Mutagenetix > Incidental Mutation

Incidental Mutation 'R8166:Aqr'

633758

Institutional Source

Beutler Lab

Gene Symbol

Aqr

Ensembl Gene

ENSMUSG00000040383

Gene Name

aquarius

Synonyms

MMRRC Submission

067592-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8166 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

113931642-114005788 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 113943806 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Leucine at position 1111 (M1111L)

Ref Sequence

ENSEMBL: ENSMUSP00000047157 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000043160] [ENSMUST00000102543]

AlphaFold

Q8CFQ3

Predicted Effect

possibly damaging
Transcript: ENSMUST00000043160
AA Change: M1111L

PolyPhen 2 Score 0.955 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000047157
Gene: ENSMUSG00000040383
AA Change: M1111L

Domain	Start	End	E-Value	Type
Pfam:Aquarius_N	18	802	N/A	PFAM
Pfam:ResIII	797	911	8.2e-7	PFAM
Pfam:AAA_11	801	1111	9.6e-32	PFAM
Pfam:AAA_19	807	894	3.7e-11	PFAM
Pfam:AAA_12	1119	1312	2.1e-27	PFAM
low complexity region	1394	1417	N/A	INTRINSIC
low complexity region	1455	1468	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000102543
AA Change: M1111L

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)

SMART Domains

Protein: ENSMUSP00000099602
Gene: ENSMUSG00000040383
AA Change: M1111L

Domain	Start	End	E-Value	Type
low complexity region	43	56	N/A	INTRINSIC
low complexity region	112	124	N/A	INTRINSIC
low complexity region	762	776	N/A	INTRINSIC
Pfam:AAA_11	801	1111	3.2e-32	PFAM
Pfam:AAA_19	807	893	6.5e-11	PFAM
Pfam:AAA_12	1119	1312	2.6e-27	PFAM
low complexity region	1348	1359	N/A	INTRINSIC
low complexity region	1371	1382	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.5%

Validation Efficiency

100% (59/59)

