Incidental Mutation 'R0497:Krt73'
ID 40562
Institutional Source Beutler Lab
Gene Symbol Krt73
Ensembl Gene ENSMUSG00000063661
Gene Name keratin 73
Synonyms
MMRRC Submission 038693-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.161) question?
Stock # R0497 (G1)
Quality Score 95
Status Validated
Chromosome 15
Chromosomal Location 101793308-101802346 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 101802230 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 23 (L23P)
Ref Sequence ENSEMBL: ENSMUSP00000065349 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063292]
AlphaFold Q6NXH9
Predicted Effect probably damaging
Transcript: ENSMUST00000063292
AA Change: L23P

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000065349
Gene: ENSMUSG00000063661
AA Change: L23P

DomainStartEndE-ValueType
low complexity region 17 57 N/A INTRINSIC
Pfam:Keratin_2_head 59 127 1.4e-19 PFAM
Filament 130 443 5.39e-159 SMART
low complexity region 450 461 N/A INTRINSIC
low complexity region 466 481 N/A INTRINSIC
Meta Mutation Damage Score 0.2075 question?
Coding Region Coverage
  • 1x: 99.6%
  • 3x: 98.7%
  • 10x: 96.6%
  • 20x: 93.1%
Validation Efficiency 100% (68/68)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene encodes a protein that is expressed in the inner root sheath of hair follicles. The type II keratins are clustered in a region of chromosome 12q13.[provided by RefSeq, Jun 2009]
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aatk A C 11: 120,018,780 (GRCm38) V110G probably damaging Het
Adcy6 A C 15: 98,597,725 (GRCm38) probably null Het
Adm A G 7: 110,629,121 (GRCm38) T170A probably benign Het
Afap1l2 G T 19: 56,930,209 (GRCm38) N171K probably benign Het
Aph1b G T 9: 66,790,618 (GRCm38) S112* probably null Het
Arhgap23 A G 11: 97,452,163 (GRCm38) S424G probably damaging Het
Asah2 T A 19: 32,054,631 (GRCm38) N46I probably benign Het
Braf G A 6: 39,640,549 (GRCm38) probably benign Het
Brd2 C T 17: 34,114,360 (GRCm38) R47Q probably damaging Het
C2cd5 A G 6: 143,012,093 (GRCm38) V972A probably benign Het
Car9 T A 4: 43,511,881 (GRCm38) L300H probably damaging Het
Chmp3 T C 6: 71,552,411 (GRCm38) S20P probably damaging Het
Chp1 A G 2: 119,571,782 (GRCm38) N79S possibly damaging Het
Cnot2 A T 10: 116,498,355 (GRCm38) I335N probably damaging Het
Cntnap4 T C 8: 112,570,151 (GRCm38) V6A probably benign Het
Ctcf T A 8: 105,675,040 (GRCm38) probably benign Het
Dennd1b A G 1: 139,039,986 (GRCm38) probably benign Het
Dnmbp A G 19: 43,856,640 (GRCm38) probably benign Het
Eef2 T C 10: 81,181,586 (GRCm38) F782L probably benign Het
Eogt T A 6: 97,135,233 (GRCm38) Y153F probably benign Het
Fam81a G T 9: 70,096,119 (GRCm38) Q237K possibly damaging Het
Fat2 T A 11: 55,283,402 (GRCm38) T2162S probably benign Het
Fcgbpl1 T A 7: 28,147,465 (GRCm38) C1158S probably damaging Het
Gas6 T C 8: 13,470,387 (GRCm38) I434V possibly damaging Het
Gm42417 A T 1: 36,532,167 (GRCm38) L77Q probably damaging Het
Grik3 A T 4: 125,623,510 (GRCm38) N49Y possibly damaging Het
Gucy2e A T 11: 69,224,159 (GRCm38) V974E probably damaging Het
Helz2 A G 2: 181,229,656 (GRCm38) V2721A probably damaging Het
Klhl6 GT G 16: 19,956,966 (GRCm38) 279 probably null Het
L3mbtl3 T C 10: 26,282,874 (GRCm38) probably benign Het
Lrrc15 A T 16: 30,272,892 (GRCm38) V543E probably damaging Het
Med13 G A 11: 86,276,983 (GRCm38) probably benign Het
Med25 T C 7: 44,892,100 (GRCm38) D60G probably damaging Het
Mgam T A 6: 40,664,892 (GRCm38) Y560N probably damaging Het
Mlkl A G 8: 111,327,873 (GRCm38) Y211H probably damaging Het
Msl2 A G 9: 101,101,294 (GRCm38) N289S probably benign Het
Nwd2 G T 5: 63,806,343 (GRCm38) W1090L probably damaging Het
Omt2b T C 9: 78,328,231 (GRCm38) probably benign Het
Or4k37 A G 2: 111,328,830 (GRCm38) D137G probably benign Het
Pald1 A G 10: 61,341,315 (GRCm38) L652P probably damaging Het
Pard3b T A 1: 62,440,008 (GRCm38) probably null Het
Prdm15 G A 16: 97,794,334 (GRCm38) T1098I possibly damaging Het
Rock2 A G 12: 16,954,953 (GRCm38) T436A probably benign Het
