Mutagenetix > Incidental Mutation

Incidental Mutation 'R2253:Ep400'

241803

Institutional Source

Beutler Lab

Gene Symbol

Ep400

Ensembl Gene

ENSMUSG00000029505

Gene Name

E1A binding protein p400

Synonyms

mDomino, 1700020J09Rik, p400

MMRRC Submission

040253-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R2253 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

110664373-110770717 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 110719091 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 1062 (N1062K)

Ref Sequence

ENSEMBL: ENSMUSP00000108055 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041558] [ENSMUST00000112435] [ENSMUST00000112436]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000041558
AA Change: N1098K

SMART Domains

Protein: ENSMUSP00000049038
Gene: ENSMUSG00000029505
AA Change: N1098K

Domain	Start	End	E-Value	Type
Pfam:EP400_N	1	461	1.6e-232	PFAM
low complexity region	519	532	N/A	INTRINSIC
low complexity region	550	561	N/A	INTRINSIC
low complexity region	598	620	N/A	INTRINSIC
low complexity region	631	645	N/A	INTRINSIC
low complexity region	658	686	N/A	INTRINSIC
HSA	762	833	1.31e-31	SMART
low complexity region	908	925	N/A	INTRINSIC
DEXDc	1049	1238	2.76e-15	SMART
Blast:DEXDc	1276	1317	2e-15	BLAST
low complexity region	1407	1417	N/A	INTRINSIC
HELICc	1807	1893	1.17e-4	SMART
low complexity region	2006	2019	N/A	INTRINSIC
low complexity region	2080	2100	N/A	INTRINSIC
low complexity region	2214	2223	N/A	INTRINSIC
SANT	2243	2310	3.57e-1	SMART
low complexity region	2402	2489	N/A	INTRINSIC
low complexity region	2596	2608	N/A	INTRINSIC
low complexity region	2644	2679	N/A	INTRINSIC
low complexity region	2694	2738	N/A	INTRINSIC
low complexity region	2769	2806	N/A	INTRINSIC
low complexity region	2846	2883	N/A	INTRINSIC
low complexity region	2933	2947	N/A	INTRINSIC
low complexity region	2974	2986	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000112435
AA Change: N1135K

SMART Domains

Protein: ENSMUSP00000108054
Gene: ENSMUSG00000029505
AA Change: N1135K

Domain	Start	End	E-Value	Type
low complexity region	28	53	N/A	INTRINSIC
low complexity region	121	145	N/A	INTRINSIC
low complexity region	262	287	N/A	INTRINSIC
low complexity region	298	308	N/A	INTRINSIC
low complexity region	313	329	N/A	INTRINSIC
coiled coil region	418	447	N/A	INTRINSIC
low complexity region	471	485	N/A	INTRINSIC
low complexity region	556	569	N/A	INTRINSIC
low complexity region	587	598	N/A	INTRINSIC
low complexity region	635	657	N/A	INTRINSIC
low complexity region	668	682	N/A	INTRINSIC
low complexity region	695	723	N/A	INTRINSIC
HSA	799	870	1.31e-31	SMART
low complexity region	945	962	N/A	INTRINSIC
DEXDc	1086	1275	2.76e-15	SMART
Blast:DEXDc	1313	1354	2e-15	BLAST
low complexity region	1444	1454	N/A	INTRINSIC
internal_repeat_1	1556	1646	6.82e-5	PROSPERO
low complexity region	1887	1900	N/A	INTRINSIC
low complexity region	1961	1981	N/A	INTRINSIC
low complexity region	2095	2104	N/A	INTRINSIC
SANT	2124	2191	3.57e-1	SMART
low complexity region	2283	2370	N/A	INTRINSIC
internal_repeat_1	2371	2463	6.82e-5	PROSPERO
low complexity region	2477	2489	N/A	INTRINSIC
low complexity region	2525	2560	N/A	INTRINSIC
low complexity region	2575	2619	N/A	INTRINSIC
low complexity region	2645	2659	N/A	INTRINSIC
low complexity region	2660	2680	N/A	INTRINSIC
low complexity region	2720	2757	N/A	INTRINSIC
low complexity region	2807	2821	N/A	INTRINSIC
low complexity region	2848	2860	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000112436
AA Change: N1062K

