Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02370:Yeats2'

290908

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Yeats2

Ensembl Gene

ENSMUSG00000041215

Gene Name

YEATS domain containing 2

Synonyms

Accession Numbers

Essential gene?

Probably essential (E-score: 0.960) question?

Stock #

IGL02370

Quality Score

Status

Chromosome

Chromosomal Location

19959813-20051323 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 19969221 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 4 (I4N)

Ref Sequence

ENSEMBL: ENSMUSP00000156060 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000090052] [ENSMUST00000115560] [ENSMUST00000231705] [ENSMUST00000232019] [ENSMUST00000232338]

AlphaFold

Q3TUF7

Predicted Effect

probably benign
Transcript: ENSMUST00000090052

SMART Domains

Protein: ENSMUSP00000087506
Gene: ENSMUSG00000041215

Domain	Start	End	E-Value	Type
Pfam:YEATS	179	262	2.6e-27	PFAM
low complexity region	299	309	N/A	INTRINSIC
low complexity region	312	333	N/A	INTRINSIC
low complexity region	409	429	N/A	INTRINSIC
low complexity region	458	467	N/A	INTRINSIC
internal_repeat_1	471	675	3.72e-6	PROSPERO
low complexity region	683	702	N/A	INTRINSIC
low complexity region	738	775	N/A	INTRINSIC
internal_repeat_1	785	978	3.72e-6	PROSPERO
low complexity region	1240	1249	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000115560
AA Change: I4N

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000111222
Gene: ENSMUSG00000041215
AA Change: I4N

Domain	Start	End	E-Value	Type
Pfam:YEATS	232	314	2.1e-28	PFAM
low complexity region	352	362	N/A	INTRINSIC
low complexity region	365	386	N/A	INTRINSIC
low complexity region	462	482	N/A	INTRINSIC
low complexity region	511	520	N/A	INTRINSIC
internal_repeat_1	524	728	4.68e-6	PROSPERO
low complexity region	736	755	N/A	INTRINSIC
low complexity region	791	828	N/A	INTRINSIC
internal_repeat_1	838	1031	4.68e-6	PROSPERO
low complexity region	1293	1302	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000231705
AA Change: I4N

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

Predicted Effect

probably benign
Transcript: ENSMUST00000232019

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000232172

Predicted Effect

probably benign
Transcript: ENSMUST00000232338

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] YEATS2 is a scaffolding subunit of the ADA2A (TADA2A; MIM 602276)-containing (ATAC) histone acetyltransferase complex (Wang et al., 2008 [PubMed 18838386]).[supplied by OMIM, Apr 2010]

Allele List at MGI

All alleles(34) : Targeted(1) Gene trapped(33)