Sema4c A T 1: 36,549,608 (GRCm38) D812E probably benign Het
Sla A T 15: 66,792,249 (GRCm38) I91K probably benign Het
Slc22a16 T G 10: 40,584,967 (GRCm38) M255R probably damaging Het
Slc49a4 A T 16: 35,735,604 (GRCm38) V162D probably benign Het
Smg8 C T 11: 87,086,084 (GRCm38) D224N possibly damaging Het
Spdef A T 17: 27,718,058 (GRCm38) D190E probably benign Het
Taok1 A G 11: 77,573,804 (GRCm38) I152T probably damaging Het
Tmem220 A G 11: 67,025,922 (GRCm38) D36G probably damaging Het
Tmem235 A C 11: 117,864,351 (GRCm38) I210L probably benign Het
Tmem266 C T 9: 55,380,884 (GRCm38) probably null Het
Tmprss12 A G 15: 100,281,039 (GRCm38) probably benign Het
Trim32 G A 4: 65,613,254 (GRCm38) R16Q probably damaging Het
Usp38 T A 8: 80,984,424 (GRCm38) probably benign Het
Usp44 C T 10: 93,846,806 (GRCm38) P373S possibly damaging Het
Vmn1r209 G T 13: 22,805,948 (GRCm38) Q191K probably damaging Het
Vmn1r70 T C 7: 10,634,026 (GRCm38) I147T probably benign Het
Vmn2r107 T A 17: 20,375,132 (GRCm38) I649N probably damaging Het
Vmn2r12 A T 5: 109,091,889 (GRCm38) Y269* probably null Het
Zan C T 5: 137,412,676 (GRCm38) probably benign Het
Zfp616 G T 11: 74,083,480 (GRCm38) V192L probably benign Het
Zfp644 A T 5: 106,638,333 (GRCm38) V116D probably damaging Het
Zgrf1 T C 3: 127,584,650 (GRCm38) probably benign Het
Zhx3 A T 2: 160,779,994 (GRCm38) L751* probably null Het
Znfx1 T A 2: 167,055,411 (GRCm38) Q531L probably benign Het
Other mutations in Krt73
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01082:Krt73 APN 15 101,798,937 (GRCm38) critical splice acceptor site probably null
IGL01768:Krt73 APN 15 101,798,856 (GRCm38) missense probably benign 0.01
IGL01836:Krt73 APN 15 101,795,896 (GRCm38) missense probably benign 0.38
IGL02058:Krt73 APN 15 101,802,021 (GRCm38) missense probably benign
IGL02063:Krt73 APN 15 101,795,769 (GRCm38) splice site probably benign
IGL02076:Krt73 APN 15 101,799,935 (GRCm38) missense probably damaging 1.00
IGL02878:Krt73 APN 15 101,798,826 (GRCm38) missense probably damaging 1.00
IGL03127:Krt73 APN 15 101,795,840 (GRCm38) missense probably benign
R0032:Krt73 UTSW 15 101,794,052 (GRCm38) missense probably benign 0.30
R0109:Krt73 UTSW 15 101,796,395 (GRCm38) nonsense probably null
R0143:Krt73 UTSW 15 101,800,773 (GRCm38) missense probably damaging 1.00
R0233:Krt73 UTSW 15 101,802,016 (GRCm38) missense probably benign 0.12
R0233:Krt73 UTSW 15 101,802,016 (GRCm38) missense probably benign 0.12
R0254:Krt73 UTSW 15 101,799,889 (GRCm38) splice site probably benign
R0256:Krt73 UTSW 15 101,801,936 (GRCm38) missense probably damaging 1.00
R1592:Krt73 UTSW 15 101,802,239 (GRCm38) nonsense probably null
R1681:Krt73 UTSW 15 101,802,047 (GRCm38) missense possibly damaging 0.70
R1696:Krt73 UTSW 15 101,799,909 (GRCm38) missense probably damaging 1.00
R1766:Krt73 UTSW 15 101,793,928 (GRCm38) missense probably damaging 1.00
R2031:Krt73 UTSW 15 101,798,764 (GRCm38) splice site probably benign
R2171:Krt73 UTSW 15 101,800,910 (GRCm38) missense possibly damaging 0.88
R4674:Krt73 UTSW 15 101,802,075 (GRCm38) missense probably benign 0.22
R4777:Krt73 UTSW 15 101,794,001 (GRCm38) missense probably benign
R4869:Krt73 UTSW 15 101,796,398 (GRCm38) missense probably damaging 1.00
R4892:Krt73 UTSW 15 101,795,809 (GRCm38) missense probably damaging 0.99
R5794:Krt73 UTSW 15 101,794,829 (GRCm38) missense probably benign 0.00
R6807:Krt73 UTSW 15 101,796,407 (GRCm38) missense probably damaging 1.00
R6885:Krt73 UTSW 15 101,796,398 (GRCm38) missense probably damaging 1.00
R7489:Krt73 UTSW 15 101,793,859 (GRCm38) missense probably benign 0.00
R7682:Krt73 UTSW 15 101,802,045 (GRCm38) missense probably benign 0.08
R9167:Krt73 UTSW 15 101,793,970 (GRCm38) missense probably benign 0.00
R9795:Krt73 UTSW 15 101,802,290 (GRCm38) missense probably damaging 1.00
Z1177:Krt73 UTSW 15 101,793,811 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGACTGTTACCTGGTGGATGCCTC -3'
(R):5'- ACGGCCTAGCTAATTACCCCATGC -3'

Sequencing Primer
(F):5'- ATTTGAAGGCCCCAGAGC -3'
(R):5'- TGCAAGCCCAGCACTTTG -3'
Posted On 2013-05-23