Mutagenetix > Incidental Mutation

Incidental Mutation 'R4579:Cul2'

343545

Institutional Source

Beutler Lab

Gene Symbol

Cul2

Ensembl Gene

ENSMUSG00000024231

Gene Name

cullin 2

Synonyms

4932411N15Rik, 1300003D18Rik

MMRRC Submission

041801-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.941) question?

Stock #

R4579 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

3382988-3436377 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 3430957 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 577 (V577A)

Ref Sequence

ENSEMBL: ENSMUSP00000125403 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025073] [ENSMUST00000080089] [ENSMUST00000161317] [ENSMUST00000162301]

AlphaFold

Q9D4H8

Predicted Effect

probably benign
Transcript: ENSMUST00000025073
AA Change: V577A

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000025073
Gene: ENSMUSG00000024231
AA Change: V577A

Domain	Start	End	E-Value	Type
SCOP:d1ldja2	11	386	1e-109	SMART
CULLIN	416	568	1.19e-84	SMART
low complexity region	636	646	N/A	INTRINSIC
Pfam:Cullin_Nedd8	651	700	9.2e-14	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000080089

SMART Domains

Protein: ENSMUSP00000078988
Gene: ENSMUSG00000024231

Domain	Start	End	E-Value	Type
Pfam:Cullin	14	88	2.1e-9	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159443

Predicted Effect

probably benign
Transcript: ENSMUST00000161317
AA Change: V514A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000123903
Gene: ENSMUSG00000024231
AA Change: V514A

Domain	Start	End	E-Value	Type
CULLIN	353	505	1.19e-84	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000161852

Predicted Effect

probably benign
Transcript: ENSMUST00000162301
AA Change: V577A

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000125403
Gene: ENSMUSG00000024231
AA Change: V577A

Domain	Start	End	E-Value	Type
SCOP:d1ldja2	11	386	1e-108	SMART
CULLIN	416	568	1.19e-84	SMART
low complexity region	636	646	N/A	INTRINSIC
Cullin_Nedd8	672	739	1.01e-33	SMART

Meta Mutation Damage Score

0.2834

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.3%

Validation Efficiency

97% (88/91)

