Mutagenetix > Incidental Mutation

Incidental Mutation 'R4982:Greb1'

384937

Institutional Source

Beutler Lab

Gene Symbol

Greb1

Ensembl Gene

ENSMUSG00000036523

Gene Name

gene regulated by estrogen in breast cancer protein

Synonyms

5730583K22Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4982 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

16670615-16800886 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 16724761 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 212 (S212P)

Ref Sequence

ENSEMBL: ENSMUSP00000124348 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000048064] [ENSMUST00000159120] [ENSMUST00000162112]

AlphaFold

Q3UHK3

Predicted Effect

probably damaging
Transcript: ENSMUST00000048064
AA Change: S212P

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000044454
Gene: ENSMUSG00000036523
AA Change: S212P

Domain	Start	End	E-Value	Type
Pfam:GREB1	1	1954	N/A	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000159120
AA Change: S212P

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000125339
Gene: ENSMUSG00000036523
AA Change: S212P

Domain	Start	End	E-Value	Type
low complexity region	52	71	N/A	INTRINSIC
low complexity region	292	303	N/A	INTRINSIC
low complexity region	437	453	N/A	INTRINSIC
low complexity region	480	503	N/A	INTRINSIC
low complexity region	631	643	N/A	INTRINSIC
low complexity region	1100	1118	N/A	INTRINSIC
low complexity region	1196	1207	N/A	INTRINSIC
low complexity region	1251	1265	N/A	INTRINSIC
low complexity region	1596	1607	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159573

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000161036

Predicted Effect

probably damaging
Transcript: ENSMUST00000162112
AA Change: S212P

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000124348
Gene: ENSMUSG00000036523
AA Change: S212P

