Mutagenetix > Incidental Mutation

Incidental Mutation 'R7090:Krt35'

568537

Institutional Source

Beutler Lab

Gene Symbol

Krt35

Ensembl Gene

ENSMUSG00000048013

Gene Name

keratin 35

Synonyms

Ha5, Krt1-24

MMRRC Submission

045184-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.143) question?

Stock #

R7090 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

99983018-99987050 bp(-) (GRCm39)

Type of Mutation

splice site (44 bp from exon)

DNA Base Change (assembly)

A to T at 99986498 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000099416 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000103127]

AlphaFold

Q497I4

Predicted Effect

probably null
Transcript: ENSMUST00000103127

SMART Domains

Protein: ENSMUSP00000099416
Gene: ENSMUSG00000048013

Domain	Start	End	E-Value	Type
low complexity region	33	43	N/A	INTRINSIC
low complexity region	74	86	N/A	INTRINSIC
Filament	96	407	3.32e-159	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (66/66)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the keratin gene family. This type I hair keratin is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Calm3	A	T	7: 16,651,004 (GRCm39)	Y139*	probably null	Het
Ccdc27	T	C	4: 154,112,523 (GRCm39)	N584S	probably benign	Het
Cdh24	C	G	14: 54,876,964 (GRCm39)	G13A	probably damaging	Het
Chd8	T	C	14: 52,452,677 (GRCm39)	K1281E	probably damaging	Het
Clasp1	G	T	1: 118,409,816 (GRCm39)	G4C	probably benign	Het
Cul9	G	T	17: 46,811,765 (GRCm39)	P2488T	probably damaging	Het
Daam2	A	G	17: 49,789,973 (GRCm39)	V428A	probably damaging	Het
Dcaf8	A	G	1: 172,016,535 (GRCm39)	S441G	probably damaging	Het
Dchs2	A	G	3: 83,255,581 (GRCm39)	T2426A	probably benign	Het
Dnai3	C	A	3: 145,746,582 (GRCm39)	K881N	possibly damaging	Het
Dpys	A	G	15: 39,690,279 (GRCm39)	V358A	probably damaging	Het
Efhd1	A	G	1: 87,217,219 (GRCm39)	D112G	probably damaging	Het
Exoc1	T	C	5: 76,714,800 (GRCm39)	S120P	unknown	Het
Fyco1	A	G	9: 123,626,784 (GRCm39)	L1309S	probably damaging	Het
Gm14403	A	G	2: 177,201,114 (GRCm39)	N111S	possibly damaging	Het
Gm5901	A	G	7: 105,026,555 (GRCm39)	T108A	probably benign	Het
Idh2	TCCCAGG	T	7: 79,748,079 (GRCm39)		probably benign	Het
Itgb5	T	G	16: 33,705,464 (GRCm39)	D251E	probably damaging	Het
Kcnk15	T	C	2: 163,700,637 (GRCm39)	V292A	probably benign	Het
Kdm2a	A	T	19: 4,369,169 (GRCm39)	Y1149N	probably damaging	Het
Kdm3a	T	C	6: 71,572,529 (GRCm39)	T1011A	possibly damaging	Het
Lipn	T	A	19: 34,049,180 (GRCm39)	D115E	possibly damaging	Het
Lpin3	T	G	2: 160,738,672 (GRCm39)	L208R	probably damaging	Het
Ltf	C	A	9: 110,855,048 (GRCm39)	Q354K	probably benign	Het
Marf1	C	A	16: 13,929,566 (GRCm39)	C1680F	possibly damaging	Het
Mtss2	T	A	8: 111,456,656 (GRCm39)	V242E	probably damaging	Het
Myo7b	T	C	18: 32,131,765 (GRCm39)	Y477C	probably damaging	Het
Nbn	T	A	4: 15,981,350 (GRCm39)	S481T	probably benign	Het
Ncoa2	A	G	1: 13,257,062 (GRCm39)	Y146H	probably damaging	Het
Ntng1	A	T	3: 109,842,496 (GRCm39)	C92*	probably null	Het
Or10ad1b	C	T	15: 98,125,083 (GRCm39)	V150I	probably benign	Het
Or2n1b	G	A	17: 38,460,385 (GRCm39)	G302D	probably benign	Het
Or8k18	T	A	2: 86,085,420 (GRCm39)	N206Y	probably damaging	Het
Or8k31-ps1	T	C	2: 86,356,471 (GRCm39)	I17V	probably benign	Het
Os9	A	T	10: 126,935,547 (GRCm39)	S308T	probably benign	Het
Otx2	T	A	14: 48,896,192 (GRCm39)	T289S	probably benign	Het
Pakap	C	T	4: 57,648,042 (GRCm39)	A60V	probably benign	Het
Pigg	A	G	5: 108,484,378 (GRCm39)	T675A	possibly damaging	Het
Pink1	C	T	4: 138,042,912 (GRCm39)	E461K	probably damaging	Het
Pip5k1a	A	G	3: 94,967,809 (GRCm39)	S543P	possibly damaging	Het
Prkaa1	A	G	15: 5,206,611 (GRCm39)	T454A	probably benign	Het
Ptk2	G	A	15: 73,093,658 (GRCm39)	P854S	possibly damaging	Het
Rab31	C	T	17: 66,005,012 (GRCm39)	V83I	possibly damaging	Het
Rabggtb	G	T	3: 153,615,986 (GRCm39)	D117E	probably benign	Het
Rbl1	T	C	2: 156,994,820 (GRCm39)	H951R	probably benign	Het
Sapcd2	A	G	2: 25,266,091 (GRCm39)	S314G	probably benign	Het
Septin4	T	C	11: 87,475,264 (GRCm39)	L164P	probably damaging	Het
Shroom1	A	G	11: 53,356,760 (GRCm39)	E541G	probably damaging	Het
Slc26a7	C	A	4: 14,565,460 (GRCm39)	G208*	probably null	Het
Smco2	A	G	6: 146,772,711 (GRCm39)	I304M	probably damaging	Het
Spg7	T	C	8: 123,818,491 (GRCm39)		probably null	Het
Spocd1	T	C	4: 129,847,691 (GRCm39)	F552L		Het
St6galnac2	T	C	11: 116,568,461 (GRCm39)	D334G	probably damaging	Het
Sub1	A	G	15: 11,986,572 (GRCm39)	S92P	probably benign	Het
Syne2	T	C	12: 75,989,125 (GRCm39)	F1829L	probably benign	Het
Tdrd1	T	C	19: 56,839,833 (GRCm39)	V631A	probably benign	Het
Tdrd9	T	C	12: 111,958,904 (GRCm39)	S113P	probably benign	Het
Tgfbrap1	A	C	1: 43,110,725 (GRCm39)	V260G	probably damaging	Het
Tyw3	G	C	3: 154,299,426 (GRCm39)	S94R	probably benign	Het
Urb2	T	C	8: 124,757,338 (GRCm39)	V1015A	probably benign	Het
Usp5	A	G	6: 124,806,357 (GRCm39)	M1T	probably null	Het
Utrn	T	C	10: 12,560,260 (GRCm39)	D1343G	possibly damaging	Het
Vmn2r56	T	C	7: 12,449,254 (GRCm39)	Y328C	probably damaging	Het
Vmn2r99	A	T	17: 19,613,972 (GRCm39)	E564V	possibly damaging	Het
Zc3h8	T	C	2: 128,777,241 (GRCm39)	T133A	possibly damaging	Het