SMART Domains

Protein: ENSMUSP00000108055
Gene: ENSMUSG00000029505
AA Change: N1062K

Domain	Start	End	E-Value	Type
low complexity region	28	53	N/A	INTRINSIC
low complexity region	121	145	N/A	INTRINSIC
low complexity region	262	287	N/A	INTRINSIC
low complexity region	298	308	N/A	INTRINSIC
low complexity region	313	329	N/A	INTRINSIC
coiled coil region	418	449	N/A	INTRINSIC
low complexity region	472	482	N/A	INTRINSIC
low complexity region	483	496	N/A	INTRINSIC
low complexity region	514	525	N/A	INTRINSIC
low complexity region	562	584	N/A	INTRINSIC
low complexity region	595	609	N/A	INTRINSIC
low complexity region	622	650	N/A	INTRINSIC
HSA	726	797	1.31e-31	SMART
low complexity region	872	889	N/A	INTRINSIC
DEXDc	1013	1202	2.76e-15	SMART
Blast:DEXDc	1240	1281	2e-15	BLAST
low complexity region	1371	1381	N/A	INTRINSIC
internal_repeat_1	1483	1573	6.76e-5	PROSPERO
HELICc	1771	1857	1.17e-4	SMART
low complexity region	1970	1983	N/A	INTRINSIC
low complexity region	2044	2064	N/A	INTRINSIC
low complexity region	2178	2187	N/A	INTRINSIC
SANT	2207	2274	3.57e-1	SMART
low complexity region	2366	2453	N/A	INTRINSIC
internal_repeat_1	2454	2546	6.76e-5	PROSPERO
low complexity region	2560	2572	N/A	INTRINSIC
low complexity region	2608	2643	N/A	INTRINSIC
low complexity region	2658	2702	N/A	INTRINSIC
low complexity region	2733	2770	N/A	INTRINSIC
low complexity region	2810	2847	N/A	INTRINSIC
low complexity region	2897	2911	N/A	INTRINSIC
low complexity region	2938	2950	N/A	INTRINSIC

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.2%
20x: 94.9%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele die at E11.5 and display severe defects in yolk sac erythropoiesis, anemia, and a slight deformity of the neural tube. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700129C05Rik	G	A	14: 59,142,612 (GRCm38)	S79F	probably damaging	Het
Acss3	G	A	10: 107,004,748 (GRCm38)	A384V	probably damaging	Het
Aff2	G	A	X: 69,834,803 (GRCm38)	E732K	possibly damaging	Het
Atp12a	A	G	14: 56,376,258 (GRCm38)	T496A	probably benign	Het
B3gnt3	A	T	8: 71,692,818 (GRCm38)	M302K	probably damaging	Het
Bptf	G	T	11: 107,111,322 (GRCm38)	D321E	probably damaging	Het
C1ql3	C	T	2: 13,010,319 (GRCm38)	V177I	possibly damaging	Het
C2cd5	A	T	6: 143,036,316 (GRCm38)	Y607*	probably null	Het
