Mutagenetix > Incidental Mutation

Incidental Mutation 'R7203:Ackr2'

560802

Institutional Source

Beutler Lab

Gene Symbol

Ackr2

Ensembl Gene

ENSMUSG00000044534

Gene Name

atypical chemokine receptor 2

Synonyms

Ccbp2, chemokine decoy receptor D6, D6

MMRRC Submission

045281-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7203 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

121898355-121911074 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 121908967 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Tyrosine at position 136 (C136Y)

Ref Sequence

ENSEMBL: ENSMUSP00000050119 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000050327] [ENSMUST00000214340] [ENSMUST00000215664] [ENSMUST00000216326]

AlphaFold

O08707

Predicted Effect

probably damaging
Transcript: ENSMUST00000050327
AA Change: C136Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000050119
Gene: ENSMUSG00000044534
AA Change: C136Y

Domain	Start	End	E-Value	Type
low complexity region	18	29	N/A	INTRINSIC
Pfam:7tm_1	62	311	1e-40	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000214340
AA Change: C136Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Predicted Effect

probably benign
Transcript: ENSMUST00000215664

Predicted Effect

probably benign
Transcript: ENSMUST00000216326

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (108/108)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a beta chemokine receptor, which is predicted to be a seven transmembrane protein similar to G protein-coupled receptors. Chemokines and their receptor-mediated signal transduction are critical for the recruitment of effector immune cells to the inflammation site. This gene is expressed in a range of tissues and hemopoietic cells. The expression of this receptor in lymphatic endothelial cells and overexpression in vascular tumors suggested its function in chemokine-driven recirculation of leukocytes and possible chemokine effects on the development and growth of vascular tumors. This receptor appears to bind the majority of beta-chemokine family members; however, its specific function remains unknown. This gene is mapped to chromosome 3p21.3, a region that includes a cluster of chemokine receptor genes. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null mice display increased inflammatory responses but are viable and fertile without any other gross abnormalities. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 108 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930544G11Rik	T	C	6: 65,953,333 (GRCm38)	V184A	probably benign	Het
4932415D10Rik	G	A	10: 82,293,414 (GRCm38)	T1254I	probably benign	Het
Aars2	A	G	17: 45,516,571 (GRCm38)	Y513C	probably damaging	Het
Aldh1l1	A	G	6: 90,570,800 (GRCm38)	K414R	probably benign	Het
Arl9	A	G	5: 77,007,271 (GRCm38)	Y83C	possibly damaging	Het
Atp10a	G	T	7: 58,786,473 (GRCm38)	R337L	probably benign	Het
Atp6v1g3	A	T	1: 138,287,800 (GRCm38)	Q66L	probably damaging	Het
Atp7b	A	T	8: 21,997,335 (GRCm38)	N1321K	probably damaging	Het
