Incidental Mutation 'IGL01662:Ccdc169'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ccdc169
Ensembl Gene ENSMUSG00000048655
Gene Namecoiled-coil domain containing 169
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.110) question?
Stock #IGL01662
Quality Score
Chromosomal Location55137339-55172935 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to A at 55163311 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000112414 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000052904] [ENSMUST00000061099] [ENSMUST00000118963] [ENSMUST00000159904] [ENSMUST00000161120]
Predicted Effect probably null
Transcript: ENSMUST00000052904
SMART Domains Protein: ENSMUSP00000049698
Gene: ENSMUSG00000048655

Pfam:DUF4600 1 100 2e-38 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000061099
SMART Domains Protein: ENSMUSP00000054771
Gene: ENSMUSG00000048655

Pfam:DUF4600 54 181 1.8e-58 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000116940
Predicted Effect probably null
Transcript: ENSMUST00000118963
SMART Domains Protein: ENSMUSP00000112414
Gene: ENSMUSG00000048655

Pfam:DUF4600 53 182 1.2e-55 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000159904
SMART Domains Protein: ENSMUSP00000123900
Gene: ENSMUSG00000048655

Pfam:DUF4600 1 79 1.1e-32 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000161120
SMART Domains Protein: ENSMUSP00000125131
Gene: ENSMUSG00000048655

Pfam:DUF4600 1 79 1.1e-32 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsm5 A T 7: 119,538,288 I402F probably damaging Het
Acvr2b T C 9: 119,432,504 Y388H probably damaging Het
Adh1 G A 3: 138,282,751 D162N possibly damaging Het
C6 G T 15: 4,792,754 R585I probably damaging Het
Cdh13 T A 8: 118,675,177 M106K probably damaging Het
Cep78 C T 19: 15,960,995 E530K probably damaging Het
Cyfip1 T A 7: 55,896,739 L533Q probably damaging Het
Etl4 T C 2: 20,806,649 V1181A probably benign Het
Fam105a C T 15: 27,658,065 D290N probably damaging Het
Fam122a A G 19: 24,476,584 V258A probably benign Het
Galnt7 T G 8: 57,531,735 probably benign Het
Gm11595 G A 11: 99,772,672 R61C unknown Het
Gucy1a1 T A 3: 82,109,253 I143F possibly damaging Het
Hmcn1 T C 1: 150,737,299 N1410D possibly damaging Het
Ltbp2 G A 12: 84,809,246 T741I probably benign Het
Mdc1 T C 17: 35,852,505 S982P probably benign Het
Mfsd4b2 A G 10: 39,922,197 probably benign Het
Mrgprb5 T G 7: 48,168,424 I188L probably benign Het
Naip6 T A 13: 100,300,354 S554C probably damaging Het
Nav2 A G 7: 49,571,209 N1715D probably damaging Het
Nav3 A T 10: 109,769,258 S985T possibly damaging Het
Nme7 A G 1: 164,328,297 Q22R probably benign Het
Olfr556 T C 7: 102,670,720 W267R probably damaging Het
Ppp1r9a A G 6: 5,115,322 E815G probably damaging Het
Ppp2r2c T A 5: 36,926,400 I95N probably damaging Het
Ppp4r4 G A 12: 103,602,966 E717K possibly damaging Het
Prdm2 A G 4: 143,133,568 S1051P possibly damaging Het
Rnf214 T C 9: 45,899,786 D193G probably damaging Het
Sirpb1b G T 3: 15,543,184 T167K probably damaging Het
Slc16a3 C A 11: 120,956,706 S240* probably null Het
Snx14 T A 9: 88,385,838 probably benign Het
Sorbs2 A G 8: 45,803,829 probably benign Het
Stk-ps2 A T 1: 46,029,362 noncoding transcript Het
Taar7b A T 10: 23,999,976 D13V probably benign Het
Trp53bp1 T C 2: 121,236,025 E740G probably damaging Het
Unc79 C T 12: 103,149,020 A2054V possibly damaging Het
Zfp106 A G 2: 120,523,553 V211A probably benign Het
Zfp112 A G 7: 24,125,954 H449R probably benign Het
Other mutations in Ccdc169
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01017:Ccdc169 APN 3 55171318 missense possibly damaging 0.85
IGL02223:Ccdc169 APN 3 55142300 missense probably benign
IGL02272:Ccdc169 APN 3 55150748 missense probably damaging 0.99
IGL02329:Ccdc169 APN 3 55171281 missense probably benign
R4603:Ccdc169 UTSW 3 55150805 missense probably benign 0.01
R5347:Ccdc169 UTSW 3 55142319 splice site probably benign
R5798:Ccdc169 UTSW 3 55140124 missense possibly damaging 0.94
R5951:Ccdc169 UTSW 3 55140141 missense probably damaging 0.99
R6562:Ccdc169 UTSW 3 55150814 missense probably damaging 0.98
R7599:Ccdc169 UTSW 3 55140109 missense probably damaging 0.99
X0011:Ccdc169 UTSW 3 55157082 missense probably damaging 1.00
Posted On2014-01-21