Incidental Mutation 'R7510:Ccdc177'
ID582045
Institutional Source Beutler Lab
Gene Symbol Ccdc177
Ensembl Gene ENSMUSG00000062961
Gene Namecoiled-coil domain containing 177
SynonymsGm1568, LOC380768
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.110) question?
Stock #R7510 (G1)
Quality Score223.009
Status Validated
Chromosome12
Chromosomal Location80754043-80760687 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 80757683 bp
ZygosityHeterozygous
Amino Acid Change Valine to Leucine at position 606 (V606L)
Ref Sequence ENSEMBL: ENSMUSP00000072982 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073251]
Predicted Effect unknown
Transcript: ENSMUST00000073251
AA Change: V606L
SMART Domains Protein: ENSMUSP00000072982
Gene: ENSMUSG00000062961
AA Change: V606L

DomainStartEndE-ValueType
low complexity region 7 20 N/A INTRINSIC
low complexity region 28 49 N/A INTRINSIC
internal_repeat_1 116 139 2.91e-5 PROSPERO
low complexity region 146 159 N/A INTRINSIC
low complexity region 165 227 N/A INTRINSIC
low complexity region 229 263 N/A INTRINSIC
Pfam:DUF4659 332 705 1.9e-115 PFAM
Meta Mutation Damage Score 0.0979 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.0%
Validation Efficiency 97% (65/67)
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp2b1 C T 10: 98,993,896 R320C probably benign Het
Bend4 A G 5: 67,427,384 F66L unknown Het
Brca2 T C 5: 150,536,691 V477A possibly damaging Het
Brms1l A T 12: 55,845,322 K134* probably null Het
Catsper1 A T 19: 5,339,550 T498S probably benign Het
D030056L22Rik G T 19: 18,713,489 A56S possibly damaging Het
Disp1 T C 1: 183,088,411 N815S probably damaging Het
Dsc2 C T 18: 20,032,274 G881R possibly damaging Het
Fancf A G 7: 51,862,205 V17A probably damaging Het
Fastkd2 T A 1: 63,737,789 H361Q possibly damaging Het
Furin A G 7: 80,393,585 S293P probably damaging Het
Ghsr A T 3: 27,372,374 D193V probably benign Het
Gm14403 T A 2: 177,508,610 N116K probably benign Het
Gpr31b A G 17: 13,051,670 L204P probably damaging Het
Hexim1 A G 11: 103,117,241 E107G probably benign Het
Hspa14 T C 2: 3,498,122 S212G probably benign Het
Il18r1 T A 1: 40,474,875 H80Q probably benign Het
Itpr3 A G 17: 27,089,039 T267A probably damaging Het
Kidins220 T A 12: 24,992,269 H146Q possibly damaging Het
Larp4 T C 15: 99,993,377 F228L probably benign Het
Ltbp1 T A 17: 75,352,717 V1288E probably damaging Het
Madd T C 2: 91,177,976 T194A possibly damaging Het
Mlana G A 19: 29,704,672 G42S probably benign Het
Mlxipl A G 5: 135,133,118 E548G possibly damaging Het
Mmab A T 5: 114,435,222 C228S probably benign Het
Mmp1a TG TGG 9: 7,465,083 probably null Het
Nrf1 C T 6: 30,151,634 T490I possibly damaging Het
Numbl A G 7: 27,271,987 probably null Het
Olfr1014 T A 2: 85,776,809 V75D probably damaging Het
Olfr111 T A 17: 37,530,589 I204N probably damaging Het
Olfr1148 T A 2: 87,833,528 I163K probably damaging Het
Olfr1350 C T 7: 6,569,961 probably benign Het
Olfr155 A G 4: 43,854,482 T58A probably benign Het
Olfr803 G T 10: 129,691,920 N40K probably damaging Het
Papln G A 12: 83,772,173 D96N probably damaging Het
Pcdhb14 T C 18: 37,449,592 Y584H probably damaging Het
Pde7b T C 10: 20,413,015 D310G possibly damaging Het
Plin5 T A 17: 56,113,975 H230L probably damaging Het
Ppp1r13l A C 7: 19,368,801 E47A possibly damaging Het
Prdm5 C T 6: 65,927,992 H536Y probably damaging Het
Prickle2 T C 6: 92,376,470 R728G possibly damaging Het
Prkca A T 11: 107,983,994 V374E possibly damaging Het
Prss3 A T 6: 41,375,110 L73* probably null Het
Prss51 G A 14: 64,096,040 D33N probably damaging Het
Rfwd3 A G 8: 111,280,027 V479A probably damaging Het
Rpl36a-ps1 G A 14: 98,994,230 T24I probably benign Het
Rps6ka5 T C 12: 100,616,068 I182V possibly damaging Het
Saa2 T A 7: 46,753,509 D61E probably damaging Het
Samd3 A T 10: 26,230,108 I22F probably benign Het
Sap130 C T 18: 31,667,004 P403L probably damaging Het
Sap130 A G 18: 31,711,215 T813A probably damaging Het
Scfd2 A G 5: 74,212,327 F629S probably damaging Het
Sec61a1 A T 6: 88,512,603 F119I probably benign Het
Serpinb9 T A 13: 33,010,785 F175I probably damaging Het
Slc12a3 G T 8: 94,365,849 C966F probably damaging Het
Sptbn4 A G 7: 27,428,268 V169A probably benign Het
Synj1 A G 16: 90,938,677 S1463P probably benign Het
Tfec T A 6: 16,835,233 H182L probably benign Het
Tigd5 T C 15: 75,910,419 V210A probably benign Het
Tssc4 G A 7: 143,069,981 E9K possibly damaging Het
Txk C G 5: 72,736,383 C18S unknown Het
Uaca G A 9: 60,850,205 probably null Het
Vmn2r1 A C 3: 64,086,501 K89N probably damaging Het
Zfp160 G A 17: 21,026,393 E402K probably benign Het
Other mutations in Ccdc177
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01598:Ccdc177 APN 12 80758745 missense unknown
IGL02433:Ccdc177 APN 12 80757598 missense unknown
R0829:Ccdc177 UTSW 12 80759479 missense probably damaging 0.96
R1739:Ccdc177 UTSW 12 80759239 missense probably damaging 1.00
R1970:Ccdc177 UTSW 12 80758712 missense unknown
R2337:Ccdc177 UTSW 12 80758691 missense unknown
R5001:Ccdc177 UTSW 12 80757386 missense unknown
R5164:Ccdc177 UTSW 12 80758562 missense unknown
R5249:Ccdc177 UTSW 12 80758508 missense unknown
R5461:Ccdc177 UTSW 12 80758042 missense unknown
R6802:Ccdc177 UTSW 12 80759283 missense probably damaging 1.00
R7051:Ccdc177 UTSW 12 80759153 missense probably damaging 0.98
R7412:Ccdc177 UTSW 12 80759018 missense possibly damaging 0.85
R7511:Ccdc177 UTSW 12 80757683 missense unknown
R7712:Ccdc177 UTSW 12 80757938 nonsense probably null
R8036:Ccdc177 UTSW 12 80758123 missense unknown
Z1177:Ccdc177 UTSW 12 80757736 missense unknown
Predicted Primers PCR Primer
(F):5'- AAAGAGCGCGTGTTGGTCTC -3'
(R):5'- AGAGAACTACGAGCAGCTGC -3'

Sequencing Primer
(F):5'- TTCTCCCGCACATGGAAGGAG -3'
(R):5'- CTACGAGCAGCTGCAGGAAC -3'
Posted On2019-10-17