Axdnd1	A	T	1: 156,382,389 (GRCm38)	M437K	probably damaging	Het
Bap1	C	A	14: 31,254,169 (GRCm38)	P147Q	probably damaging	Het
Bicd1	C	T	6: 149,512,905 (GRCm38)	T372I	possibly damaging	Het
Brix1	T	C	15: 10,483,292 (GRCm38)		probably null	Het
Btrc	A	G	19: 45,513,528 (GRCm38)		probably null	Het
C130050O18Rik	A	C	5: 139,414,374 (GRCm38)	I61L	probably benign	Het
Cfap161	A	G	7: 83,776,050 (GRCm38)	S278P	probably damaging	Het
Cgnl1	T	C	9: 71,724,533 (GRCm38)	D512G	possibly damaging	Het
Chat	T	C	14: 32,419,057 (GRCm38)	D461G	probably damaging	Het
Chl1	T	A	6: 103,691,674 (GRCm38)	V456D	probably benign	Het
Cib1	T	C	7: 80,232,372 (GRCm38)	T20A	possibly damaging	Het
Cubn	T	G	2: 13,351,003 (GRCm38)	H1806P	probably benign	Het
Dapk1	T	A	13: 60,696,335 (GRCm38)	V56E	possibly damaging	Het
Dennd4a	A	G	9: 64,896,474 (GRCm38)	N1032D	probably benign	Het
Dlg5	T	A	14: 24,138,655 (GRCm38)	E1756V	probably damaging	Het
Dnah1	T	C	14: 31,274,382 (GRCm38)	T2666A	probably benign	Het
Dnah11	A	T	12: 118,045,522 (GRCm38)	I2135N	possibly damaging	Het
Dnah6	T	A	6: 73,173,545 (GRCm38)	E745V	probably benign	Het
Dock8	A	T	19: 25,181,563 (GRCm38)	N1695I	probably damaging	Het
Esf1	C	T	2: 140,164,219 (GRCm38)	R336Q	possibly damaging	Het
Fam161a	A	G	11: 23,021,664 (GRCm38)		probably null	Het
Fam89a	T	C	8: 124,751,679 (GRCm38)	E44G	possibly damaging	Het
Fndc3b	A	T	3: 27,456,485 (GRCm38)	D829E	probably benign	Het
Fxr1	C	T	3: 34,046,540 (GRCm38)	T125I	possibly damaging	Het
Gfer	T	C	17: 24,695,862 (GRCm38)	D69G	probably damaging	Het
Gm16486	A	T	8: 70,716,948 (GRCm38)	E1229V	probably benign	Het
Gm2000	A	T	1: 156,366,087 (GRCm38)	I4F	probably damaging	Het
Gpatch2l	T	A	12: 86,288,937 (GRCm38)	S471T	probably benign	Het
Grm7	T	G	6: 111,358,569 (GRCm38)	I647S	possibly damaging	Het
Gsn	A	G	2: 35,298,795 (GRCm38)	I447V	probably benign	Het
H2al2c	C	T	Y: 2,599,234 (GRCm38)	L46F	possibly damaging	Het
Hao2	A	C	3: 98,877,282 (GRCm38)		probably null	Het
Ifitm10	T	C	7: 142,328,568 (GRCm38)	E155G	probably benign	Het
Igkv8-16	C	A	6: 70,386,810 (GRCm38)	W76L	probably benign	Het
Igsf21	A	T	4: 140,107,337 (GRCm38)	F75I	possibly damaging	Het
Ints14	T	A	9: 64,964,419 (GRCm38)	M13K	probably damaging	Het
Ipmk	A	T	10: 71,363,468 (GRCm38)	D53V	possibly damaging	Het
Itga8	A	G	2: 12,230,095 (GRCm38)	F451L	possibly damaging	Het
Jup	A	G	11: 100,381,734 (GRCm38)	F284S	probably damaging	Het
Kctd5	T	C	17: 24,073,235 (GRCm38)	D65G	probably benign	Het
Klrc1	A	T	6: 129,677,221 (GRCm38)	S148T	probably benign	Het
Kmt5b	A	G	19: 3,814,147 (GRCm38)	K404E	probably damaging	Het
Krt9	A	C	11: 100,190,791 (GRCm38)	M304R	probably damaging	Het
Krtap5-1	A	T	7: 142,296,562 (GRCm38)	S143T	unknown	Het
Kyat3	A	G	3: 142,720,401 (GRCm38)	N68D	probably damaging	Het
Kynu	A	G	2: 43,681,353 (GRCm38)	D427G	probably damaging	Het
Leo1	A	G	9: 75,445,996 (GRCm38)		probably null	Het
Loxhd1	A	G	18: 77,414,196 (GRCm38)	D1737G	probably damaging	Het
Lpo	C	A	11: 87,809,251 (GRCm38)	L521F	possibly damaging	Het
Lrrk1	A	G	7: 66,270,825 (GRCm38)	S1477P	probably damaging	Het
