Mutagenetix > Incidental Mutation

Incidental Mutation 'R7524:Asns'

585943

Institutional Source

Beutler Lab

Gene Symbol

Asns

Ensembl Gene

ENSMUSG00000029752

Gene Name

asparagine synthetase

Synonyms

MMRRC Submission

045596-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.235) question?

Stock #

R7524 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

7675169-7693209 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

G to T at 7677259 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000111204 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031766] [ENSMUST00000115542]

AlphaFold

Q61024

Predicted Effect

probably null
Transcript: ENSMUST00000031766

SMART Domains

Protein: ENSMUSP00000031766
Gene: ENSMUSG00000029752

Domain	Start	End	E-Value	Type
Pfam:GATase_6	29	160	4.3e-21	PFAM
Pfam:GATase_7	47	166	9.1e-26	PFAM
Pfam:DUF3700	68	178	5.5e-6	PFAM
Pfam:GATase_2	91	161	3.3e-5	PFAM
Pfam:Asn_synthase	234	467	1.7e-61	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000115542

SMART Domains

Protein: ENSMUSP00000111204
Gene: ENSMUSG00000029752

Domain	Start	End	E-Value	Type
Pfam:GATase_6	29	160	1.2e-19	PFAM
Pfam:GATase_7	47	166	4.8e-25	PFAM
Pfam:DUF3700	64	180	3.3e-6	PFAM
Pfam:Asn_synthase	234	390	2.4e-46	PFAM
Pfam:Asn_synthase	382	547	1.5e-35	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (79/79)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is involved in the synthesis of asparagine. This gene complements a mutation in the temperature-sensitive hamster mutant ts11, which blocks progression through the G1 phase of the cell cycle at nonpermissive temperature. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2010]
PHENOTYPE: Mice homozygous for a hypomophic allele exhibit structural brain abnormalities, including enlarged ventricles and reduced cortical thickness, and deficits in short- and long-term memory. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam29	C	T	8: 56,325,395 (GRCm39)	C353Y	probably damaging	Het
Afap1l2	T	A	19: 56,906,543 (GRCm39)	E452V	probably damaging	Het
Ak6	A	G	13: 100,800,415 (GRCm39)	D45G	probably benign	Het
Arhgap17	G	A	7: 122,905,643 (GRCm39)	P334L	probably damaging	Het
Bend7	A	G	2: 4,804,791 (GRCm39)	T424A	probably benign	Het
Btbd2	C	T	10: 80,482,278 (GRCm39)	E241K	probably damaging	Het
Commd2	A	C	3: 57,557,569 (GRCm39)	L99W	probably damaging	Het
Cpne9	A	T	6: 113,279,025 (GRCm39)	D473V	probably damaging	Het
Cuzd1	A	T	7: 130,913,347 (GRCm39)	F423L	probably damaging	Het
Cyp2d9	T	C	15: 82,340,146 (GRCm39)	F390L	probably damaging	Het
Dcaf5	T	A	12: 80,423,470 (GRCm39)	Q234L	probably benign	Het
Dennd3	T	G	15: 73,396,095 (GRCm39)	Y201*	probably null	Het
Dnah17	T	C	11: 118,012,307 (GRCm39)	D485G	probably benign	Het
Dnah5	A	T	15: 28,297,212 (GRCm39)	T1469S	possibly damaging	Het
Dnah6	T	C	6: 73,095,082 (GRCm39)	D2167G	probably damaging	Het
Dst	T	C	1: 34,330,974 (GRCm39)	V4921A	possibly damaging	Het
Ephb2	A	G	4: 136,387,020 (GRCm39)	Y736H	probably damaging	Het
Eri2	C	G	7: 119,384,972 (GRCm39)	V510L	probably benign	Het
Eya2	G	A	2: 165,611,246 (GRCm39)		probably null	Het
Fastkd5	G	T	2: 130,458,048 (GRCm39)	Q181K	probably benign	Het
Fcgbp	T	C	7: 27,802,391 (GRCm39)	S1440P	probably damaging	Het
Fkbp9	G	A	6: 56,845,725 (GRCm39)	V354M	probably damaging	Het
Frmpd1	T	A	4: 45,271,181 (GRCm39)	S304T	probably benign	Het