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A930004D18Rik	A	G	2: 18,031,848 (GRCm39)	I90T	probably damaging	Het
Acox3	A	G	5: 35,761,987 (GRCm39)	N444D	probably damaging	Het
Adamts16	A	G	13: 70,927,743 (GRCm39)	Y499H	probably damaging	Het
Ajm1	T	A	2: 25,469,661 (GRCm39)	R83S	possibly damaging	Het
Ank2	A	T	3: 126,752,612 (GRCm39)	V368D	probably damaging	Het
Atad5	T	C	11: 79,986,017 (GRCm39)	V368A	probably damaging	Het
Atp13a5	T	C	16: 29,067,090 (GRCm39)		probably null	Het
Bdh1	A	T	16: 31,254,954 (GRCm39)		probably benign	Het
Bmp6	A	T	13: 38,653,701 (GRCm39)	Y256F	probably damaging	Het
Bub1b	C	A	2: 118,453,657 (GRCm39)	S496*	probably null	Het
Capn15	C	T	17: 26,178,811 (GRCm39)	R1128H	probably damaging	Het
Ccnf	T	A	17: 24,450,303 (GRCm39)	R461*	probably null	Het
Col6a1	C	T	10: 76,547,191 (GRCm39)	V725I	unknown	Het
Cp	T	C	3: 20,011,599 (GRCm39)		probably null	Het
Cux2	A	T	5: 121,998,716 (GRCm39)	I1408K	probably benign	Het
Cyp2c69	T	A	19: 39,869,630 (GRCm39)	T130S	possibly damaging	Het
Cyp3a57	A	G	5: 145,311,074 (GRCm39)	T278A	probably benign	Het
Dchs1	T	G	7: 105,403,972 (GRCm39)	T2857P	probably damaging	Het
Dchs1	A	G	7: 105,408,180 (GRCm39)	M1884T	probably benign	Het
Dnah3	T	C	7: 119,608,554 (GRCm39)	S1802G	probably damaging	Het
Dner	T	C	1: 84,361,537 (GRCm39)	S691G	probably damaging	Het
Dzip1l	A	T	9: 99,529,267 (GRCm39)	Q332L	probably damaging	Het
Eprs1	A	G	1: 185,133,804 (GRCm39)	Y827C	probably damaging	Het
Ermp1	A	T	19: 29,594,051 (GRCm39)	N706K	probably damaging	Het
F830045P16Rik	A	G	2: 129,305,423 (GRCm39)	L317S	probably damaging	Het
Fam120c	G	T	X: 150,219,179 (GRCm39)	G696W	probably damaging	Het
Fance	T	A	17: 28,536,125 (GRCm39)		probably null	Het
Fancl	G	T	11: 26,418,423 (GRCm39)		probably null	Het
Fbxo30	T	A	10: 11,165,293 (GRCm39)	V5E	probably benign	Het
Foxn4	A	T	5: 114,394,886 (GRCm39)	I347N	possibly damaging	Het
Galr2	A	T	11: 116,172,325 (GRCm39)	D5V	probably benign	Het
Gm4845	T	G	1: 141,184,865 (GRCm39)		noncoding transcript	Het
Gnao1	A	T	8: 94,693,532 (GRCm39)	Q73L	probably damaging	Het
Gnpat	T	A	8: 125,605,241 (GRCm39)		probably null	Het
H2-T5	C	T	17: 36,472,649 (GRCm39)		probably benign	Het
Hectd1	A	G	12: 51,791,356 (GRCm39)	M2594T	probably damaging	Het
Hint3	T	C	10: 30,486,428 (GRCm39)	H117R	probably damaging	Het
Hsd3b6	A	G	3: 98,713,541 (GRCm39)	F253L	probably damaging	Het
Itgal	A	G	7: 126,904,466 (GRCm39)	D313G	possibly damaging	Het
Kbtbd2	A	T	6: 56,755,893 (GRCm39)	D614E	probably damaging	Het
Ksr2	A	T	5: 117,894,335 (GRCm39)	I825F	probably damaging	Het
L3mbtl4	A	T	17: 69,071,635 (GRCm39)	S521C	probably benign	Het
Lamc1	T	C	1: 153,123,015 (GRCm39)	N725S	probably damaging	Het
Med1	T	G	11: 98,049,248 (GRCm39)	E516A	possibly damaging	Het
Mical3	A	T	6: 120,935,660 (GRCm39)	V1622E	probably benign	Het
Miip	G	A	4: 147,945,518 (GRCm39)	P373S	probably damaging	Het
Myo7a	C	A	7: 97,722,400 (GRCm39)	S1175I	probably damaging	Het
Ndst3	A	T	3: 123,340,474 (GRCm39)	D781E	probably benign	Het
Nf1	T	A	11: 79,359,583 (GRCm39)	V1407E	probably damaging	Het
Opalin	A	G	19: 41,056,196 (GRCm39)	L33P	probably damaging	Het
Or2f2	A	T	6: 42,767,458 (GRCm39)	I162F	probably benign	Het
Or2n1b	G	C	17: 38,460,296 (GRCm39)	K272N	probably damaging	Het
Or4c111	T	C	2: 88,843,488 (GRCm39)	I307V	probably benign	Het
Or8b12i	G	T	9: 20,082,410 (GRCm39)	S152R	probably damaging	Het
Or8k28	T	C	2: 86,285,859 (GRCm39)	Y252C	probably damaging	Het
Or8s10	A	T	15: 98,335,560 (GRCm39)	D70V	probably damaging	Het
Pcdhb2	T	A	18: 37,429,168 (GRCm39)	N23K	probably damaging	Het
Pdap1	A	G	5: 145,073,691 (GRCm39)		probably benign	Het
Pds5b	A	G	5: 150,670,197 (GRCm39)	E395G	probably damaging	Het
Pex1	C	A	5: 3,668,880 (GRCm39)	R624S	probably benign	Het
Pitrm1	G	A	13: 6,608,261 (GRCm39)	V329I	probably benign	Het
Pop1	G	A	15: 34,515,970 (GRCm39)		probably benign	Het
Prkaa1	A	G	15: 5,190,082 (GRCm39)		probably null	Het
Slc38a6	G	T	12: 73,335,298 (GRCm39)		probably null	Het
Slc5a9	T	A	4: 111,750,384 (GRCm39)	Y158F	probably damaging	Het
Spata3	T	A	1: 85,954,175 (GRCm39)	V114E	probably damaging	Het
Tbcb	T	A	7: 29,931,019 (GRCm39)	I34F	possibly damaging	Het
Tek	T	A	4: 94,751,903 (GRCm39)	Y1014*	probably null	Het
Togaram1	G	T	12: 65,014,681 (GRCm39)	C644F	probably damaging	Het
Trim56	A	C	5: 137,142,918 (GRCm39)	D199E	possibly damaging	Het
Tssk3	A	T	4: 129,383,110 (GRCm39)	D187E	probably benign	Het
Ttn	G	A	2: 76,727,147 (GRCm39)		probably benign	Het
Twf2	G	A	9: 106,090,025 (GRCm39)	R126Q	probably benign	Het
Ugt1a10	T	C	1: 87,983,838 (GRCm39)	M212T	probably benign	Het
Vmn1r177	A	T	7: 23,565,772 (GRCm39)	F35I	possibly damaging	Het
Vmn1r44	T	A	6: 89,870,915 (GRCm39)	H77Q	possibly damaging	Het
Zfp1004	T	A	2: 150,034,143 (GRCm39)	Y186N	probably damaging	Het
Zfp524	G	A	7: 5,021,347 (GRCm39)	V292I	probably benign	Het
Zfp788	T	G	7: 41,297,018 (GRCm39)	I56S	probably benign	Het