MGI Phenotype

PHENOTYPE: Homozygotes for a targeted null mutation exhibit severe defects in placental vascularization with few vessels entering the placenta and little branching. Mutants die between embryonic days 9.5 and 10.5. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acad9	T	C	3: 36,144,232 (GRCm39)	V569A	probably benign	Het
Actrt3	A	G	3: 30,652,674 (GRCm39)	F140S	probably damaging	Het
Alx1	T	A	10: 102,845,224 (GRCm39)	Q269L	probably damaging	Het
Amph	G	T	13: 19,132,660 (GRCm39)	A20S	possibly damaging	Het
Atp10a	A	T	7: 58,457,270 (GRCm39)	H923L	possibly damaging	Het
Bmpr1a	A	C	14: 34,147,026 (GRCm39)	W249G	probably damaging	Het
Bmpr2	A	T	1: 59,906,740 (GRCm39)	N611I	probably damaging	Het
Cadm2	A	G	16: 66,750,197 (GRCm39)	L9S	probably benign	Het
Ccdc102a	C	A	8: 95,639,944 (GRCm39)	A117S	possibly damaging	Het
Clec4f	G	T	6: 83,629,624 (GRCm39)	S311R	possibly damaging	Het
Dchs2	T	A	3: 83,261,640 (GRCm39)	I2636N	probably benign	Het
Dync2h1	T	A	9: 7,129,089 (GRCm39)	K1809*	probably null	Het
Efs	C	T	14: 55,158,077 (GRCm39)	R108Q	probably damaging	Het
Eif5b	A	G	1: 38,087,901 (GRCm39)	T966A	probably benign	Het
Entrep2	A	G	7: 64,409,153 (GRCm39)	S414P	probably benign	Het
Flnc	A	C	6: 29,433,731 (GRCm39)	N92H	probably damaging	Het
Gm13030	A	T	4: 138,598,533 (GRCm39)	L130H	unknown	Het
Gm17190	A	C	13: 96,219,142 (GRCm39)	R159S	unknown	Het
Hipk1	T	C	3: 103,685,489 (GRCm39)	Y42C	possibly damaging	Het
Ifi207	C	A	1: 173,557,166 (GRCm39)	C524F	possibly damaging	Het
Ifi207	A	C	1: 173,557,504 (GRCm39)	S411R	probably benign	Het
Ighv8-9	G	T	12: 115,432,212 (GRCm39)	P33H	probably damaging	Het
Igkv8-34	A	G	6: 70,021,619 (GRCm39)	V15A	probably benign	Het
Irx5	T	A	8: 93,086,712 (GRCm39)		probably null	Het
Kcnh4	A	G	11: 100,632,712 (GRCm39)	L925P	probably benign	Het
Kctd9	G	A	14: 67,967,141 (GRCm39)	R153H	possibly damaging	Het
Lats1	A	G	10: 7,577,880 (GRCm39)	T335A	probably benign	Het
Med20	A	G	17: 47,924,027 (GRCm39)	T52A	probably benign	Het
Msantd4	A	T	9: 4,384,095 (GRCm39)	T139S	possibly damaging	Het
Mtif3	T	C	5: 146,896,052 (GRCm39)	T12A	probably benign	Het
N4bp2	T	G	5: 65,977,655 (GRCm39)	S1518A	probably benign	Het
Naip2	T	C	13: 100,298,515 (GRCm39)	N507S	probably benign	Het
Nasp	A	T	4: 116,468,112 (GRCm39)	V291E	probably benign	Het
Ncapg2	T	G	12: 116,376,036 (GRCm39)	D40E	probably benign	Het
Nipsnap1	A	G	11: 4,834,057 (GRCm39)	D103G	probably benign	Het
Nsmce1	A	G	7: 125,070,319 (GRCm39)	L164P	probably damaging	Het
Ogdhl	G	A	14: 32,059,763 (GRCm39)	V426I	probably damaging	Het
Or5p66	A	G	7: 107,885,904 (GRCm39)	V143A	probably benign	Het
P3h2	T	C	16: 25,811,572 (GRCm39)	E217G	possibly damaging	Het
Pnpt1	A	G	11: 29,106,875 (GRCm39)	I649V	probably benign	Het
Prxl2c	A	T	13: 64,456,921 (GRCm39)	Y101N		Het
Pum2	G	A	12: 8,771,739 (GRCm39)	A361T	possibly damaging	Het
Rictor	G	A	15: 6,798,815 (GRCm39)		probably null	Het
Rps6ka4	G	A	19: 6,814,811 (GRCm39)	R264W	possibly damaging	Het
Rsf1	G	GACGGCGGCA	7: 97,229,116 (GRCm39)		probably benign	Het
Sall1	T	C	8: 89,755,146 (GRCm39)	T1278A	probably benign	Het
Scg2	T	A	1: 79,413,300 (GRCm39)	K434N	possibly damaging	Het
Suclg1	T	A	6: 73,237,555 (GRCm39)	V100D	probably damaging	Het
Tarbp1	T	G	8: 127,153,867 (GRCm39)	E1528D	possibly damaging	Het
Trgc1	A	G	13: 19,400,772 (GRCm39)	N167S		Het
Tshz2	C	A	2: 169,725,575 (GRCm39)	T57K	probably benign	Het
Ttc22	G	A	4: 106,491,673 (GRCm39)	R229H	probably damaging	Het
Vcan	A	G	13: 89,840,855 (GRCm39)	V1563A	probably benign	Het
Vmn1r68	A	T	7: 10,261,888 (GRCm39)	M70K	probably benign	Het
Vmn2r105	A	T	17: 20,428,904 (GRCm39)	I724N	probably benign	Het
Vmn2r96	T	C	17: 18,802,744 (GRCm39)	L26P	probably damaging	Het
Wdr72	G	A	9: 74,120,610 (GRCm39)	S955N	probably benign	Het
Zfp518b	C	A	5: 38,831,838 (GRCm39)	A56S	probably damaging	Het

