Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01700:Ear2'

104419

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Ear2

Ensembl Gene

ENSMUSG00000072596

Gene Name

eosinophil-associated, ribonuclease A family, member 2

Synonyms

Rnase2, eosinophil-derived neurotoxin, liver

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.055) question?

Stock #

IGL01700

Quality Score

Status

Chromosome

Chromosomal Location

44340111-44340988 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 44340716 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Stop codon at position 125 (R125*)

Ref Sequence

ENSEMBL: ENSMUSP00000074386 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000074839]

AlphaFold

P97425

Predicted Effect

probably null
Transcript: ENSMUST00000074839
AA Change: R125*

SMART Domains

Protein: ENSMUSP00000074386
Gene: ENSMUSG00000072596
AA Change: R125*

Domain	Start	End	E-Value	Type
low complexity region	5	26	N/A	INTRINSIC
RNAse_Pc	27	156	1.09e-57	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000226587

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca12	T	A	1: 71,319,549 (GRCm39)	M1778L	probably benign	Het
Aldh6a1	C	T	12: 84,486,312 (GRCm39)	C202Y	probably damaging	Het
Ankrd36	A	G	11: 5,582,198 (GRCm39)	T276A	probably benign	Het
Ankrd55	T	C	13: 112,517,702 (GRCm39)	I556T	probably benign	Het
Aqp4	A	G	18: 15,532,922 (GRCm39)	I57T	probably benign	Het
Atp1a1	T	C	3: 101,501,574 (GRCm39)	D43G	possibly damaging	Het
Cyld	G	A	8: 89,433,727 (GRCm39)	R172H	probably damaging	Het
Efcab9	T	C	11: 32,477,451 (GRCm39)	R24G	probably damaging	Het
F7	C	A	8: 13,078,685 (GRCm39)	Q39K	probably benign	Het
Galntl6	A	T	8: 58,411,494 (GRCm39)		probably benign	Het
Kcnj5	A	G	9: 32,233,925 (GRCm39)	V130A	probably damaging	Het
Magee2	A	G	X: 103,899,574 (GRCm39)	I359T	possibly damaging	Het
Myh1	T	G	11: 67,102,238 (GRCm39)	I843S	probably damaging	Het
Nfat5	T	A	8: 108,065,762 (GRCm39)	M98K	probably damaging	Het
Nrip3	T	A	7: 109,361,074 (GRCm39)	N200I	possibly damaging	Het
Or6c219	A	T	10: 129,781,810 (GRCm39)	N40K	probably damaging	Het
Phkb	A	T	8: 86,744,094 (GRCm39)	Q581L	probably benign	Het
Plxdc2	T	C	2: 16,516,926 (GRCm39)	V69A	probably benign	Het
Pou3f1	G	T	4: 124,552,650 (GRCm39)	W384L	probably damaging	Het
Prrc2a	G	A	17: 35,369,643 (GRCm39)	S1890L	possibly damaging	Het
Psmc1	C	A	12: 100,079,337 (GRCm39)	P27H	probably damaging	Het
Pvr	C	A	7: 19,643,157 (GRCm39)	A359S	probably benign	Het
Rasal1	A	T	5: 120,814,882 (GRCm39)	I711F	probably benign	Het
Ror1	C	T	4: 100,266,968 (GRCm39)	A223V	probably damaging	Het
Slc22a16	A	T	10: 40,479,904 (GRCm39)	I638L	unknown	Het
Slfn10-ps	C	T	11: 82,919,938 (GRCm39)		noncoding transcript	Het
Sptbn4	A	G	7: 27,103,693 (GRCm39)	L1176P	probably damaging	Het
Usp21	A	T	1: 171,110,975 (GRCm39)	F421I	probably damaging	Het
Utp25	G	A	1: 192,800,573 (GRCm39)	P416S	probably damaging	Het
Vmn1r61	T	A	7: 5,614,202 (GRCm39)	R37S	possibly damaging	Het
Vps13a	G	A	19: 16,722,221 (GRCm39)	R364*	probably null	Het
Vps29	A	G	5: 122,500,930 (GRCm39)	Y165C	probably damaging	Het
Wdfy4	T	C	14: 32,742,195 (GRCm39)		probably benign	Het
Wdr24	A	G	17: 26,044,802 (GRCm39)	D219G	probably damaging	Het
Xpo1	T	C	11: 23,226,422 (GRCm39)		probably benign	Het
Zfp831	C	A	2: 174,486,711 (GRCm39)	T462K	possibly damaging	Het
Zswim5	T	C	4: 116,843,658 (GRCm39)		probably benign	Het

Other mutations in Ear2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01729:Ear2	APN	14	44,340,701 (GRCm39)	nonsense	probably null
R0346:Ear2	UTSW	14	44,340,363 (GRCm39)	missense	probably damaging	1.00
R0458:Ear2	UTSW	14	44,340,705 (GRCm39)	missense	probably damaging	1.00
R1035:Ear2	UTSW	14	44,340,344 (GRCm39)	start codon destroyed	possibly damaging	0.59
R4920:Ear2	UTSW	14	44,340,582 (GRCm39)	missense	probably damaging	0.97
R5845:Ear2	UTSW	14	44,340,618 (GRCm39)	missense	probably benign	0.00
R6008:Ear2	UTSW	14	44,340,546 (GRCm39)	missense	probably damaging	1.00
R6432:Ear2	UTSW	14	44,340,660 (GRCm39)	missense	probably damaging	1.00
R6720:Ear2	UTSW	14	44,340,416 (GRCm39)	missense	probably damaging	0.99
R7721:Ear2	UTSW	14	44,340,495 (GRCm39)	missense	probably damaging	1.00
R8251:Ear2	UTSW	14	44,340,477 (GRCm39)	missense	probably benign	0.00
R8719:Ear2	UTSW	14	44,340,734 (GRCm39)	missense	possibly damaging	0.94
R9659:Ear2	UTSW	14	44,340,705 (GRCm39)	missense	probably damaging	1.00
R9776:Ear2	UTSW	14	44,340,729 (GRCm39)	missense	probably benign	0.02
R9788:Ear2	UTSW	14	44,340,705 (GRCm39)	missense	probably damaging	1.00

Posted On

2014-01-21