Domain	Start	End	E-Value	Type
low complexity region	52	71	N/A	INTRINSIC
low complexity region	292	303	N/A	INTRINSIC
low complexity region	437	453	N/A	INTRINSIC
low complexity region	480	503	N/A	INTRINSIC
low complexity region	631	643	N/A	INTRINSIC
low complexity region	1128	1146	N/A	INTRINSIC
low complexity region	1224	1235	N/A	INTRINSIC
low complexity region	1279	1293	N/A	INTRINSIC
low complexity region	1624	1635	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.6%
20x: 93.1%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is an estrogen-responsive gene that is an early response gene in the estrogen receptor-regulated pathway. It is thought to play an important role in hormone-responsive tissues and cancer. Three alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	A	T	11: 9,292,348 (GRCm38)	I1404L	possibly damaging	Het
Adra1b	A	G	11: 43,835,230 (GRCm38)	S287P	probably damaging	Het
Atxn2	G	T	5: 121,814,343 (GRCm38)	A1280S	possibly damaging	Het
Bbip1	T	C	19: 53,932,208 (GRCm38)		probably null	Het
Bbs2	A	G	8: 94,082,354 (GRCm38)		probably null	Het
Bcl11b	A	T	12: 107,965,772 (GRCm38)	C180*	probably null	Het
Bod1l	A	G	5: 41,820,473 (GRCm38)	V1166A	probably benign	Het
Bora	C	T	14: 99,047,352 (GRCm38)	P13S	probably damaging	Het
C2cd4c	T	C	10: 79,613,241 (GRCm38)	E24G	probably benign	Het
Ccne1	A	T	7: 38,100,571 (GRCm38)	I196N	probably damaging	Het
Chsy3	C	T	18: 59,409,575 (GRCm38)	S595L	probably benign	Het
Chsy3	T	A	18: 59,409,767 (GRCm38)	I659N	possibly damaging	Het
Cntrob	T	A	11: 69,311,362 (GRCm38)		probably null	Het
Col5a2	G	A	1: 45,389,458 (GRCm38)	P983S	possibly damaging	Het
Crat	T	A	2: 30,407,136 (GRCm38)		probably null	Het
Ctnnbl1	C	T	2: 157,836,553 (GRCm38)	H359Y	probably benign	Het
D430041D05Rik	A	G	2: 104,255,387 (GRCm38)	V83A	possibly damaging	Het
Dixdc1	A	G	9: 50,682,602 (GRCm38)	S488P	possibly damaging	Het
Dmrta1	T	C	4: 89,688,564 (GRCm38)	C86R	probably damaging	Het
Dnase1l1	C	T	X: 74,277,038 (GRCm38)		probably null	Homo
Fam171a1	G	A	2: 3,178,468 (GRCm38)		probably null	Het
Fam222b	T	C	11: 78,154,743 (GRCm38)	C249R	probably damaging	Het
Fbxw18	T	A	9: 109,702,651 (GRCm38)		probably benign	Het
Fes	T	C	7: 80,387,204 (GRCm38)	Y44C	probably damaging	Het
Gimap6	A	G	6: 48,707,999 (GRCm38)	V51A	probably benign	Het
Gpr75	C	A	11: 30,891,462 (GRCm38)	H122Q	probably damaging	Het
Gpr75	C	T	11: 30,891,463 (GRCm38)	L123F	possibly damaging	Het
Grin3a	T	C	4: 49,665,512 (GRCm38)	H1041R	probably benign	Het
Ifna5	A	G	4: 88,835,624 (GRCm38)	N34D	probably damaging	Het