Other mutations in Aqr

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00572:Aqr	APN	2	113,956,423 (GRCm39)	missense	possibly damaging	0.90
IGL00694:Aqr	APN	2	113,982,006 (GRCm39)	missense	probably damaging	1.00
IGL02113:Aqr	APN	2	113,950,508 (GRCm39)	nonsense	probably null
IGL02297:Aqr	APN	2	113,980,962 (GRCm39)	missense	probably benign	0.24
IGL02380:Aqr	APN	2	113,940,417 (GRCm39)	missense	probably damaging	1.00
IGL02410:Aqr	APN	2	113,967,398 (GRCm39)	missense	possibly damaging	0.85
IGL02413:Aqr	APN	2	113,949,261 (GRCm39)	missense	possibly damaging	0.87
IGL02474:Aqr	APN	2	113,943,127 (GRCm39)	missense	probably damaging	1.00
IGL02941:Aqr	APN	2	113,943,835 (GRCm39)	missense	probably damaging	1.00
IGL02981:Aqr	APN	2	113,965,305 (GRCm39)	splice site	probably benign
IGL03001:Aqr	APN	2	113,977,400 (GRCm39)	missense	probably benign
IGL03092:Aqr	APN	2	113,989,424 (GRCm39)	missense	probably benign	0.38
IGL03222:Aqr	APN	2	113,951,737 (GRCm39)	missense	probably damaging	1.00
capricorn	UTSW	2	113,936,363 (GRCm39)	missense	probably damaging	1.00
Goat	UTSW	2	113,988,056 (GRCm39)	missense	probably damaging	1.00
Pliades	UTSW	2	113,963,457 (GRCm39)	missense	probably damaging	1.00
sagittarius	UTSW	2	113,979,497 (GRCm39)	missense	probably damaging	1.00
Zodiac	UTSW	2	113,938,590 (GRCm39)	missense	probably damaging	0.96
PIT4531001:Aqr	UTSW	2	113,961,215 (GRCm39)	missense	possibly damaging	0.94
R0103:Aqr	UTSW	2	113,979,497 (GRCm39)	missense	probably damaging	1.00
R0103:Aqr	UTSW	2	113,979,497 (GRCm39)	missense	probably damaging	1.00
R0152:Aqr	UTSW	2	113,989,491 (GRCm39)	missense	probably benign	0.07
R0352:Aqr	UTSW	2	114,000,533 (GRCm39)	missense	probably damaging	1.00
R0371:Aqr	UTSW	2	113,988,085 (GRCm39)	missense	possibly damaging	0.80
R0374:Aqr	UTSW	2	113,961,092 (GRCm39)	missense	probably damaging	1.00
R0550:Aqr	UTSW	2	113,963,457 (GRCm39)	missense	probably damaging	1.00
R0604:Aqr	UTSW	2	113,961,085 (GRCm39)	missense	probably benign	0.00
R0685:Aqr	UTSW	2	113,971,458 (GRCm39)	missense	probably damaging	1.00
R1236:Aqr	UTSW	2	113,947,136 (GRCm39)	missense	probably damaging	1.00
R1434:Aqr	UTSW	2	113,980,890 (GRCm39)	missense	probably damaging	1.00
R1806:Aqr	UTSW	2	113,992,133 (GRCm39)	missense	probably damaging	1.00
R2154:Aqr	UTSW	2	113,967,485 (GRCm39)	missense	probably damaging	1.00
R2185:Aqr	UTSW	2	113,961,015 (GRCm39)	critical splice donor site	probably null
R2377:Aqr	UTSW	2	113,971,421 (GRCm39)	missense	possibly damaging	0.58
R2862:Aqr	UTSW	2	113,967,398 (GRCm39)	missense	probably damaging	1.00
R3615:Aqr	UTSW	2	113,967,368 (GRCm39)	missense	probably damaging	1.00
R3616:Aqr	UTSW	2	113,967,368 (GRCm39)	missense	probably damaging	1.00
R3713:Aqr	UTSW	2	113,949,150 (GRCm39)	splice site	probably benign
R3715:Aqr	UTSW	2	113,949,150 (GRCm39)	splice site	probably benign
R4586:Aqr	UTSW	2	113,943,058 (GRCm39)	missense	probably benign	0.06
R4663:Aqr	UTSW	2	113,992,147 (GRCm39)	nonsense	probably null
