Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02511:Krtap31-2'

296546

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Krtap31-2

Ensembl Gene

ENSMUSG00000051481

Gene Name

keratin associated protein 31-2

Synonyms

OTTMUSG00000002177

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.089) question?

Stock #

IGL02511

Quality Score

Status

Chromosome

Chromosomal Location

99827117-99828051 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 99827518 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 117 (C117S)

Ref Sequence

ENSEMBL: ENSMUSP00000055035 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000058761]

AlphaFold

Q8CAY5

Predicted Effect

possibly damaging
Transcript: ENSMUST00000058761
AA Change: C117S

PolyPhen 2 Score 0.711 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000055035
Gene: ENSMUSG00000051481
AA Change: C117S

Domain	Start	End	E-Value	Type
low complexity region	8	29	N/A	INTRINSIC
low complexity region	40	56	N/A	INTRINSIC
Pfam:Keratin_B2_2	64	107	1.7e-9	PFAM
Pfam:Keratin_B2_2	110	156	7.3e-6	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000117567

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Accsl	A	T	2: 93,692,111 (GRCm39)		probably benign	Het
Adam3	T	A	8: 25,185,192 (GRCm39)	D502V	probably damaging	Het
Adss2	T	C	1: 177,598,700 (GRCm39)		probably benign	Het
Ankrd36	T	A	11: 5,610,845 (GRCm39)		probably null	Het
Atf6b	T	C	17: 34,873,615 (GRCm39)	S692P	probably benign	Het
Cap2	T	C	13: 46,684,498 (GRCm39)	M1T	probably null	Het
Cdc45	C	T	16: 18,617,479 (GRCm39)	M200I	probably benign	Het
Cntn1	A	T	15: 92,114,266 (GRCm39)		probably benign	Het
Copg2	A	T	6: 30,835,757 (GRCm39)	F218Y	probably benign	Het
Dll4	G	A	2: 119,156,947 (GRCm39)	G73E	probably damaging	Het
Dzip3	T	C	16: 48,757,343 (GRCm39)	M897V	possibly damaging	Het
Ehbp1	T	C	11: 22,039,653 (GRCm39)	R816G	probably damaging	Het
Enoph1	T	C	5: 100,208,894 (GRCm39)	L83P	probably benign	Het
Enpep	A	G	3: 129,115,059 (GRCm39)	S238P	probably damaging	Het
Fermt1	A	C	2: 132,775,086 (GRCm39)		probably benign	Het
Gm6619	T	A	6: 131,467,330 (GRCm39)	I65K	possibly damaging	Het
Ksr1	T	C	11: 78,936,046 (GRCm39)	D106G	possibly damaging	Het
Lgr4	A	T	2: 109,841,617 (GRCm39)	Y534F	probably benign	Het
Mamdc2	T	C	19: 23,356,095 (GRCm39)	T118A	probably benign	Het
Myo10	T	A	15: 25,723,975 (GRCm39)	I170N	probably damaging	Het
Myom2	T	C	8: 15,115,743 (GRCm39)	S53P	probably benign	Het
Npl	T	A	1: 153,391,227 (GRCm39)	D176V	probably damaging	Het
Nrm	T	C	17: 36,172,316 (GRCm39)	S14P	probably damaging	Het
Or5al7	A	G	2: 85,992,363 (GRCm39)	I310T	probably benign	Het
Or5p70	T	A	7: 107,995,265 (GRCm39)	F313I	probably benign	Het
Or5v1b	A	G	17: 37,840,870 (GRCm39)	M1V	probably null	Het
Papola	T	A	12: 105,775,604 (GRCm39)	C204S	probably damaging	Het
Pard3	A	T	8: 127,888,070 (GRCm39)		probably benign	Het
Pdzd4	T	A	X: 72,838,206 (GRCm39)	M701L	probably damaging	Het
Pkhd1	A	T	1: 20,143,731 (GRCm39)	V3865E	possibly damaging	Het
Plxna3	C	A	X: 73,378,991 (GRCm39)	Q712K	probably damaging	Het
Pon1	A	G	6: 5,193,724 (GRCm39)	L9P	probably damaging	Het
Pygm	A	T	19: 6,435,718 (GRCm39)	I83F	probably benign	Het
Scyl2	A	G	10: 89,476,681 (GRCm39)	S815P	probably benign	Het
Serpina1a	C	T	12: 103,822,226 (GRCm39)	W212*	probably null	Het
Slc38a9	C	A	13: 112,834,541 (GRCm39)	D239E	possibly damaging	Het
Smad6	A	G	9: 63,860,859 (GRCm39)	F479L	probably damaging	Het
Smarcc2	T	C	10: 128,297,251 (GRCm39)	S48P	probably damaging	Het
Ttn	T	A	2: 76,768,034 (GRCm39)	M3022L	unknown	Het
Tulp1	C	A	17: 28,575,142 (GRCm39)	R441L	probably benign	Het
Ugt1a10	T	C	1: 87,983,585 (GRCm39)	F128L	probably damaging	Het
Ulk4	A	G	9: 121,017,420 (GRCm39)	V686A	probably damaging	Het
Ush2a	T	C	1: 188,475,884 (GRCm39)		probably null	Het
Ushbp1	T	C	8: 71,843,581 (GRCm39)	M286V	probably null	Het
Usp51	T	G	X: 151,791,726 (GRCm39)	I440R	probably damaging	Het
Wee1	G	T	7: 109,738,483 (GRCm39)	R532L	possibly damaging	Het
Zfhx4	A	G	3: 5,464,243 (GRCm39)	E1467G	probably damaging	Het
Zfp13	C	T	17: 23,795,072 (GRCm39)	A493T	probably benign	Het
Zfp551	A	G	7: 12,150,602 (GRCm39)	V269A	possibly damaging	Het

Other mutations in Krtap31-2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
PIT4378001:Krtap31-2	UTSW	11	99,827,542 (GRCm39)	missense	possibly damaging	0.71
R0243:Krtap31-2	UTSW	11	99,827,572 (GRCm39)	missense	possibly damaging	0.71
R4751:Krtap31-2	UTSW	11	99,827,402 (GRCm39)	missense	possibly damaging	0.71
R4987:Krtap31-2	UTSW	11	99,827,396 (GRCm39)	missense	possibly damaging	0.92
R5500:Krtap31-2	UTSW	11	99,827,173 (GRCm39)	missense	possibly damaging	0.53
R6789:Krtap31-2	UTSW	11	99,827,549 (GRCm39)	missense	possibly damaging	0.86
R7519:Krtap31-2	UTSW	11	99,827,501 (GRCm39)	missense	possibly damaging	0.96
R7614:Krtap31-2	UTSW	11	99,827,429 (GRCm39)	missense	possibly damaging	0.52
R7890:Krtap31-2	UTSW	11	99,827,377 (GRCm39)	missense	possibly damaging	0.71

Posted On

2015-04-16