Mutagenetix > Incidental Mutations

Incidental Mutation 'R6834:Eml5'

534523

Institutional Source

Beutler Lab

Gene Symbol

Eml5

Ensembl Gene

ENSMUSG00000051166

Gene Name

echinoderm microtubule associated protein like 5

Synonyms

C130068M19Rik

MMRRC Submission

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.339) question?

Stock #

R6834 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

98786805-98901484 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 98887024 bp

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 105 (H105Q)

Ref Sequence

ENSEMBL: ENSMUSP00000065643 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000065716] [ENSMUST00000223282]

Predicted Effect

probably damaging
Transcript: ENSMUST00000065716
AA Change: H105Q

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

SMART Domains

Protein: ENSMUSP00000065643
Gene: ENSMUSG00000051166
AA Change: H105Q

Domain	Start	End	E-Value	Type
Pfam:HELP	1	49	3.3e-21	PFAM
WD40	50	91	6.42e-1	SMART
WD40	94	136	1.08e-4	SMART
WD40	139	178	1.27e-1	SMART
WD40	184	224	2.75e1	SMART
WD40	225	263	2.65e-4	SMART
Blast:WD40	265	312	2e-22	BLAST
WD40	313	353	4.69e-5	SMART
WD40	356	394	2.2e2	SMART
WD40	397	436	8.59e-1	SMART
WD40	444	479	6.6e1	SMART
WD40	505	546	2.74e2	SMART
WD40	552	592	4.8e-2	SMART
low complexity region	609	632	N/A	INTRINSIC
Pfam:HELP	656	715	1.4e-20	PFAM
WD40	716	757	1.18e-1	SMART
WD40	760	802	2.84e-4	SMART
WD40	805	844	1.91e1	SMART
WD40	853	891	2.64e2	SMART
WD40	892	929	3.45e-3	SMART
WD40	985	1026	4.55e-3	SMART
WD40	1029	1068	6.39e0	SMART
WD40	1071	1111	5.15e-2	SMART
WD40	1180	1221	1.9e2	SMART
WD40	1227	1267	1.38e0	SMART
low complexity region	1280	1297	N/A	INTRINSIC
Pfam:HELP	1335	1410	2.4e-16	PFAM
Blast:WD40	1412	1462	8e-28	BLAST
WD40	1465	1507	1.56e-1	SMART
WD40	1510	1549	2.06e0	SMART
WD40	1558	1597	8.22e1	SMART
WD40	1599	1644	4.26e1	SMART
WD40	1690	1730	2.19e-5	SMART
WD40	1774	1813	5.97e-1	SMART
WD40	1884	1925	2.39e0	SMART
WD40	1931	1971	2.88e-1	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000223282
AA Change: H105Q

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)

