Ms4a4b T A 19: 11,438,629 (GRCm39) D149E probably damaging Het
Myom2 G A 8: 15,164,278 (GRCm39) D1058N probably benign Het
Ncam2 C T 16: 81,234,571 (GRCm39) P142L probably damaging Het
Nek9 A G 12: 85,379,330 (GRCm39) L192P probably damaging Het
Nol10 T C 12: 17,418,390 (GRCm39) probably null Het
Nrcam T C 12: 44,591,538 (GRCm39) V194A probably damaging Het
Nudt6 A G 3: 37,466,549 (GRCm39) V82A probably benign Het
Odf2l A T 3: 144,856,809 (GRCm39) N492I probably damaging Het
Or2a12 T C 6: 42,904,764 (GRCm39) S200P probably damaging Het
Or51f1d T C 7: 102,701,189 (GRCm39) I228T probably benign Het
Pkn3 T C 2: 29,972,840 (GRCm39) V276A probably damaging Het
Prl3b1 T G 13: 27,431,886 (GRCm39) L137R possibly damaging Het
Rab11fip2 A G 19: 59,925,762 (GRCm39) F10L probably damaging Het
Rab3b T A 4: 108,786,649 (GRCm39) V133E probably damaging Het
Rnf111 A T 9: 70,383,520 (GRCm39) S138T probably damaging Het
Rsf1 G A 7: 97,229,117 (GRCm39) probably benign Het
Runx1t1 A G 4: 13,835,767 (GRCm39) T75A probably benign Het
Ryr2 T G 13: 11,753,242 (GRCm39) K1693T probably damaging Het
Sdha A T 13: 74,481,255 (GRCm39) I317N probably damaging Het
Serpina1d T A 12: 103,732,037 (GRCm39) D274V possibly damaging Het
Setd2 T G 9: 110,385,486 (GRCm39) probably null Het
Sh3tc2 A G 18: 62,141,646 (GRCm39) Y1109C probably damaging Het
Sik3 C G 9: 46,132,387 (GRCm39) H1276Q probably benign Het
Slc22a2 A G 17: 12,833,713 (GRCm39) probably benign Het
Slc35f4 A T 14: 49,551,091 (GRCm39) W108R probably damaging Het
Slc4a1ap A G 5: 31,691,524 (GRCm39) E440G probably damaging Het
Slc6a4 A G 11: 76,904,201 (GRCm39) T219A probably benign Het
Stxbp5 C A 10: 9,688,042 (GRCm39) V420F possibly damaging Het
Svil T G 18: 5,094,640 (GRCm39) V1440G possibly damaging Het
Tas2r126 A T 6: 42,411,961 (GRCm39) T165S probably benign Het
Tbck T C 3: 132,430,677 (GRCm39) probably null Het
Tnxb T A 17: 34,908,539 (GRCm39) D1520E probably benign Het
Top1mt C T 15: 75,539,750 (GRCm39) R287H possibly damaging Het
Trdn A G 10: 33,133,091 (GRCm39) K314E probably benign Het
Troap T A 15: 98,975,779 (GRCm39) C233S probably benign Het
Usp28 T C 9: 48,947,247 (GRCm39) M571T probably damaging Het
Vac14 A G 8: 111,438,319 (GRCm39) H644R probably damaging Het
Vipr1 C T 9: 121,494,930 (GRCm39) P327L possibly damaging Het
Vmn1r31 C T 6: 58,449,029 (GRCm39) V279I probably damaging Het
Vmn1r69 G A 7: 10,314,678 (GRCm39) R18W probably benign Het
Vmn2r18 G T 5: 151,499,190 (GRCm39) Q425K probably benign Het
Vmn2r60 T C 7: 41,786,094 (GRCm39) V299A probably damaging Het
Vps13b A T 15: 35,430,437 (GRCm39) probably benign Het
Zfp157 A G 5: 138,443,102 (GRCm39) D31G probably damaging Het
Zfp385c A C 11: 100,521,532 (GRCm39) V176G probably benign Het
Zfp831 A G 2: 174,545,870 (GRCm39) H1325R possibly damaging Het
Other mutations in Coro7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00428:Coro7 APN 16 4,452,500 (GRCm39) missense possibly damaging 0.83
IGL00885:Coro7 APN 16 4,452,890 (GRCm39) missense probably benign 0.00
IGL02944:Coro7 APN 16 4,453,276 (GRCm39) missense probably benign 0.14
IGL03104:Coro7 APN 16 4,446,990 (GRCm39) missense probably damaging 1.00
IGL03153:Coro7 APN 16 4,453,246 (GRCm39) critical splice donor site probably null
R0022:Coro7 UTSW 16 4,451,168 (GRCm39) missense probably benign 0.01
R0022:Coro7 UTSW 16 4,451,168 (GRCm39) missense probably benign 0.01
