Mutagenetix > Incidental Mutation

Incidental Mutation 'R3736:Ang2'

270139

Institutional Source

Beutler Lab

Gene Symbol

Ang2

Ensembl Gene

ENSMUSG00000047894

Gene Name

angiogenin, ribonuclease A family, member 2

Synonyms

Rnase5b, Angrp

MMRRC Submission

040723-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.065) question?

Stock #

R3736 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

51432781-51436400 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 51433113 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Stop codon at position 90 (R90*)

Ref Sequence

ENSEMBL: ENSMUSP00000154100 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000051274] [ENSMUST00000228835]

AlphaFold

Q64438

Predicted Effect

probably null
Transcript: ENSMUST00000051274
AA Change: R90*

SMART Domains

Protein: ENSMUSP00000062902
Gene: ENSMUSG00000047894
AA Change: R90*

Domain	Start	End	E-Value	Type
low complexity region	5	18	N/A	INTRINSIC
RNAse_Pc	26	142	3.11e-62	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000228835
AA Change: R90*

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 94.6%

Validation Efficiency

100% (53/53)

Allele List at MGI

Other mutations in this stock

Total: 47 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930432E11Rik	G	A	7: 29,273,996 (GRCm39)		noncoding transcript	Het
Acot12	T	A	13: 91,932,465 (GRCm39)	I487N	probably benign	Het
Acox3	A	G	5: 35,768,497 (GRCm39)	K686R	probably benign	Het
Adgrf2	T	C	17: 43,021,903 (GRCm39)	E307G	probably benign	Het
Ankrd11	A	T	8: 123,618,524 (GRCm39)	V1776D	probably damaging	Het
Atp12a	G	A	14: 56,611,884 (GRCm39)	V353I	possibly damaging	Het
Bbs7	A	G	3: 36,661,819 (GRCm39)	Y127H	possibly damaging	Het
C8a	T	C	4: 104,674,812 (GRCm39)	E509G	probably benign	Het
Ccdc158	A	C	5: 92,780,283 (GRCm39)	L930R	possibly damaging	Het
Ccdc162	T	C	10: 41,465,564 (GRCm39)		probably null	Het
Cep170b	A	T	12: 112,707,438 (GRCm39)	I395F	probably damaging	Het
Cimip2c	A	T	5: 30,639,442 (GRCm39)	Y123F	probably benign	Het
Clcn3	T	A	8: 61,436,686 (GRCm39)		probably benign	Het
Ctps1	T	C	4: 120,400,943 (GRCm39)	T459A	probably benign	Het
Cyp2j8	T	A	4: 96,332,836 (GRCm39)	R503S	probably damaging	Het
Dync1h1	G	A	12: 110,598,109 (GRCm39)	V1767I	probably benign	Het
Evi5	A	T	5: 107,966,849 (GRCm39)	V224D	probably damaging	Het
F8	G	A	X: 74,254,981 (GRCm39)	P2138S	probably damaging	Het
Helq	T	G	5: 100,938,054 (GRCm39)	D464A	possibly damaging	Het
Irag1	A	G	7: 110,523,170 (GRCm39)	V297A	probably benign	Het
Irag2	G	A	6: 145,106,596 (GRCm39)		probably benign	Het
Kcnk10	A	G	12: 98,456,171 (GRCm39)	V203A	probably benign	Het
Lef1	C	T	3: 130,984,715 (GRCm39)	P160S	possibly damaging	Het
Lyn	G	T	4: 3,745,330 (GRCm39)	W78C	probably damaging	Het
Med12l	T	A	3: 58,998,916 (GRCm39)	H614Q	probably damaging	Het
Mogs	C	A	6: 83,093,757 (GRCm39)	T242K	possibly damaging	Het
Morc3	T	A	16: 93,671,700 (GRCm39)	V910E	probably damaging	Het
Ncapg	A	T	5: 45,853,469 (GRCm39)	Q906L	probably benign	Het
Nup210l	A	G	3: 90,027,320 (GRCm39)	Y234C	probably damaging	Het
Olr1	T	A	6: 129,476,838 (GRCm39)		probably benign	Het
Or5p76	A	G	7: 108,122,626 (GRCm39)	V177A	possibly damaging	Het
Osmr	A	T	15: 6,851,561 (GRCm39)	Y656N	probably damaging	Het
Pde4dip	A	T	3: 97,631,427 (GRCm39)	F1161I	probably damaging	Het
Poc5	A	G	13: 96,533,324 (GRCm39)	S151G	probably damaging	Het
Rmnd5a	T	C	6: 71,373,846 (GRCm39)	D316G	possibly damaging	Het
Shroom3	T	C	5: 93,112,303 (GRCm39)	V1888A	possibly damaging	Het
Shtn1	A	T	19: 59,010,700 (GRCm39)	S256T	probably benign	Het
Sptlc2	G	A	12: 87,388,339 (GRCm39)	A381V	probably benign	Het
Suclg2	T	A	6: 95,474,677 (GRCm39)	I363F	probably damaging	Het
Tas2r134	C	A	2: 51,517,786 (GRCm39)	N88K	probably damaging	Het
Tbc1d32	A	G	10: 56,005,189 (GRCm39)	Y815H	probably damaging	Het
Tnrc6b	G	C	15: 80,773,364 (GRCm39)		probably benign	Het
Vti1a	T	A	19: 55,369,364 (GRCm39)		probably null	Het
Zfp273	T	A	13: 67,973,626 (GRCm39)	C251*	probably null	Het
Zfp683	C	A	4: 133,784,742 (GRCm39)	Q330K	probably benign	Het
Zfpm1	G	A	8: 123,050,475 (GRCm39)	C117Y	possibly damaging	Het
Zscan4d	T	C	7: 10,896,803 (GRCm39)	N189S	probably benign	Het

Other mutations in Ang2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0276:Ang2	UTSW	14	51,432,975 (GRCm39)	missense	probably damaging	0.98
R1319:Ang2	UTSW	14	51,433,164 (GRCm39)	missense	probably benign	0.02
R1548:Ang2	UTSW	14	51,432,990 (GRCm39)	nonsense	probably null
R4329:Ang2	UTSW	14	51,433,325 (GRCm39)	missense	possibly damaging	0.77
R4754:Ang2	UTSW	14	51,432,974 (GRCm39)	missense	probably damaging	1.00
R5457:Ang2	UTSW	14	51,433,292 (GRCm39)	missense	probably damaging	1.00
R7718:Ang2	UTSW	14	51,433,217 (GRCm39)	missense	probably benign
R8317:Ang2	UTSW	14	51,433,349 (GRCm39)	missense	probably benign	0.34
R8325:Ang2	UTSW	14	51,432,960 (GRCm39)	missense	probably damaging	1.00
R8725:Ang2	UTSW	14	51,432,996 (GRCm39)	missense	probably benign	0.40
R8727:Ang2	UTSW	14	51,432,996 (GRCm39)	missense	probably benign	0.40
R9487:Ang2	UTSW	14	51,433,071 (GRCm39)	missense	probably damaging	1.00
R9697:Ang2	UTSW	14	51,433,326 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AAAGAGAGCTAGGCCTGTGC -3'
(R):5'- TCTCAGGATGACTCCAGGTAC -3'

Sequencing Primer
(F):5'- CAGGGGTCTGCTGTCTATGGAC -3'
(R):5'- GGATGACTCCAGGTACACAAAATTC -3'

Posted On

2015-03-18