Incidental Mutation 'R2188:Klk14'
ID 237923
Institutional Source Beutler Lab
Gene Symbol Klk14
Ensembl Gene ENSMUSG00000044737
Gene Name kallikrein related-peptidase 14
Synonyms
MMRRC Submission 040190-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R2188 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 43339842-43344960 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 43341501 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Tyrosine at position 51 (C51Y)
Ref Sequence ENSEMBL: ENSMUSP00000056935 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056329]
AlphaFold Q8CGR5
Predicted Effect probably damaging
Transcript: ENSMUST00000056329
AA Change: C51Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000056935
Gene: ENSMUSG00000044737
AA Change: C51Y

DomainStartEndE-ValueType
signal peptide 1 16 N/A INTRINSIC
Tryp_SPc 23 243 2.02e-93 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181454
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205416
Meta Mutation Damage Score 0.7935 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency
MGI Phenotype FUNCTION: This gene encodes a member of the kallikrein subfamily of serine proteases that have diverse physiological functions such as regulation of blood pressure and desquamation. The encoded protein is a precursor that undergoes proteolytic cleavage of the activation peptide to generate the functional enzyme. The encoded enzyme was found to activate the complement pathway by cleavage of C3 to release C3a anaphylotoxin. This gene is one of the several glandular kallikrein genes located in a cluster on chromosome 7. [provided by RefSeq, Aug 2015]
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca7 T C 10: 79,838,367 (GRCm39) L547P probably damaging Het
Arhgap29 A C 3: 121,784,658 (GRCm39) D195A probably damaging Het
Atad3a A T 4: 155,835,976 (GRCm39) I274N probably damaging Het
Ccdc12 G T 9: 110,485,699 (GRCm39) K23N possibly damaging Het
Ccpg1 A G 9: 72,920,388 (GRCm39) T668A probably benign Het
Cdc34b T C 11: 94,632,998 (GRCm39) I66T probably benign Het
Dnah1 A G 14: 31,001,121 (GRCm39) I2408T probably damaging Het
Fam91a1 A C 15: 58,302,512 (GRCm39) N284T probably damaging Het
Gbp2b A T 3: 142,314,040 (GRCm39) E440V probably benign Het
Gm5134 T C 10: 75,831,670 (GRCm39) S370P probably damaging Het
Hmcn2 G A 2: 31,309,947 (GRCm39) A3238T probably benign Het
Hmg20a A G 9: 56,384,584 (GRCm39) E118G possibly damaging Het
Itprid2 T C 2: 79,475,267 (GRCm39) S409P probably benign Het
Kdm5a T A 6: 120,383,601 (GRCm39) F781I possibly damaging Het
Kmt2d A G 15: 98,737,181 (GRCm39) probably benign Het
Lrp1b T C 2: 41,298,971 (GRCm39) T857A probably benign Het
Mucl2 T A 15: 103,927,840 (GRCm39) N39I probably damaging Het
Myl6 A G 10: 128,328,566 (GRCm39) I27T possibly damaging Het
Ndor1 A T 2: 25,141,765 (GRCm39) probably null Het
Nlrp9a A G 7: 26,264,354 (GRCm39) E758G probably damaging Het
Or52h7 G A 7: 104,213,883 (GRCm39) A152T probably benign Het
Or8u8 A T 2: 86,011,780 (GRCm39) I225N probably damaging Het
Parp3 G A 9: 106,353,051 (GRCm39) R42W probably damaging Het
Pik3c2g A G 6: 139,798,600 (GRCm39) I495V probably damaging Het
Qrfprl C A 6: 65,418,260 (GRCm39) H143N probably damaging Het
Sdsl C T 5: 120,596,485 (GRCm39) G310S probably damaging Het
Sec24a A G 11: 51,614,411 (GRCm39) L531P probably damaging Het
Slc2a12 C T 10: 22,540,736 (GRCm39) S197F probably benign Het
Snapc1 T A 12: 74,017,001 (GRCm39) I213N probably damaging Het
Srpk1 A T 17: 28,813,163 (GRCm39) I527N probably damaging Het
Steap2 G T 5: 5,723,643 (GRCm39) Y412* probably null Het
Tbk1 A C 10: 121,399,836 (GRCm39) Y329* probably null Het
Tekt5 T C 16: 10,176,189 (GRCm39) E452G probably damaging Het
Tmc5 G T 7: 118,254,178 (GRCm39) C672F probably damaging Het
Trim27 T C 13: 21,367,987 (GRCm39) L201S probably damaging Het
Vil1 A C 1: 74,466,724 (GRCm39) D638A probably benign Het
Vmn2r68 TCC TC 7: 84,870,758 (GRCm39) probably null Het
Zfp583 C T 7: 6,320,610 (GRCm39) R134H probably benign Het
Other mutations in Klk14
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0309:Klk14 UTSW 7 43,343,769 (GRCm39) missense probably benign 0.01
R0467:Klk14 UTSW 7 43,343,534 (GRCm39) missense probably benign 0.33
R1432:Klk14 UTSW 7 43,344,342 (GRCm39) missense probably damaging 1.00
R1575:Klk14 UTSW 7 43,343,377 (GRCm39) critical splice acceptor site probably null
R2160:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R2185:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R2189:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R2472:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R2474:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R2961:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R2962:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R2968:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3147:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3148:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3176:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3177:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3276:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3277:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3418:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3419:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3430:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R3956:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4080:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4081:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4152:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4153:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4169:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4205:Klk14 UTSW 7 43,344,358 (GRCm39) missense probably benign 0.00
R4284:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4285:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4287:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4356:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4359:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4379:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4380:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4381:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4611:Klk14 UTSW 7 43,343,781 (GRCm39) missense probably damaging 1.00
R4684:Klk14 UTSW 7 43,341,392 (GRCm39) missense probably benign
R4784:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4792:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4793:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4825:Klk14 UTSW 7 43,341,500 (GRCm39) missense probably damaging 1.00
R4844:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4847:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4884:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4898:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4941:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4942:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4943:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4972:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R4997:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5021:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5022:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5024:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5053:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5054:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5056:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5057:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5097:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5253:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5257:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5459:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5489:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5490:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5493:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R5543:Klk14 UTSW 7 43,341,501 (GRCm39) missense probably damaging 1.00
R6823:Klk14 UTSW 7 43,343,880 (GRCm39) nonsense probably null
R7960:Klk14 UTSW 7 43,341,467 (GRCm39) missense probably damaging 1.00
R7993:Klk14 UTSW 7 43,344,367 (GRCm39) missense probably benign 0.01
R8220:Klk14 UTSW 7 43,343,498 (GRCm39) missense probably damaging 1.00
R8701:Klk14 UTSW 7 43,343,566 (GRCm39) missense possibly damaging 0.49
R8880:Klk14 UTSW 7 43,343,459 (GRCm39) missense probably damaging 0.99
X0064:Klk14 UTSW 7 43,343,534 (GRCm39) missense probably benign 0.33
Predicted Primers PCR Primer
(F):5'- AAAGATCTCTGTCTGCTGGGC -3'
(R):5'- GGCAAGGGTTCTACATACACTC -3'

Sequencing Primer
(F):5'- ATCTCTGTCTGCTGGGCATTGG -3'
(R):5'- TGAATTATGCCTCTCAGCCTAG -3'
Posted On 2014-10-02