Ift140	A	T	17: 25,036,994 (GRCm38)	H221L	probably damaging	Het
Igsf3	T	C	3: 101,435,667 (GRCm38)	V540A	probably benign	Het
Il10ra	A	G	9: 45,269,059 (GRCm38)	L5S	probably damaging	Het
Klra2	A	T	6: 131,220,189 (GRCm38)	D282E	probably benign	Het
Lyst	T	A	13: 13,725,954 (GRCm38)	H3138Q	probably damaging	Het
Malrd1	A	G	2: 16,042,129 (GRCm38)	T1689A	probably benign	Het
Mon2	A	T	10: 122,995,789 (GRCm38)	L1671M	probably damaging	Het
Mpped1	T	C	15: 83,836,327 (GRCm38)	F71S	probably damaging	Het
Mtpap	C	A	18: 4,396,332 (GRCm38)	H541Q	probably benign	Het
Muc5ac	T	A	7: 141,809,456 (GRCm38)		probably benign	Het
Mybbp1a	T	C	11: 72,445,214 (GRCm38)	I451T	probably damaging	Het
Myh7	T	A	14: 54,972,767 (GRCm38)	E1827V	probably damaging	Het
Olfr132	A	T	17: 38,130,577 (GRCm38)	I205N	probably damaging	Het
Olfr145	C	A	9: 37,897,515 (GRCm38)	T37N	probably damaging	Het
Olfr342	A	T	2: 36,527,397 (GRCm38)		probably null	Het
Olfr501-ps1	T	A	7: 108,508,648 (GRCm38)	Y197*	probably null	Het
Os9	C	T	10: 127,121,051 (GRCm38)	R23H	possibly damaging	Het
Otud6b	A	G	4: 14,815,607 (GRCm38)	L261P	probably damaging	Het
Pcdhga2	A	G	18: 37,669,423 (GRCm38)	N107D	probably benign	Het
Pclo	C	T	5: 14,679,294 (GRCm38)		probably benign	Het
Peg10	T	TCCG	6: 4,756,451 (GRCm38)		probably benign	Het
Phtf1	T	A	3: 103,998,708 (GRCm38)	S524T	probably damaging	Het
Pkdrej	A	C	15: 85,818,996 (GRCm38)	L913R	probably damaging	Het
Pld1	C	A	3: 28,031,298 (GRCm38)	A201D	probably damaging	Het
Rorb	T	A	19: 18,977,688 (GRCm38)	Q103L	probably benign	Het
Sec24d	C	T	3: 123,299,606 (GRCm38)	T284M	probably benign	Het
Serpinb3b	T	C	1: 107,157,754 (GRCm38)	I86V	probably benign	Het
Serpinb6a	A	T	13: 33,918,874 (GRCm38)	M201K	probably damaging	Het
Snx8	A	G	5: 140,352,234 (GRCm38)	S219P	probably benign	Het
Sp8	C	T	12: 118,848,425 (GRCm38)	T5I	probably damaging	Het
Tanc1	A	G	2: 59,799,943 (GRCm38)	N749D	probably damaging	Het
Tarm1	G	C	7: 3,489,096 (GRCm38)	P284A	probably damaging	Het
Tbx15	A	T	3: 99,254,074 (GRCm38)	E65V	probably benign	Het
Ticam1	T	A	17: 56,272,020 (GRCm38)	H25L	probably benign	Het
Tmprss11g	T	A	5: 86,492,815 (GRCm38)	L170F	probably damaging	Het
Tnfsf9	A	G	17: 57,107,504 (GRCm38)	*310W	probably null	Het
Tsks	C	T	7: 44,943,994 (GRCm38)	T128I	possibly damaging	Het
Uhrf1bp1	T	C	17: 27,886,606 (GRCm38)	F702S	probably benign	Het
Vmn1r175	A	T	7: 23,809,069 (GRCm38)	N44K	possibly damaging	Het
Vmn1r45	A	G	6: 89,933,865 (GRCm38)	I41T	probably damaging	Het
Ythdc2	A	G	18: 44,871,465 (GRCm38)	N1102S	probably benign	Het
Zswim4	C	T	8: 84,226,667 (GRCm38)		probably null	Het

