Mutagenetix > Incidental Mutation

Incidental Mutation 'R4936:Cnot6l'

380364

Institutional Source

Beutler Lab

Gene Symbol

Cnot6l

Ensembl Gene

ENSMUSG00000034724

Gene Name

CCR4-NOT transcription complex, subunit 6-like

Synonyms

MMRRC Submission

042536-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.438) question?

Stock #

R4936 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

96070333-96164171 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 96079937 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 479 (F479S)

Ref Sequence

ENSEMBL: ENSMUSP00000119415 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000036646] [ENSMUST00000113005] [ENSMUST00000122003] [ENSMUST00000155901]

AlphaFold

Q8VEG6

Predicted Effect

probably benign
Transcript: ENSMUST00000036646

Predicted Effect

probably damaging
Transcript: ENSMUST00000113005
AA Change: F484S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000108629
Gene: ENSMUSG00000034724
AA Change: F484S

Domain	Start	End	E-Value	Type
LRR	55	77	4.34e-1	SMART
LRR	78	100	1.01e-1	SMART
LRR	101	124	7.55e-1	SMART
Pfam:Exo_endo_phos	192	529	7.3e-22	PFAM
low complexity region	532	545	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000122003

SMART Domains

Protein: ENSMUSP00000113821
Gene: ENSMUSG00000034724

Domain	Start	End	E-Value	Type
LRR	50	72	4.34e-1	SMART
LRR	73	95	1.01e-1	SMART
LRR	96	119	7.55e-1	SMART
Pfam:Exo_endo_phos	187	433	1.3e-18	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152490

Predicted Effect

probably damaging
Transcript: ENSMUST00000155901
AA Change: F479S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000119415
Gene: ENSMUSG00000034724
AA Change: F479S

Domain	Start	End	E-Value	Type
LRR	50	72	4.34e-1	SMART
LRR	73	95	1.01e-1	SMART
LRR	96	119	7.55e-1	SMART
Pfam:Exo_endo_phos	187	524	2.2e-23	PFAM
low complexity region	527	540	N/A	INTRINSIC

