Incidental Mutation 'R2392:Krtap14'
ID 247837
Institutional Source Beutler Lab
Gene Symbol Krtap14
Ensembl Gene ENSMUSG00000074928
Gene Name keratin associated protein 14
Synonyms mKAP13, Pmg1
MMRRC Submission 040360-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R2392 (G1)
Quality Score 225
Status Not validated
Chromosome 16
Chromosomal Location 88622179-88623033 bp(-) (GRCm39)
Type of Mutation splice site (10 bp from exon)
DNA Base Change (assembly) T to A at 88622597 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000136883 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023648] [ENSMUST00000099562] [ENSMUST00000187823] [ENSMUST00000189774]
AlphaFold O08640
Predicted Effect probably benign
Transcript: ENSMUST00000023648
SMART Domains Protein: ENSMUSP00000023648
Gene: ENSMUSG00000022931

DomainStartEndE-ValueType
Pfam:PMG 1 126 1.8e-35 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000099562
SMART Domains Protein: ENSMUSP00000136883
Gene: ENSMUSG00000074928

DomainStartEndE-ValueType
Pfam:PMG 1 67 5.7e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000187823
SMART Domains Protein: ENSMUSP00000140888
Gene: ENSMUSG00000022931

DomainStartEndE-ValueType
Pfam:PMG 1 145 3.3e-38 PFAM
Predicted Effect silent
Transcript: ENSMUST00000189774
SMART Domains Protein: ENSMUSP00000139983
Gene: ENSMUSG00000074928

DomainStartEndE-ValueType
Pfam:PMG 1 166 1.3e-53 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000232467
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.1%
Validation Efficiency 96% (53/55)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 A T 1: 71,297,264 (GRCm39) S2409T probably damaging Het
Acap2 A G 16: 30,958,458 (GRCm39) F120S probably damaging Het
Akr1c6 A G 13: 4,484,477 (GRCm39) probably null Het
Bptf C A 11: 106,963,573 (GRCm39) A1874S probably damaging Het
Ccnl1 A G 3: 65,856,173 (GRCm39) V244A probably damaging Het
Cenpe T G 3: 134,953,874 (GRCm39) L1628R probably damaging Het
Cfap54 A G 10: 92,860,873 (GRCm39) probably null Het
Chchd7 T A 4: 3,943,381 (GRCm39) probably null Het
Col9a2 C G 4: 120,911,455 (GRCm39) R599G probably damaging Het
Crybg2 G T 4: 133,799,925 (GRCm39) V362L probably benign Het
Ddx11 T A 17: 66,456,968 (GRCm39) V791E probably damaging Het
Disp1 G A 1: 182,868,731 (GRCm39) P1230S probably benign Het
Elp5 T C 11: 69,865,928 (GRCm39) H116R probably benign Het
Epb42 T C 2: 120,860,468 (GRCm39) E177G possibly damaging Het
F13a1 T A 13: 37,127,971 (GRCm39) I336F possibly damaging Het
Fabp3 C T 4: 130,206,180 (GRCm39) T57I probably benign Het
Fcsk A G 8: 111,616,356 (GRCm39) M453T probably benign Het
Hacd2 A T 16: 34,926,748 (GRCm39) E249V probably benign Het
Hnrnpf C A 6: 117,901,829 (GRCm39) A371D possibly damaging Het
Jmjd1c A G 10: 67,065,683 (GRCm39) T1703A probably damaging Het
Kcnj13 G A 1: 87,314,622 (GRCm39) T200I possibly damaging Het
Kif1b G A 4: 149,305,077 (GRCm39) T949M possibly damaging Het
Klhl35 G A 7: 99,123,031 (GRCm39) A552T possibly damaging Het
Krt74 A G 15: 101,665,236 (GRCm39) noncoding transcript Het
Lrrc45 A G 11: 120,610,365 (GRCm39) N492S probably benign Het
Lrrcc1 T A 3: 14,601,580 (GRCm39) N114K probably damaging Het
Mfsd2b T C 12: 4,915,164 (GRCm39) D375G possibly damaging Het
Mgat4a A G 1: 37,537,785 (GRCm39) L44P probably damaging Het
Mttp A C 3: 137,800,782 (GRCm39) D774E probably damaging Het
Myo5a T C 9: 75,116,521 (GRCm39) V1554A probably benign Het
Nes C T 3: 87,883,250 (GRCm39) A503V probably benign Het
Nme8 A G 13: 19,873,113 (GRCm39) probably null Het
Nr4a1 A G 15: 101,172,075 (GRCm39) D583G possibly damaging Het
Or12d17 A G 17: 37,777,310 (GRCm39) Y71C probably damaging Het
Or5k14 A G 16: 58,692,797 (GRCm39) S239P probably damaging Het
Pnpla8 T A 12: 44,358,287 (GRCm39) L746I probably damaging Het
Ppp1r7 A T 1: 93,282,063 (GRCm39) I205F probably benign Het
Psd4 C A 2: 24,284,679 (GRCm39) P181Q probably damaging Het
Ripor2 G A 13: 24,890,206 (GRCm39) V694I probably benign Het
Scn10a A G 9: 119,456,268 (GRCm39) S1185P possibly damaging Het
Sec23b T A 2: 144,427,507 (GRCm39) probably null Het
Slfn2 A G 11: 82,956,154 (GRCm39) N12S possibly damaging Het
Slfn4 A G 11: 83,076,248 (GRCm39) K38R possibly damaging Het
Smarca2 G T 19: 26,618,050 (GRCm39) probably null Het
Taar4 A G 10: 23,837,172 (GRCm39) T261A possibly damaging Het
Tbl2 A G 5: 135,185,368 (GRCm39) D159G probably benign Het
Tmem120a T C 5: 135,770,892 (GRCm39) E55G probably damaging Het
Ttc21b A G 2: 66,037,794 (GRCm39) probably null Het
Vill A T 9: 118,896,628 (GRCm39) probably benign Het
Vmn2r28 A T 7: 5,487,130 (GRCm39) M511K probably damaging Het
Vmn2r81 A T 10: 79,110,516 (GRCm39) D543V probably damaging Het
Wdr95 A G 5: 149,504,135 (GRCm39) T314A probably benign Het
Zbtb8b A G 4: 129,326,982 (GRCm39) I61T probably damaging Het
Other mutations in Krtap14
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01298:Krtap14 APN 16 88,622,615 (GRCm39) missense probably benign 0.35
PIT4810001:Krtap14 UTSW 16 88,622,515 (GRCm39) missense probably damaging 1.00
R1471:Krtap14 UTSW 16 88,622,515 (GRCm39) missense probably damaging 1.00
R4927:Krtap14 UTSW 16 88,622,919 (GRCm39) missense possibly damaging 0.90
R5339:Krtap14 UTSW 16 88,622,747 (GRCm39) missense probably benign 0.05
R9442:Krtap14 UTSW 16 88,622,865 (GRCm39) missense possibly damaging 0.68
Predicted Primers
Posted On 2014-11-11