Mutagenetix > Incidental Mutation

Incidental Mutation 'R2190:Aspg'

238051

Institutional Source

Beutler Lab

Gene Symbol

Aspg

Ensembl Gene

ENSMUSG00000037686

Gene Name

asparaginase

Synonyms

A530050D06Rik

MMRRC Submission

040192-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.137) question?

Stock #

R2190 (G1)

Quality Score

173

Status

Not validated

Chromosome

Chromosomal Location

112073113-112093993 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 112091322 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Aspartic acid at position 501 (E501D)

Ref Sequence

ENSEMBL: ENSMUSP00000078369 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000079400] [ENSMUST00000223184]

AlphaFold

A0JNU3

Predicted Effect

probably damaging
Transcript: ENSMUST00000079400
AA Change: E501D

PolyPhen 2 Score 0.960 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000078369
Gene: ENSMUSG00000037686
AA Change: E501D

Domain	Start	End	E-Value	Type
Asparaginase	10	348	2.67e-111	SMART
ANK	396	426	4.05e2	SMART
ANK	430	459	4.46e-7	SMART
ANK	463	494	1.1e2	SMART
ANK	530	559	4.73e2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222645

Predicted Effect

unknown
Transcript: ENSMUST00000222970
AA Change: A135S

Predicted Effect

probably benign
Transcript: ENSMUST00000223184

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aars1	A	T	8: 111,766,785 (GRCm39)	T56S	probably damaging	Het
Acbd6	A	T	1: 155,500,652 (GRCm39)	H204L	probably damaging	Het
Acnat2	T	A	4: 49,383,551 (GRCm39)	M1L	probably benign	Het
Adgrg5	A	T	8: 95,660,579 (GRCm39)	I73F	probably damaging	Het
Ankrd52	A	G	10: 128,219,487 (GRCm39)	T474A	probably benign	Het
Arid3a	A	G	10: 79,782,365 (GRCm39)	D252G	possibly damaging	Het
Bicral	A	G	17: 47,136,049 (GRCm39)	I387T	probably damaging	Het
Bub1	T	C	2: 127,652,645 (GRCm39)	N574S	probably benign	Het
Casr	G	A	16: 36,315,778 (GRCm39)	T764M	probably damaging	Het
Ccdc60	A	G	5: 116,295,639 (GRCm39)	S259P	probably damaging	Het
Ccne2	A	T	4: 11,197,241 (GRCm39)	N181I	probably benign	Het
Chd4	A	G	6: 125,091,260 (GRCm39)	D89G	probably benign	Het
Col25a1	C	T	3: 130,378,364 (GRCm39)	P606S	probably damaging	Het
Dcc	A	G	18: 71,680,491 (GRCm39)	S582P	possibly damaging	Het
Dlg4	A	G	11: 69,933,430 (GRCm39)	D619G	probably damaging	Het
Elavl2	C	T	4: 91,152,331 (GRCm39)	V129I	probably benign	Het
Epha3	A	G	16: 63,366,552 (GRCm39)	I965T	probably benign	Het
Fbxw16	G	A	9: 109,265,739 (GRCm39)	S360L	probably damaging	Het
Fgf14	T	C	14: 124,221,330 (GRCm39)	Y158C	probably damaging	Het
Gm44511	A	G	6: 128,803,163 (GRCm39)	I16T	possibly damaging	Het
Has2	C	A	15: 56,531,183 (GRCm39)	V511F	probably benign	Het
Heatr5b	G	A	17: 79,109,185 (GRCm39)	R1025C	probably damaging	Het
Hsd17b12	T	C	2: 93,864,408 (GRCm39)	Y233C	probably benign	Het
Il36rn	A	T	2: 24,170,831 (GRCm39)	I43F	probably damaging	Het
Inpp5b	T	A	4: 124,678,988 (GRCm39)	I465N	probably damaging	Het
Irak2	T	A	6: 113,663,904 (GRCm39)	N423K	probably damaging	Het
Itga2	C	A	13: 115,007,141 (GRCm39)	V396L	probably benign	Het
Itprid1	A	G	6: 55,874,685 (GRCm39)	T212A	possibly damaging	Het
Lipo2	A	T	19: 33,725,969 (GRCm39)	N94K	probably damaging	Het
Lrrc37a	T	C	11: 103,390,869 (GRCm39)	T1519A	possibly damaging	Het
Macf1	A	G	4: 123,353,005 (GRCm39)	V1558A	probably benign	Het
Mocos	C	A	18: 24,797,114 (GRCm39)	H91Q	probably benign	Het
Myh14	G	A	7: 44,310,487 (GRCm39)	T132I	probably damaging	Het
Nlrp2	A	T	7: 5,322,237 (GRCm39)	D803E	possibly damaging	Het
Ntsr2	T	A	12: 16,704,018 (GRCm39)	I173N	probably damaging	Het
Or14c43	A	G	7: 86,115,573 (GRCm39)	Y318C	possibly damaging	Het
Or5b105	T	G	19: 13,079,857 (GRCm39)	K270N	probably damaging	Het
Pitx3	T	C	19: 46,125,486 (GRCm39)	Y86C	probably damaging	Het
Pkp1	T	C	1: 135,807,709 (GRCm39)	S520G	probably benign	Het
Pygo1	C	T	9: 72,852,529 (GRCm39)	Q239*	probably null	Het
Rab13	A	G	3: 90,130,851 (GRCm39)	E68G	probably damaging	Het
Rfx7	A	G	9: 72,525,201 (GRCm39)	E797G	probably benign	Het
Slc5a1	T	C	5: 33,261,937 (GRCm39)		probably null	Het
Slco1c1	A	G	6: 141,508,893 (GRCm39)	T518A	probably benign	Het
Spint1	A	G	2: 119,068,661 (GRCm39)	I132V	probably benign	Het
Stard9	T	A	2: 120,544,601 (GRCm39)	I4514N	probably benign	Het
Tenm3	T	G	8: 48,848,579 (GRCm39)	S87R	probably damaging	Het
Thap4	G	T	1: 93,678,381 (GRCm39)	P135Q	probably damaging	Het
Tmed9	A	G	13: 55,741,156 (GRCm39)	E57G	probably benign	Het
Tnrc18	C	T	5: 142,761,644 (GRCm39)	V594I	unknown	Het
Trmt1	A	T	8: 85,416,470 (GRCm39)	K64*	probably null	Het
Usf2	A	G	7: 30,654,606 (GRCm39)	V198A	probably damaging	Het
Usp14	A	T	18: 10,007,835 (GRCm39)	C168S	probably damaging	Het
Vav3	C	A	3: 109,470,130 (GRCm39)	T525K	probably damaging	Het
Vmn1r52	A	G	6: 90,156,151 (GRCm39)	I152V	probably benign	Het
Vmn2r81	A	G	10: 79,104,085 (GRCm39)	D236G	possibly damaging	Het
Wdr19	G	A	5: 65,401,509 (GRCm39)	V975I	possibly damaging	Het

