Mutagenetix > Incidental Mutation

Incidental Mutation 'R6911:Xkr4'

538997

Institutional Source

Beutler Lab

Gene Symbol

Xkr4

Ensembl Gene

ENSMUSG00000051951

Gene Name

X-linked Kx blood group related 4

Synonyms

MMRRC Submission

045003-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6911 (G1)

Quality Score

137.008

Status

Validated

Chromosome

Chromosomal Location

3276124-3741721 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 3741544 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Glutamic Acid at position 10 (K10E)

Ref Sequence

ENSEMBL: ENSMUSP00000070648 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000070533]

AlphaFold

Q5GH67

Predicted Effect

possibly damaging
Transcript: ENSMUST00000070533
AA Change: K10E

PolyPhen 2 Score 0.907 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000070648
Gene: ENSMUSG00000051951
AA Change: K10E

Domain	Start	End	E-Value	Type
low complexity region	49	99	N/A	INTRINSIC
Pfam:XK-related	111	513	2.6e-128	PFAM
low complexity region	573	586	N/A	INTRINSIC

Meta Mutation Damage Score

0.0998

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.1%
20x: 97.1%

Validation Efficiency

98% (60/61)

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930407I10Rik	T	A	15: 81,948,068 (GRCm39)	M655K	probably benign	Het
Adam34l	A	T	8: 44,078,146 (GRCm39)	F693I	probably benign	Het
Amt	G	T	9: 108,178,428 (GRCm39)		probably null	Het
Anapc7	A	T	5: 122,578,343 (GRCm39)	K443*	probably null	Het
Apcs	A	G	1: 172,721,752 (GRCm39)	V198A	probably benign	Het
Atp2a1	A	G	7: 126,056,008 (GRCm39)	V271A	probably damaging	Het
Bltp2	T	A	11: 78,159,179 (GRCm39)	I459N	probably damaging	Het
Cdh20	T	C	1: 104,912,411 (GRCm39)	I555T	possibly damaging	Het
Cgnl1	T	C	9: 71,563,497 (GRCm39)	E810G	possibly damaging	Het
Cntnap5c	A	G	17: 58,199,009 (GRCm39)	D101G	probably damaging	Het
Coq7	T	A	7: 118,109,385 (GRCm39)	H221L	unknown	Het
Depdc5	A	T	5: 33,081,536 (GRCm39)	Q566L	probably damaging	Het
Dync1i2	G	A	2: 71,077,446 (GRCm39)	V233I	probably benign	Het
Erp44	G	T	4: 48,204,268 (GRCm39)	H298N	probably benign	Het
Fam162a	A	G	16: 35,866,747 (GRCm39)		probably null	Het
Fancd2	A	G	6: 113,525,346 (GRCm39)	E274G	probably damaging	Het
Fkbp15	G	T	4: 62,258,527 (GRCm39)	Q147K	probably damaging	Het
Ganab	T	A	19: 8,885,152 (GRCm39)		probably null	Het
Gfm1	T	C	3: 67,358,636 (GRCm39)	V409A	possibly damaging	Het
Gnptab	G	A	10: 88,267,258 (GRCm39)	G450S	probably damaging	Het
Gpatch2l	G	A	12: 86,290,958 (GRCm39)	R47H	probably damaging	Het
Grid1	A	T	14: 34,542,185 (GRCm39)	M1L	probably benign	Het
Helz	C	T	11: 107,510,051 (GRCm39)	T558I	probably benign	Het
Htra4	A	G	8: 25,515,721 (GRCm39)	V439A	probably damaging	Het
Kctd17	A	G	15: 78,318,206 (GRCm39)	E95G	probably damaging	Het
Kif18b	T	C	11: 102,807,206 (GRCm39)	D43G	probably damaging	Het
Lrpprc	G	A	17: 85,063,711 (GRCm39)	S550L	possibly damaging	Het
Lrrfip1	T	A	1: 91,042,529 (GRCm39)	C311*	probably null	Het
Mcoln2	C	T	3: 145,898,011 (GRCm39)	T44I	probably damaging	Het
Med13l	A	G	5: 118,893,723 (GRCm39)	T2010A	possibly damaging	Het
Med23	C	T	10: 24,778,079 (GRCm39)	T803M	probably damaging	Het
Mfsd13a	T	C	19: 46,357,716 (GRCm39)	F290S	probably damaging	Het
Myh13	C	T	11: 67,245,753 (GRCm39)	Q1095*	probably null	Het
Nktr	C	A	9: 121,583,392 (GRCm39)	Y93*	probably null	Het
Nox3	A	G	17: 3,736,198 (GRCm39)	S143P	probably damaging	Het
Ntrk2	A	T	13: 59,007,029 (GRCm39)	E210D	probably damaging	Het
Nup210	G	T	6: 91,007,112 (GRCm39)	A568E	probably damaging	Het
Or10ak9	T	A	4: 118,726,335 (GRCm39)	M119K	probably damaging	Het
Or2y1g	A	G	11: 49,171,634 (GRCm39)	I220V	probably benign	Het
Or4g16	A	G	2: 111,136,618 (GRCm39)	T23A	probably benign	Het
Or5as1	T	A	2: 86,980,111 (GRCm39)	K298I	probably damaging	Het
Pdlim5	T	C	3: 142,010,076 (GRCm39)	I289V	probably damaging	Het
Peg10	GC	GCTCC	6: 4,756,452 (GRCm39)		probably benign	Het
Per1	C	T	11: 68,994,083 (GRCm39)	T443M	probably damaging	Het
Plxna1	A	G	6: 89,297,956 (GRCm39)	V1774A	probably damaging	Het
Poteg	A	G	8: 27,940,326 (GRCm39)	Y165C	probably damaging	Het
Prlr	A	G	15: 10,329,270 (GRCm39)	T582A	probably benign	Het
Psma5	A	G	3: 108,172,464 (GRCm39)	E60G	probably damaging	Het
Rsrc1	C	T	3: 66,901,982 (GRCm39)	P44L	unknown	Het
Ryr2	T	C	13: 11,842,445 (GRCm39)	N484S	possibly damaging	Het
Sec31a	A	G	5: 100,541,123 (GRCm39)	I328T	possibly damaging	Het
Slc12a2	G	T	18: 58,052,541 (GRCm39)	V787L	probably benign	Het
St14	C	T	9: 31,018,081 (GRCm39)	R177Q	probably benign	Het
Tcof1	G	C	18: 60,962,123 (GRCm39)	A702G	possibly damaging	Het
Tom1l1	G	T	11: 90,534,987 (GRCm39)		probably null	Het
Ttf1	A	G	2: 28,954,863 (GRCm39)	R76G	probably benign	Het
Ube4a	C	T	9: 44,854,056 (GRCm39)	E581K	probably damaging	Het
Vmn2r114	A	G	17: 23,510,104 (GRCm39)	V792A	probably damaging	Het
Wdr11	T	C	7: 129,208,819 (GRCm39)	I430T	probably benign	Het
Zfp451	T	C	1: 33,842,537 (GRCm39)		probably benign	Het