Gtf2a2	T	A	9: 69,922,629 (GRCm39)	Y3*	probably null	Het
Hagh	G	A	17: 25,080,314 (GRCm39)	V226I	probably benign	Het
Hemk1	T	A	9: 107,205,484 (GRCm39)	I293F	probably benign	Het
Kcna3	A	G	3: 106,944,523 (GRCm39)	E262G	probably damaging	Het
Kcnt2	A	T	1: 140,511,793 (GRCm39)	T983S	probably damaging	Het
Klhdc3	A	T	17: 46,989,340 (GRCm39)	H7Q	probably damaging	Het
Knl1	A	T	2: 118,896,460 (GRCm39)	Q94L	probably damaging	Het
Krt12	T	C	11: 99,310,485 (GRCm39)	D224G	probably damaging	Het
Lats1	T	A	10: 7,577,742 (GRCm39)	S289T	possibly damaging	Het
Man2a2	G	C	7: 80,018,613 (GRCm39)	A82G	probably benign	Het
Map1a	G	A	2: 121,120,293 (GRCm39)	V60M	probably damaging	Het
Mms22l	T	A	4: 24,536,138 (GRCm39)	F536I	possibly damaging	Het
Ms4a14	T	C	19: 11,281,200 (GRCm39)	T453A	unknown	Het
Muc3a	A	C	5: 137,245,020 (GRCm39)	I151S	probably benign	Het
Myorg	C	A	4: 41,498,779 (GRCm39)	V284L	probably benign	Het
Oaf	G	A	9: 43,134,077 (GRCm39)	R215C	probably damaging	Het
Or4c112	T	A	2: 88,854,315 (GRCm39)	I11L	probably benign	Het
Or4c125	A	G	2: 89,170,221 (GRCm39)	C142R	probably benign	Het
Or4e5	T	C	14: 52,727,750 (GRCm39)	I224V	probably damaging	Het
Or5ar1	T	A	2: 85,671,701 (GRCm39)	M145L	probably benign	Het
Or6z7	T	C	7: 6,483,586 (GRCm39)	N190D	probably benign	Het
Or7a42	T	A	10: 78,791,325 (GRCm39)	Y95*	probably null	Het
Pcdhgb4	A	T	18: 37,854,661 (GRCm39)	D352V	probably benign	Het
Pced1a	A	G	2: 130,263,948 (GRCm39)	F235L	probably benign	Het
Pclo	A	G	5: 14,728,317 (GRCm39)	I2392V	unknown	Het
Pld1	A	T	3: 28,078,470 (GRCm39)	D43V	possibly damaging	Het
Ppp1r1b	C	A	11: 98,241,720 (GRCm39)	A51D	possibly damaging	Het
Prr23a1	T	A	9: 98,724,917 (GRCm39)	L93H	probably damaging	Het
Psg20	T	C	7: 18,418,584 (GRCm39)	D61G	probably benign	Het
Rab40b	T	A	11: 121,278,878 (GRCm39)	I31F	probably damaging	Het
Rasd2	T	C	8: 75,948,709 (GRCm39)	F212L	probably benign	Het
Rbl2	A	G	8: 91,841,821 (GRCm39)	I1006V	probably benign	Het
Sema6c	A	G	3: 95,074,371 (GRCm39)	E59G	probably benign	Het
Slc22a2	G	T	17: 12,824,944 (GRCm39)	V269L	possibly damaging	Het
Slc2a1	C	T	4: 118,989,809 (GRCm39)	P149S	probably damaging	Het
Smad4	T	G	18: 73,808,942 (GRCm39)	E108D	probably damaging	Het
Sorbs2	T	A	8: 46,248,693 (GRCm39)	I648K	probably benign	Het
Suclg1	A	T	6: 73,240,824 (GRCm39)	I118F	probably damaging	Het
Tasor	T	A	14: 27,188,160 (GRCm39)	C869S	probably damaging	Het
Tet2	A	G	3: 133,185,990 (GRCm39)	I1149T	probably benign	Het
Tfr2	T	A	5: 137,569,751 (GRCm39)	Y82*	probably null	Het
Tfr2	G	T	5: 137,581,751 (GRCm39)	V613L	probably benign	Het
Tg	A	T	15: 66,568,010 (GRCm39)	M1305L	probably benign	Het
Tmem176a	A	T	6: 48,821,039 (GRCm39)	M170L	probably benign	Het
Trim71	T	C	9: 114,342,230 (GRCm39)	N684S	probably benign	Het
Tspan9	A	G	6: 127,942,214 (GRCm39)	I212T	probably benign	Het
Ttn	A	G	2: 76,773,319 (GRCm39)	V2361A	possibly damaging	Het
Uqcrc1	C	T	9: 108,765,827 (GRCm39)	T14M	possibly damaging	Het
Vmn2r11	T	C	5: 109,201,848 (GRCm39)	I219V	probably benign	Het
Vmn2r76	T	C	7: 85,874,577 (GRCm39)	H800R	probably benign	Het
Vmn2r76	C	T	7: 85,879,374 (GRCm39)	G309R	probably benign	Het
Xpc	A	T	6: 91,476,513 (GRCm39)	C529S	probably benign	Het
Zfp455	T	A	13: 67,355,688 (GRCm39)	S254T	possibly damaging	Het
Zfp746	T	C	6: 48,041,823 (GRCm39)	H301R	possibly damaging	Het
Zyg11a	A	T	4: 108,049,271 (GRCm39)	I490N	probably damaging	Het