Coding Region Coverage

1x: 98.9%
3x: 98.0%
10x: 95.0%
20x: 87.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2300002M23Rik	T	A	17: 35,568,315 (GRCm38)	F183L	possibly damaging	Het
4930590J08Rik	T	A	6: 91,944,264 (GRCm38)	M775K	probably damaging	Het
Actn1	T	G	12: 80,172,998 (GRCm38)	I700L	probably benign	Het
Adam5	T	C	8: 24,786,271 (GRCm38)	Y460C	probably damaging	Het
Akna	C	T	4: 63,395,265 (GRCm38)	G207E	probably damaging	Het
Ank2	T	A	3: 126,955,039 (GRCm38)	H527L	possibly damaging	Het
Anks1	C	A	17: 27,988,805 (GRCm38)	N383K	probably damaging	Het
Apba3	C	T	10: 81,269,370 (GRCm38)		probably null	Het
Atp9b	C	A	18: 80,736,093 (GRCm38)	V1121F	possibly damaging	Het
Bsn	T	C	9: 108,111,761 (GRCm38)	Y2264C	probably damaging	Het
Bst1	A	G	5: 43,840,457 (GRCm38)	D266G	probably damaging	Het
Cep55	A	G	19: 38,071,754 (GRCm38)		probably null	Het
Ces4a	G	A	8: 105,138,097 (GRCm38)	G69S	probably damaging	Het
Ckb	T	C	12: 111,671,230 (GRCm38)	K156E	probably benign	Het
Cln3	T	A	7: 126,575,221 (GRCm38)	H315L	probably damaging	Het
Col1a1	A	G	11: 94,947,132 (GRCm38)	D826G	unknown	Het
Cyp27a1	T	C	1: 74,735,405 (GRCm38)	V194A	probably benign	Het
Dis3l2	C	T	1: 87,044,168 (GRCm38)	P643S	probably benign	Het
Dpf3	T	C	12: 83,331,966 (GRCm38)	D108G	probably damaging	Het
Eif2b4	C	T	5: 31,192,897 (GRCm38)	G27D	probably benign	Het
Eif4a1	T	G	11: 69,672,425 (GRCm38)		probably benign	Het
Espl1	A	T	15: 102,304,937 (GRCm38)	D566V	probably damaging	Het
Ext2	T	A	2: 93,813,679 (GRCm38)	R86*	probably null	Het
Fasn	A	T	11: 120,816,085 (GRCm38)	F914I	probably damaging	Het
Fbf1	A	G	11: 116,152,552 (GRCm38)	L477P	probably benign	Het
Fsd1	A	T	17: 55,996,452 (GRCm38)	K441N	possibly damaging	Het
Fsip2	T	A	2: 82,985,040 (GRCm38)	S3706T	probably benign	Het
Gabra5	A	T	7: 57,408,799 (GRCm38)	N400K	probably benign	Het
Gimap8	G	T	6: 48,656,134 (GRCm38)	G296W	probably damaging	Het
Gli2	A	G	1: 118,836,140 (GRCm38)	V1427A	probably benign	Het
Gm7334	A	T	17: 50,698,827 (GRCm38)	Y47F	probably damaging	Het
Gm8674	T	G	13: 49,900,755 (GRCm38)		noncoding transcript	Het
Gmeb2	G	T	2: 181,254,246 (GRCm38)	T377K	probably benign	Het
Gp9	T	A	6: 87,779,247 (GRCm38)	D81E	probably benign	Het
Il5ra	T	A	6: 106,738,162 (GRCm38)	I212F	possibly damaging	Het
Klhl18	G	T	9: 110,428,961 (GRCm38)	N470K	possibly damaging	Het
Lfng	G	T	5: 140,612,395 (GRCm38)		probably null	Het
Lpo	A	G	11: 87,810,340 (GRCm38)	I430T	probably benign	Het
Lrrc31	C	T	3: 30,689,268 (GRCm38)	D183N	probably damaging	Het
Meis2	T	C	2: 115,864,412 (GRCm38)	T410A	probably benign	Het
Myo6	A	G	9: 80,307,681 (GRCm38)	D1232G	probably damaging	Het
Ncapd2	C	T	6: 125,169,840 (GRCm38)	R1261H	probably benign	Het
Nfkb1	C	T	3: 135,613,982 (GRCm38)	V251M	probably damaging	Het
Nmbr	C	A	10: 14,766,986 (GRCm38)	H96Q	probably damaging	Het
Nop14	C	T	5: 34,652,393 (GRCm38)	R256H	probably damaging	Het
Nqo2	T	A	13: 33,981,518 (GRCm38)	Y133N	probably damaging	Het
Olfr1153	A	G	2: 87,896,813 (GRCm38)	I213V	probably benign	Het
Olfr1366	T	C	13: 21,537,187 (GRCm38)	I273V	probably benign	Het
Pbld2	C	A	10: 63,052,238 (GRCm38)	S168R	probably damaging	Het
Pcdhb7	G	T	18: 37,342,149 (GRCm38)	G113*	probably null	Het
Pcdhb7	G	T	18: 37,342,150 (GRCm38)	G113V	probably damaging	Het
Pdgfra	A	T	5: 75,195,026 (GRCm38)	T1066S	probably damaging	Het
Prdm8	G	T	5: 98,185,023 (GRCm38)		probably null	Het
Prdm8	A	T	5: 98,185,022 (GRCm38)		probably null	Het
Prkg1	T	C	19: 30,586,375 (GRCm38)	Y479C	probably benign	Het
Pudp	T	C	18: 50,568,468 (GRCm38)	T65A	probably benign	Het
Rbbp6	C	T	7: 122,999,703 (GRCm38)		probably benign	Het
Rcc1	C	G	4: 132,335,735 (GRCm38)	V187L	probably damaging	Het
Rims2	T	A	15: 39,437,728 (GRCm38)	M285K	probably damaging	Het
Rtkn2	T	C	10: 68,041,915 (GRCm38)	*602Q	probably null	Het
Rxfp3	T	G	15: 11,036,780 (GRCm38)	S169R	probably damaging	Het
Sardh	T	C	2: 27,228,241 (GRCm38)		probably null	Het
Slc24a2	A	T	4: 87,227,347 (GRCm38)	F157I	probably damaging	Het
Slc25a20	T	C	9: 108,681,992 (GRCm38)	Y186H	probably damaging	Het
Slc25a24	A	G	3: 109,163,548 (GRCm38)	R408G	probably damaging	Het
Slc44a5	T	G	3: 154,253,716 (GRCm38)	I348S	probably damaging	Het
Slc8a2	A	T	7: 16,134,175 (GRCm38)	K111*	probably null	Het
Smc5	A	G	19: 23,234,003 (GRCm38)	V589A	probably damaging	Het
Thbd	A	T	2: 148,407,735 (GRCm38)	I71N	probably damaging	Het
Thsd7b	T	C	1: 129,678,145 (GRCm38)	M541T	probably benign	Het
Tie1	T	A	4: 118,484,771 (GRCm38)		silent	Het
Tln1	A	G	4: 43,547,522 (GRCm38)	F813S	possibly damaging	Het
Tnrc18	A	T	5: 142,765,977 (GRCm38)	L1191*	probably null	Het
Tubb2a	A	C	13: 34,075,257 (GRCm38)	Y183*	probably null	Het
Ubr4	T	A	4: 139,396,566 (GRCm38)	V343E	probably damaging	Het
Vmn2r93	A	T	17: 18,304,065 (GRCm38)	D107V	possibly damaging	Het
Vwa5a	T	G	9: 38,736,198 (GRCm38)	S624R	probably benign	Het
Wwox	G	A	8: 114,706,358 (GRCm38)	V255I	probably benign	Het
Wwp1	T	C	4: 19,638,804 (GRCm38)	K546E	probably damaging	Het
Xirp2	T	A	2: 67,509,819 (GRCm38)	F801L	possibly damaging	Het
Zfp407	T	C	18: 84,559,464 (GRCm38)	I1175V	probably benign	Het
Zfp646	T	A	7: 127,881,761 (GRCm38)	C1037S	possibly damaging	Het
Zfp786	A	T	6: 47,821,268 (GRCm38)	C245*	probably null	Het
Zfp827	T	C	8: 79,061,183 (GRCm38)	V326A	probably benign	Het