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4732471J01Rik	T	C	7: 25,084,313 (GRCm39)		probably benign	Het
Abra	T	C	15: 41,732,640 (GRCm39)	D142G	probably damaging	Het
Aldh9a1	A	G	1: 167,184,101 (GRCm39)	N199D	probably damaging	Het
Baz2b	A	T	2: 59,753,933 (GRCm39)	I1130N	possibly damaging	Het
Cacna1s	A	G	1: 136,013,085 (GRCm39)	I312V	probably damaging	Het
Chrd	A	G	16: 20,554,541 (GRCm39)	M367V	possibly damaging	Het
Clec12a	C	T	6: 129,331,539 (GRCm39)	A160V	possibly damaging	Het
Cnnm1	T	C	19: 43,460,389 (GRCm39)		probably null	Het
Cntnap3	A	T	13: 64,899,565 (GRCm39)	M976K	probably benign	Het
Cyp27b1	T	C	10: 126,886,543 (GRCm39)		probably benign	Het
Ddx54	T	A	5: 120,757,852 (GRCm39)	L226Q	probably damaging	Het
Dnah7a	A	G	1: 53,674,556 (GRCm39)	V407A	probably benign	Het
Elp4	A	G	2: 105,624,937 (GRCm39)	S201P	probably damaging	Het
Exoc3	A	T	13: 74,340,880 (GRCm39)	V308D	probably benign	Het
Exosc3	A	G	4: 45,319,671 (GRCm39)	I117T	probably damaging	Het
Gbx2	A	T	1: 89,856,871 (GRCm39)		probably benign	Het
Hnf1b	A	C	11: 83,773,559 (GRCm39)	T253P	possibly damaging	Het
Inhca	A	G	9: 103,140,273 (GRCm39)	V482A	probably benign	Het
Itih5	A	T	2: 10,191,786 (GRCm39)	Y107F	probably benign	Het
Kcnb2	A	G	1: 15,781,159 (GRCm39)	N677S	probably benign	Het
Knstrn	T	A	2: 118,654,269 (GRCm39)		probably null	Het
Lin9	G	T	1: 180,515,583 (GRCm39)	C451F	probably damaging	Het
Mast1	A	C	8: 85,638,883 (GRCm39)	V1482G	probably benign	Het
Mroh4	A	G	15: 74,497,390 (GRCm39)	F144L	probably benign	Het
Myrf	T	C	19: 10,191,504 (GRCm39)	N945D	probably benign	Het
Nfrkb	G	A	9: 31,300,308 (GRCm39)	G33D	probably benign	Het
Or5m9b	C	A	2: 85,905,132 (GRCm39)	T16K	probably damaging	Het
P2ry13	T	C	3: 59,116,886 (GRCm39)	I297M	probably damaging	Het
Pcdhb21	T	A	18: 37,647,645 (GRCm39)		probably null	Het
Pitpnm3	A	G	11: 71,942,684 (GRCm39)	Y868H	probably benign	Het
Pou2f3	G	A	9: 43,048,643 (GRCm39)	R266W	probably damaging	Het
Rcn3	T	C	7: 44,732,757 (GRCm39)	S304G	probably benign	Het
Rinl	A	G	7: 28,494,397 (GRCm39)		probably null	Het
Sema5a	T	C	15: 32,682,445 (GRCm39)		probably benign	Het
Sipa1l2	A	G	8: 126,207,008 (GRCm39)	L565P	probably damaging	Het
Slc5a9	A	G	4: 111,734,826 (GRCm39)	I656T	probably benign	Het
Sptan1	A	G	2: 29,920,752 (GRCm39)	K2404R	probably damaging	Het
Tars3	C	A	7: 65,310,913 (GRCm39)	P314Q	probably benign	Het
Tbc1d14	C	T	5: 36,652,562 (GRCm39)	V627I	possibly damaging	Het
Tdpoz8	A	G	3: 92,981,354 (GRCm39)	D124G	possibly damaging	Het
Tfcp2	A	T	15: 100,410,185 (GRCm39)	V394D	probably damaging	Het
Trerf1	C	T	17: 47,625,387 (GRCm39)		noncoding transcript	Het
Ucp2	A	G	7: 100,147,591 (GRCm39)	N190S	probably damaging	Het
Vmn2r124	A	G	17: 18,284,453 (GRCm39)	Q498R	probably benign	Het
Zfp574	T	G	7: 24,779,014 (GRCm39)	I12S	possibly damaging	Het
Zscan29	T	A	2: 120,994,314 (GRCm39)	E522V	probably benign	Het

