Mutagenetix > Incidental Mutations

Incidental Mutation 'R5377:Crebrf'

425649

Institutional Source

Beutler Lab

Gene Symbol

Crebrf

Ensembl Gene

ENSMUSG00000048249

Gene Name

CREB3 regulatory factor

Synonyms

A930001N09Rik

MMRRC Submission

042845-MU

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.385) question?

Stock #

R5377 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

26715650-26776635 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 26759865 bp

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 509 (V509A)

Ref Sequence

ENSEMBL: ENSMUSP00000059102 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000062519] [ENSMUST00000142539] [ENSMUST00000151681]

Predicted Effect

probably damaging
Transcript: ENSMUST00000062519
AA Change: V509A

PolyPhen 2 Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000059102
Gene: ENSMUSG00000048249
AA Change: V509A

Domain	Start	End	E-Value	Type
low complexity region	317	330	N/A	INTRINSIC
low complexity region	356	407	N/A	INTRINSIC
Blast:BRLZ	520	584	3e-35	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132972

Predicted Effect

probably benign
Transcript: ENSMUST00000142539
AA Change: V501A

PolyPhen 2 Score 0.235 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000114274
Gene: ENSMUSG00000048249
AA Change: V501A

Domain	Start	End	E-Value	Type
low complexity region	309	322	N/A	INTRINSIC
low complexity region	348	399	N/A	INTRINSIC
Blast:BRLZ	512	576	3e-35	BLAST
low complexity region	617	630	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000151681
AA Change: V89A

PolyPhen 2 Score 0.807 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000119186
Gene: ENSMUSG00000048249
AA Change: V89A

Domain	Start	End	E-Value	Type
Blast:BRLZ	100	137	2e-18	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000176845

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.5%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit impaired social recognition, increased vertical and horizontal activity, abnormal maternal nurturing, decreased prolactin and corticosterone serum levels, and abnormal mammary gland growth during lactation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2m	G	T	6: 121,645,253	V372F	probably benign	Het
Adcy10	G	A	1: 165,519,895	C393Y	probably damaging	Het
Adgrg7	A	C	16: 56,730,306	I681S	possibly damaging	Het
Akap8l	T	C	17: 32,321,511		probably benign	Het
Akr1a1	A	T	4: 116,639,895	V156E	probably damaging	Het
Alk	T	G	17: 71,895,739	D1167A	probably damaging	Het
Ankrd11	T	C	8: 122,893,714		probably null	Het
Aspm	A	G	1: 139,470,395		probably null	Het
Aspm	T	A	1: 139,457,483	N288K	probably damaging	Het
Asxl2	G	A	12: 3,474,618		probably null	Het
Atp6v0a1	A	G	11: 101,055,587	H802R	probably damaging	Het
B4galnt1	A	G	10: 127,171,822	T531A	possibly damaging	Het
Ccdc114	C	T	7: 45,942,082	R257*	probably null	Het
Cecr2	A	G	6: 120,756,569	N506D	possibly damaging	Het
Cyp4f40	A	T	17: 32,675,616	I413F	probably null	Het
Defb12	C	A	8: 19,114,326		probably null	Het
Dnah2	T	C	11: 69,421,848	E4297G	probably damaging	Het
Dpysl5	A	T	5: 30,791,513	N371Y	probably damaging	Het
Eef1d	G	T	15: 75,903,189	T207N	probably benign	Het
Esrrb	C	T	12: 86,519,009	Q416*	probably null	Het
Exd2	T	C	12: 80,489,448	L284P	probably damaging	Het
Fat3	T	A	9: 16,376,443	I595F	probably benign	Het
Gm9920	A	G	15: 55,108,975		probably benign	Het
Hephl1	T	C	9: 15,069,788	K783E	probably damaging	Het
Irs2	A	G	8: 11,005,277	S1052P	probably benign	Het
Kctd18	T	C	1: 57,963,093	I192V	probably benign	Het
Lama3	A	G	18: 12,453,746	D722G	probably damaging	Het
Lepr	T	C	4: 101,815,019	V1080A	possibly damaging	Het
Lpin1	C	T	12: 16,563,655	G504S	probably damaging	Het
Lrit2	A	C	14: 37,069,183	Q273P	possibly damaging	Het
Mgea5	A	T	19: 45,758,022	Y779*	probably null	Het
Mlkl	T	A	8: 111,327,937	E189D	probably benign	Het
Mttp	C	T	3: 138,105,029	R608H	probably benign	Het
Nav2	T	C	7: 49,589,160	V2011A	probably benign	Het
Nos2	A	T	11: 78,957,491	I1075F	probably benign	Het
Npat	A	G	9: 53,550,036		probably null	Het
Nucks1	T	C	1: 131,919,033	F16L	probably damaging	Het
Nus1	T	C	10: 52,429,213	S150P	possibly damaging	Het
Olfr1230	G	T	2: 89,297,162	T36K	probably damaging	Het
Olfr881	A	T	9: 37,992,612	Y40F	probably benign	Het
Pclo	A	G	5: 14,681,353	T3290A	unknown	Het
Pign	A	T	1: 105,657,812	F4Y	probably benign	Het
Rfx4	A	G	10: 84,860,542	N233D	possibly damaging	Het
Rpgrip1	A	T	14: 52,160,195	M1325L	possibly damaging	Het
Rufy4	T	C	1: 74,147,663	C537R	probably damaging	Het
Scaf11	T	A	15: 96,417,120	H1227L	possibly damaging	Het
Sec31b	G	T	19: 44,518,637	P840T	probably damaging	Het
Slc16a9	T	A	10: 70,283,128	L426I	probably damaging	Het
Slc17a2	T	C	13: 23,812,592	S27P	probably damaging	Het
Slc22a30	G	A	19: 8,344,393	Q436*	probably null	Het
Tacc1	A	G	8: 25,182,283	S310P	possibly damaging	Het
Tmem245	G	A	4: 56,947,084	R110C	probably damaging	Het
Trip12	T	C	1: 84,757,431	Y953C	probably damaging	Het
Trpm7	C	A	2: 126,842,855		probably null	Het
Ush2a	G	A	1: 188,912,123	V4561I	probably benign	Het
Vmn1r192	C	T	13: 22,187,631	V140I	probably benign	Het
Vmn2r66	A	T	7: 85,006,818	I330N	probably damaging	Het
Vmn2r99	T	C	17: 19,379,269	V405A	probably damaging	Het
Wdhd1	A	C	14: 47,272,221	V172G	probably benign	Het
Zfhx3	C	T	8: 108,951,185	R2956C	possibly damaging	Het
Zfp446	T	C	7: 12,982,251	L283P	possibly damaging	Het
Zfp82	T	C	7: 30,057,166	K164E	probably damaging	Het