Meta Mutation Damage Score

0.4576

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	T	A	11: 9,275,110	W530R	possibly damaging	Het
Aco1	A	G	4: 40,164,747	K79R	probably benign	Het
Adam15	C	T	3: 89,340,083	G426R	probably damaging	Het
Angptl1	A	T	1: 156,844,693	I30L	probably benign	Het
Ankrd35	A	G	3: 96,683,283	E295G	possibly damaging	Het
Ap5m1	T	A	14: 49,073,737	V88E	probably damaging	Het
Astn1	A	T	1: 158,664,122	Q47L	probably benign	Het
Atf6b	T	C	17: 34,649,157	S135P	probably damaging	Het
AU018091	T	A	7: 3,157,955	I589F	probably benign	Het
BC052040	T	C	2: 115,674,784	S179P	probably benign	Het
Cenpf	T	C	1: 189,659,446	K730E	probably damaging	Het
Chrna6	C	T	8: 27,408,310		probably null	Het
Dmxl1	A	T	18: 49,955,823	I2790F	probably damaging	Het
Ell	A	G	8: 70,579,134	D116G	probably damaging	Het
Epb41l2	T	A	10: 25,493,604	V23D	possibly damaging	Het
Gatad2b	T	A	3: 90,348,643	S139T	probably benign	Het
Glb1l	A	G	1: 75,201,753	V347A	possibly damaging	Het
Gm4846	A	T	1: 166,494,578	I140N	possibly damaging	Het
Gm7534	A	C	4: 134,193,165	V563G	possibly damaging	Het
Gm9268	G	C	7: 43,023,580	A143P	probably damaging	Het
Gng11	A	G	6: 4,008,068	I44V	probably benign	Het
H2-Ke6	T	C	17: 34,027,217	S161G	probably damaging	Het
Hsp90ab1	T	C	17: 45,570,467	I250V	probably benign	Het
Igkv4-79	A	G	6: 69,043,272	S20P	probably damaging	Het
Il11ra1	A	G	4: 41,765,454	H183R	probably benign	Het
Kcnip3	A	T	2: 127,458,358	F252I	probably damaging	Het
Klk11	T	C	7: 43,778,912	I242T	probably damaging	Het
Klk12	T	C	7: 43,773,348	V233A	possibly damaging	Het
Lama3	G	A	18: 12,491,548	C1450Y	probably damaging	Het
Lmod2	A	T	6: 24,597,783		probably benign	Het
Loxhd1	T	A	18: 77,441,526	V1089E	probably damaging	Het
Lrba	C	T	3: 86,350,286	P1286S	probably benign	Het
Lrrc41	T	C	4: 116,096,529	V804A	possibly damaging	Het
Lrrc8a	T	A	2: 30,255,647	S158T	possibly damaging	Het
Mcm3	A	T	1: 20,810,096	M504K	possibly damaging	Het
Med24	A	T	11: 98,705,024		probably null	Het
Mrgprx1	T	C	7: 48,021,637	S121G	probably damaging	Het
Mvb12a	G	A	8: 71,545,252	M103I	probably benign	Het
Olfr726	A	G	14: 50,084,228	V151A	probably damaging	Het
Olfr730	T	C	14: 50,186,483	I245V	probably benign	Het
Otx1	C	A	11: 21,997,037	A91S	probably damaging	Het
Pacsin3	T	A	2: 91,262,835	M224K	probably damaging	Het
Pam	T	A	1: 97,837,992	I771F	probably damaging	Het
Pamr1	C	T	2: 102,614,931	R270C	probably damaging	Het
Pcdhgb8	G	T	18: 37,762,089	A71S	probably benign	Het
Poc1b	C	T	10: 99,192,804	A336V	probably benign	Het
Prss39	G	T	1: 34,498,616	V54F	possibly damaging	Het
Ptar1	A	G	19: 23,717,924	T252A	probably benign	Het
Ptprz1	A	G	6: 22,999,633	D574G	probably benign	Het
Rnf40	G	A	7: 127,596,406	D635N	probably benign	Het
Scn1a	T	A	2: 66,327,742	Q429L	probably damaging	Het
Sf1	G	T	19: 6,374,097	G386C	probably damaging	Het
Shank2	A	T	7: 144,409,894	Y623F	probably damaging	Het
Slc9a5	G	T	8: 105,364,684	A699S	probably benign	Het
Sox9	A	T	11: 112,784,000	Q208L	probably benign	Het
Synpo2l	A	T	14: 20,660,634	D865E	probably damaging	Het
Szt2	A	G	4: 118,388,325	S1097P	probably benign	Het
Tmc1	C	A	19: 20,795,610	E676*	probably null	Het
Ubr3	T	C	2: 70,000,481	I158T	possibly damaging	Het
Ush2a	T	C	1: 188,356,792	Y315H	probably damaging	Het
Vmn1r85	T	C	7: 13,084,644	D191G	probably damaging	Het
Zfp358	A	G	8: 3,495,613	D92G	probably benign	Het
Zfp735	G	A	11: 73,710,608	G126D	probably damaging	Het

