Incidental Mutation 'R1615:Mtcl2'
ID 177033
Institutional Source Beutler Lab
Gene Symbol Mtcl2
Ensembl Gene ENSMUSG00000055485
Gene Name microtubule crosslinking factor 2
Synonyms 9830001H06Rik, D430036N24Rik, Soga1
MMRRC Submission 039652-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.388) question?
Stock # R1615 (G1)
Quality Score 224
Status Validated
Chromosome 2
Chromosomal Location 156857719-156921174 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 156862663 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Proline at position 1422 (H1422P)
Ref Sequence ENSEMBL: ENSMUSP00000066556 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000069098]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000069098
AA Change: H1422P

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000066556
Gene: ENSMUSG00000055485
AA Change: H1422P

DomainStartEndE-ValueType
low complexity region 15 23 N/A INTRINSIC
low complexity region 51 66 N/A INTRINSIC
low complexity region 97 112 N/A INTRINSIC
low complexity region 132 148 N/A INTRINSIC
low complexity region 155 174 N/A INTRINSIC
Blast:BRLZ 212 246 4e-8 BLAST
SCOP:d1fxkc_ 216 350 1e-3 SMART
Pfam:DUF3166 378 472 2.3e-31 PFAM
Pfam:DUF3166 504 593 5.3e-31 PFAM
low complexity region 637 649 N/A INTRINSIC
coiled coil region 807 867 N/A INTRINSIC
low complexity region 872 884 N/A INTRINSIC
low complexity region 938 950 N/A INTRINSIC
Pfam:DUF4482 1065 1205 3.9e-28 PFAM
low complexity region 1311 1321 N/A INTRINSIC
low complexity region 1363 1377 N/A INTRINSIC
low complexity region 1389 1418 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153229
Meta Mutation Damage Score 0.1160 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.0%
  • 10x: 95.3%
  • 20x: 88.8%
Validation Efficiency 98% (64/65)
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy8 A T 15: 64,743,625 (GRCm39) C328S probably benign Het
Adgrv1 G T 13: 81,572,407 (GRCm39) T4918K probably benign Het
Aen T C 7: 78,555,660 (GRCm39) Y108H probably damaging Het
Amer3 T C 1: 34,627,252 (GRCm39) M497T probably damaging Het
Arid2 C T 15: 96,269,535 (GRCm39) T1216M possibly damaging Het
Birc6 A G 17: 74,916,404 (GRCm39) probably null Het
Bzw2 A G 12: 36,169,126 (GRCm39) probably benign Het
Ccr1 T C 9: 123,763,573 (GRCm39) H319R probably benign Het
Dnah11 A G 12: 118,014,457 (GRCm39) I2010T probably damaging Het
Dnhd1 A G 7: 105,352,413 (GRCm39) Y2522C probably benign Het
Dnhd1 T A 7: 105,362,913 (GRCm39) I3825K possibly damaging Het
Dst A T 1: 34,238,452 (GRCm39) D3718V probably damaging Het
Esp36 A G 17: 38,730,330 (GRCm39) probably benign Het
Fbxw21 T C 9: 108,972,794 (GRCm39) Y380C probably damaging Het
Fhad1 G A 4: 141,649,634 (GRCm39) T836M probably damaging Het
Fhod1 C T 8: 106,074,463 (GRCm39) probably benign Het
Flt1 A G 5: 147,576,098 (GRCm39) C637R probably damaging Het
Fmnl2 A G 2: 53,008,436 (GRCm39) K809E probably damaging Het
Grm1 G T 10: 10,617,252 (GRCm39) Y510* probably null Het
Hey1 A T 3: 8,729,898 (GRCm39) H186Q possibly damaging Het
Insyn1 C T 9: 58,406,351 (GRCm39) A87V probably damaging Het
Itga2b C T 11: 102,350,963 (GRCm39) probably null Het
Kcnv1 G A 15: 44,977,840 (GRCm39) T66M probably damaging Het