Other mutations in Yeats2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01118:Yeats2	APN	16	20,005,054 (GRCm39)	missense	probably damaging	0.99
IGL01128:Yeats2	APN	16	19,980,718 (GRCm39)	splice site	probably benign
IGL01139:Yeats2	APN	16	20,033,143 (GRCm39)	missense	probably damaging	1.00
IGL01394:Yeats2	APN	16	19,980,782 (GRCm39)	missense	probably damaging	0.99
IGL01482:Yeats2	APN	16	20,041,671 (GRCm39)	missense	probably damaging	1.00
IGL01924:Yeats2	APN	16	20,024,917 (GRCm39)	missense	probably damaging	1.00
IGL01925:Yeats2	APN	16	19,998,430 (GRCm39)	splice site	probably benign
IGL02106:Yeats2	APN	16	20,011,970 (GRCm39)	missense	possibly damaging	0.79
IGL02447:Yeats2	APN	16	20,012,429 (GRCm39)	missense	probably benign	0.00
IGL02669:Yeats2	APN	16	20,005,033 (GRCm39)	missense	probably benign	0.13
IGL03155:Yeats2	APN	16	20,048,323 (GRCm39)	critical splice donor site	probably null
tyrion	UTSW	16	20,032,151 (GRCm39)	splice site	probably benign
P0045:Yeats2	UTSW	16	19,975,695 (GRCm39)	missense	possibly damaging	0.47
R0051:Yeats2	UTSW	16	20,012,474 (GRCm39)	nonsense	probably null
R0051:Yeats2	UTSW	16	20,012,474 (GRCm39)	nonsense	probably null
R0118:Yeats2	UTSW	16	19,975,692 (GRCm39)	nonsense	probably null
R0157:Yeats2	UTSW	16	20,040,427 (GRCm39)	makesense	probably null
R0184:Yeats2	UTSW	16	20,022,435 (GRCm39)	missense	possibly damaging	0.79
R0194:Yeats2	UTSW	16	19,971,719 (GRCm39)	start codon destroyed	probably null	1.00
R0612:Yeats2	UTSW	16	20,005,175 (GRCm39)	missense	probably benign	0.00
R0655:Yeats2	UTSW	16	20,012,574 (GRCm39)	nonsense	probably null
R0826:Yeats2	UTSW	16	20,011,966 (GRCm39)	nonsense	probably null
R1526:Yeats2	UTSW	16	20,024,836 (GRCm39)	missense	probably damaging	1.00
R1535:Yeats2	UTSW	16	20,008,115 (GRCm39)	missense	probably damaging	0.99
R1749:Yeats2	UTSW	16	20,005,018 (GRCm39)	nonsense	probably null
R1842:Yeats2	UTSW	16	19,989,988 (GRCm39)	missense	probably damaging	1.00
R1843:Yeats2	UTSW	16	20,048,314 (GRCm39)	missense	probably benign	0.01
R1926:Yeats2	UTSW	16	20,033,176 (GRCm39)	missense	probably benign
R2000:Yeats2	UTSW	16	20,005,141 (GRCm39)	missense	probably benign	0.20
R2017:Yeats2	UTSW	16	19,977,931 (GRCm39)	missense	probably benign	0.01
R2076:Yeats2	UTSW	16	20,005,032 (GRCm39)	missense	possibly damaging	0.47
R2153:Yeats2	UTSW	16	19,972,916 (GRCm39)	missense	probably damaging	1.00
R2167:Yeats2	UTSW	16	20,032,151 (GRCm39)	splice site	probably benign
R2981:Yeats2	UTSW	16	20,005,051 (GRCm39)	missense	probably damaging	0.99
R3160:Yeats2	UTSW	16	20,012,395 (GRCm39)	missense	probably damaging	1.00
R3161:Yeats2	UTSW	16	20,012,395 (GRCm39)	missense	probably damaging	1.00
R3162:Yeats2	UTSW	16	20,012,395 (GRCm39)	missense	probably damaging	1.00
R3774:Yeats2	UTSW	16	19,969,245 (GRCm39)	missense	probably damaging	1.00