Other mutations in Greb1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00155:Greb1	APN	12	16,711,961 (GRCm38)	missense	probably damaging	1.00
IGL01316:Greb1	APN	12	16,698,586 (GRCm38)	missense	probably benign	0.04
IGL01464:Greb1	APN	12	16,714,826 (GRCm38)	missense	probably damaging	0.99
IGL01474:Greb1	APN	12	16,684,501 (GRCm38)	missense	probably benign
IGL01522:Greb1	APN	12	16,701,201 (GRCm38)	missense	probably damaging	1.00
IGL01824:Greb1	APN	12	16,711,716 (GRCm38)	nonsense	probably null
IGL01837:Greb1	APN	12	16,684,451 (GRCm38)	missense	probably benign	0.19
IGL01991:Greb1	APN	12	16,699,681 (GRCm38)	missense	probably damaging	1.00
IGL01996:Greb1	APN	12	16,690,845 (GRCm38)	missense	possibly damaging	0.70
IGL02213:Greb1	APN	12	16,706,232 (GRCm38)	missense	probably damaging	1.00
IGL02267:Greb1	APN	12	16,717,208 (GRCm38)	missense	probably benign	0.00
IGL02512:Greb1	APN	12	16,692,712 (GRCm38)	missense	possibly damaging	0.79
IGL02583:Greb1	APN	12	16,706,295 (GRCm38)	splice site	probably benign
IGL02613:Greb1	APN	12	16,739,888 (GRCm38)	critical splice donor site	probably null
IGL02648:Greb1	APN	12	16,708,682 (GRCm38)	missense	probably damaging	1.00
IGL02679:Greb1	APN	12	16,708,723 (GRCm38)	missense	probably damaging	1.00
begraben	UTSW	12	16,684,373 (GRCm38)	missense	possibly damaging	0.51
Eared	UTSW	12	16,673,863 (GRCm38)	missense	probably damaging	1.00
Humpback	UTSW	12	16,701,171 (GRCm38)	missense	probably damaging	1.00
pied_billed	UTSW	12	16,724,857 (GRCm38)	missense	possibly damaging	0.79
rednecked	UTSW	12	16,682,152 (GRCm38)	missense	probably damaging	0.99
G1patch:Greb1	UTSW	12	16,688,567 (GRCm38)	missense	probably damaging	1.00
IGL03048:Greb1	UTSW	12	16,733,331 (GRCm38)	missense	probably damaging	1.00
R0083:Greb1	UTSW	12	16,696,451 (GRCm38)	missense	probably benign
R0100:Greb1	UTSW	12	16,680,224 (GRCm38)	missense	probably benign	0.41
R0100:Greb1	UTSW	12	16,680,224 (GRCm38)	missense	probably benign	0.41
R0220:Greb1	UTSW	12	16,682,286 (GRCm38)	missense	probably damaging	1.00
R0245:Greb1	UTSW	12	16,696,456 (GRCm38)	missense	probably damaging	1.00
R0540:Greb1	UTSW	12	16,682,193 (GRCm38)	missense	probably damaging	1.00
R0547:Greb1	UTSW	12	16,723,411 (GRCm38)	missense	probably benign
R0563:Greb1	UTSW	12	16,680,267 (GRCm38)	missense	probably benign	0.23
R0607:Greb1	UTSW	12	16,682,193 (GRCm38)	missense	probably damaging	1.00
R0610:Greb1	UTSW	12	16,696,442 (GRCm38)	missense	probably benign
R0652:Greb1	UTSW	12	16,696,456 (GRCm38)	missense	probably damaging	1.00
R0659:Greb1	UTSW	12	16,680,212 (GRCm38)	missense	probably damaging	0.99
R0945:Greb1	UTSW	12	16,673,802 (GRCm38)	missense	probably benign	0.31
R1055:Greb1	UTSW	12	16,682,251 (GRCm38)	missense	probably damaging	0.98
R1445:Greb1	UTSW	12	16,707,851 (GRCm38)	missense	probably damaging	1.00
R1471:Greb1	UTSW	12	16,711,774 (GRCm38)	missense	probably damaging	0.97
R1503:Greb1	UTSW	12	16,724,819 (GRCm38)	nonsense	probably null
R1566:Greb1	UTSW	12	16,711,828 (GRCm38)	missense	possibly damaging	0.94
R1614:Greb1	UTSW	12	16,701,171 (GRCm38)	missense	probably damaging	1.00
R1623:Greb1	UTSW	12	16,674,770 (GRCm38)	missense	probably damaging	1.00
R1751:Greb1	UTSW	12	16,723,438 (GRCm38)	splice site	probably benign
