Incidental Mutation 'R5546:Ctsq'
ID 436307
Institutional Source Beutler Lab
Gene Symbol Ctsq
Ensembl Gene ENSMUSG00000021439
Gene Name cathepsin Q
Synonyms 1600010J02Rik
MMRRC Submission 043104-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R5546 (G1)
Quality Score 225
Status Not validated
Chromosome 13
Chromosomal Location 61182852-61188411 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 61185702 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 146 (C146*)
Ref Sequence ENSEMBL: ENSMUSP00000021888 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021888]
AlphaFold Q91ZF4
Predicted Effect probably null
Transcript: ENSMUST00000021888
AA Change: C146*
SMART Domains Protein: ENSMUSP00000021888
Gene: ENSMUSG00000021439
AA Change: C146*

DomainStartEndE-ValueType
Inhibitor_I29 29 88 3.76e-24 SMART
Pept_C1 125 342 3.46e-103 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144401
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.5%
Validation Efficiency
Allele List at MGI

All alleles(2) : Targeted(2)

Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actl11 A G 9: 107,806,832 (GRCm39) N385S probably benign Het
Ahctf1 A T 1: 179,581,633 (GRCm39) I1523N probably benign Het
Akna C T 4: 63,313,196 (GRCm39) G309E probably benign Het
Akna T C 4: 63,313,803 (GRCm39) N107D probably benign Het
Arhgef15 G A 11: 68,844,877 (GRCm39) P240L probably benign Het
Brd1 T A 15: 88,585,325 (GRCm39) E836D probably benign Het
Brf2 A G 8: 27,614,311 (GRCm39) S292P possibly damaging Het
C3 A G 17: 57,529,976 (GRCm39) L500P probably damaging Het
Cblif T C 19: 11,725,859 (GRCm39) S50P possibly damaging Het
Ccdc107 T C 4: 43,495,685 (GRCm39) L196P probably damaging Het
Cdcp1 G T 9: 123,007,094 (GRCm39) P551Q probably damaging Het
Ckap5 T C 2: 91,425,161 (GRCm39) L1224P probably damaging Het
Csnk1g2 C A 10: 80,474,232 (GRCm39) T178K probably benign Het
Cyp2ab1 T A 16: 20,132,507 (GRCm39) I264F probably damaging Het
Daxx TGATGATGACGATGATGACGATGATGA TGATGATGACGATGATGA 17: 34,131,615 (GRCm39) probably benign Het
Dnah11 G A 12: 117,939,583 (GRCm39) T3179M possibly damaging Het
Dnah7c A T 1: 46,705,477 (GRCm39) T2497S probably damaging Het
Eif4enif1 T C 11: 3,193,989 (GRCm39) V776A probably damaging Het
Erbb4 G T 1: 68,337,452 (GRCm39) T622N probably damaging Het
Erich6 A G 3: 58,526,218 (GRCm39) Y595H probably benign Het
Fam107a C T 14: 8,298,764 (GRCm38) A121T probably benign Het
Gpatch11 C T 17: 79,149,548 (GRCm39) Q183* probably null Het
Gpr161 C A 1: 165,133,982 (GRCm39) F81L possibly damaging Het
Hook1 G T 4: 95,890,765 (GRCm39) E291D probably benign Het
Hsf2bp T A 17: 32,165,669 (GRCm39) I309F probably damaging Het
Hspg2 T C 4: 137,275,485 (GRCm39) probably null Het
Ide T G 19: 37,249,623 (GRCm39) M910L unknown Het
Igdcc4 A G 9: 65,036,077 (GRCm39) Y712C probably damaging Het
Kmt2d T C 15: 98,750,949 (GRCm39) probably benign Het
Lats1 T C 10: 7,581,518 (GRCm39) Y768H probably damaging Het
Mageb3 A G 2: 121,784,868 (GRCm39) V278A probably damaging Het
Mapkbp1 G A 2: 119,849,724 (GRCm39) R732H probably damaging Het
Marveld2 T C 13: 100,737,446 (GRCm39) I148V probably benign Het
Mast1 G C 8: 85,642,889 (GRCm39) P969A probably damaging Het
Myh10 T G 11: 68,689,206 (GRCm39) V1261G possibly damaging Het
Nlrp1b A T 11: 71,108,102 (GRCm39) H466Q probably benign Het
Npr2 T G 4: 43,650,150 (GRCm39) V905G probably damaging Het
Oip5 T A 2: 119,440,808 (GRCm39) I240F unknown Het
Or4c12 A G 2: 89,773,929 (GRCm39) C177R probably damaging Het
Or5k8 G T 16: 58,644,516 (GRCm39) Y185* probably null Het
Or8b12 T A 9: 37,657,820 (GRCm39) M130K probably benign Het
Pcsk2 G A 2: 143,388,480 (GRCm39) A24T probably benign Het
