Incidental Mutation 'R7830:Cc2d2b'
ID602410
Institutional Source Beutler Lab
Gene Symbol Cc2d2b
Ensembl Gene ENSMUSG00000108929
Gene Namecoiled-coil and C2 domain containing 2B
SynonymsEG668310
Accession Numbers

NCBI RefSeq: XM_001000795; MGI: 3645359

Is this an essential gene? Probably non essential (E-score: 0.118) question?
Stock #R7830 (G1)
Quality Score225.009
Status Not validated
Chromosome19
Chromosomal Location40748753-40827743 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 40765357 bp
ZygosityHeterozygous
Amino Acid Change Valine to Glutamic Acid at position 108 (V108E)
Ref Sequence ENSEMBL: ENSMUSP00000153384 (fasta)
Predicted Effect unknown
Transcript: ENSMUST00000207801
AA Change: V108E
Predicted Effect possibly damaging
Transcript: ENSMUST00000224596
AA Change: V108E

PolyPhen 2 Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3110002H16Rik A G 18: 12,168,871 N24S probably benign Het
4932438A13Rik CCAGATTCATGTAGCA CCA 3: 36,964,932 probably null Het
Adat3 T C 10: 80,606,820 L164P probably damaging Het
Aldh16a1 A T 7: 45,146,225 L388Q probably damaging Het
Angpt1 T C 15: 42,676,268 N65S probably damaging Het
Ankrd54 G A 15: 79,054,050 T287I probably damaging Het
Cntnap5c A T 17: 58,162,250 D609V probably damaging Het
Col6a4 G T 9: 106,075,390 D436E probably damaging Het
Cul9 A T 17: 46,540,311 D394E probably benign Het
Cyfip1 A G 7: 55,873,462 E75G probably damaging Het
Efr3a G A 15: 65,829,830 V198I probably benign Het
Eif2ak2 C T 17: 78,866,403 G249S probably damaging Het
Erich4 A T 7: 25,615,724 M42K probably benign Het
Fig4 A C 10: 41,256,466 V448G probably benign Het
Gas1 T C 13: 60,176,034 D303G probably damaging Het
Gm609 A T 16: 45,442,554 I187N probably damaging Het
Golgb1 T G 16: 36,898,721 Y330D possibly damaging Het
Gpr146 C T 5: 139,392,602 A53V probably benign Het
Klk1b27 A C 7: 44,055,726 M106L probably benign Het
Lipc T C 9: 70,812,901 T190A probably damaging Het
Lrrc4b A G 7: 44,461,807 I368V possibly damaging Het
Mmp10 A T 9: 7,507,283 Q368L probably benign Het
Myo10 T A 15: 25,737,971 Y501* probably null Het
Neb T A 2: 52,165,189 H6445L probably benign Het
Numa1 T A 7: 101,999,285 M741K probably benign Het
Nxn T A 11: 76,273,993 I231F probably damaging Het
Olfr1471 T C 19: 13,445,621 L203S probably benign Het
Olfr341 A G 2: 36,479,380 L250P probably damaging Het
Osbp2 A G 11: 3,863,414 S152P probably benign Het
P3h4 T C 11: 100,414,043 T173A probably damaging Het
Pcdh15 C A 10: 74,385,901 R678S probably damaging Het
Pcdhb6 C A 18: 37,336,312 T762K probably benign Het
Pnrc1 G A 4: 33,248,057 P114L probably damaging Het
Ppp3ca T A 3: 136,868,720 S126R probably damaging Het
Prl3d2 C T 13: 27,126,017 T155I probably benign Het
Prune2 C A 19: 17,122,674 N1847K probably benign Het
Psg21 A T 7: 18,647,298 V440E probably damaging Het
Rag1 A G 2: 101,642,059 S913P probably damaging Het
Ros1 T A 10: 52,154,934 H525L probably damaging Het
Scarb1 T C 5: 125,287,383 Y94C probably damaging Het
Serpinb6a T G 13: 33,930,047 D120A probably benign Het
Sik3 ACAGCAGCAGCAGCAGCAGCAGCAGCA ACAGCAGCAGCAGCAGCAGCAGCA 9: 46,212,057 probably benign Het
Slc39a14 T C 14: 70,310,117 D299G probably benign Het
Sox1 G A 8: 12,396,955 A199T probably damaging Het
Strc T A 2: 121,375,049 I867F probably damaging Het
Tfrc A G 16: 32,619,167 K346R probably benign Het
Usf3 C T 16: 44,219,779 Q1541* probably null Het
Wrn G A 8: 33,269,054 L716F probably damaging Het
Zfp141 G A 7: 42,475,188 T620I probably benign Het
Zfp354b A T 11: 50,923,309 I263K probably benign Het
Zfp804b T A 5: 6,771,124 E646D probably benign Het
Zfp970 G T 2: 177,475,545 C304F probably damaging Het
Other mutations in Cc2d2b
AlleleSourceChrCoordTypePredicted EffectPPH Score
1mM(1):Cc2d2b UTSW 19 40795685 missense possibly damaging 0.60
R6163:Cc2d2b UTSW 19 40756506 missense probably benign 0.31
R6481:Cc2d2b UTSW 19 40802395 missense possibly damaging 0.95
R6651:Cc2d2b UTSW 19 40778129 missense probably damaging 0.97
R6747:Cc2d2b UTSW 19 40795667 missense probably benign 0.03
R6799:Cc2d2b UTSW 19 40791208 missense possibly damaging 0.69
R6857:Cc2d2b UTSW 19 40770865 missense possibly damaging 0.62
R6869:Cc2d2b UTSW 19 40809454 missense probably benign 0.06
R6881:Cc2d2b UTSW 19 40825039 missense probably damaging 0.99
R6900:Cc2d2b UTSW 19 40825074 missense probably null 0.08
R6902:Cc2d2b UTSW 19 40816289 missense possibly damaging 0.93
R6960:Cc2d2b UTSW 19 40785062 missense possibly damaging 0.85
R7016:Cc2d2b UTSW 19 40795804 missense possibly damaging 0.85
R7039:Cc2d2b UTSW 19 40802401 missense probably damaging 1.00
R7072:Cc2d2b UTSW 19 40760359 missense unknown
R7192:Cc2d2b UTSW 19 40774437 missense unknown
R7226:Cc2d2b UTSW 19 40791307 missense unknown
R7303:Cc2d2b UTSW 19 40808994 missense unknown
R7324:Cc2d2b UTSW 19 40809108 missense unknown
R7503:Cc2d2b UTSW 19 40794612 missense unknown
R7727:Cc2d2b UTSW 19 40756530 missense probably benign 0.03
R7774:Cc2d2b UTSW 19 40765717 missense unknown
Predicted Primers PCR Primer
(F):5'- TGAGTTCCTCTTTATTCAGCCAAAC -3'
(R):5'- CCTGGAGAACTACTTGGCAC -3'

Sequencing Primer
(F):5'- CCTCTTTATTCAGCCAAACCTTATC -3'
(R):5'- CTGCAGCTTTCACTTCAAA -3'
Posted On2019-12-03