R4250:Yeats2	UTSW	16	19,975,685 (GRCm39)	missense	possibly damaging	0.90
R4305:Yeats2	UTSW	16	20,027,172 (GRCm39)	missense	probably damaging	1.00
R4455:Yeats2	UTSW	16	19,980,743 (GRCm39)	missense	possibly damaging	0.88
R4458:Yeats2	UTSW	16	20,032,071 (GRCm39)	missense	probably damaging	0.99
R4811:Yeats2	UTSW	16	19,971,645 (GRCm39)	splice site	probably null
R4902:Yeats2	UTSW	16	20,026,418 (GRCm39)	missense	probably benign	0.00
R5043:Yeats2	UTSW	16	20,027,215 (GRCm39)	missense	probably damaging	1.00
R5047:Yeats2	UTSW	16	20,027,215 (GRCm39)	missense	probably damaging	1.00
R5319:Yeats2	UTSW	16	20,005,175 (GRCm39)	missense	probably benign	0.01
R5328:Yeats2	UTSW	16	19,989,955 (GRCm39)	missense	probably damaging	1.00
R5360:Yeats2	UTSW	16	19,972,912 (GRCm39)	missense	probably damaging	0.97
R5416:Yeats2	UTSW	16	20,030,319 (GRCm39)	missense	probably benign	0.01
R5672:Yeats2	UTSW	16	19,980,779 (GRCm39)	missense	probably damaging	1.00
R5684:Yeats2	UTSW	16	20,012,553 (GRCm39)	missense	possibly damaging	0.94
R5932:Yeats2	UTSW	16	20,011,913 (GRCm39)	missense	probably benign	0.06
R5946:Yeats2	UTSW	16	20,026,513 (GRCm39)	nonsense	probably null
R6168:Yeats2	UTSW	16	19,998,308 (GRCm39)	missense	probably benign	0.01
R6169:Yeats2	UTSW	16	20,038,417 (GRCm39)	missense	probably damaging	1.00
R6179:Yeats2	UTSW	16	20,033,225 (GRCm39)	missense	probably benign	0.16
R6371:Yeats2	UTSW	16	20,040,460 (GRCm39)	missense	possibly damaging	0.54
R6877:Yeats2	UTSW	16	19,998,344 (GRCm39)	missense	probably benign	0.00
R7149:Yeats2	UTSW	16	19,972,939 (GRCm39)	missense	probably damaging	1.00
R7405:Yeats2	UTSW	16	20,041,663 (GRCm39)	missense	probably damaging	1.00
R8353:Yeats2	UTSW	16	20,041,637 (GRCm39)	nonsense	probably null
R8367:Yeats2	UTSW	16	20,041,575 (GRCm39)	missense	probably damaging	1.00
R8453:Yeats2	UTSW	16	20,041,637 (GRCm39)	nonsense	probably null
R8506:Yeats2	UTSW	16	19,971,684 (GRCm39)	missense	probably damaging	0.98
R8535:Yeats2	UTSW	16	19,977,926 (GRCm39)	missense	probably damaging	1.00
R8828:Yeats2	UTSW	16	19,969,260 (GRCm39)	missense	probably benign	0.45
R8905:Yeats2	UTSW	16	20,009,144 (GRCm39)	missense	probably benign	0.02
R8924:Yeats2	UTSW	16	19,969,312 (GRCm39)	critical splice donor site	probably null
R9087:Yeats2	UTSW	16	20,030,500 (GRCm39)	critical splice donor site	probably null
R9276:Yeats2	UTSW	16	19,975,786 (GRCm39)	missense	probably benign	0.34
R9338:Yeats2	UTSW	16	20,041,533 (GRCm39)	missense	probably damaging	0.99
R9338:Yeats2	UTSW	16	20,032,078 (GRCm39)	missense	possibly damaging	0.69
R9378:Yeats2	UTSW	16	20,033,228 (GRCm39)	missense	probably benign
R9569:Yeats2	UTSW	16	19,972,902 (GRCm39)	missense	probably damaging	1.00
R9664:Yeats2	UTSW	16	20,047,491 (GRCm39)	nonsense	probably null

Posted On

2015-04-16