Plxnb1 G T 9: 108,929,818 (GRCm39) G225W probably damaging Het
Polr1a T C 6: 71,906,350 (GRCm39) S389P possibly damaging Het
Prkca A G 11: 107,944,806 (GRCm39) V175A probably benign Het
Rassf7 C A 7: 140,796,973 (GRCm39) probably null Het
Rbl2 A G 8: 91,805,560 (GRCm39) I206V probably benign Het
Rnf111 A T 9: 70,366,378 (GRCm39) H353Q probably benign Het
Rpn1 T G 6: 88,070,841 (GRCm39) V237G probably damaging Het
Sec61a2 T A 2: 5,881,351 (GRCm39) I267F possibly damaging Het
Spop G T 11: 95,376,669 (GRCm39) V241F probably damaging Het
Sptbn2 C T 19: 4,775,978 (GRCm39) A178V probably damaging Het
Stard13 A G 5: 150,969,366 (GRCm39) Y791H probably benign Het
Susd2 T A 10: 75,478,052 (GRCm39) I113L probably benign Het
Tcof1 T C 18: 60,964,628 (GRCm39) E666G possibly damaging Het
Tekt5 G T 16: 10,179,254 (GRCm39) A371E possibly damaging Het
Thap11 G A 8: 106,582,548 (GRCm39) E186K probably damaging Het
Tk2 A T 8: 104,974,315 (GRCm39) D45E possibly damaging Het
Tuba8 C A 6: 121,199,872 (GRCm39) Y185* probably null Het
Usp24 T A 4: 106,273,244 (GRCm39) Y2210N probably damaging Het
Wfdc8 A T 2: 164,439,239 (GRCm39) probably benign Het
Zar1l T C 5: 150,436,365 (GRCm39) N237S probably damaging Het
Zfp607b A T 7: 27,402,032 (GRCm39) T163S probably benign Het
Zfp619 C A 7: 39,184,577 (GRCm39) H202Q probably benign Het
Other mutations in Ctsq
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00428:Ctsq APN 13 61,185,528 (GRCm39) missense probably damaging 0.96
IGL00585:Ctsq APN 13 61,184,941 (GRCm39) missense probably benign 0.00
IGL00743:Ctsq APN 13 61,183,998 (GRCm39) missense probably damaging 1.00
IGL00897:Ctsq APN 13 61,185,539 (GRCm39) missense probably damaging 1.00
IGL01679:Ctsq APN 13 61,186,722 (GRCm39) missense probably benign 0.00
IGL01982:Ctsq APN 13 61,187,335 (GRCm39) missense probably benign 0.05
IGL01982:Ctsq APN 13 61,186,732 (GRCm39) missense probably benign
IGL02448:Ctsq APN 13 61,184,044 (GRCm39) missense probably damaging 1.00
R0036:Ctsq UTSW 13 61,185,485 (GRCm39) critical splice donor site probably null
R0036:Ctsq UTSW 13 61,185,485 (GRCm39) critical splice donor site probably null
R0741:Ctsq UTSW 13 61,184,019 (GRCm39) missense probably damaging 0.99
R1192:Ctsq UTSW 13 61,186,859 (GRCm39) missense probably damaging 1.00
R1593:Ctsq UTSW 13 61,183,986 (GRCm39) splice site probably null
R3906:Ctsq UTSW 13 61,186,585 (GRCm39) missense probably damaging 1.00
R4483:Ctsq UTSW 13 61,186,726 (GRCm39) missense probably benign 0.01
R4590:Ctsq UTSW 13 61,184,028 (GRCm39) missense probably benign 0.17
R5157:Ctsq UTSW 13 61,184,913 (GRCm39) missense probably benign 0.00
R5365:Ctsq UTSW 13 61,185,632 (GRCm39) missense possibly damaging 0.95
R5366:Ctsq UTSW 13 61,184,913 (GRCm39) missense probably benign 0.00
R5595:Ctsq UTSW 13 61,184,874 (GRCm39) missense probably benign 0.41
R6046:Ctsq UTSW 13 61,186,955 (GRCm39) missense probably benign 0.00
R6049:Ctsq UTSW 13 61,186,572 (GRCm39) critical splice donor site probably null
R6535:Ctsq UTSW 13 61,183,140 (GRCm39) missense probably damaging 1.00
R6537:Ctsq UTSW 13 61,183,140 (GRCm39) missense probably damaging 1.00
R7159:Ctsq UTSW 13 61,186,737 (GRCm39) missense probably benign 0.00
R8189:Ctsq UTSW 13 61,184,969 (GRCm39) missense probably damaging 1.00
R8890:Ctsq UTSW 13 61,185,502 (GRCm39) missense probably damaging 1.00
Z1176:Ctsq UTSW 13 61,184,937 (GRCm39) missense probably benign 0.01
Z1177:Ctsq UTSW 13 61,184,910 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGACAACATAGGAAGTCCACTTAC -3'
(R):5'- ATCGGGTACATATTGGCTGC -3'

Sequencing Primer
(F):5'- CATAAGGATAGGTTGCCTGAGCCTC -3'
(R):5'- TGCATCCAAGTCCTCTAGGAG -3'
Posted On 2016-10-24