Mutagenetix > Incidental Mutation

Incidental Mutation 'R0610:Greb1'

54641

Institutional Source

Beutler Lab

Gene Symbol

Greb1

Ensembl Gene

ENSMUSG00000036523

Gene Name

gene regulated by estrogen in breast cancer protein

Synonyms

5730583K22Rik

MMRRC Submission

038799-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0610 (G1)

Quality Score

157

Status

Validated

Chromosome

Chromosomal Location

16670615-16800886 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 16696442 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Alanine at position 1276 (S1276A)

Ref Sequence

ENSEMBL: ENSMUSP00000124348 (fasta)

Gene Model

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

AlphaFold

Q3UHK3

Predicted Effect

probably benign
Transcript: ENSMUST00000048064
AA Change: S1276A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000044454
Gene: ENSMUSG00000036523
AA Change: S1276A

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

Predicted Effect

probably benign
Transcript: ENSMUST00000159120
AA Change: S1248A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000125339
Gene: ENSMUSG00000036523
AA Change: S1248A

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: ENSMUST00000161036

Predicted Effect

probably benign
Transcript: ENSMUST00000162112
AA Change: S1276A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000124348
Gene: ENSMUSG00000036523
AA Change: S1276A

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

Meta Mutation Damage Score

0.0758

Coding Region Coverage

1x: 99.4%
3x: 98.9%
10x: 97.4%
20x: 94.7%

Validation Efficiency

99% (97/98)