Lrrtm1	C	A	6: 77,243,601 (GRCm38)	L14M	probably damaging	Het
Ly75	G	A	2: 60,323,852 (GRCm38)	R1084*	probably null	Het
Mcf2l	A	G	8: 13,010,456 (GRCm38)	D764G	probably benign	Het
Mrgprd	A	T	7: 145,322,349 (GRCm38)	D319V	probably benign	Het
Mut	A	T	17: 40,938,673 (GRCm38)	M180L	probably benign	Het
Myom3	T	C	4: 135,795,179 (GRCm38)	L897P	possibly damaging	Het
Ncapd2	A	T	6: 125,184,328 (GRCm38)	M247K	possibly damaging	Het
Nlrp2	T	C	7: 5,317,534 (GRCm38)	D868G	probably damaging	Het
Npy6r	A	G	18: 44,275,932 (GRCm38)	N140S	probably damaging	Het
Nsmce4a	T	C	7: 130,539,872 (GRCm38)	K196E	probably benign	Het
Nup88	T	C	11: 70,945,254 (GRCm38)	K532R	probably benign	Het
Olfr424	T	A	1: 174,137,114 (GRCm38)	Y123*	probably null	Het
Olfr947-ps1	A	T	9: 39,289,293 (GRCm38)	I199N	unknown	Het
Olfr974	T	A	9: 39,942,509 (GRCm38)	V83E	probably benign	Het
Pbxip1	A	T	3: 89,447,428 (GRCm38)	D418V	possibly damaging	Het
Pde2a	C	A	7: 101,509,944 (GRCm38)	R761S	possibly damaging	Het
Phf10	A	T	17: 14,946,313 (GRCm38)	C432S	probably damaging	Het
Pitpnm2	T	C	5: 124,121,459 (GRCm38)	D1271G	probably damaging	Het
Plin1	A	T	7: 79,723,444 (GRCm38)	L259Q	probably damaging	Het
Pmpca	G	C	2: 26,395,034 (GRCm38)	E424Q	possibly damaging	Het
Pou6f2	T	A	13: 18,239,794 (GRCm38)	Q132L	unknown	Het
Ppa2	A	T	3: 133,330,438 (GRCm38)	N118Y	possibly damaging	Het
Prickle2	T	C	6: 92,410,978 (GRCm38)	E537G	possibly damaging	Het
Prl3d1	A	G	13: 27,098,701 (GRCm38)	I141V	possibly damaging	Het
Prl8a1	A	T	13: 27,574,189 (GRCm38)	V179D	probably damaging	Het
Prr14l	A	G	5: 32,827,145 (GRCm38)	F1669L	probably benign	Het
Prrg4	T	A	2: 104,839,442 (GRCm38)	E110V	possibly damaging	Het
Rfx5	C	A	3: 94,958,876 (GRCm38)	H495Q	unknown	Het
Rgl2	C	T	17: 33,933,429 (GRCm38)	R367W	probably damaging	Het
Rpe65	A	G	3: 159,622,854 (GRCm38)	Y433C	probably damaging	Het
Rtn4rl1	C	T	11: 75,265,750 (GRCm38)	S336F	possibly damaging	Het
Scn2a	A	G	2: 65,748,319 (GRCm38)	D1446G	probably benign	Het
Sdk1	C	A	5: 142,046,176 (GRCm38)	T1002K	probably benign	Het
Slc9b2	T	C	3: 135,330,661 (GRCm38)	S409P	probably benign	Het
Sowahc	A	G	10: 59,222,278 (GRCm38)	T79A	probably benign	Het
Stk35	T	A	2: 129,801,593 (GRCm38)	C166S	probably benign	Het
Tarbp2	A	G	15: 102,522,487 (GRCm38)	H225R	probably benign	Het
Tdrd12	T	A	7: 35,489,223 (GRCm38)	K530*	probably null	Het
Terf2ip	A	G	8: 112,017,986 (GRCm38)	I312V	probably benign	Het
Tgfb1	T	C	7: 25,692,539 (GRCm38)		probably null	Het
Thbs2	T	C	17: 14,671,458 (GRCm38)	D939G	probably damaging	Het
Ube4b	A	T	4: 149,398,610 (GRCm38)	I67K	probably benign	Het
Ubn1	G	T	16: 5,077,216 (GRCm38)	V709F	possibly damaging	Het
Ugt2b5	T	C	5: 87,128,399 (GRCm38)	K339E	possibly damaging	Het
Vax2	T	C	6: 83,737,900 (GRCm38)	S266P	probably damaging	Het
Vmn2r108	A	G	17: 20,462,776 (GRCm38)	I722T	probably benign	Het
Vmn2r95	A	G	17: 18,441,315 (GRCm38)	K441R	probably benign	Het
Wapl	C	A	14: 34,736,691 (GRCm38)	D903E	probably benign	Het
Wee1	T	A	7: 110,134,794 (GRCm38)	V442D	probably benign	Het
Zan	T	C	5: 137,434,096 (GRCm38)	N2313S	unknown	Het