R1778:Greb1	UTSW	12	16,690,894 (GRCm38)	missense	probably benign
R1842:Greb1	UTSW	12	16,696,243 (GRCm38)	missense	probably damaging	1.00
R2040:Greb1	UTSW	12	16,702,650 (GRCm38)	missense	probably damaging	1.00
R2153:Greb1	UTSW	12	16,699,532 (GRCm38)	missense	probably damaging	1.00
R2178:Greb1	UTSW	12	16,696,387 (GRCm38)	missense	probably damaging	1.00
R2194:Greb1	UTSW	12	16,690,908 (GRCm38)	missense	probably benign	0.08
R2248:Greb1	UTSW	12	16,680,378 (GRCm38)	missense	possibly damaging	0.90
R2474:Greb1	UTSW	12	16,714,953 (GRCm38)	missense	possibly damaging	0.93
R2509:Greb1	UTSW	12	16,724,922 (GRCm38)	missense	probably damaging	1.00
R2860:Greb1	UTSW	12	16,711,745 (GRCm38)	missense	probably benign	0.28
R2861:Greb1	UTSW	12	16,711,745 (GRCm38)	missense	probably benign	0.28
R2862:Greb1	UTSW	12	16,711,745 (GRCm38)	missense	probably benign	0.28
R2866:Greb1	UTSW	12	16,699,550 (GRCm38)	missense	probably damaging	1.00
R2890:Greb1	UTSW	12	16,704,478 (GRCm38)	missense	probably damaging	1.00
R3056:Greb1	UTSW	12	16,688,591 (GRCm38)	missense	probably damaging	0.96
R3863:Greb1	UTSW	12	16,702,420 (GRCm38)	missense	probably damaging	1.00
R3864:Greb1	UTSW	12	16,702,420 (GRCm38)	missense	probably damaging	1.00
R3956:Greb1	UTSW	12	16,682,299 (GRCm38)	missense	probably damaging	1.00
R4493:Greb1	UTSW	12	16,698,610 (GRCm38)	missense	probably benign	0.14
R4548:Greb1	UTSW	12	16,699,675 (GRCm38)	missense	probably damaging	1.00
R4683:Greb1	UTSW	12	16,711,773 (GRCm38)	missense	possibly damaging	0.75
R4739:Greb1	UTSW	12	16,696,328 (GRCm38)	missense	probably damaging	1.00
R4770:Greb1	UTSW	12	16,681,356 (GRCm38)	missense	probably benign	0.03
R4838:Greb1	UTSW	12	16,684,360 (GRCm38)	critical splice donor site	probably null
R4925:Greb1	UTSW	12	16,681,471 (GRCm38)	missense	probably damaging	1.00
R5009:Greb1	UTSW	12	16,724,857 (GRCm38)	missense	possibly damaging	0.79
R5086:Greb1	UTSW	12	16,708,022 (GRCm38)	intron	probably benign
R5213:Greb1	UTSW	12	16,714,790 (GRCm38)	nonsense	probably null
R5310:Greb1	UTSW	12	16,716,759 (GRCm38)	missense	probably benign	0.09
R5353:Greb1	UTSW	12	16,688,566 (GRCm38)	nonsense	probably null
R5544:Greb1	UTSW	12	16,673,796 (GRCm38)	missense	probably damaging	1.00
R5605:Greb1	UTSW	12	16,708,726 (GRCm38)	missense	probably damaging	0.96
R5708:Greb1	UTSW	12	16,673,842 (GRCm38)	missense	probably benign	0.11
R5837:Greb1	UTSW	12	16,688,585 (GRCm38)	missense	probably damaging	1.00
R5890:Greb1	UTSW	12	16,733,421 (GRCm38)	missense	possibly damaging	0.90
R5938:Greb1	UTSW	12	16,717,258 (GRCm38)	missense	probably damaging	1.00
R6049:Greb1	UTSW	12	16,681,394 (GRCm38)	missense	probably damaging	0.99
R6093:Greb1	UTSW	12	16,684,486 (GRCm38)	missense	probably benign
R6120:Greb1	UTSW	12	16,708,621 (GRCm38)	missense	probably damaging	0.99
R6175:Greb1	UTSW	12	16,674,770 (GRCm38)	missense	probably damaging	1.00
R6247:Greb1	UTSW	12	16,716,675 (GRCm38)	missense	probably damaging	1.00
R6274:Greb1	UTSW	12	16,735,151 (GRCm38)	missense	probably damaging	0.97
R6376:Greb1	UTSW	12	16,699,579 (GRCm38)	missense	probably damaging	0.97
R6523:Greb1	UTSW	12	16,684,373 (GRCm38)	missense	possibly damaging	0.51
R6557:Greb1	UTSW	12	16,710,383 (GRCm38)	missense	probably benign	0.00