Other mutations in Asns

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00264:Asns	APN	6	7,680,179 (GRCm39)	missense	probably damaging	1.00
IGL00656:Asns	APN	6	7,680,215 (GRCm39)	unclassified	probably benign
IGL01534:Asns	APN	6	7,675,397 (GRCm39)	missense	probably benign	0.03
IGL01996:Asns	APN	6	7,682,378 (GRCm39)	missense	possibly damaging	0.56
IGL02058:Asns	APN	6	7,685,184 (GRCm39)	missense	probably damaging	1.00
IGL02311:Asns	APN	6	7,676,233 (GRCm39)	critical splice donor site	probably null
IGL02367:Asns	APN	6	7,685,411 (GRCm39)	splice site	probably benign
IGL03263:Asns	APN	6	7,689,404 (GRCm39)	missense	probably benign	0.07
IGL03341:Asns	APN	6	7,682,002 (GRCm39)	missense	probably damaging	0.98
PIT4445001:Asns	UTSW	6	7,689,277 (GRCm39)	missense	probably damaging	1.00
R0034:Asns	UTSW	6	7,676,299 (GRCm39)	missense	probably damaging	1.00
R0034:Asns	UTSW	6	7,676,299 (GRCm39)	missense	probably damaging	1.00
R0050:Asns	UTSW	6	7,676,019 (GRCm39)	missense	probably benign	0.02
R0627:Asns	UTSW	6	7,675,516 (GRCm39)	missense	probably benign	0.05
R1075:Asns	UTSW	6	7,676,076 (GRCm39)	nonsense	probably null
R1591:Asns	UTSW	6	7,678,007 (GRCm39)	missense	probably damaging	0.97
R2047:Asns	UTSW	6	7,680,093 (GRCm39)	missense	probably damaging	0.99
R2232:Asns	UTSW	6	7,689,316 (GRCm39)	missense	possibly damaging	0.82
R2907:Asns	UTSW	6	7,675,506 (GRCm39)	missense	probably benign	0.03
R3907:Asns	UTSW	6	7,682,270 (GRCm39)	critical splice donor site	probably null
R4373:Asns	UTSW	6	7,677,978 (GRCm39)	missense	probably damaging	0.98
R4438:Asns	UTSW	6	7,675,320 (GRCm39)	missense	probably benign	0.15
R4660:Asns	UTSW	6	7,678,012 (GRCm39)	missense	probably benign	0.05
R4784:Asns	UTSW	6	7,678,029 (GRCm39)	missense	probably benign	0.12
R5655:Asns	UTSW	6	7,685,309 (GRCm39)	missense	probably benign	0.31
R5752:Asns	UTSW	6	7,689,365 (GRCm39)	missense	probably damaging	1.00
R5863:Asns	UTSW	6	7,675,443 (GRCm39)	nonsense	probably null
R5864:Asns	UTSW	6	7,675,443 (GRCm39)	nonsense	probably null
R5953:Asns	UTSW	6	7,682,285 (GRCm39)	missense	probably benign	0.00
R6773:Asns	UTSW	6	7,676,284 (GRCm39)	missense	probably benign	0.01
R6789:Asns	UTSW	6	7,675,344 (GRCm39)	missense	probably benign
R7389:Asns	UTSW	6	7,689,291 (GRCm39)	missense	probably damaging	1.00
R7783:Asns	UTSW	6	7,677,978 (GRCm39)	missense	probably damaging	1.00
R7949:Asns	UTSW	6	7,685,328 (GRCm39)	missense	probably damaging	0.97
R8722:Asns	UTSW	6	7,676,085 (GRCm39)	missense	probably damaging	1.00
R9405:Asns	UTSW	6	7,689,283 (GRCm39)	missense	probably damaging	0.99
R9663:Asns	UTSW	6	7,680,132 (GRCm39)	missense	probably damaging	1.00
R9697:Asns	UTSW	6	7,689,268 (GRCm39)	missense	probably damaging	1.00
R9798:Asns	UTSW	6	7,689,395 (GRCm39)	missense	possibly damaging	0.92

Predicted Primers

PCR Primer
(F):5'- CAGGCCATAGCACAGCTTTTAG -3'
(R):5'- AAAACATTGCTGGCCTCTGAAG -3'

Sequencing Primer
(F):5'- CCATAGCACAGCTTTTAGGGGAC -3'
(R):5'- GCTGGCCTCTGAAGTCATTTAC -3'

Posted On

2019-10-18