Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01522:Greb1'

89455

Institutional Source

Australian Phenomics Network (link to record)

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 #

IGL01522

Quality Score

Status

Chromosome

Chromosomal Location

16670615-16800886 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 16701201 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 1003 (I1003V)

Ref Sequence

ENSEMBL: ENSMUSP00000125339 (fasta)

Gene Model

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

AlphaFold

Q3UHK3

Predicted Effect

probably damaging
Transcript: ENSMUST00000048064
AA Change: I1031V

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000044454
Gene: ENSMUSG00000036523
AA Change: I1031V

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159044

Predicted Effect

probably damaging
Transcript: ENSMUST00000159120
AA Change: I1003V

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000125339
Gene: ENSMUSG00000036523
AA Change: I1003V

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

probably benign
Transcript: ENSMUST00000160347

SMART Domains

Protein: ENSMUSP00000124897
Gene: ENSMUSG00000036523

Domain	Start	End	E-Value	Type
Pfam:GREB1	1	121	4.5e-61	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160575

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000161036

Predicted Effect

probably damaging
Transcript: ENSMUST00000162112
AA Change: I1031V

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000124348
Gene: ENSMUSG00000036523
AA Change: I1031V

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

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: 41 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts12	T	C	15: 11,065,159 (GRCm38)		probably null	Het
Adamts3	T	C	5: 89,702,943 (GRCm38)	N579S	probably benign	Het
Akr1c19	A	G	13: 4,239,099 (GRCm38)		probably benign	Het
Ankrd39	T	A	1: 36,542,061 (GRCm38)	H69L	probably damaging	Het
Apcdd1	T	A	18: 62,952,115 (GRCm38)	M461K	possibly damaging	Het
Bpifa3	G	A	2: 154,137,582 (GRCm38)	C209Y	probably damaging	Het
Cep131	T	C	11: 120,067,163 (GRCm38)	E779G	probably benign	Het
Cep85	G	T	4: 134,152,256 (GRCm38)	Q394K	probably damaging	Het
Cep85	T	C	4: 134,152,255 (GRCm38)	Q394R	probably damaging	Het
Clcn6	T	C	4: 148,017,535 (GRCm38)	Y364C	probably benign	Het
Fetub	G	A	16: 22,929,641 (GRCm38)	M1I	probably null	Het
Hsf3	A	G	X: 96,320,594 (GRCm38)		probably benign	Het
Jcad	A	G	18: 4,673,312 (GRCm38)	N358S	probably damaging	Het
Kndc1	T	C	7: 139,913,972 (GRCm38)		probably benign	Het
Lama1	A	T	17: 67,752,774 (GRCm38)		probably benign	Het
Mark2	A	G	19: 7,281,238 (GRCm38)	V50A	probably benign	Het
Mmp7	T	C	9: 7,692,228 (GRCm38)	W35R	probably damaging	Het
Ndc80	A	G	17: 71,499,325 (GRCm38)	V578A	probably benign	Het
Nfyc	T	C	4: 120,781,524 (GRCm38)	E42G	probably damaging	Het
Or1j15	A	G	2: 36,569,221 (GRCm38)	T208A	probably benign	Het
Or52b4	A	T	7: 102,535,184 (GRCm38)	I146F	probably damaging	Het
Or5d37	T	C	2: 88,093,016 (GRCm38)	K307E	possibly damaging	Het
Or8g21	A	T	9: 38,995,100 (GRCm38)	C112S	probably benign	Het
Or9i16	A	T	19: 13,887,358 (GRCm38)	L284*	probably null	Het
Pcdha11	T	C	18: 37,185,008 (GRCm38)	F925L	probably damaging	Het
Pdcd1	T	G	1: 94,040,846 (GRCm38)	R154S	probably benign	Het
Pepd	T	A	7: 34,924,440 (GRCm38)	D87E	probably benign	Het
Pfn4	A	G	12: 4,770,240 (GRCm38)	T30A	probably benign	Het
Pgpep1l	A	G	7: 68,237,708 (GRCm38)	M48T	possibly damaging	Het
Pla2g15	A	G	8: 106,163,116 (GRCm38)	N340S	probably benign	Het
Plcb4	A	G	2: 136,002,627 (GRCm38)	D155G	probably damaging	Het
Plg	G	A	17: 12,404,069 (GRCm38)	G499S	probably damaging	Het
Plin3	C	T	17: 56,280,799 (GRCm38)	W305*	probably null	Het
Polq	C	A	16: 37,027,903 (GRCm38)	L291I	probably damaging	Het
Sanbr	A	G	11: 23,582,865 (GRCm38)		probably null	Het
Sdf2l1	T	A	16: 17,132,150 (GRCm38)	H54L	probably damaging	Het
Slc38a2	C	T	15: 96,693,055 (GRCm38)	D276N	possibly damaging	Het
Syk	A	G	13: 52,643,061 (GRCm38)	T576A	probably benign	Het
Tas2r119	G	A	15: 32,178,193 (GRCm38)	V302I	probably benign	Het
Uso1	T	C	5: 92,181,419 (GRCm38)	F389L	probably damaging	Het
Wwc2	T	A	8: 47,868,633 (GRCm38)	Y482F	unknown	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
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
R4982:Greb1	UTSW	12	16,724,761 (GRCm38)	missense	probably damaging	0.98
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

Posted On

2013-12-03