Incidental Mutation 'R1478:Jkampl'
ID 165618
Institutional Source Beutler Lab
Gene Symbol Jkampl
Ensembl Gene ENSMUSG00000056197
Gene Name JNK1/MAPK8 associated membrane protein like
Synonyms 4931417E11Rik
MMRRC Submission 039531-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.111) question?
Stock # R1478 (G1)
Quality Score 225
Status Not validated
Chromosome 6
Chromosomal Location 73445563-73446621 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 73446039 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Glutamine at position 170 (L170Q)
Ref Sequence ENSEMBL: ENSMUSP00000068770 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070163]
AlphaFold Q9CR05
Predicted Effect probably damaging
Transcript: ENSMUST00000070163
AA Change: L170Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000068770
Gene: ENSMUSG00000056197
AA Change: L170Q

DomainStartEndE-ValueType
Pfam:DUF766 3 294 3.1e-113 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204006
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204961
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205241
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 95.7%
  • 20x: 90.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 63 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aacs T A 5: 125,580,287 (GRCm39) I204N possibly damaging Het
Acaca A G 11: 84,263,453 (GRCm39) T2025A probably damaging Het
B4galt3 C T 1: 171,103,938 (GRCm39) R170C probably benign Het
BC028528 T C 3: 95,799,271 (GRCm39) probably null Het
Ccdc73 A T 2: 104,737,955 (GRCm39) Q17L possibly damaging Het
Ccdc73 A G 2: 104,745,012 (GRCm39) T50A possibly damaging Het
Ccdc83 T C 7: 89,908,677 (GRCm39) D19G probably damaging Het
Ccn6 G A 10: 39,029,239 (GRCm39) R230W probably damaging Het
Cct8l1 T C 5: 25,722,767 (GRCm39) V494A probably benign Het
Chd1 T C 17: 15,959,769 (GRCm39) F663L probably damaging Het
Chn2 A T 6: 54,270,065 (GRCm39) E319V probably damaging Het
Cnnm1 T C 19: 43,460,295 (GRCm39) V679A probably damaging Het
Cntn6 C T 6: 104,753,389 (GRCm39) T447I probably benign Het
Cyp3a11 G T 5: 145,795,581 (GRCm39) L457I probably benign Het
Dera T A 6: 137,807,193 (GRCm39) S214T possibly damaging Het
Dmtf1 A G 5: 9,171,404 (GRCm39) V501A possibly damaging Het
Dnpep A G 1: 75,292,671 (GRCm39) V114A probably damaging Het
Dscam C T 16: 96,592,110 (GRCm39) V722M probably benign Het
Dsp A G 13: 38,365,114 (GRCm39) N499S probably damaging Het
Ecd A T 14: 20,396,725 (GRCm39) Y53* probably null Het
Esyt3 T C 9: 99,200,119 (GRCm39) T692A probably benign Het
Fat1 T A 8: 45,478,659 (GRCm39) N2545K probably damaging Het
Fndc3a A G 14: 72,795,072 (GRCm39) probably null Het
Fscn3 A G 6: 28,430,567 (GRCm39) M246V probably benign Het
Gde1 G T 7: 118,291,007 (GRCm39) T106K probably benign Het
Gjc2 A G 11: 59,068,434 (GRCm39) I16T possibly damaging Het
Hacd4 A T 4: 88,341,260 (GRCm39) M168K probably damaging Het
Hmx3 A G 7: 131,145,826 (GRCm39) E178G probably damaging Het
Htt A G 5: 34,961,171 (GRCm39) Y266C probably damaging Het
Kif27 G T 13: 58,451,359 (GRCm39) R990S probably damaging Het
Krtap22-2 A T 16: 88,807,534 (GRCm39) Y21* probably null Het
Lrrc41 T A 4: 115,952,405 (GRCm39) L661* probably null Het
Lrrc63 T C 14: 75,363,424 (GRCm39) T236A probably benign Het
Mmp13 T C 9: 7,272,892 (GRCm39) L84P probably damaging Het
