Mutagenetix > Incidental Mutation

Incidental Mutation 'R0497:Krt73'

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

Status

Validated

Chromosome

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

Domain	Start	End	E-Value	Type
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

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
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
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

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH 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