R0071:Coro7 UTSW 16 4,488,391 (GRCm39) missense probably damaging 1.00
R0071:Coro7 UTSW 16 4,488,391 (GRCm39) missense probably damaging 1.00
R0080:Coro7 UTSW 16 4,448,328 (GRCm39) missense probably damaging 1.00
R0193:Coro7 UTSW 16 4,445,368 (GRCm39) unclassified probably benign
R0242:Coro7 UTSW 16 4,448,042 (GRCm39) splice site probably benign
R0318:Coro7 UTSW 16 4,493,671 (GRCm39) missense probably benign 0.09
R0554:Coro7 UTSW 16 4,450,121 (GRCm39) missense possibly damaging 0.63
R0666:Coro7 UTSW 16 4,449,775 (GRCm39) missense possibly damaging 0.70
R0835:Coro7 UTSW 16 4,450,118 (GRCm39) missense probably benign 0.12
R0968:Coro7 UTSW 16 4,487,919 (GRCm39) splice site probably benign
R1670:Coro7 UTSW 16 4,446,097 (GRCm39) missense possibly damaging 0.76
R1709:Coro7 UTSW 16 4,452,305 (GRCm39) splice site probably null
R1848:Coro7 UTSW 16 4,448,298 (GRCm39) missense probably damaging 0.99
R1935:Coro7 UTSW 16 4,446,596 (GRCm39) missense probably benign
R1937:Coro7 UTSW 16 4,446,596 (GRCm39) missense probably benign
R1939:Coro7 UTSW 16 4,446,596 (GRCm39) missense probably benign
R1967:Coro7 UTSW 16 4,452,753 (GRCm39) missense probably damaging 1.00
R1969:Coro7 UTSW 16 4,451,620 (GRCm39) missense probably benign 0.19
R1970:Coro7 UTSW 16 4,451,620 (GRCm39) missense probably benign 0.19
R3034:Coro7 UTSW 16 4,450,155 (GRCm39) missense probably damaging 0.99
R4638:Coro7 UTSW 16 4,450,151 (GRCm39) missense probably damaging 0.96
R4710:Coro7 UTSW 16 4,452,797 (GRCm39) intron probably benign
R4723:Coro7 UTSW 16 4,449,858 (GRCm39) missense probably benign 0.00
R4789:Coro7 UTSW 16 4,446,085 (GRCm39) missense probably damaging 1.00
R5493:Coro7 UTSW 16 4,450,351 (GRCm39) missense probably damaging 0.99
R5619:Coro7 UTSW 16 4,494,799 (GRCm39) critical splice donor site probably null
R5756:Coro7 UTSW 16 4,450,148 (GRCm39) missense probably damaging 0.97
R5974:Coro7 UTSW 16 4,449,753 (GRCm39) missense possibly damaging 0.83
R6010:Coro7 UTSW 16 4,487,820 (GRCm39) missense possibly damaging 0.68
R6038:Coro7 UTSW 16 4,497,414 (GRCm39) critical splice donor site probably null
R6038:Coro7 UTSW 16 4,497,414 (GRCm39) critical splice donor site probably null
R6906:Coro7 UTSW 16 4,451,168 (GRCm39) missense probably benign 0.00
R6925:Coro7 UTSW 16 4,446,538 (GRCm39) critical splice donor site probably null
R7069:Coro7 UTSW 16 4,497,475 (GRCm39) start codon destroyed probably damaging 0.99
R7326:Coro7 UTSW 16 4,449,912 (GRCm39) missense probably damaging 0.96
R7421:Coro7 UTSW 16 4,486,615 (GRCm39) missense probably benign 0.19
R7521:Coro7 UTSW 16 4,449,346 (GRCm39) missense probably benign 0.00
R7773:Coro7 UTSW 16 4,449,870 (GRCm39) missense probably damaging 1.00
R7846:Coro7 UTSW 16 4,488,400 (GRCm39) missense probably damaging 1.00
R8240:Coro7 UTSW 16 4,486,660 (GRCm39) missense probably damaging 0.96
R8726:Coro7 UTSW 16 4,486,619 (GRCm39) missense possibly damaging 0.95
R8762:Coro7 UTSW 16 4,452,203 (GRCm39) missense probably benign
R9383:Coro7 UTSW 16 4,452,888 (GRCm39) missense probably damaging 1.00
R9451:Coro7 UTSW 16 4,488,402 (GRCm39) missense probably damaging 1.00
R9553:Coro7 UTSW 16 4,486,624 (GRCm39) missense possibly damaging 0.55
Predicted Primers PCR Primer
(F):5'- ACGAAGGACTGTACTTGGGC -3'
(R):5'- ACCTGTTCTTGCACCCAAAC -3'

Sequencing Primer
(F):5'- GACTGTACTTGGGCCTCCTG -3'
(R):5'- AAACCTCCCAGCTGTCTACTTTGG -3'
Posted On 2014-06-30