Casp3	G	T	8: 46,637,955 (GRCm38)	W214L	probably damaging	Het
Cd248	A	G	19: 5,068,126 (GRCm38)	M1V	probably null	Het
Cdh18	A	G	15: 23,410,805 (GRCm38)	T405A	probably benign	Het
Cldn24	G	T	8: 47,822,328 (GRCm38)	R62S	probably benign	Het
Cnot1	A	G	8: 95,763,186 (GRCm38)	V463A	probably benign	Het
Cul2	A	T	18: 3,399,876 (GRCm38)	L3F	probably damaging	Het
Gch1	T	C	14: 47,189,341 (GRCm38)		probably benign	Het
Gzf1	T	C	2: 148,683,936 (GRCm38)	M109T	probably damaging	Het
Itch	T	A	2: 155,212,339 (GRCm38)	M701K	probably benign	Het
Kank4	A	T	4: 98,779,226 (GRCm38)	I328N	probably damaging	Het
Krt9	A	T	11: 100,190,859 (GRCm38)	N281K	possibly damaging	Het
Lgals12	T	A	19: 7,606,765 (GRCm38)		probably benign	Het
Lrrc37a	T	C	11: 103,501,467 (GRCm38)	Q1044R	probably benign	Het
Mbtps2	A	T	X: 157,559,033 (GRCm38)	F270L	probably benign	Het
Nr3c1	G	T	18: 39,486,751 (GRCm38)	T161K	probably benign	Het
Or2w3b	T	C	11: 58,732,995 (GRCm38)	T57A	probably benign	Het
Or4g16	A	G	2: 111,306,310 (GRCm38)	Y35C	probably damaging	Het
Or5ak20	A	G	2: 85,353,858 (GRCm38)	S23P	possibly damaging	Het
Or5b116	T	C	19: 13,445,185 (GRCm38)	Y58H	probably damaging	Het
Pla2g4d	T	C	2: 120,271,141 (GRCm38)	K453E	probably damaging	Het
Plcb2	T	C	2: 118,723,765 (GRCm38)	N69S	probably benign	Het
Prl3d1	T	C	13: 27,094,998 (GRCm38)	Y59H	possibly damaging	Het
Rnf133	T	C	6: 23,649,175 (GRCm38)	M252V	probably benign	Het
Rnf181	G	T	6: 72,361,484 (GRCm38)	H14N	possibly damaging	Het
Sash1	A	T	10: 8,729,977 (GRCm38)	M883K	probably benign	Het
Secisbp2l	C	T	2: 125,740,737 (GRCm38)	G933D	possibly damaging	Het
Slc13a4	A	G	6: 35,280,483 (GRCm38)	V240A	probably benign	Het
Slc2a5	T	C	4: 150,139,990 (GRCm38)	Y315H	possibly damaging	Het
Slc7a2	T	C	8: 40,905,621 (GRCm38)	Y334H	probably benign	Het
Spib	A	G	7: 44,529,968 (GRCm38)	S23P	probably benign	Het
Tbc1d1	A	G	5: 64,284,800 (GRCm38)	N721S	probably benign	Het
Tcf25	A	G	8: 123,374,033 (GRCm38)	E54G	probably benign	Het
Tesl2	G	A	X: 23,958,711 (GRCm38)	A75V	probably benign	Het
Tns2	C	T	15: 102,108,934 (GRCm38)	R281C	probably damaging	Het
Uba7	A	G	9: 107,976,364 (GRCm38)	H131R	probably benign	Het
Vmn2r6	C	T	3: 64,559,718 (GRCm38)	C120Y	probably damaging	Het
Zdhhc18	A	T	4: 133,633,077 (GRCm38)		probably null	Het
Zfp970	T	A	2: 177,474,821 (GRCm38)		probably null	Het