Other mutations in Ackr2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01743:Ackr2	APN	9	121,909,500 (GRCm38)	missense	probably benign	0.02
IGL01744:Ackr2	APN	9	121,909,119 (GRCm38)	missense	probably benign	0.06
IGL03019:Ackr2	APN	9	121,909,182 (GRCm38)	missense	probably benign	0.43
IGL03143:Ackr2	APN	9	121,909,267 (GRCm38)	missense	probably damaging	1.00
IGL03398:Ackr2	APN	9	121,908,588 (GRCm38)	missense	probably damaging	1.00
R0180:Ackr2	UTSW	9	121,908,916 (GRCm38)	missense	probably benign	0.44
R0366:Ackr2	UTSW	9	121,909,360 (GRCm38)	missense	probably damaging	1.00
R1295:Ackr2	UTSW	9	121,908,717 (GRCm38)	missense	possibly damaging	0.94
R1596:Ackr2	UTSW	9	121,909,212 (GRCm38)	missense	probably damaging	1.00
R1827:Ackr2	UTSW	9	121,909,515 (GRCm38)	missense	probably benign	0.36
R2109:Ackr2	UTSW	9	121,908,960 (GRCm38)	missense	probably damaging	0.98
R2125:Ackr2	UTSW	9	121,908,786 (GRCm38)	nonsense	probably null
R2414:Ackr2	UTSW	9	121,908,974 (GRCm38)	missense	probably damaging	1.00
R4161:Ackr2	UTSW	9	121,909,522 (GRCm38)	missense	probably benign	0.05
R4524:Ackr2	UTSW	9	121,909,543 (GRCm38)	missense	probably benign
R4732:Ackr2	UTSW	9	121,909,183 (GRCm38)	missense	probably damaging	0.98
R4733:Ackr2	UTSW	9	121,909,183 (GRCm38)	missense	probably damaging	0.98
R5809:Ackr2	UTSW	9	121,909,474 (GRCm38)	missense	probably damaging	1.00
R7210:Ackr2	UTSW	9	121,908,877 (GRCm38)	missense	possibly damaging	0.64
R7267:Ackr2	UTSW	9	121,908,808 (GRCm38)	missense	probably damaging	1.00
R7665:Ackr2	UTSW	9	121,909,308 (GRCm38)	missense	probably benign
R8090:Ackr2	UTSW	9	121,908,979 (GRCm38)	missense	possibly damaging	0.53
R9074:Ackr2	UTSW	9	121,908,663 (GRCm38)	missense	probably damaging	1.00
R9598:Ackr2	UTSW	9	121,908,591 (GRCm38)	missense	possibly damaging	0.89

Predicted Primers

PCR Primer
(F):5'- AGACGGACGATGGAGCTTTAC -3'
(R):5'- CGCAGGTACAGCTTCCAAATG -3'

Sequencing Primer
(F):5'- GATGGAGCTTTACCTGCTGAACC -3'
(R):5'- AGCTTCCAAATGGTCGCATG -3'

Posted On

2019-06-26