Other mutations in Aspg

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01462:Aspg	APN	12	112,089,387 (GRCm39)	missense	probably benign
IGL02199:Aspg	APN	12	112,087,426 (GRCm39)	missense	probably benign	0.39
R0704:Aspg	UTSW	12	112,080,906 (GRCm39)	missense	probably damaging	1.00
R0730:Aspg	UTSW	12	112,078,693 (GRCm39)	nonsense	probably null
R1196:Aspg	UTSW	12	112,082,958 (GRCm39)	missense	possibly damaging	0.94
R1270:Aspg	UTSW	12	112,082,881 (GRCm39)	missense	probably damaging	1.00
R1466:Aspg	UTSW	12	112,088,286 (GRCm39)	missense	probably benign	0.20
R1466:Aspg	UTSW	12	112,088,286 (GRCm39)	missense	probably benign	0.20
R1592:Aspg	UTSW	12	112,086,406 (GRCm39)	missense	probably benign	0.17
R1826:Aspg	UTSW	12	112,089,852 (GRCm39)	missense	probably damaging	0.99
R1859:Aspg	UTSW	12	112,087,606 (GRCm39)	missense	possibly damaging	0.86
R2124:Aspg	UTSW	12	112,087,608 (GRCm39)	missense	probably benign	0.15
R2154:Aspg	UTSW	12	112,087,408 (GRCm39)	missense	probably benign	0.01
R2221:Aspg	UTSW	12	112,080,868 (GRCm39)	missense	probably damaging	1.00
R2223:Aspg	UTSW	12	112,080,868 (GRCm39)	missense	probably damaging	1.00
R3907:Aspg	UTSW	12	112,078,693 (GRCm39)	nonsense	probably null
R4234:Aspg	UTSW	12	112,089,750 (GRCm39)	nonsense	probably null
R4258:Aspg	UTSW	12	112,087,687 (GRCm39)	missense	probably benign	0.00
R4270:Aspg	UTSW	12	112,087,629 (GRCm39)	missense	probably damaging	1.00
R4271:Aspg	UTSW	12	112,087,629 (GRCm39)	missense	probably damaging	1.00
R5386:Aspg	UTSW	12	112,089,466 (GRCm39)	missense	probably benign	0.01
R5431:Aspg	UTSW	12	112,089,846 (GRCm39)	missense	probably benign	0.13
R5458:Aspg	UTSW	12	112,086,436 (GRCm39)	missense	probably damaging	0.99
R5941:Aspg	UTSW	12	112,079,519 (GRCm39)	missense	probably benign	0.02
R6003:Aspg	UTSW	12	112,079,476 (GRCm39)	missense	probably damaging	1.00
R6057:Aspg	UTSW	12	112,087,432 (GRCm39)	missense	probably damaging	0.96
R6928:Aspg	UTSW	12	112,093,123 (GRCm39)	missense	possibly damaging	0.52
R6979:Aspg	UTSW	12	112,087,378 (GRCm39)	missense	possibly damaging	0.77
R6998:Aspg	UTSW	12	112,078,628 (GRCm39)	missense	probably damaging	1.00
R7054:Aspg	UTSW	12	112,092,824 (GRCm39)	missense	probably damaging	0.98
R7060:Aspg	UTSW	12	112,089,387 (GRCm39)	missense	probably benign
R7124:Aspg	UTSW	12	112,089,417 (GRCm39)	missense	probably damaging	0.99
R7137:Aspg	UTSW	12	112,078,632 (GRCm39)	missense	possibly damaging	0.92
R7439:Aspg	UTSW	12	112,091,255 (GRCm39)	missense	possibly damaging	0.90
R7441:Aspg	UTSW	12	112,091,255 (GRCm39)	missense	possibly damaging	0.90
R8922:Aspg	UTSW	12	112,089,830 (GRCm39)	missense	possibly damaging	0.86
R9463:Aspg	UTSW	12	112,089,824 (GRCm39)	missense	probably damaging	1.00
Z1176:Aspg	UTSW	12	112,079,515 (GRCm39)	missense	possibly damaging	0.58
Z1177:Aspg	UTSW	12	112,087,455 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGAGTCGCCCCAGTTCTCAC -3'
(R):5'- CTCCAGGACCCAGGATGAAC -3'

Sequencing Primer
(F):5'- GCCCCAGTTCTCACCCCAC -3'
(R):5'- GGACCCAGGATGAACACCTTATG -3'

Posted On

2014-10-02