Other mutations in Ep400

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00231:Ep400	APN	5	110,687,841 (GRCm38)	missense	unknown
IGL00585:Ep400	APN	5	110,755,905 (GRCm38)	missense	possibly damaging	0.70
IGL00586:Ep400	APN	5	110,739,594 (GRCm38)	missense	probably damaging	1.00
IGL00816:Ep400	APN	5	110,735,490 (GRCm38)	unclassified	probably benign
IGL01066:Ep400	APN	5	110,668,199 (GRCm38)	splice site	probably benign
IGL01302:Ep400	APN	5	110,742,048 (GRCm38)	missense	probably benign	0.00
IGL01568:Ep400	APN	5	110,719,495 (GRCm38)	missense	unknown
IGL01833:Ep400	APN	5	110,680,008 (GRCm38)	missense	unknown
IGL02086:Ep400	APN	5	110,676,943 (GRCm38)	splice site	probably benign
IGL02266:Ep400	APN	5	110,695,297 (GRCm38)	unclassified	probably benign
IGL02288:Ep400	APN	5	110,683,836 (GRCm38)	splice site	probably benign
IGL02301:Ep400	APN	5	110,674,960 (GRCm38)	missense	probably damaging	1.00
IGL02377:Ep400	APN	5	110,720,825 (GRCm38)	missense	unknown
IGL02382:Ep400	APN	5	110,701,728 (GRCm38)	missense	unknown
IGL02419:Ep400	APN	5	110,697,376 (GRCm38)	splice site	probably null
IGL02591:Ep400	APN	5	110,733,772 (GRCm38)	unclassified	probably benign
IGL02981:Ep400	APN	5	110,691,610 (GRCm38)	splice site	probably benign
IGL02981:Ep400	APN	5	110,756,103 (GRCm38)	missense	possibly damaging	0.79
IGL03173:Ep400	APN	5	110,708,871 (GRCm38)	unclassified	probably benign
IGL03244:Ep400	APN	5	110,727,563 (GRCm38)	missense	unknown
IGL03333:Ep400	APN	5	110,703,566 (GRCm38)	missense	unknown
santol	UTSW	5	110,701,671 (GRCm38)	missense	unknown
PIT4243001:Ep400	UTSW	5	110,735,580 (GRCm38)	missense	unknown
PIT4260001:Ep400	UTSW	5	110,693,171 (GRCm38)	nonsense	probably null
R0017:Ep400	UTSW	5	110,673,529 (GRCm38)	missense	probably damaging	1.00
R0179:Ep400	UTSW	5	110,668,649 (GRCm38)	missense	probably damaging	0.99
R0243:Ep400	UTSW	5	110,724,407 (GRCm38)	splice site	probably benign
R0366:Ep400	UTSW	5	110,701,671 (GRCm38)	missense	unknown
R0508:Ep400	UTSW	5	110,739,508 (GRCm38)	missense	probably benign	0.00
R0541:Ep400	UTSW	5	110,705,016 (GRCm38)	missense	unknown
R0558:Ep400	UTSW	5	110,685,067 (GRCm38)	splice site	probably benign
R0576:Ep400	UTSW	5	110,711,093 (GRCm38)	unclassified	probably benign
R0595:Ep400	UTSW	5	110,703,542 (GRCm38)	missense	unknown
R0671:Ep400	UTSW	5	110,688,196 (GRCm38)	missense	unknown
R0763:Ep400	UTSW	5	110,665,837 (GRCm38)	missense	probably damaging	1.00
R1078:Ep400	UTSW	5	110,735,522 (GRCm38)	unclassified	probably benign
R1300:Ep400	UTSW	5	110,673,560 (GRCm38)	missense	probably damaging	1.00
R1439:Ep400	UTSW	5	110,685,478 (GRCm38)	missense	unknown
R1520:Ep400	UTSW	5	110,691,778 (GRCm38)	intron	probably benign
R1529:Ep400	UTSW	5	110,739,445 (GRCm38)	missense	probably benign	0.00
R1535:Ep400	UTSW	5	110,708,166 (GRCm38)	unclassified	probably benign
R1560:Ep400	UTSW	5	110,671,106 (GRCm38)	splice site	probably null
R1587:Ep400	UTSW	5	110,726,902 (GRCm38)	missense	probably benign	0.23
R1596:Ep400	UTSW	5	110,708,861 (GRCm38)	unclassified	probably benign
R1653:Ep400	UTSW	5	110,693,174 (GRCm38)	nonsense	probably null
R1711:Ep400	UTSW	5	110,693,308 (GRCm38)	unclassified	probably benign
R1774:Ep400	UTSW	5	110,685,491 (GRCm38)	missense	unknown
R1836:Ep400	UTSW	5	110,705,054 (GRCm38)	missense	unknown
R1905:Ep400	UTSW	5	110,670,948 (GRCm38)	missense	probably damaging	1.00