Other mutations in Xkr4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03398:Xkr4	APN	1	3,286,798 (GRCm39)	missense	probably damaging	1.00
R0200:Xkr4	UTSW	1	3,740,886 (GRCm39)	missense	probably benign	0.00
R0829:Xkr4	UTSW	1	3,741,469 (GRCm39)	missense	possibly damaging	0.59
R0830:Xkr4	UTSW	1	3,740,968 (GRCm39)	missense	possibly damaging	0.48
R0959:Xkr4	UTSW	1	3,286,897 (GRCm39)	missense	probably damaging	1.00
R1242:Xkr4	UTSW	1	3,286,360 (GRCm39)	missense	probably damaging	1.00
R1257:Xkr4	UTSW	1	3,287,036 (GRCm39)	missense	probably benign	0.29
R2002:Xkr4	UTSW	1	3,741,318 (GRCm39)	missense	probably benign
R3896:Xkr4	UTSW	1	3,286,414 (GRCm39)	missense	probably damaging	0.99
R4006:Xkr4	UTSW	1	3,491,998 (GRCm39)	missense	probably benign	0.01
R4173:Xkr4	UTSW	1	3,286,711 (GRCm39)	missense	probably damaging	1.00
R4770:Xkr4	UTSW	1	3,286,714 (GRCm39)	missense	probably damaging	1.00
R4868:Xkr4	UTSW	1	3,287,074 (GRCm39)	missense	probably damaging	1.00
R5103:Xkr4	UTSW	1	3,740,911 (GRCm39)	missense	probably benign
R5548:Xkr4	UTSW	1	3,287,153 (GRCm39)	missense	probably damaging	1.00
R5602:Xkr4	UTSW	1	3,286,751 (GRCm39)	missense	probably benign	0.18
R5608:Xkr4	UTSW	1	3,741,603 (GRCm39)	start gained	probably benign
R5668:Xkr4	UTSW	1	3,741,258 (GRCm39)	missense	probably damaging	1.00
R5901:Xkr4	UTSW	1	3,286,901 (GRCm39)	missense	probably damaging	0.99
R6296:Xkr4	UTSW	1	3,286,793 (GRCm39)	missense	probably benign	0.01
R6302:Xkr4	UTSW	1	3,286,961 (GRCm39)	missense	probably damaging	0.99
R6326:Xkr4	UTSW	1	3,741,261 (GRCm39)	missense	possibly damaging	0.75
R6341:Xkr4	UTSW	1	3,741,001 (GRCm39)	missense	probably benign
R7086:Xkr4	UTSW	1	3,287,185 (GRCm39)	missense	probably damaging	1.00
R7249:Xkr4	UTSW	1	3,287,033 (GRCm39)	missense	probably damaging	1.00
R7571:Xkr4	UTSW	1	3,740,911 (GRCm39)	missense	probably benign	0.00
R7881:Xkr4	UTSW	1	3,286,487 (GRCm39)	missense	probably damaging	1.00
R7952:Xkr4	UTSW	1	3,740,842 (GRCm39)	missense	possibly damaging	0.94
R8332:Xkr4	UTSW	1	3,492,122 (GRCm39)	missense	probably damaging	1.00
R9076:Xkr4	UTSW	1	3,286,358 (GRCm39)	nonsense	probably null
R9134:Xkr4	UTSW	1	3,740,860 (GRCm39)	missense	probably benign
R9618:Xkr4	UTSW	1	3,741,201 (GRCm39)	missense	probably damaging	1.00
R9663:Xkr4	UTSW	1	3,286,519 (GRCm39)	missense	probably benign	0.01
Z1176:Xkr4	UTSW	1	3,741,205 (GRCm39)	missense	probably damaging	1.00
Z1176:Xkr4	UTSW	1	3,741,204 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCAGTCCCACAGCGAGTAA -3'
(R):5'- AGGTCATCCTCTCCCTCGGA -3'

Sequencing Primer
(F):5'- AGTAACGCCGCTGCTCC -3'
(R):5'- ATGTGCAGGTCCGAGGAGC -3'

Posted On

2018-11-06