R6602:Greb1	UTSW	12	16,709,440 (GRCm38)	missense	probably benign	0.44
R6621:Greb1	UTSW	12	16,692,717 (GRCm38)	missense	probably damaging	1.00
R6645:Greb1	UTSW	12	16,698,579 (GRCm38)	missense	probably benign	0.07
R6725:Greb1	UTSW	12	16,688,567 (GRCm38)	missense	probably damaging	1.00
R6750:Greb1	UTSW	12	16,688,583 (GRCm38)	missense	probably benign	0.05
R6863:Greb1	UTSW	12	16,684,420 (GRCm38)	missense	probably damaging	1.00
R6914:Greb1	UTSW	12	16,707,902 (GRCm38)	missense	probably damaging	0.97
R6996:Greb1	UTSW	12	16,723,354 (GRCm38)	missense	probably benign	0.00
R7083:Greb1	UTSW	12	16,723,314 (GRCm38)	missense	probably benign
R7147:Greb1	UTSW	12	16,733,427 (GRCm38)	missense	probably damaging	1.00
R7238:Greb1	UTSW	12	16,674,672 (GRCm38)	missense	probably damaging	0.99
R7290:Greb1	UTSW	12	16,711,738 (GRCm38)	missense	probably damaging	1.00
R7358:Greb1	UTSW	12	16,724,881 (GRCm38)	missense	probably damaging	1.00
R7395:Greb1	UTSW	12	16,709,430 (GRCm38)	critical splice donor site	probably null
R7526:Greb1	UTSW	12	16,716,765 (GRCm38)	missense	probably benign	0.00
R7530:Greb1	UTSW	12	16,717,206 (GRCm38)	missense	probably benign	0.02
R7536:Greb1	UTSW	12	16,682,185 (GRCm38)	missense	probably damaging	1.00
R7643:Greb1	UTSW	12	16,711,996 (GRCm38)	missense	probably damaging	0.99
R7732:Greb1	UTSW	12	16,673,863 (GRCm38)	missense	probably damaging	1.00
R7740:Greb1	UTSW	12	16,740,121 (GRCm38)	start gained	probably benign
R7747:Greb1	UTSW	12	16,674,795 (GRCm38)	missense	probably benign	0.01
R7760:Greb1	UTSW	12	16,723,416 (GRCm38)	missense	probably benign
R7937:Greb1	UTSW	12	16,716,669 (GRCm38)	missense	probably damaging	0.99
R8043:Greb1	UTSW	12	16,711,789 (GRCm38)	missense	probably damaging	1.00
R8259:Greb1	UTSW	12	16,724,924 (GRCm38)	nonsense	probably null
R8553:Greb1	UTSW	12	16,723,327 (GRCm38)	missense	probably benign	0.00
R8559:Greb1	UTSW	12	16,696,435 (GRCm38)	missense	probably damaging	1.00
R8690:Greb1	UTSW	12	16,696,547 (GRCm38)	missense	probably benign	0.03
R8830:Greb1	UTSW	12	16,688,519 (GRCm38)	missense	probably benign	0.35
R8911:Greb1	UTSW	12	16,690,902 (GRCm38)	missense	possibly damaging	0.84
R8963:Greb1	UTSW	12	16,724,884 (GRCm38)	missense	probably damaging	1.00
R8986:Greb1	UTSW	12	16,684,456 (GRCm38)	missense	probably damaging	0.99
R9013:Greb1	UTSW	12	16,739,969 (GRCm38)	missense	probably damaging	1.00
R9279:Greb1	UTSW	12	16,682,152 (GRCm38)	missense	probably damaging	0.99
R9360:Greb1	UTSW	12	16,740,036 (GRCm38)	missense	probably damaging	1.00
R9563:Greb1	UTSW	12	16,724,823 (GRCm38)	missense	probably benign	0.06
R9616:Greb1	UTSW	12	16,740,037 (GRCm38)	missense	probably damaging	1.00
R9627:Greb1	UTSW	12	16,706,166 (GRCm38)	missense	probably damaging	1.00
R9731:Greb1	UTSW	12	16,688,597 (GRCm38)	missense	probably damaging	1.00
R9761:Greb1	UTSW	12	16,701,274 (GRCm38)	missense	probably benign	0.05
Z1176:Greb1	UTSW	12	16,696,756 (GRCm38)	missense	probably benign	0.00
Z1177:Greb1	UTSW	12	16,702,491 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGTTTACCCAGCCCAGTGAG -3'
(R):5'- AGAGGCTCATGGCATGCTTC -3'

Sequencing Primer
(F):5'- GCCCAGTGAGTCTGTAATTATAACC -3'
(R):5'- GGCTCATGGCATGCTTCTTTCTG -3'

Posted On

2016-05-10