R1917:Ep400	UTSW	5	110,703,575 (GRCm38)	missense	unknown
R2064:Ep400	UTSW	5	110,735,404 (GRCm38)	unclassified	probably benign
R2122:Ep400	UTSW	5	110,708,850 (GRCm38)	unclassified	probably benign
R2144:Ep400	UTSW	5	110,703,518 (GRCm38)	missense	unknown
R2215:Ep400	UTSW	5	110,693,555 (GRCm38)	unclassified	probably benign
R2252:Ep400	UTSW	5	110,719,091 (GRCm38)	missense	unknown
R2483:Ep400	UTSW	5	110,719,236 (GRCm38)	missense	unknown
R2504:Ep400	UTSW	5	110,668,645 (GRCm38)	missense	probably damaging	1.00
R2512:Ep400	UTSW	5	110,708,915 (GRCm38)	unclassified	probably benign
R2842:Ep400	UTSW	5	110,698,815 (GRCm38)	nonsense	probably null
R2920:Ep400	UTSW	5	110,755,914 (GRCm38)	missense	probably damaging	1.00
R3082:Ep400	UTSW	5	110,693,230 (GRCm38)	unclassified	probably benign
R3151:Ep400	UTSW	5	110,703,569 (GRCm38)	missense	unknown
R3552:Ep400	UTSW	5	110,729,287 (GRCm38)	missense	unknown
R3623:Ep400	UTSW	5	110,719,236 (GRCm38)	missense	unknown
R3779:Ep400	UTSW	5	110,691,649 (GRCm38)	missense	unknown
R3923:Ep400	UTSW	5	110,756,523 (GRCm38)	missense	possibly damaging	0.55
R4062:Ep400	UTSW	5	110,741,981 (GRCm38)	missense	probably benign	0.10
R4508:Ep400	UTSW	5	110,703,615 (GRCm38)	missense	unknown
R4584:Ep400	UTSW	5	110,733,897 (GRCm38)	unclassified	probably benign
R4585:Ep400	UTSW	5	110,753,859 (GRCm38)	missense	probably damaging	1.00
R4586:Ep400	UTSW	5	110,753,859 (GRCm38)	missense	probably damaging	1.00
R4807:Ep400	UTSW	5	110,695,578 (GRCm38)	splice site	probably null
R4921:Ep400	UTSW	5	110,665,810 (GRCm38)	missense	probably damaging	1.00
R4976:Ep400	UTSW	5	110,720,756 (GRCm38)	missense	unknown
R4976:Ep400	UTSW	5	110,698,812 (GRCm38)	missense	unknown
R5075:Ep400	UTSW	5	110,685,485 (GRCm38)	missense	unknown
R5120:Ep400	UTSW	5	110,756,358 (GRCm38)	missense	probably damaging	1.00
R5122:Ep400	UTSW	5	110,668,170 (GRCm38)	missense	probably damaging	1.00
R5223:Ep400	UTSW	5	110,668,630 (GRCm38)	missense	probably damaging	1.00
R5284:Ep400	UTSW	5	110,668,124 (GRCm38)	missense	probably damaging	1.00
R5388:Ep400	UTSW	5	110,701,728 (GRCm38)	missense	unknown
R5401:Ep400	UTSW	5	110,683,171 (GRCm38)	missense	unknown
R5431:Ep400	UTSW	5	110,676,554 (GRCm38)	missense	unknown
R5461:Ep400	UTSW	5	110,676,684 (GRCm38)	nonsense	probably null
R5568:Ep400	UTSW	5	110,756,205 (GRCm38)	missense	probably damaging	1.00
R5650:Ep400	UTSW	5	110,695,952 (GRCm38)	critical splice donor site	probably null
R5778:Ep400	UTSW	5	110,719,584 (GRCm38)	missense	unknown
R5806:Ep400	UTSW	5	110,755,554 (GRCm38)	nonsense	probably null
R5814:Ep400	UTSW	5	110,695,578 (GRCm38)	splice site	probably null
R5830:Ep400	UTSW	5	110,683,996 (GRCm38)	missense	unknown
R5882:Ep400	UTSW	5	110,755,587 (GRCm38)	missense	probably benign	0.00
R5931:Ep400	UTSW	5	110,735,520 (GRCm38)	unclassified	probably benign
R5945:Ep400	UTSW	5	110,682,866 (GRCm38)	missense	unknown
R5966:Ep400	UTSW	5	110,676,900 (GRCm38)	missense	unknown
R5973:Ep400	UTSW	5	110,729,831 (GRCm38)	missense	unknown
R5980:Ep400	UTSW	5	110,733,729 (GRCm38)	unclassified	probably benign
R6000:Ep400	UTSW	5	110,683,201 (GRCm38)	missense	unknown
R6006:Ep400	UTSW	5	110,704,959 (GRCm38)	missense	unknown
R6053:Ep400	UTSW	5	110,755,795 (GRCm38)	missense	probably benign	0.22
R6145:Ep400	UTSW	5	110,756,703 (GRCm38)	missense	possibly damaging	0.95
R6154:Ep400	UTSW	5	110,755,933 (GRCm38)	missense	probably damaging	0.97
