Incidental Mutation 'R5533:Krtap19-2'
ID433778
Institutional Source Beutler Lab
Gene Symbol Krtap19-2
Ensembl Gene ENSMUSG00000057650
Gene Namekeratin associated protein 19-2
Synonyms
MMRRC Submission 043091-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.072) question?
Stock #R5533 (G1)
Quality Score225
Status Not validated
Chromosome16
Chromosomal Location88873627-88874269 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 88874108 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000132718 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075284] [ENSMUST00000076186] [ENSMUST00000081334]
Predicted Effect probably benign
Transcript: ENSMUST00000075284
SMART Domains Protein: ENSMUSP00000133176
Gene: ENSMUSG00000060469

DomainStartEndE-ValueType
Pfam:KRTAP 1 56 4.4e-14 PFAM
Pfam:KRTAP 49 81 1.7e-7 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000076186
AA Change: F50L
SMART Domains Protein: ENSMUSP00000075543
Gene: ENSMUSG00000057650
AA Change: F50L

DomainStartEndE-ValueType
Pfam:KRTAP 1 52 3e-11 PFAM
transmembrane domain 83 105 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000081334
SMART Domains Protein: ENSMUSP00000132718
Gene: ENSMUSG00000060691

DomainStartEndE-ValueType
Pfam:KRTAP 1 57 9e-16 PFAM
Coding Region Coverage
  • 1x: 98.4%
  • 3x: 97.1%
  • 10x: 94.5%
  • 20x: 88.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agap2 A G 10: 127,083,042 E429G unknown Het
Akap12 T A 10: 4,357,405 V1405D probably damaging Het
Akap7 C T 10: 25,283,982 D107N possibly damaging Het
Arfgef1 A G 1: 10,199,727 probably null Het
Cacna1s T A 1: 136,098,375 probably null Het
Casc4 AGATGGTGATGGTG AGATGGTG 2: 121,925,697 probably benign Het
Ctsd T C 7: 142,377,333 Q274R probably benign Het
Dysf G A 6: 84,186,471 R1575Q probably damaging Het
Erich6b A T 14: 75,658,834 L53F possibly damaging Het
Exoc6 A C 19: 37,593,770 probably null Het
Fbxw19 A T 9: 109,486,065 V143E probably benign Het
Fkbpl G A 17: 34,645,329 A24T probably benign Het
Fndc1 A G 17: 7,772,776 F696S unknown Het
Foxa3 G T 7: 19,015,015 Y102* probably null Het
Foxn1 A G 11: 78,365,966 M301T probably damaging Het
Foxp2 C T 6: 15,197,120 Q54* probably null Het
Glra1 T C 11: 55,532,382 E117G possibly damaging Het
Glt1d1 A T 5: 127,691,031 D234V probably damaging Het
Gm597 T A 1: 28,778,082 I290F probably damaging Het
Gulp1 T C 1: 44,773,281 I137T probably damaging Het
Itga8 A G 2: 12,160,350 V816A possibly damaging Het
Kdm4c G A 4: 74,315,649 probably benign Het
Lcorl T C 5: 45,733,877 N378S possibly damaging Het
Ltbr G A 6: 125,312,794 R146W probably damaging Het
Mocos T C 18: 24,674,300 L363P probably damaging Het
Mycbp2 G T 14: 103,282,645 Y745* probably null Het
Nav3 A C 10: 109,883,678 N141K possibly damaging Het
Ncor1 T C 11: 62,343,011 N779S probably benign Het
Nebl G T 2: 17,393,268 Y414* probably null Het
Nf1 T G 11: 79,445,789 C1065G probably damaging Het
Nfib A G 4: 82,359,767 V216A probably damaging Het
Nub1 A T 5: 24,702,381 N354I possibly damaging Het
Nyap1 C T 5: 137,735,464 V436I probably benign Het
Olfr1029 A G 2: 85,975,453 D70G possibly damaging Het
Olfr498 T C 7: 108,466,262 F313L probably benign Het
Pde2a T A 7: 101,505,980 M570K probably damaging Het
Pfas T C 11: 68,991,470 S856G probably benign Het
Pkd1l2 T C 8: 117,068,116 E368G probably benign Het
Ptf1a G A 2: 19,447,158 V323M probably damaging Het
Ptprh T C 7: 4,549,505 Y920C probably damaging Het
Sergef T A 7: 46,614,776 D229V possibly damaging Het
Slc1a4 T C 11: 20,304,417 K483R probably benign Het
Slc26a6 G A 9: 108,857,956 R351H probably damaging Het
Slc6a19 G A 13: 73,685,829 T370I possibly damaging Het
Smpd5 T C 15: 76,294,557 S42P possibly damaging Het
Snx13 G A 12: 35,123,026 probably null Het
Sox10 G A 15: 79,156,302 S185L probably benign Het
Srpk1 T C 17: 28,602,759 Y227C probably damaging Het
Stambpl1 T A 19: 34,233,916 probably null Het
Stk36 A G 1: 74,626,591 R698G possibly damaging Het
Tas2r122 T A 6: 132,711,430 T167S probably damaging Het
Tlr12 A G 4: 128,615,863 S865P probably damaging Het
Trp53bp1 A G 2: 121,207,746 L1537P probably damaging Het
Vstm2a C A 11: 16,263,125 T170K possibly damaging Het
Xpo7 A T 14: 70,693,967 F304I probably damaging Het
Zfp286 T C 11: 62,780,970 probably benign Het
Zfp985 A T 4: 147,582,983 K103* probably null Het
Other mutations in Krtap19-2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03372:Krtap19-2 APN 16 88873886 unclassified probably benign
R0520:Krtap19-2 UTSW 16 88873861 unclassified probably benign
R4779:Krtap19-2 UTSW 16 88873874 unclassified probably benign
R5038:Krtap19-2 UTSW 16 88874028 nonsense probably null
R5810:Krtap19-2 UTSW 16 88874236 unclassified probably benign
X0028:Krtap19-2 UTSW 16 88874002 unclassified probably benign
Predicted Primers PCR Primer
(F):5'- GCCAGAGCCATATCCATAGC -3'
(R):5'- GCTGATGCTCACACTCACAATC -3'

Sequencing Primer
(F):5'- AAGCCAGAGCCATATCCATAG -3'
(R):5'- GATGTAACAGCATCCGCA -3'
Posted On2016-10-06