Lmcd1 A G 6: 112,250,911 (GRCm39) D7G probably benign Het
Lrrc1 T C 9: 77,342,400 (GRCm39) D358G possibly damaging Het
Lyn A G 4: 3,748,765 (GRCm39) K248E probably benign Het
Map4k4 A G 1: 40,045,990 (GRCm39) probably benign Het
Map4k5 A T 12: 69,891,187 (GRCm39) L160H probably damaging Het
Myo6 C T 9: 80,215,007 (GRCm39) R1247C probably damaging Het
Myo9a A G 9: 59,695,739 (GRCm39) E347G possibly damaging Het
Ndfip1 C T 18: 38,593,672 (GRCm39) P213S probably benign Het
Neurl3 T C 1: 36,308,470 (GRCm39) E114G possibly damaging Het
Nlrp14 A T 7: 106,795,370 (GRCm39) I877F probably benign Het
Obscn A G 11: 58,990,651 (GRCm39) S1733P probably benign Het
Oxgr1 A T 14: 120,260,185 (GRCm39) S7R probably benign Het
Plcb1 A T 2: 135,204,364 (GRCm39) probably benign Het
Prkag2 G T 5: 25,080,176 (GRCm39) N120K possibly damaging Het
Rnf43 C T 11: 87,622,485 (GRCm39) R529* probably null Het
Saraf A G 8: 34,632,442 (GRCm39) K174E possibly damaging Het
Scrib T C 15: 75,938,054 (GRCm39) Q264R probably benign Het
Sh3rf3 T A 10: 58,966,899 (GRCm39) M747K probably benign Het
Shf T C 2: 122,179,913 (GRCm39) H421R probably damaging Het
Slc35g3 A G 11: 69,651,368 (GRCm39) S228P probably damaging Het
Slit1 A G 19: 41,639,110 (GRCm39) probably benign Het
Srrm4 A G 5: 116,585,359 (GRCm39) probably benign Het
Stfa1 T G 16: 36,100,829 (GRCm39) V23G probably damaging Het
Swap70 A G 7: 109,872,498 (GRCm39) D371G probably benign Het
Tada2a T C 11: 83,993,926 (GRCm39) D186G probably damaging Het
Tdpoz3 C A 3: 93,733,618 (GRCm39) Q98K probably benign Het
Tgfbrap1 A G 1: 43,091,145 (GRCm39) V660A probably benign Het
Tnn A G 1: 159,945,978 (GRCm39) Y947H possibly damaging Het
Trim60 A T 8: 65,453,162 (GRCm39) C362* probably null Het
Vmn1r81 T A 7: 11,994,441 (GRCm39) N56Y probably damaging Het
Vsig8 A G 1: 172,387,280 (GRCm39) D52G probably damaging Het
Wdfy4 G A 14: 32,764,469 (GRCm39) R2140C probably damaging Het
Other mutations in Mtcl2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00429:Mtcl2 APN 2 156,872,784 (GRCm39) missense probably damaging 1.00
IGL00924:Mtcl2 APN 2 156,882,625 (GRCm39) missense probably damaging 0.99
IGL01723:Mtcl2 APN 2 156,872,534 (GRCm39) missense probably benign 0.00
IGL01749:Mtcl2 APN 2 156,863,461 (GRCm39) splice site probably benign
IGL02199:Mtcl2 APN 2 156,872,865 (GRCm39) missense probably damaging 1.00
IGL02262:Mtcl2 APN 2 156,872,826 (GRCm39) missense probably damaging 1.00
IGL02618:Mtcl2 APN 2 156,882,486 (GRCm39) missense probably damaging 1.00
IGL02643:Mtcl2 APN 2 156,882,663 (GRCm39) missense probably damaging 1.00
deglutition UTSW 2 156,881,784 (GRCm39) missense possibly damaging 0.63
gulp UTSW 2 156,865,737 (GRCm39) nonsense probably null
IGL02835:Mtcl2 UTSW 2 156,883,854 (GRCm39) missense possibly damaging 0.91
R0528:Mtcl2 UTSW 2 156,862,612 (GRCm39) missense probably damaging 1.00
R0535:Mtcl2 UTSW 2 156,875,209 (GRCm39) missense possibly damaging 0.89
R0726:Mtcl2 UTSW 2 156,902,182 (GRCm39) missense probably damaging 1.00
R1473:Mtcl2 UTSW 2 156,862,368 (GRCm39) nonsense probably null
R1589:Mtcl2 UTSW 2 156,869,557 (GRCm39) missense probably benign 0.05
R1681:Mtcl2 UTSW 2 156,872,450 (GRCm39) missense possibly damaging 0.70
R1701:Mtcl2 UTSW 2 156,872,539 (GRCm39) missense probably damaging 1.00