Other mutations in Crebrf

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00490:Crebrf	APN	17	26743093	missense	probably damaging	1.00
IGL03106:Crebrf	APN	17	26771319	missense	probably damaging	1.00
R0046:Crebrf	UTSW	17	26763334	missense	probably damaging	1.00
R0046:Crebrf	UTSW	17	26763334	missense	probably damaging	1.00
R0254:Crebrf	UTSW	17	26739594	missense	probably benign	0.01
R0448:Crebrf	UTSW	17	26743102	missense	probably benign	0.42
R1268:Crebrf	UTSW	17	26739596	frame shift	probably null
R1857:Crebrf	UTSW	17	26742963	missense	probably benign	0.00
R1858:Crebrf	UTSW	17	26742963	missense	probably benign	0.00
R1937:Crebrf	UTSW	17	26742468	missense	probably damaging	1.00
R2005:Crebrf	UTSW	17	26742883	missense	possibly damaging	0.53
R2006:Crebrf	UTSW	17	26742883	missense	possibly damaging	0.53
R2031:Crebrf	UTSW	17	26742921	missense	probably damaging	0.97
R2323:Crebrf	UTSW	17	26763607	unclassified	probably benign
R2352:Crebrf	UTSW	17	26742346	missense	probably damaging	1.00
R4510:Crebrf	UTSW	17	26742964	missense	probably benign
R4511:Crebrf	UTSW	17	26742964	missense	probably benign
R4585:Crebrf	UTSW	17	26762255	missense	probably damaging	1.00
R4642:Crebrf	UTSW	17	26743061	missense	probably benign	0.23
R4896:Crebrf	UTSW	17	26742420	missense	possibly damaging	0.75
R5227:Crebrf	UTSW	17	26759765	missense	probably damaging	1.00
R5443:Crebrf	UTSW	17	26742354	missense	probably damaging	1.00
R5540:Crebrf	UTSW	17	26742097	missense	possibly damaging	0.90
R6017:Crebrf	UTSW	17	26757849	missense	probably benign	0.04
R6132:Crebrf	UTSW	17	26763403	missense	probably benign	0.03
R7464:Crebrf	UTSW	17	26763487	missense	unknown
R7956:Crebrf	UTSW	17	26742657	missense	probably benign	0.21
R8378:Crebrf	UTSW	17	26762289	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGAGCTATAGAAATTGCATGTCTTG -3'
(R):5'- GTGTACTTACTGTAGTCACCTACCC -3'

Sequencing Primer
(F):5'- GCATGTCTTGTTCACTAAAATGATG -3'
(R):5'- CCCCAAACTTCTTAAAAGCATAAATG -3'

Posted On

2016-08-04