Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03375:Krtap6-5'

420468

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Krtap6-5

Ensembl Gene

ENSMUSG00000062400

Gene Name

keratin associated protein 6-5

Synonyms

Krtap16-8, 1110002D05Rik

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL03375

Quality Score

Status

Chromosome

Chromosomal Location

88844177-88844771 bp(-) (GRCm39)

Type of Mutation

utr 5 prime

DNA Base Change (assembly)

T to G at 88844740 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000074211 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000074637]

AlphaFold

Q925H3

Predicted Effect

probably benign
Transcript: ENSMUST00000074637

SMART Domains

Protein: ENSMUSP00000074211
Gene: ENSMUSG00000062400

Domain	Start	End	E-Value	Type
Pfam:KRTAP	1	62	6.6e-8	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 36 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arhgap31	A	G	16: 38,423,190 (GRCm39)	S959P	probably damaging	Het
Arrb2	G	A	11: 70,327,005 (GRCm39)	G24D	probably damaging	Het
Catsper4	A	G	4: 133,945,519 (GRCm39)	I180T	probably damaging	Het
Chst15	G	A	7: 131,872,186 (GRCm39)	Q32*	probably null	Het
Cntnap5c	A	T	17: 58,469,200 (GRCm39)	Y594F	possibly damaging	Het
Cse1l	T	A	2: 166,784,977 (GRCm39)		probably benign	Het
Dab1	A	T	4: 104,538,798 (GRCm39)	I201F	possibly damaging	Het
Eif2ak4	T	C	2: 118,252,799 (GRCm39)	V457A	probably benign	Het
Fkbp1b	T	C	12: 4,888,220 (GRCm39)		probably benign	Het
Fryl	C	A	5: 73,245,792 (GRCm39)	V1122F	possibly damaging	Het
Gas2l2	A	G	11: 83,317,036 (GRCm39)		probably benign	Het
Gstt2	A	T	10: 75,668,655 (GRCm39)		probably null	Het
H4c14	T	C	3: 96,170,458 (GRCm39)	T55A	possibly damaging	Het
Hcst	T	G	7: 30,118,036 (GRCm39)		probably benign	Het
Hectd4	A	G	5: 121,466,445 (GRCm39)	E2420G	possibly damaging	Het
Ifi206	A	T	1: 173,308,344 (GRCm39)	S551T	probably benign	Het
Itgb3bp	A	G	4: 99,657,724 (GRCm39)		probably benign	Het
Krtap6-2	A	G	16: 89,216,644 (GRCm39)	Y108H	unknown	Het
Muc5b	A	G	7: 141,415,699 (GRCm39)	T2882A	possibly damaging	Het
Nup214	C	T	2: 31,900,233 (GRCm39)	T854M	probably damaging	Het
Olfml2b	A	G	1: 170,477,401 (GRCm39)	K179E	probably benign	Het
Or10d1b	A	G	9: 39,613,871 (GRCm39)	S65P	probably damaging	Het
Or4k37	A	T	2: 111,159,229 (GRCm39)	H155L	probably damaging	Het
Per2	A	T	1: 91,351,950 (GRCm39)	I852K	possibly damaging	Het
Pkhd1	A	T	1: 20,187,247 (GRCm39)	I3687N	probably damaging	Het
Slc7a2	A	T	8: 41,369,410 (GRCm39)	S622C	probably damaging	Het
Smarcc2	G	A	10: 128,318,781 (GRCm39)	V719I	probably damaging	Het
Syne2	T	C	12: 75,972,209 (GRCm39)	I1033T	possibly damaging	Het
Tmod1	T	C	4: 46,096,999 (GRCm39)	I264T	probably damaging	Het
Tmtc3	G	A	10: 100,283,581 (GRCm39)	A658V	possibly damaging	Het
Top6bl	T	C	19: 4,748,206 (GRCm39)	E164G	probably benign	Het
Tpm3	A	G	3: 89,981,079 (GRCm39)	E56G	possibly damaging	Het
Tra2b	T	C	16: 22,065,993 (GRCm39)		probably benign	Het
Trmu	T	A	15: 85,779,138 (GRCm39)	Y262N	possibly damaging	Het
Uox	C	T	3: 146,331,590 (GRCm39)	T213I	probably damaging	Het
Vps13d	A	G	4: 144,818,517 (GRCm39)	W2R	probably damaging	Het

Other mutations in Krtap6-5

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02377:Krtap6-5	APN	16	88,844,734 (GRCm39)	utr 5 prime	probably benign
IGL03378:Krtap6-5	APN	16	88,844,677 (GRCm39)	missense	unknown
R1259:Krtap6-5	UTSW	16	88,844,607 (GRCm39)	missense	unknown
R8972:Krtap6-5	UTSW	16	88,844,607 (GRCm39)	missense	unknown
R9221:Krtap6-5	UTSW	16	88,844,655 (GRCm39)	missense	unknown

Posted On

2016-08-02