Other mutations in Eml5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00091:Eml5	APN	12	98873209	splice site	probably benign
IGL00473:Eml5	APN	12	98805492	splice site	probably benign
IGL01120:Eml5	APN	12	98844019	missense	probably benign
IGL01308:Eml5	APN	12	98802313	missense	probably damaging	1.00
IGL01790:Eml5	APN	12	98798932	missense	probably damaging	1.00
IGL01973:Eml5	APN	12	98863280	missense	probably benign
IGL02182:Eml5	APN	12	98802322	missense	probably damaging	1.00
IGL02201:Eml5	APN	12	98794424	splice site	probably benign
IGL02375:Eml5	APN	12	98844087	missense	probably damaging	1.00
IGL02397:Eml5	APN	12	98790674	missense	probably benign	0.07
IGL02480:Eml5	APN	12	98876243	missense	probably damaging	1.00
IGL02801:Eml5	APN	12	98817845	missense	possibly damaging	0.88
IGL02876:Eml5	APN	12	98858841	missense	probably damaging	1.00
IGL03104:Eml5	APN	12	98861245	nonsense	probably null
IGL03158:Eml5	APN	12	98827514	splice site	probably benign
IGL03286:Eml5	APN	12	98860503	missense	probably damaging	1.00
IGL03380:Eml5	APN	12	98874647	splice site	probably benign
BB010:Eml5	UTSW	12	98844020	missense	possibly damaging	0.87
BB020:Eml5	UTSW	12	98844020	missense	possibly damaging	0.87
R0573:Eml5	UTSW	12	98824772	splice site	probably null
R0624:Eml5	UTSW	12	98865479	missense	probably damaging	1.00
R0993:Eml5	UTSW	12	98861183	missense	probably benign	0.25
R1073:Eml5	UTSW	12	98830973	missense	probably damaging	1.00
R1183:Eml5	UTSW	12	98792046	missense	probably benign	0.31
R1352:Eml5	UTSW	12	98831003	splice site	probably benign
R1469:Eml5	UTSW	12	98858823	missense	probably benign
R1469:Eml5	UTSW	12	98858823	missense	probably benign
R1503:Eml5	UTSW	12	98831174	missense	probably damaging	0.99
R1538:Eml5	UTSW	12	98794276	missense	probably damaging	0.99
R1689:Eml5	UTSW	12	98830935	missense	probably damaging	1.00
R1773:Eml5	UTSW	12	98798839	missense	probably damaging	1.00
R1775:Eml5	UTSW	12	98852704	splice site	probably null
R1791:Eml5	UTSW	12	98887056	missense	probably benign	0.31
R1856:Eml5	UTSW	12	98810584	missense	probably damaging	1.00
R1919:Eml5	UTSW	12	98798839	missense	probably damaging	1.00
R1957:Eml5	UTSW	12	98859961	missense	probably damaging	1.00
R1962:Eml5	UTSW	12	98876311	missense	probably damaging	0.99
R2033:Eml5	UTSW	12	98791386	missense	possibly damaging	0.71
R2035:Eml5	UTSW	12	98794266	missense	probably benign	0.33
R2073:Eml5	UTSW	12	98802446	missense	probably damaging	0.99
R2143:Eml5	UTSW	12	98810605	missense	probably damaging	1.00
R2144:Eml5	UTSW	12	98810605	missense	probably damaging	1.00
R2158:Eml5	UTSW	12	98843946	splice site	probably benign
R2164:Eml5	UTSW	12	98887097	missense	probably damaging	0.99
R2175:Eml5	UTSW	12	98876223	nonsense	probably null
R2200:Eml5	UTSW	12	98825417	missense	probably damaging	1.00
R2234:Eml5	UTSW	12	98841581	missense	probably damaging	1.00
R2504:Eml5	UTSW	12	98844105	missense	possibly damaging	0.71
R2871:Eml5	UTSW	12	98865401	missense	probably damaging	1.00
R2871:Eml5	UTSW	12	98865401	missense	probably damaging	1.00
R2958:Eml5	UTSW	12	98876178	missense	possibly damaging	0.74
