Mutagenetix > Incidental Mutation

Incidental Mutation 'R2392:Krt74'

247833

Institutional Source

Beutler Lab

Gene Symbol

Krt74

Ensembl Gene

ENSMUSG00000067596

Gene Name

keratin 74

Synonyms

Kb37

MMRRC Submission

040360-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2392 (G1)

Quality Score

197

Status

Validated

Chromosome

Chromosomal Location

101662694-101671939 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 101665236 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000088018]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000088018

SMART Domains

Protein: ENSMUSP00000085335
Gene: ENSMUSG00000067596

Domain	Start	End	E-Value	Type
Pfam:Keratin_2_head	1	102	9e-21	PFAM
Filament	105	418	6.41e-143	SMART
low complexity region	425	440	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000229279

Meta Mutation Damage Score

0.0869

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
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
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
Krtap14	T	A	16: 88,622,597 (GRCm39)		probably null	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 Krt74

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02027:Krt74	APN	15	101,665,229 (GRCm39)	exon	noncoding transcript
IGL02376:Krt74	APN	15	101,662,938 (GRCm39)	exon	noncoding transcript
IGL02507:Krt74	APN	15	101,669,059 (GRCm39)	exon	noncoding transcript
IGL03374:Krt74	APN	15	101,668,937 (GRCm39)	splice site	noncoding transcript
R0032:Krt74	UTSW	15	101,669,887 (GRCm39)	exon	noncoding transcript
R0032:Krt74	UTSW	15	101,669,887 (GRCm39)	exon	noncoding transcript
R0110:Krt74	UTSW	15	101,671,751 (GRCm39)	exon	noncoding transcript
R0450:Krt74	UTSW	15	101,671,751 (GRCm39)	exon	noncoding transcript
R0469:Krt74	UTSW	15	101,671,751 (GRCm39)	exon	noncoding transcript
R0510:Krt74	UTSW	15	101,671,751 (GRCm39)	exon	noncoding transcript
R0550:Krt74	UTSW	15	101,669,114 (GRCm39)	splice site	noncoding transcript
R0558:Krt74	UTSW	15	101,669,398 (GRCm39)	exon	noncoding transcript
R1663:Krt74	UTSW	15	101,665,109 (GRCm39)	exon	noncoding transcript
R3772:Krt74	UTSW	15	101,670,630 (GRCm39)	exon	noncoding transcript
R4167:Krt74	UTSW	15	101,667,304 (GRCm39)	exon	noncoding transcript
R4670:Krt74	UTSW	15	101,667,304 (GRCm39)	exon	noncoding transcript
R4741:Krt74	UTSW	15	101,669,876 (GRCm39)	exon	noncoding transcript
R5470:Krt74	UTSW	15	101,662,900 (GRCm39)	exon	noncoding transcript
R5639:Krt74	UTSW	15	101,665,195 (GRCm39)	exon	noncoding transcript
R5664:Krt74	UTSW	15	101,669,014 (GRCm39)	exon	noncoding transcript
R6274:Krt74	UTSW	15	101,671,872 (GRCm39)	exon	noncoding transcript

Predicted Primers

PCR Primer
(F):5'- ACGTCCAGTGACAGCTTCAG -3'
(R):5'- AAGGCTACTCTGTTACTCTACCACAG -3'

Sequencing Primer
(F):5'- TGACAGCTTCAGGCCCATGAG -3'
(R):5'- AGTCTATCATGACAGGCTGC -3'

Posted On

2014-11-11