R4809:Aqr	UTSW	2	114,005,695 (GRCm39)	utr 5 prime	probably benign
R4887:Aqr	UTSW	2	113,980,990 (GRCm39)	missense	probably damaging	1.00
R4888:Aqr	UTSW	2	113,980,990 (GRCm39)	missense	probably damaging	1.00
R4952:Aqr	UTSW	2	113,940,418 (GRCm39)	missense	probably damaging	1.00
R4974:Aqr	UTSW	2	113,943,832 (GRCm39)	missense	probably damaging	1.00
R5050:Aqr	UTSW	2	114,000,506 (GRCm39)	critical splice donor site	probably null
R5050:Aqr	UTSW	2	113,943,090 (GRCm39)	nonsense	probably null
R5213:Aqr	UTSW	2	113,943,808 (GRCm39)	missense	probably damaging	1.00
R5263:Aqr	UTSW	2	113,947,059 (GRCm39)	missense	probably damaging	1.00
R5470:Aqr	UTSW	2	113,988,056 (GRCm39)	missense	probably damaging	1.00
R5488:Aqr	UTSW	2	113,963,554 (GRCm39)	missense	probably damaging	1.00
R5489:Aqr	UTSW	2	113,963,554 (GRCm39)	missense	probably damaging	1.00
R5567:Aqr	UTSW	2	113,979,451 (GRCm39)	missense	probably damaging	1.00
R5570:Aqr	UTSW	2	113,979,451 (GRCm39)	missense	probably damaging	1.00
R5641:Aqr	UTSW	2	113,979,515 (GRCm39)	missense	probably damaging	1.00
R5685:Aqr	UTSW	2	113,986,746 (GRCm39)	missense	possibly damaging	0.87
R5963:Aqr	UTSW	2	113,957,442 (GRCm39)	missense	probably damaging	1.00
R5992:Aqr	UTSW	2	113,973,530 (GRCm39)	nonsense	probably null
R6015:Aqr	UTSW	2	114,005,646 (GRCm39)	start codon destroyed	probably null	0.53
R6253:Aqr	UTSW	2	113,986,758 (GRCm39)	missense	possibly damaging	0.93
R6264:Aqr	UTSW	2	113,940,445 (GRCm39)	missense	probably damaging	1.00
R6773:Aqr	UTSW	2	113,979,477 (GRCm39)	missense	possibly damaging	0.64
R6877:Aqr	UTSW	2	113,947,052 (GRCm39)	nonsense	probably null
R7211:Aqr	UTSW	2	113,965,204 (GRCm39)	missense	probably benign	0.01
R7232:Aqr	UTSW	2	113,936,363 (GRCm39)	missense	probably damaging	1.00
R7308:Aqr	UTSW	2	113,934,543 (GRCm39)	missense	possibly damaging	0.86
R7396:Aqr	UTSW	2	113,950,427 (GRCm39)	nonsense	probably null
R7490:Aqr	UTSW	2	113,989,349 (GRCm39)	critical splice donor site	probably null
R7526:Aqr	UTSW	2	113,938,590 (GRCm39)	missense	probably damaging	0.96
R7629:Aqr	UTSW	2	113,945,074 (GRCm39)	missense	probably damaging	1.00
R7828:Aqr	UTSW	2	113,979,497 (GRCm39)	missense	probably damaging	1.00
R8037:Aqr	UTSW	2	113,992,161 (GRCm39)	missense	probably damaging	1.00
R8712:Aqr	UTSW	2	113,949,358 (GRCm39)	missense	probably damaging	1.00
R8904:Aqr	UTSW	2	113,967,474 (GRCm39)	missense	probably damaging	0.98
R9487:Aqr	UTSW	2	113,934,528 (GRCm39)	missense	probably benign	0.04
R9527:Aqr	UTSW	2	113,932,037 (GRCm39)	missense	probably benign	0.02
R9664:Aqr	UTSW	2	113,971,396 (GRCm39)	nonsense	probably null
Z1176:Aqr	UTSW	2	113,940,472 (GRCm39)	missense	probably benign	0.25
Z1176:Aqr	UTSW	2	113,938,603 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- TCCTAGGTTTGTAGAGGAGGCTAAAAC -3'
(R):5'- GCTGCTGAAGGTTGGGAATC -3'

Sequencing Primer
(F):5'- GAGGAGGCTAAAACTTTTTGTAACAG -3'
(R):5'- CATGATGTCGTCTGATGAACAG -3'

Posted On

2020-07-13