Other mutations in Cnot6l

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01346:Cnot6l	APN	5	96,086,246 (GRCm38)	missense	probably damaging	1.00
IGL02102:Cnot6l	APN	5	96,091,659 (GRCm38)	missense	probably damaging	0.98
BB005:Cnot6l	UTSW	5	96,131,068 (GRCm38)	missense	possibly damaging	0.95
BB015:Cnot6l	UTSW	5	96,131,068 (GRCm38)	missense	possibly damaging	0.95
R0443:Cnot6l	UTSW	5	96,091,745 (GRCm38)	splice site	probably benign
R0448:Cnot6l	UTSW	5	96,080,046 (GRCm38)	missense	probably benign	0.00
R1436:Cnot6l	UTSW	5	96,134,112 (GRCm38)	missense	probably damaging	1.00
R2198:Cnot6l	UTSW	5	96,079,941 (GRCm38)	missense	possibly damaging	0.79
R4240:Cnot6l	UTSW	5	96,077,362 (GRCm38)	missense	probably benign
R4506:Cnot6l	UTSW	5	96,086,174 (GRCm38)	missense	possibly damaging	0.93
R4624:Cnot6l	UTSW	5	96,077,211 (GRCm38)	missense	probably benign	0.05
R4627:Cnot6l	UTSW	5	96,077,211 (GRCm38)	missense	probably benign	0.05
R4629:Cnot6l	UTSW	5	96,077,211 (GRCm38)	missense	probably benign	0.05
R4868:Cnot6l	UTSW	5	96,083,023 (GRCm38)	missense	probably damaging	1.00
R5597:Cnot6l	UTSW	5	96,131,119 (GRCm38)	missense	probably damaging	1.00
R5781:Cnot6l	UTSW	5	96,086,165 (GRCm38)	missense	probably benign	0.31
R6142:Cnot6l	UTSW	5	96,082,978 (GRCm38)	missense	probably benign	0.00
R6166:Cnot6l	UTSW	5	96,079,940 (GRCm38)	missense	possibly damaging	0.79
R6189:Cnot6l	UTSW	5	96,098,277 (GRCm38)	missense	probably benign	0.18
R6382:Cnot6l	UTSW	5	96,128,999 (GRCm38)	missense	probably damaging	0.99
R6515:Cnot6l	UTSW	5	96,161,678 (GRCm38)	intron	probably benign
R6773:Cnot6l	UTSW	5	96,094,299 (GRCm38)	missense	probably damaging	1.00
R7326:Cnot6l	UTSW	5	96,077,299 (GRCm38)	missense	probably benign	0.00
R7466:Cnot6l	UTSW	5	96,131,128 (GRCm38)	missense	probably benign	0.01
R7832:Cnot6l	UTSW	5	96,094,225 (GRCm38)	missense	possibly damaging	0.90
R7928:Cnot6l	UTSW	5	96,131,068 (GRCm38)	missense	possibly damaging	0.95
R8310:Cnot6l	UTSW	5	96,091,676 (GRCm38)	missense	probably benign
R8499:Cnot6l	UTSW	5	96,077,317 (GRCm38)	missense	probably damaging	1.00
R8698:Cnot6l	UTSW	5	96,077,290 (GRCm38)	missense	probably damaging	1.00
R9029:Cnot6l	UTSW	5	96,098,277 (GRCm38)	missense	probably benign	0.18
R9100:Cnot6l	UTSW	5	96,083,016 (GRCm38)	missense	probably damaging	1.00
R9377:Cnot6l	UTSW	5	96,128,967 (GRCm38)	missense	probably benign	0.01
R9485:Cnot6l	UTSW	5	96,082,999 (GRCm38)	missense	probably damaging	0.99
R9685:Cnot6l	UTSW	5	96,082,890 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCCAACAAAGTTCCTTGTTTAGTTG -3'
(R):5'- TTAAGCAACGGTGGAGTAGC -3'

Sequencing Primer
(F):5'- CCTGCATGTATGTCTGTGAAAC -3'
(R):5'- CGGTGGAGTAGCTGACAACC -3'

Posted On

2016-04-15