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: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930433I11Rik	A	T	7: 40,993,056 (GRCm38)	T141S	probably benign	Het
4930578I06Rik	G	A	14: 63,986,265 (GRCm38)	R21*	probably null	Het
Abca15	A	G	7: 120,365,786 (GRCm38)	E757G	possibly damaging	Het
Abca5	T	C	11: 110,301,527 (GRCm38)	T720A	probably benign	Het
Actr5	T	A	2: 158,632,456 (GRCm38)		probably null	Het
Adgrl3	T	C	5: 81,693,716 (GRCm38)		probably benign	Het
Adra1a	A	G	14: 66,637,792 (GRCm38)	D72G	probably damaging	Het
Ahcyl	T	C	16: 46,153,901 (GRCm38)	E371G	probably damaging	Het
Ahnak	G	T	19: 9,007,878 (GRCm38)	L2175F	probably benign	Het
AK157302	A	G	13: 21,495,663 (GRCm38)	T120A	possibly damaging	Het
Apol7a	G	A	15: 77,389,254 (GRCm38)	A336V	probably benign	Het
Asic1	C	A	15: 99,698,899 (GRCm38)	H525Q	probably benign	Het
Atxn7l2	T	C	3: 108,204,774 (GRCm38)	D335G	possibly damaging	Het
Bpgm	G	T	6: 34,504,349 (GRCm38)	R227L	possibly damaging	Het
Calm4	T	A	13: 3,838,320 (GRCm38)	V142E	possibly damaging	Het
Catsperg1	A	T	7: 29,190,619 (GRCm38)	L721Q	probably damaging	Het
Cdh26	A	G	2: 178,449,898 (GRCm38)	I83M	probably damaging	Het
Cep295	A	C	9: 15,322,754 (GRCm38)	S2249A	possibly damaging	Het
Cfhr4	G	A	1: 139,701,846 (GRCm38)	T799I	probably benign	Het
Cln3	A	G	7: 126,580,189 (GRCm38)	F139L	probably damaging	Het
Cmpk2	T	A	12: 26,478,056 (GRCm38)	L424Q	possibly damaging	Het
Col12a1	A	T	9: 79,707,848 (GRCm38)	V53E	probably benign	Het
Csmd1	G	A	8: 15,918,208 (GRCm38)	R3140C	possibly damaging	Het
Dagla	A	G	19: 10,271,558 (GRCm38)	W11R	probably damaging	Het
Dbx2	C	T	15: 95,624,897 (GRCm38)	V310M	probably benign	Het
Disp2	T	A	2: 118,792,236 (GRCm38)	C1150S	probably benign	Het
Dock3	T	C	9: 107,023,788 (GRCm38)	D326G	probably damaging	Het
Dph1	G	T	11: 75,185,957 (GRCm38)		probably benign	Het
Dyrk1b	C	A	7: 28,186,634 (GRCm38)	T594K	probably damaging	Het
Evx2	C	A	2: 74,655,987 (GRCm38)	A353S	probably benign	Het
Garin1b	T	A	6: 29,326,577 (GRCm38)	V231E	probably benign	Het
Hhipl1	T	A	12: 108,319,402 (GRCm38)	C490*	probably null	Het
Hmmr	G	T	11: 40,715,902 (GRCm38)	T231K	probably damaging	Het
Hspa4l	A	C	3: 40,779,400 (GRCm38)	E526D	probably benign	Het
Ibsp	A	G	5: 104,310,134 (GRCm38)	E179G	probably benign	Het
Ift140	C	T	17: 25,035,803 (GRCm38)	A150V	probably benign	Het
Igf2bp2	A	G	16: 22,070,309 (GRCm38)	S416P	probably benign	Het
Ighe	T	C	12: 113,271,743 (GRCm38)	K294E	unknown	Het
Ino80	G	A	2: 119,382,960 (GRCm38)	R1249C	probably damaging	Het
Iqca1	C	A	1: 90,142,731 (GRCm38)	G133V	probably null	Het
Kng2	T	A	16: 23,000,594 (GRCm38)	N231Y	possibly damaging	Het
Lca5	A	T	9: 83,399,739 (GRCm38)	C331S	probably benign	Het
Lrrc1	A	G	9: 77,472,206 (GRCm38)	I101T	possibly damaging	Het
Lrrk2	A	T	15: 91,815,416 (GRCm38)	I2489L	probably benign	Het
Lyz3	A	G	10: 117,237,730 (GRCm38)	F66S	probably benign	Het
Mapk9	A	C	11: 49,863,573 (GRCm38)	N51T	probably benign	Het
Marf1	C	T	16: 14,142,534 (GRCm38)	A549T	probably damaging	Het
Nek2	T	A	1: 191,822,515 (GRCm38)	V113D	probably damaging	Het
Nr4a3	C	A	4: 48,051,903 (GRCm38)	A248E	probably benign	Het
Nrp1	T	C	8: 128,502,618 (GRCm38)	I859T	probably damaging	Het
Olfm5	A	T	7: 104,154,445 (GRCm38)	Y195*	probably null	Het
Or13j1	T	A	4: 43,706,400 (GRCm38)	H56L	possibly damaging	Het
Or1n2	T	A	2: 36,907,659 (GRCm38)	W238R	probably damaging	Het
Or8g35	A	G	9: 39,469,823 (GRCm38)	L301P	probably damaging	Het
Oxtr	C	T	6: 112,477,177 (GRCm38)	R42Q	probably benign	Het
Pcnx2	A	G	8: 125,839,687 (GRCm38)	W1006R	probably damaging	Het
Pdpk1	T	C	17: 24,098,171 (GRCm38)		probably null	Het
Ryr2	T	A	13: 11,622,952 (GRCm38)	H3731L	probably damaging	Het
Sdr16c5	T	G	4: 4,016,116 (GRCm38)	E103D	possibly damaging	Het
Setdb2	A	C	14: 59,417,470 (GRCm38)	S324A	possibly damaging	Het
Slc17a3	C	T	13: 23,855,858 (GRCm38)	S293F	probably damaging	Het
Slc17a8	A	T	10: 89,576,626 (GRCm38)	I499K	probably damaging	Het
Slc2a9	T	A	5: 38,379,942 (GRCm38)	I389F	probably damaging	Het
Slc30a1	T	C	1: 191,909,424 (GRCm38)	V394A	probably damaging	Het
Slc41a2	A	G	10: 83,283,728 (GRCm38)	I390T	possibly damaging	Het
Slco1a1	A	G	6: 141,918,461 (GRCm38)		probably null	Het
Slit2	A	G	5: 48,275,674 (GRCm38)	K1053E	possibly damaging	Het
Smarca2	T	A	19: 26,691,391 (GRCm38)	L930Q	probably damaging	Het
Snx6	T	C	12: 54,751,789 (GRCm38)	H387R	probably damaging	Het
Sox5	A	T	6: 143,833,439 (GRCm38)	M622K	possibly damaging	Het
Ston1	C	A	17: 88,635,281 (GRCm38)	N38K	possibly damaging	Het
Strbp	C	T	2: 37,584,077 (GRCm38)	V658I	probably damaging	Het
Strn3	T	C	12: 51,610,448 (GRCm38)		probably null	Het
Suco	A	G	1: 161,864,032 (GRCm38)		probably benign	Het
Suco	T	G	1: 161,859,503 (GRCm38)	D96A	probably benign	Het
Sytl2	A	T	7: 90,380,853 (GRCm38)		probably benign	Het
Tmem41b	T	A	7: 109,981,085 (GRCm38)	D91V	probably damaging	Het
Tmem41b	T	A	7: 109,981,083 (GRCm38)	M25L	probably benign	Het
Tmem50b	C	T	16: 91,583,286 (GRCm38)	A68T	probably damaging	Het
Tmprss11e	G	A	5: 86,707,347 (GRCm38)	Q400*	probably null	Het
Tnfsf13b	G	A	8: 10,031,661 (GRCm38)		probably null	Het
Trappc8	A	G	18: 20,837,188 (GRCm38)	V916A	probably damaging	Het
Trdn	G	T	10: 33,474,453 (GRCm38)	V673F	probably damaging	Het
Trim28	G	T	7: 13,025,784 (GRCm38)		probably benign	Het
Txnrd2	T	C	16: 18,472,882 (GRCm38)	V427A	probably damaging	Het
Uggt1	T	C	1: 36,165,506 (GRCm38)		probably benign	Het
Vmn1r36	A	G	6: 66,716,420 (GRCm38)	L51P	probably damaging	Het
Vmn1r63	T	A	7: 5,803,064 (GRCm38)	M190L	possibly damaging	Het
Vmn2r116	T	A	17: 23,387,312 (GRCm38)	N399K	probably damaging	Het
Vmn2r117	T	C	17: 23,475,514 (GRCm38)	N453S	probably benign	Het
Wbp1l	T	A	19: 46,654,670 (GRCm38)	I370N	probably damaging	Het
Zfp445	T	C	9: 122,852,981 (GRCm38)	K632E	probably benign	Het
Zfp850	C	T	7: 27,989,394 (GRCm38)	R463H	probably damaging	Het
Zyg11a	A	G	4: 108,204,857 (GRCm38)	L249P	probably damaging	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
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

Predicted Primers

PCR Primer
(F):5'- TCTGGCAGTAAAACTGAAGACGACC -3'
(R):5'- ACAGCCTGATTCTAGCCTCAGGAC -3'

Sequencing Primer
(F):5'- GGCATGATACCCACCTGAG -3'
(R):5'- TGGTCGGAGGAGCTTGC -3'

Posted On

2013-07-11