Other mutations in Krt35

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00742:Krt35	APN	11	99,984,785 (GRCm39)	missense	probably damaging	1.00
IGL01528:Krt35	APN	11	99,985,420 (GRCm39)	missense	probably damaging	1.00
IGL02552:Krt35	APN	11	99,983,899 (GRCm39)	missense	probably benign	0.39
IGL02583:Krt35	APN	11	99,983,360 (GRCm39)	missense	possibly damaging	0.66
IGL03276:Krt35	APN	11	99,983,953 (GRCm39)	missense	probably benign	0.39
R0011:Krt35	UTSW	11	99,984,502 (GRCm39)	missense	probably benign	0.10
R0282:Krt35	UTSW	11	99,986,573 (GRCm39)	missense	probably damaging	0.99
R0692:Krt35	UTSW	11	99,983,896 (GRCm39)	missense	possibly damaging	0.92
R0737:Krt35	UTSW	11	99,984,620 (GRCm39)	missense	probably benign	0.33
R0750:Krt35	UTSW	11	99,986,979 (GRCm39)	missense	possibly damaging	0.69
R1815:Krt35	UTSW	11	99,986,565 (GRCm39)	missense	probably benign	0.02
R2218:Krt35	UTSW	11	99,986,988 (GRCm39)	missense	probably null
R2262:Krt35	UTSW	11	99,986,593 (GRCm39)	missense	probably benign	0.01
R4519:Krt35	UTSW	11	99,985,453 (GRCm39)	missense	possibly damaging	0.50
R4575:Krt35	UTSW	11	99,986,725 (GRCm39)	missense	probably benign	0.40
R4599:Krt35	UTSW	11	99,984,834 (GRCm39)	missense	probably damaging	1.00
R4887:Krt35	UTSW	11	99,983,956 (GRCm39)	missense	probably damaging	1.00
R5140:Krt35	UTSW	11	99,985,343 (GRCm39)	missense	probably damaging	1.00
R5159:Krt35	UTSW	11	99,984,875 (GRCm39)	missense	probably damaging	1.00
R5575:Krt35	UTSW	11	99,985,450 (GRCm39)	missense	probably damaging	1.00
R5909:Krt35	UTSW	11	99,986,639 (GRCm39)	missense	probably damaging	0.99
R6738:Krt35	UTSW	11	99,984,535 (GRCm39)	missense	probably damaging	1.00
R7163:Krt35	UTSW	11	99,986,984 (GRCm39)	missense	probably damaging	0.99
R7797:Krt35	UTSW	11	99,985,713 (GRCm39)	missense	probably damaging	1.00
R8716:Krt35	UTSW	11	99,987,011 (GRCm39)	start codon destroyed	probably null	0.98
R9480:Krt35	UTSW	11	99,986,609 (GRCm39)	missense	probably benign	0.24
Z1177:Krt35	UTSW	11	99,986,883 (GRCm39)	missense	probably benign	0.05

Predicted Primers

PCR Primer
(F):5'- AAAGGTGTCTTCTCTGCTTTACAG -3'
(R):5'- AGCTATCTGGAGAAGGTGCG -3'

Sequencing Primer
(F):5'- TGCCTCTTTAGAACAAGGGC -3'
(R):5'- AGAAGGTGCGCCAGCTG -3'

Posted On

2019-08-16