Incidental Mutation 'IGL03182:Ccdc157'
ID412300
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ccdc157
Ensembl Gene ENSMUSG00000051427
Gene Namecoiled-coil domain containing 157
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.061) question?
Stock #IGL03182
Quality Score
Status
Chromosome11
Chromosomal Location4141123-4160293 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 4151832 bp
ZygosityHeterozygous
Amino Acid Change Serine to Proline at position 30 (S30P)
Ref Sequence ENSEMBL: ENSMUSP00000091074 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000093381] [ENSMUST00000101626]
Predicted Effect probably damaging
Transcript: ENSMUST00000093381
AA Change: S30P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000091074
Gene: ENSMUSG00000051427
AA Change: S30P

DomainStartEndE-ValueType
low complexity region 76 88 N/A INTRINSIC
low complexity region 321 343 N/A INTRINSIC
low complexity region 385 414 N/A INTRINSIC
SCOP:d1fxkc_ 452 595 4e-5 SMART
low complexity region 639 659 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000101626
SMART Domains Protein: ENSMUSP00000099148
Gene: ENSMUSG00000051427

DomainStartEndE-ValueType
low complexity region 219 241 N/A INTRINSIC
low complexity region 283 312 N/A INTRINSIC
SCOP:d1fxkc_ 350 493 3e-4 SMART
low complexity region 537 557 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132712
Predicted Effect noncoding transcript
Transcript: ENSMUST00000133962
Predicted Effect noncoding transcript
Transcript: ENSMUST00000137060
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139099
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agbl3 A T 6: 34,803,500 K469N probably damaging Het
Aldh2 A G 5: 121,580,724 probably benign Het
Ankfy1 T C 11: 72,728,754 probably benign Het
Ankhd1 C T 18: 36,578,774 T209I probably benign Het
Aox3 G A 1: 58,165,887 V754I probably benign Het
Arfgef3 C T 10: 18,600,544 R1509H probably damaging Het
AU019823 T C 9: 50,612,398 N50S possibly damaging Het
Cept1 T A 3: 106,504,550 E369D probably damaging Het
Clcnka T C 4: 141,394,487 Y236C probably damaging Het
Ddx42 A T 11: 106,247,527 L717F probably benign Het
Dnah11 A T 12: 118,030,291 I2340N probably damaging Het
Dsel T C 1: 111,860,138 E889G probably damaging Het
Fasn T C 11: 120,812,726 Y1560C probably damaging Het
Fermt2 A T 14: 45,461,768 M623K possibly damaging Het
Gm21970 T A 16: 91,393,838 S110T possibly damaging Het
Gm826 T A 2: 160,327,115 R91S unknown Het
Lrrn3 A G 12: 41,454,021 L99S probably damaging Het
Megf8 T A 7: 25,347,348 M1552K possibly damaging Het
Mgll G T 6: 88,823,191 V191F probably damaging Het
Nol8 C A 13: 49,664,081 H778N probably damaging Het
Olfr1090 A T 2: 86,754,022 S239T probably damaging Het
Olfr1471 A C 19: 13,445,443 T144P possibly damaging Het
Olfr385 T A 11: 73,589,442 T99S probably benign Het
Olfr948 A T 9: 39,318,981 M211K probably benign Het
Pfkfb3 A T 2: 11,501,663 I13N probably damaging Het
Pim1 T A 17: 29,491,766 D114E possibly damaging Het
Pkd1 T C 17: 24,573,818 L1493P probably damaging Het
Plb1 A T 5: 32,344,915 probably benign Het
Plch1 A T 3: 63,702,594 Y872* probably null Het
Rictor A G 15: 6,789,598 D1434G probably benign Het
Rptor G A 11: 119,725,145 G162R probably damaging Het
Serping1 T C 2: 84,765,818 D424G probably damaging Het
Slit2 A G 5: 48,220,053 I475V possibly damaging Het
Snx31 G T 15: 36,525,687 Q289K probably benign Het
Tbc1d13 G A 2: 30,147,367 A254T probably damaging Het
Tek T C 4: 94,851,765 I750T probably damaging Het
Tet2 A T 3: 133,471,398 L1296* probably null Het
Tmem145 T A 7: 25,314,879 F459I probably damaging Het
Uba5 A T 9: 104,054,129 V247D possibly damaging Het
Vmn1r83 T C 7: 12,321,690 M147V probably benign Het
Vwde T C 6: 13,187,139 D783G probably damaging Het
Zfp609 A G 9: 65,701,005 S1198P probably benign Het
Other mutations in Ccdc157
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01599:Ccdc157 APN 11 4148781 missense probably damaging 1.00
IGL02267:Ccdc157 APN 11 4144035 missense probably benign 0.00
R0282:Ccdc157 UTSW 11 4146708 missense probably damaging 0.98
R0360:Ccdc157 UTSW 11 4146663 missense probably damaging 0.98
R1349:Ccdc157 UTSW 11 4149056 missense probably benign 0.20
R1527:Ccdc157 UTSW 11 4151795 missense probably damaging 1.00
R1691:Ccdc157 UTSW 11 4149030 missense probably benign 0.07
R1932:Ccdc157 UTSW 11 4146549 missense probably damaging 1.00
R2132:Ccdc157 UTSW 11 4150004 missense probably damaging 1.00
R4361:Ccdc157 UTSW 11 4146550 missense probably damaging 0.99
R4754:Ccdc157 UTSW 11 4148994 missense possibly damaging 0.46
R4786:Ccdc157 UTSW 11 4151861 missense probably damaging 1.00
R5314:Ccdc157 UTSW 11 4150078 nonsense probably null
R5564:Ccdc157 UTSW 11 4148765 missense probably damaging 1.00
R5625:Ccdc157 UTSW 11 4151888 missense probably damaging 0.99
R5898:Ccdc157 UTSW 11 4144538 missense probably benign 0.23
R6193:Ccdc157 UTSW 11 4151912 missense probably damaging 1.00
R6936:Ccdc157 UTSW 11 4144030 missense probably benign
R7057:Ccdc157 UTSW 11 4144586 missense probably benign 0.33
R7113:Ccdc157 UTSW 11 4148889 missense possibly damaging 0.94
R7136:Ccdc157 UTSW 11 4148592 missense possibly damaging 0.94
T0975:Ccdc157 UTSW 11 4146246 missense probably damaging 0.99
Posted On2016-08-02