Other mutations in Cul2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00704:Cul2	APN	18	3,423,487 (GRCm39)	missense	probably benign
IGL01293:Cul2	APN	18	3,419,426 (GRCm39)	missense	probably damaging	0.99
IGL02719:Cul2	APN	18	3,434,052 (GRCm39)	missense	probably damaging	1.00
IGL02886:Cul2	APN	18	3,426,920 (GRCm39)	splice site	probably benign
IGL03190:Cul2	APN	18	3,429,634 (GRCm39)	missense	possibly damaging	0.95
IGL03389:Cul2	APN	18	3,431,029 (GRCm39)	missense	probably benign	0.00
IGL03409:Cul2	APN	18	3,429,593 (GRCm39)	missense	probably damaging	1.00
R0238:Cul2	UTSW	18	3,414,115 (GRCm39)	splice site	probably benign
R1013:Cul2	UTSW	18	3,425,535 (GRCm39)	nonsense	probably null
R1119:Cul2	UTSW	18	3,419,335 (GRCm39)	splice site	probably benign
R1743:Cul2	UTSW	18	3,426,851 (GRCm39)	missense	probably damaging	1.00
R1897:Cul2	UTSW	18	3,414,164 (GRCm39)	missense	probably benign
R2252:Cul2	UTSW	18	3,399,876 (GRCm39)	missense	probably damaging	1.00
R2253:Cul2	UTSW	18	3,399,876 (GRCm39)	missense	probably damaging	1.00
R3898:Cul2	UTSW	18	3,434,033 (GRCm39)	missense	probably benign	0.07
R4386:Cul2	UTSW	18	3,434,856 (GRCm39)	missense	probably damaging	1.00
R4828:Cul2	UTSW	18	3,431,013 (GRCm39)	missense	probably damaging	1.00
R6085:Cul2	UTSW	18	3,431,508 (GRCm39)	missense	probably benign	0.01
R6429:Cul2	UTSW	18	3,421,345 (GRCm39)	missense	probably damaging	1.00
R6480:Cul2	UTSW	18	3,417,561 (GRCm39)	missense	possibly damaging	0.89
R6805:Cul2	UTSW	18	3,421,263 (GRCm39)	missense	probably damaging	1.00
R6825:Cul2	UTSW	18	3,434,946 (GRCm39)	missense	probably damaging	0.99
R7343:Cul2	UTSW	18	3,426,873 (GRCm39)	missense	probably benign	0.08
R7690:Cul2	UTSW	18	3,419,420 (GRCm39)	missense	probably benign	0.09
R8114:Cul2	UTSW	18	3,426,164 (GRCm39)	nonsense	probably null
R8414:Cul2	UTSW	18	3,399,912 (GRCm39)	missense	probably benign	0.08
R8736:Cul2	UTSW	18	3,434,019 (GRCm39)	missense	probably damaging	0.99
R8849:Cul2	UTSW	18	3,423,551 (GRCm39)	missense	probably benign	0.00
R9199:Cul2	UTSW	18	3,423,577 (GRCm39)	missense	probably benign	0.00
R9443:Cul2	UTSW	18	3,434,041 (GRCm39)	nonsense	probably null
R9709:Cul2	UTSW	18	3,431,560 (GRCm39)	missense	probably damaging	1.00
X0067:Cul2	UTSW	18	3,419,435 (GRCm39)	missense	possibly damaging	0.62

Predicted Primers

PCR Primer
(F):5'- TCTAGGCAAGAACTTTCAAATGCC -3'
(R):5'- TCTGCTAAGGGTTGAAATCCC -3'

Sequencing Primer
(F):5'- GGCAAGAACTTTCAAATGCCTTTGC -3'
(R):5'- AAATCCCTTGGGAAGGTTACCTTTTC -3'

Posted On

2015-09-24