Mutagenetix > Incidental Mutation

Incidental Mutation 'R5406:Ino80c'

426300

Institutional Source

Beutler Lab

Gene Symbol

Ino80c

Ensembl Gene

ENSMUSG00000047989

Gene Name

INO80 complex subunit C

Synonyms

D030070L09Rik

MMRRC Submission

042976-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.921) question?

Stock #

R5406 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

24237818-24254876 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 24245819 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 92 (H92L)

Ref Sequence

ENSEMBL: ENSMUSP00000055342 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000055012] [ENSMUST00000125169] [ENSMUST00000141489] [ENSMUST00000153360]

AlphaFold

Q8BHA0

Predicted Effect

probably benign
Transcript: ENSMUST00000055012
AA Change: H92L

PolyPhen 2 Score 0.176 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000055342
Gene: ENSMUSG00000047989
AA Change: H92L

Domain	Start	End	E-Value	Type
low complexity region	31	48	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000125169
AA Change: H35L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000117684
Gene: ENSMUSG00000047989
AA Change: H35L

Domain	Start	End	E-Value	Type
YL1_C	83	112	2.99e-9	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000141489

SMART Domains

Protein: ENSMUSP00000122372
Gene: ENSMUSG00000047989

Domain	Start	End	E-Value	Type
YL1_C	43	72	1.73e0	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000153360
AA Change: H92L

PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000114643
Gene: ENSMUSG00000047989
AA Change: H92L

Domain	Start	End	E-Value	Type
low complexity region	31	48	N/A	INTRINSIC
YL1_C	140	169	2.99e-9	SMART

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.0%
20x: 94.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 44 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aasdhppt	A	T	9: 4,309,387 (GRCm39)	V17D	probably damaging	Het
Abcb1a	C	A	5: 8,752,946 (GRCm39)	Q566K	probably damaging	Het
Adam26a	A	T	8: 44,022,141 (GRCm39)	C450S	probably damaging	Het
Adar	C	T	3: 89,643,418 (GRCm39)	P433L	probably damaging	Het
Aldh1a2	G	T	9: 71,162,403 (GRCm39)	A151S	possibly damaging	Het
Arsk	T	A	13: 76,242,066 (GRCm39)	H69L	probably benign	Het
Atf6b	T	A	17: 34,872,771 (GRCm39)	Y600*	probably null	Het
Blk	C	A	14: 63,618,180 (GRCm39)	G242V	probably damaging	Het
Bmt2	A	T	6: 13,677,831 (GRCm39)	M1K	probably null	Het
Catsperg1	G	A	7: 28,884,948 (GRCm39)	T891M	probably damaging	Het
Ccdc32	A	C	2: 118,852,560 (GRCm39)	S131A	possibly damaging	Het
Cdh8	A	G	8: 99,923,002 (GRCm39)	V298A	probably damaging	Het
Cfap54	T	A	10: 92,837,720 (GRCm39)	Q1060L	probably benign	Het
Cfap58	G	A	19: 48,017,541 (GRCm39)	M800I	possibly damaging	Het
Cntn5	A	T	9: 9,833,465 (GRCm39)	V362D	probably damaging	Het
Fkbpl	G	A	17: 34,864,303 (GRCm39)	A24T	probably benign	Het
G2e3	T	C	12: 51,419,449 (GRCm39)	S699P	probably damaging	Het
Gbp4	G	T	5: 105,267,387 (GRCm39)	Q511K	possibly damaging	Het
Gdap2	T	A	3: 100,098,991 (GRCm39)	I361N	probably damaging	Het
Lipo4	A	G	19: 33,480,618 (GRCm39)	V250A	probably benign	Het
Llgl1	C	T	11: 60,604,010 (GRCm39)	R1055W	probably damaging	Het
Lrriq3	T	C	3: 154,835,138 (GRCm39)		probably null	Het
Mmp1a	A	G	9: 7,467,294 (GRCm39)	E290G	probably damaging	Het
Ncstn	A	G	1: 171,899,731 (GRCm39)	V317A	probably benign	Het
Nfxl1	G	A	5: 72,713,541 (GRCm39)	T134I	possibly damaging	Het
Nup155	A	T	15: 8,183,122 (GRCm39)		probably null	Het
Nup214	C	A	2: 31,892,619 (GRCm39)	P680T	probably damaging	Het
Or6c212	G	A	10: 129,558,799 (GRCm39)	L205F	probably damaging	Het
Or7h8	A	G	9: 20,124,454 (GRCm39)	K270E	probably benign	Het
Or8b12	A	G	9: 37,657,943 (GRCm39)	N171S	probably benign	Het
Or8b9	G	A	9: 37,766,515 (GRCm39)	V134I	probably benign	Het
Pkd2	T	C	5: 104,628,198 (GRCm39)	F424S	probably damaging	Het
Plb1	A	G	5: 32,499,259 (GRCm39)	D1074G	probably damaging	Het
Ppm1l	T	C	3: 69,224,927 (GRCm39)	S10P	possibly damaging	Het
Rnf213	A	G	11: 119,331,634 (GRCm39)	H2281R	probably damaging	Het
Rpa2	G	T	4: 132,503,559 (GRCm39)	A3S	probably benign	Het
Sardh	A	G	2: 27,101,096 (GRCm39)	V698A	possibly damaging	Het
Saxo2	A	T	7: 82,284,586 (GRCm39)	C91S	probably benign	Het
Slc3a2	T	C	19: 8,685,406 (GRCm39)	D198G	probably damaging	Het
Spata31d1d	T	A	13: 59,876,592 (GRCm39)	E314D	probably benign	Het
Sptlc3	T	C	2: 139,388,398 (GRCm39)	V130A	probably benign	Het
Stpg3	C	A	2: 25,103,580 (GRCm39)	E115*	probably null	Het
Tbcd	T	A	11: 121,342,927 (GRCm39)	D19E	probably benign	Het
Xrcc3	T	C	12: 111,778,545 (GRCm39)	D2G	probably damaging	Het