R3013:Eml5	UTSW	12	98880808	splice site	probably null
R3118:Eml5	UTSW	12	98865494	missense	probably damaging	0.97
R3735:Eml5	UTSW	12	98855989	missense	possibly damaging	0.78
R3856:Eml5	UTSW	12	98816024	missense	probably damaging	1.00
R3900:Eml5	UTSW	12	98825523	missense	probably damaging	1.00
R3973:Eml5	UTSW	12	98802465	splice site	probably benign
R3976:Eml5	UTSW	12	98802465	splice site	probably benign
R4105:Eml5	UTSW	12	98841548	splice site	probably null
R4107:Eml5	UTSW	12	98841548	splice site	probably null
R4108:Eml5	UTSW	12	98841548	splice site	probably null
R4109:Eml5	UTSW	12	98841548	splice site	probably null
R4258:Eml5	UTSW	12	98865434	missense	probably benign	0.01
R4381:Eml5	UTSW	12	98815955	missense	possibly damaging	0.93
R4590:Eml5	UTSW	12	98837341	missense	possibly damaging	0.91
R4737:Eml5	UTSW	12	98798852	missense	probably damaging	1.00
R4775:Eml5	UTSW	12	98802307	missense	probably benign	0.05
R4850:Eml5	UTSW	12	98790619	missense	probably damaging	1.00
R5007:Eml5	UTSW	12	98830965	missense	probably damaging	1.00
R5092:Eml5	UTSW	12	98792616	missense	probably damaging	1.00
R5123:Eml5	UTSW	12	98874512	missense	probably damaging	1.00
R5124:Eml5	UTSW	12	98792042	missense	probably damaging	1.00
R5273:Eml5	UTSW	12	98790688	missense	probably damaging	1.00
R5369:Eml5	UTSW	12	98858783	missense	probably damaging	1.00
R5430:Eml5	UTSW	12	98794158	missense	probably damaging	1.00
R5748:Eml5	UTSW	12	98825555	missense	probably damaging	0.99
R5769:Eml5	UTSW	12	98790619	missense	probably damaging	1.00
R5832:Eml5	UTSW	12	98876188	missense	probably benign
R6113:Eml5	UTSW	12	98824674	nonsense	probably null
R6131:Eml5	UTSW	12	98861251	missense	probably damaging	0.99
R6175:Eml5	UTSW	12	98794456	missense	possibly damaging	0.69
R6184:Eml5	UTSW	12	98863129	missense	possibly damaging	0.53
R6357:Eml5	UTSW	12	98870884	missense	probably damaging	0.98
R6375:Eml5	UTSW	12	98798868
R6528:Eml5	UTSW	12	98824637	missense	probably benign	0.18
R6657:Eml5	UTSW	12	98791405	missense	probably damaging	0.98
R6717:Eml5	UTSW	12	98827506	missense	probably damaging	1.00
R6751:Eml5	UTSW	12	98865400	missense	probably damaging	1.00
R6833:Eml5	UTSW	12	98887024	missense	probably damaging	1.00
R6972:Eml5	UTSW	12	98876180	missense	probably benign	0.00
R7091:Eml5	UTSW	12	98802474	missense	probably benign	0.16
R7353:Eml5	UTSW	12	98825424	missense
R7644:Eml5	UTSW	12	98855944	missense	probably benign	0.05
R7694:Eml5	UTSW	12	98792563	missense	probably damaging	0.99
R7842:Eml5	UTSW	12	98794135	missense	probably damaging	1.00
R7933:Eml5	UTSW	12	98844020	missense	possibly damaging	0.87
R8111:Eml5	UTSW	12	98792514	critical splice donor site	probably null
R8198:Eml5	UTSW	12	98858886	nonsense	probably null
R8482:Eml5	UTSW	12	98876301	missense	probably damaging	1.00
T0722:Eml5	UTSW	12	98841582	missense	probably null	1.00

Predicted Primers

PCR Primer
(F):5'- GTTCTGGGTAACAATGAAATCAACAAC -3'
(R):5'- GCACACTATATCACATGGAGTTTATG -3'

Sequencing Primer
(F):5'- ATCTGGGTACTGGGAATTGAACCC -3'
(R):5'- GTCATTAACCTTTTAGT -3'

Posted On

2018-09-12