R6169:Ep400	UTSW	5	110,741,997 (GRCm38)	missense	possibly damaging	0.83
R6228:Ep400	UTSW	5	110,670,942 (GRCm38)	missense	probably damaging	1.00
R6295:Ep400	UTSW	5	110,753,809 (GRCm38)	missense	probably benign	0.00
R6486:Ep400	UTSW	5	110,697,218 (GRCm38)	unclassified	probably benign
R6504:Ep400	UTSW	5	110,708,837 (GRCm38)	unclassified	probably benign
R6607:Ep400	UTSW	5	110,683,314 (GRCm38)	missense	unknown
R6657:Ep400	UTSW	5	110,693,545 (GRCm38)	unclassified	probably benign
R6660:Ep400	UTSW	5	110,719,447 (GRCm38)	nonsense	probably null
R6741:Ep400	UTSW	5	110,676,895 (GRCm38)	missense	unknown
R6933:Ep400	UTSW	5	110,665,862 (GRCm38)	missense	probably damaging	1.00
R6937:Ep400	UTSW	5	110,711,152 (GRCm38)	unclassified	probably benign
R7069:Ep400	UTSW	5	110,668,124 (GRCm38)	missense	probably damaging	1.00
R7103:Ep400	UTSW	5	110,733,785 (GRCm38)	missense	unknown
R7156:Ep400	UTSW	5	110,685,363 (GRCm38)	missense	unknown
R7272:Ep400	UTSW	5	110,755,645 (GRCm38)	nonsense	probably null
R7365:Ep400	UTSW	5	110,719,614 (GRCm38)	missense	unknown
R7581:Ep400	UTSW	5	110,756,025 (GRCm38)	missense	unknown
R7684:Ep400	UTSW	5	110,697,352 (GRCm38)	missense	unknown
R7699:Ep400	UTSW	5	110,696,032 (GRCm38)	missense	unknown
R7700:Ep400	UTSW	5	110,696,032 (GRCm38)	missense	unknown
R7856:Ep400	UTSW	5	110,666,584 (GRCm38)	missense	probably damaging	0.99
R7954:Ep400	UTSW	5	110,668,733 (GRCm38)	missense	possibly damaging	0.46
R8098:Ep400	UTSW	5	110,693,251 (GRCm38)	missense	unknown
R8108:Ep400	UTSW	5	110,687,883 (GRCm38)	missense	unknown
R8260:Ep400	UTSW	5	110,755,612 (GRCm38)	nonsense	probably null
R8293:Ep400	UTSW	5	110,708,892 (GRCm38)	missense	unknown
R8314:Ep400	UTSW	5	110,755,753 (GRCm38)	missense	unknown
R8351:Ep400	UTSW	5	110,739,334 (GRCm38)	missense	probably damaging	1.00
R8424:Ep400	UTSW	5	110,693,278 (GRCm38)	missense	unknown
R8459:Ep400	UTSW	5	110,708,891 (GRCm38)	missense	unknown
R8529:Ep400	UTSW	5	110,719,236 (GRCm38)	missense	unknown
R8688:Ep400	UTSW	5	110,720,819 (GRCm38)	missense	unknown
R8744:Ep400	UTSW	5	110,742,059 (GRCm38)	missense	unknown
R8923:Ep400	UTSW	5	110,683,998 (GRCm38)	missense	unknown
R9005:Ep400	UTSW	5	110,711,093 (GRCm38)	missense	unknown
R9087:Ep400	UTSW	5	110,667,564 (GRCm38)	nonsense	probably null
R9146:Ep400	UTSW	5	110,701,769 (GRCm38)	nonsense	probably null
R9383:Ep400	UTSW	5	110,685,485 (GRCm38)	missense	unknown
R9479:Ep400	UTSW	5	110,729,864 (GRCm38)	missense	unknown
R9496:Ep400	UTSW	5	110,707,987 (GRCm38)	missense	unknown
R9582:Ep400	UTSW	5	110,676,449 (GRCm38)	critical splice donor site	probably null
R9607:Ep400	UTSW	5	110,683,939 (GRCm38)	missense	unknown
R9712:Ep400	UTSW	5	110,756,643 (GRCm38)	missense	unknown
R9746:Ep400	UTSW	5	110,742,006 (GRCm38)	missense	unknown
X0012:Ep400	UTSW	5	110,673,196 (GRCm38)	small deletion	probably benign
X0021:Ep400	UTSW	5	110,682,864 (GRCm38)	missense	unknown
Z1176:Ep400	UTSW	5	110,756,635 (GRCm38)	missense	unknown
Z1177:Ep400	UTSW	5	110,733,743 (GRCm38)	missense	unknown
Z1177:Ep400	UTSW	5	110,683,364 (GRCm38)	missense	unknown
Z1188:Ep400	UTSW	5	110,755,683 (GRCm38)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- ACTCTGGGAAGAATGGTGTG -3'
(R):5'- GGTGTGTGCCAATTACTCACTC -3'

Sequencing Primer
(F):5'- TGGTCGAGATATAATGTATGCAAAG -3'
(R):5'- CTCTATAGGTGAAGTTTAGTGCTCC -3'

Posted On

2014-10-16