Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00870:Krtap20-2'

11704

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Krtap20-2

Ensembl Gene

ENSMUSG00000091039

Gene Name

keratin associated protein 20-2

Synonyms

1190004K03Rik, Gm6371

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.195) question?

Stock #

IGL00870

Quality Score

Status

Chromosome

Chromosomal Location

89002749-89003282 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 89002875 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Aspartic acid at position 25 (G25D)

Ref Sequence

ENSEMBL: ENSMUSP00000126264 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000169954]

AlphaFold

E9Q0A8

Predicted Effect

unknown
Transcript: ENSMUST00000169954
AA Change: G25D

SMART Domains

Protein: ENSMUSP00000126264
Gene: ENSMUSG00000091039
AA Change: G25D

Domain	Start	End	E-Value	Type
Pfam:KRTAP	1	54	3e-14	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 31 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahnak	T	A	19: 8,991,062 (GRCm39)	D4115E	probably damaging	Het
Asb5	T	C	8: 55,036,695 (GRCm39)		probably null	Het
Cpeb3	A	T	19: 37,031,695 (GRCm39)	I569N	probably damaging	Het
Cpsf7	T	C	19: 10,517,014 (GRCm39)		probably null	Het
Dlat	A	G	9: 50,562,169 (GRCm39)	L285P	probably damaging	Het
Dytn	T	C	1: 63,716,272 (GRCm39)		probably benign	Het
Ears2	A	T	7: 121,654,899 (GRCm39)	L123Q	probably damaging	Het
Gad2	T	C	2: 22,519,983 (GRCm39)	V212A	probably benign	Het
Gon4l	T	C	3: 88,764,492 (GRCm39)	Y358H	probably damaging	Het
Gys1	T	C	7: 45,097,437 (GRCm39)		probably null	Het
Hnrnpm	C	A	17: 33,868,876 (GRCm39)	R517L	probably damaging	Het
Lrif1	T	C	3: 106,641,957 (GRCm39)		probably null	Het
Naip2	A	G	13: 100,288,568 (GRCm39)		probably benign	Het
Or8b37	A	T	9: 37,959,036 (GRCm39)	I173F	probably damaging	Het
Oxct1	T	A	15: 4,131,300 (GRCm39)	L396Q	probably damaging	Het
Pclo	A	T	5: 14,589,997 (GRCm39)	R766W	unknown	Het
Pkhd1	T	A	1: 20,641,614 (GRCm39)	I275F	probably damaging	Het
Rxfp3	A	G	15: 11,036,301 (GRCm39)	F357S	probably damaging	Het
Rxfp3	A	G	15: 11,036,391 (GRCm39)	V327A	probably damaging	Het
Serpinb2	A	G	1: 107,450,800 (GRCm39)	I181V	probably damaging	Het
Smad5	A	G	13: 56,871,480 (GRCm39)	D25G	probably benign	Het
Strada	A	G	11: 106,062,083 (GRCm39)	L82P	probably damaging	Het
Tek	T	A	4: 94,761,318 (GRCm39)	Y1079*	probably null	Het
Tenm3	T	C	8: 48,870,167 (GRCm39)	T209A	probably benign	Het
Tnks1bp1	C	T	2: 84,892,580 (GRCm39)	Q836*	probably null	Het
Toporsl	T	C	4: 52,610,172 (GRCm39)	S22P	probably benign	Het
Ttc17	T	C	2: 94,202,078 (GRCm39)		probably null	Het
Ttc39a	A	G	4: 109,299,542 (GRCm39)		probably benign	Het
Vangl1	T	C	3: 102,096,756 (GRCm39)	D60G	probably damaging	Het
Vmn1r13	A	T	6: 57,187,098 (GRCm39)	M86L	probably benign	Het
Vmn1r220	C	T	13: 23,368,647 (GRCm39)	M16I	probably null	Het

Other mutations in Krtap20-2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01634:Krtap20-2	APN	16	89,002,977 (GRCm39)	missense	unknown
R5086:Krtap20-2	UTSW	16	89,002,806 (GRCm39)	missense	unknown

Posted On

2012-12-06