Other mutations in Ino80c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0063:Ino80c	UTSW	18	24,239,681 (GRCm39)	missense	probably damaging	0.98
R2017:Ino80c	UTSW	18	24,244,810 (GRCm39)	nonsense	probably null
R3800:Ino80c	UTSW	18	24,254,752 (GRCm39)	missense	probably damaging	1.00
R4688:Ino80c	UTSW	18	24,241,903 (GRCm39)	missense	probably damaging	1.00
R4711:Ino80c	UTSW	18	24,247,222 (GRCm39)	missense	probably benign	0.00
R4966:Ino80c	UTSW	18	24,239,702 (GRCm39)	missense	probably damaging	1.00
R5144:Ino80c	UTSW	18	24,241,935 (GRCm39)	missense	probably benign	0.40
R6909:Ino80c	UTSW	18	24,241,812 (GRCm39)	intron	probably benign
R7419:Ino80c	UTSW	18	24,241,836 (GRCm39)	missense	unknown
R7470:Ino80c	UTSW	18	24,241,895 (GRCm39)	nonsense	probably null
R8071:Ino80c	UTSW	18	24,239,707 (GRCm39)	missense	unknown
R8936:Ino80c	UTSW	18	24,254,865 (GRCm39)	start gained	probably benign
R9134:Ino80c	UTSW	18	24,254,765 (GRCm39)	missense	probably benign	0.18
R9673:Ino80c	UTSW	18	24,254,856 (GRCm39)	start codon destroyed	probably null	0.01

Predicted Primers

PCR Primer
(F):5'- AGCAAATAACGTAGGCTTGTTG -3'
(R):5'- ACTTGTGGGTTTGAAGAGCC -3'

Sequencing Primer
(F):5'- CAAATAACGTAGGCTTGTTGTAAGG -3'
(R):5'- TTGATAAAGGTCACCTGTAGCCCAG -3'

Posted On

2016-09-01