R1872:Mtcl2 UTSW 2 156,882,181 (GRCm39) missense possibly damaging 0.88
R2056:Mtcl2 UTSW 2 156,864,747 (GRCm39) missense probably benign 0.00
R2118:Mtcl2 UTSW 2 156,875,245 (GRCm39) missense probably damaging 1.00
R2120:Mtcl2 UTSW 2 156,875,245 (GRCm39) missense probably damaging 1.00
R2121:Mtcl2 UTSW 2 156,875,245 (GRCm39) missense probably damaging 1.00
R2124:Mtcl2 UTSW 2 156,875,245 (GRCm39) missense probably damaging 1.00
R2249:Mtcl2 UTSW 2 156,882,013 (GRCm39) missense probably benign 0.08
R3147:Mtcl2 UTSW 2 156,862,284 (GRCm39) missense possibly damaging 0.91
R3758:Mtcl2 UTSW 2 156,862,558 (GRCm39) missense possibly damaging 0.77
R4601:Mtcl2 UTSW 2 156,881,844 (GRCm39) missense probably benign 0.41
R4646:Mtcl2 UTSW 2 156,862,426 (GRCm39) missense probably damaging 1.00
R4653:Mtcl2 UTSW 2 156,882,511 (GRCm39) missense probably damaging 1.00
R4736:Mtcl2 UTSW 2 156,862,474 (GRCm39) missense probably damaging 1.00
R4773:Mtcl2 UTSW 2 156,872,489 (GRCm39) missense probably benign 0.08
R4796:Mtcl2 UTSW 2 156,862,172 (GRCm39) missense probably benign
R4999:Mtcl2 UTSW 2 156,864,776 (GRCm39) missense probably benign 0.10
R5304:Mtcl2 UTSW 2 156,865,737 (GRCm39) nonsense probably null
R5369:Mtcl2 UTSW 2 156,882,654 (GRCm39) missense probably damaging 1.00
R5530:Mtcl2 UTSW 2 156,862,262 (GRCm39) missense probably damaging 1.00
R5712:Mtcl2 UTSW 2 156,872,841 (GRCm39) missense probably damaging 1.00
R5780:Mtcl2 UTSW 2 156,860,410 (GRCm39) missense probably damaging 0.98
R6162:Mtcl2 UTSW 2 156,881,784 (GRCm39) missense possibly damaging 0.63
R6253:Mtcl2 UTSW 2 156,863,339 (GRCm39) missense probably benign 0.00
R6303:Mtcl2 UTSW 2 156,882,684 (GRCm39) missense possibly damaging 0.91
R6304:Mtcl2 UTSW 2 156,882,684 (GRCm39) missense possibly damaging 0.91
R6523:Mtcl2 UTSW 2 156,902,263 (GRCm39) nonsense probably null
R7216:Mtcl2 UTSW 2 156,860,290 (GRCm39) missense possibly damaging 0.76
R7335:Mtcl2 UTSW 2 156,872,925 (GRCm39) missense possibly damaging 0.86
R7562:Mtcl2 UTSW 2 156,895,509 (GRCm39) missense probably damaging 1.00
R7593:Mtcl2 UTSW 2 156,882,776 (GRCm39) missense probably benign 0.40
R7788:Mtcl2 UTSW 2 156,869,504 (GRCm39) missense probably benign 0.09
R8013:Mtcl2 UTSW 2 156,872,706 (GRCm39) critical splice donor site probably null
R8263:Mtcl2 UTSW 2 156,869,510 (GRCm39) missense possibly damaging 0.94
R8299:Mtcl2 UTSW 2 156,862,651 (GRCm39) missense possibly damaging 0.93
R8814:Mtcl2 UTSW 2 156,872,451 (GRCm39) nonsense probably null
R9222:Mtcl2 UTSW 2 156,881,919 (GRCm39) missense probably benign 0.08
R9563:Mtcl2 UTSW 2 156,902,182 (GRCm39) missense probably damaging 1.00
R9607:Mtcl2 UTSW 2 156,869,488 (GRCm39) missense probably damaging 0.96
R9645:Mtcl2 UTSW 2 156,869,390 (GRCm39) missense probably damaging 1.00
R9690:Mtcl2 UTSW 2 156,862,134 (GRCm39) missense probably benign 0.06
R9727:Mtcl2 UTSW 2 156,862,168 (GRCm39) missense possibly damaging 0.89
X0019:Mtcl2 UTSW 2 156,862,184 (GRCm39) missense probably benign 0.04
Predicted Primers PCR Primer
(F):5'- AGTTTCCACACAGACTCGGTGC -3'
(R):5'- CGACATGAAGGAGATCACCAACTGC -3'

Sequencing Primer
(F):5'- GATGTTCCTCAGTACAGGGCTATC -3'
(R):5'- GAAGGTAAAGAACACATCCAGC -3'
Posted On 2014-04-24