Myh8 T C 11: 67,183,551 (GRCm39) I754T probably benign Het
Neb A C 2: 52,065,619 (GRCm39) D5961E probably benign Het
Nlrx1 T C 9: 44,175,374 (GRCm39) H134R probably benign Het
Npepps A T 11: 97,117,673 (GRCm39) M542K probably benign Het
Nup160 C T 2: 90,509,743 (GRCm39) probably benign Het
Or3a1c T A 11: 74,045,963 (GRCm39) probably null Het
Or8g33 T A 9: 39,337,888 (GRCm39) T160S possibly damaging Het
Pikfyve T C 1: 65,302,136 (GRCm39) probably null Het
Ppp6r1 A T 7: 4,643,377 (GRCm39) probably null Het
Prss33 A G 17: 24,054,072 (GRCm39) W45R probably damaging Het
Ptprf A T 4: 118,069,302 (GRCm39) Y980* probably null Het
Qrich1 T C 9: 108,436,531 (GRCm39) V743A probably benign Het
Rev3l G A 10: 39,659,329 (GRCm39) probably null Het
Samd9l A T 6: 3,376,369 (GRCm39) N297K probably benign Het
Sap130 A G 18: 31,813,527 (GRCm39) H528R possibly damaging Het
Slc9b2 T C 3: 135,031,863 (GRCm39) V241A probably benign Het
Snx14 A T 9: 88,276,581 (GRCm39) V577E probably benign Het
Srrm2 T C 17: 24,034,876 (GRCm39) S507P probably benign Het
Stat2 A G 10: 128,117,969 (GRCm39) probably null Het
Susd5 T C 9: 113,925,752 (GRCm39) F545S probably benign Het
Tafa2 T A 10: 123,429,401 (GRCm39) M5K possibly damaging Het
Tnnt2 A G 1: 135,775,764 (GRCm39) T107A probably benign Het
Trappc6b T A 12: 59,094,953 (GRCm39) I41F possibly damaging Het
Ttn T A 2: 76,682,417 (GRCm39) probably benign Het
Vmn1r88 A C 7: 12,911,878 (GRCm39) D78A probably damaging Het
Xpc C T 6: 91,485,510 (GRCm39) D122N possibly damaging Het
Xpo1 C T 11: 23,241,623 (GRCm39) A890V probably damaging Het
Zfp493 A G 13: 67,934,680 (GRCm39) H211R probably damaging Het
Zfp958 A T 8: 4,679,190 (GRCm39) H405L probably damaging Het
Other mutations in Jkampl
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01566:Jkampl APN 6 73,445,673 (GRCm39) missense probably damaging 1.00
IGL01768:Jkampl APN 6 73,445,899 (GRCm39) missense possibly damaging 0.83
IGL02903:Jkampl APN 6 73,446,103 (GRCm39) missense probably damaging 1.00
R0084:Jkampl UTSW 6 73,445,918 (GRCm39) nonsense probably null
R0123:Jkampl UTSW 6 73,446,402 (GRCm39) missense possibly damaging 0.49
R0225:Jkampl UTSW 6 73,446,402 (GRCm39) missense possibly damaging 0.49
R1640:Jkampl UTSW 6 73,445,869 (GRCm39) missense probably benign 0.13
R4616:Jkampl UTSW 6 73,446,252 (GRCm39) missense probably benign 0.02
R5451:Jkampl UTSW 6 73,445,850 (GRCm39) missense probably benign 0.00
R5875:Jkampl UTSW 6 73,446,028 (GRCm39) missense possibly damaging 0.50
R5911:Jkampl UTSW 6 73,445,674 (GRCm39) missense probably damaging 0.99
R6784:Jkampl UTSW 6 73,445,918 (GRCm39) nonsense probably null
R6982:Jkampl UTSW 6 73,446,527 (GRCm39) nonsense probably null
R7990:Jkampl UTSW 6 73,446,528 (GRCm39) missense probably damaging 1.00
R8365:Jkampl UTSW 6 73,446,329 (GRCm39) missense probably benign 0.02
R8381:Jkampl UTSW 6 73,445,895 (GRCm39) missense probably damaging 1.00
R9098:Jkampl UTSW 6 73,446,517 (GRCm39) missense probably benign 0.18
R9363:Jkampl UTSW 6 73,446,487 (GRCm39) missense possibly damaging 0.54
X0024:Jkampl UTSW 6 73,446,033 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- TGCCACCAACACAATGTATGGGAAG -3'
(R):5'- CCAGAAGTACTGTCAGCCTTGCAC -3'

Sequencing Primer
(F):5'- CAATGTATGGGAAGGCATAATATAGG -3'
(R):5'- CTGCGCTATTAGAATGCAGC -3'
Posted On 2014-03-28