Incidental Mutation 'R5111:Abhd17c'
ID 393857
Institutional Source Beutler Lab
Gene Symbol Abhd17c
Ensembl Gene ENSMUSG00000038459
Gene Name abhydrolase domain containing 17C
Synonyms 2210412D01Rik, Fam108c
MMRRC Submission 042699-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # R5111 (G1)
Quality Score 127
Status Validated
Chromosome 7
Chromosomal Location 83758564-83801101 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 83800646 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Stop codon at position 136 (L136*)
Ref Sequence ENSEMBL: ENSMUSP00000112988 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000117085]
AlphaFold Q8VCV1
Predicted Effect probably null
Transcript: ENSMUST00000117085
AA Change: L136*
SMART Domains Protein: ENSMUSP00000112988
Gene: ENSMUSG00000038459
AA Change: L136*

DomainStartEndE-ValueType
low complexity region 46 77 N/A INTRINSIC
Pfam:Hydrolase_4 120 240 8.7e-9 PFAM
Pfam:Abhydrolase_5 125 297 2.8e-30 PFAM
Pfam:DLH 162 297 4.7e-7 PFAM
Pfam:Peptidase_S9 167 317 2.7e-7 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000131505
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180424
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208101
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208236
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208271
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 95.9%
  • 20x: 91.0%
Validation Efficiency 100% (56/56)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ankrd17 A T 5: 90,390,858 (GRCm39) S2271T possibly damaging Het
Arhgef10 A G 8: 14,982,408 (GRCm39) D179G probably benign Het
Bcan G T 3: 87,901,514 (GRCm39) S396Y probably damaging Het
Btbd3 T A 2: 138,120,829 (GRCm39) M1K probably null Het
Capns1 A G 7: 29,891,944 (GRCm39) V106A probably benign Het
Ccnjl A G 11: 43,447,544 (GRCm39) T76A probably benign Het
Cdc23 C A 18: 34,784,742 (GRCm39) V7L unknown Het
Col6a6 C T 9: 105,586,673 (GRCm39) V1783I possibly damaging Het
Crisp3 T C 17: 40,536,695 (GRCm39) T207A possibly damaging Het
Crxos G A 7: 15,630,142 (GRCm39) probably benign Het
Csf3r T C 4: 125,923,861 (GRCm39) probably null Het
Cyp2a12 A G 7: 26,736,046 (GRCm39) Y485C possibly damaging Het
Echdc2 A T 4: 108,026,994 (GRCm39) probably benign Het
Elp3 A C 14: 65,797,685 (GRCm39) Y329D probably damaging Het
Fbxw16 T C 9: 109,265,796 (GRCm39) D341G probably benign Het
H2-Ab1 T A 17: 34,486,456 (GRCm39) S172T probably damaging Het
Hyal2 T C 9: 107,448,310 (GRCm39) V321A probably benign Het
Ighv6-3 A T 12: 114,355,394 (GRCm39) S98R probably benign Het
Kank3 A G 17: 34,037,155 (GRCm39) E153G possibly damaging Het
Klrb1c C T 6: 128,762,968 (GRCm39) R83H probably benign Het
Krtap16-1 T C 11: 99,877,378 (GRCm39) K9E possibly damaging Het
Liph G A 16: 21,802,820 (GRCm39) S83F probably damaging Het
Lnpep A G 17: 17,798,872 (GRCm39) I261T possibly damaging Het
Mdm2 A T 10: 117,527,126 (GRCm39) V273D possibly damaging Het
Mterf1a A G 5: 3,941,860 (GRCm39) S3P probably benign Het
Myt1 A G 2: 181,437,678 (GRCm39) T172A probably benign Het
Nufip2 T A 11: 77,582,669 (GRCm39) S194R probably benign Het
Nusap1 T A 2: 119,460,837 (GRCm39) L110* probably null Het
Palb2 A T 7: 121,716,528 (GRCm39) C488* probably null Het
Pcdhac1 A T 18: 37,224,558 (GRCm39) N457I probably damaging Het
Per1 A T 11: 68,991,612 (GRCm39) S49C probably damaging Het
Ppargc1b A T 18: 61,443,558 (GRCm39) I535N probably damaging Het
Rb1cc1 T C 1: 6,284,858 (GRCm39) probably benign Het
Rpap1 A T 2: 119,601,728 (GRCm39) L744Q probably damaging Het
Sdk1 A G 5: 142,113,600 (GRCm39) E1549G probably damaging Het
Tnr C T 1: 159,713,798 (GRCm39) T742I probably benign Het
Trp53bp1 A T 2: 121,041,868 (GRCm39) H1229Q probably damaging Het
Unc80 A G 1: 66,567,154 (GRCm39) H920R possibly damaging Het
Urb1 A C 16: 90,548,905 (GRCm39) S2268A probably benign Het
Usp32 A T 11: 84,968,157 (GRCm39) Y169N possibly damaging Het
Vmn2r18 A T 5: 151,485,913 (GRCm39) M527K possibly damaging Het
Vmn2r93 A T 17: 18,546,326 (GRCm39) I733F probably damaging Het
Vstm2l A G 2: 157,777,389 (GRCm39) D89G probably damaging Het
Zdhhc8 G T 16: 18,044,612 (GRCm39) Q303K probably benign Het
Zfand2a A G 5: 139,459,509 (GRCm39) V159A probably benign Het
Zswim6 A G 13: 107,865,170 (GRCm39) noncoding transcript Het
Other mutations in Abhd17c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01529:Abhd17c APN 7 83,800,622 (GRCm39) missense possibly damaging 0.93
IGL01824:Abhd17c APN 7 83,800,497 (GRCm39) missense probably benign 0.01
IGL02835:Abhd17c UTSW 7 83,800,731 (GRCm39) missense probably benign 0.00
R2127:Abhd17c UTSW 7 83,759,870 (GRCm39) missense probably damaging 1.00
R2151:Abhd17c UTSW 7 83,800,663 (GRCm39) missense probably damaging 1.00
R2495:Abhd17c UTSW 7 83,759,884 (GRCm39) nonsense probably null
R7812:Abhd17c UTSW 7 83,800,624 (GRCm39) nonsense probably null
R9449:Abhd17c UTSW 7 83,763,637 (GRCm39) missense probably damaging 0.99
R9640:Abhd17c UTSW 7 83,800,814 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGCAACAATCCGGGAGCAC -3'
(R):5'- ATGAACGGCTTCTCGCTCG -3'

Sequencing Primer
(F):5'- ATCCGGGAGCACAAGCC -3'
(R):5'- CTTGTCCGAGCCGCATC -3'
Posted On 2016-06-15