Mutagenetix > Incidental Mutation

Incidental Mutation 'R0130:Epb41l5'

50091

Institutional Source

Beutler Lab

Gene Symbol

Epb41l5

Ensembl Gene

ENSMUSG00000026383

Gene Name

erythrocyte membrane protein band 4.1 like 5

Synonyms

E230025E14Rik, 1700030C16Rik, NBL5, Epb4.1l5, Lulu1

MMRRC Submission

038415-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0130 (G1)

Quality Score

172

Status

Validated (trace)

Chromosome

Chromosomal Location

119472767-119576730 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 119477632 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glycine at position 705 (V705G)

Ref Sequence

ENSEMBL: ENSMUSP00000058966 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052404] [ENSMUST00000163147]

AlphaFold

Q8BGS1

Predicted Effect

possibly damaging
Transcript: ENSMUST00000052404
AA Change: V705G

PolyPhen 2 Score 0.805 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000058966
Gene: ENSMUSG00000026383
AA Change: V705G

Domain	Start	End	E-Value	Type
B41	39	235	8.64e-68	SMART
FERM_C	239	331	1.07e-34	SMART
FA	336	380	1.16e-12	SMART
low complexity region	412	421	N/A	INTRINSIC
coiled coil region	482	512	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000163147
AA Change: V713G

PolyPhen 2 Score 0.770 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000128374
Gene: ENSMUSG00000026383
AA Change: V713G

Domain	Start	End	E-Value	Type
B41	39	235	8.64e-68	SMART
FERM_C	239	331	1.07e-34	SMART
FA	336	380	1.16e-12	SMART
low complexity region	420	429	N/A	INTRINSIC
coiled coil region	490	520	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000191162

Meta Mutation Damage Score

0.1057

Coding Region Coverage

1x: 99.0%
3x: 97.7%
10x: 93.4%
20x: 80.2%

Validation Efficiency

99% (84/85)

MGI Phenotype

PHENOTYPE: Mice homozygous for a number of different mutations exhibit prenatal lethality and mesodermal and epithelial-mesenchymal transition defects during gastrulation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcg8	A	T	17: 84,994,094 (GRCm39)	Y37F	probably damaging	Het
Ablim2	G	A	5: 35,966,520 (GRCm39)		probably benign	Het
Anxa9	A	G	3: 95,209,733 (GRCm39)	S129P	probably benign	Het
Apol7c	A	G	15: 77,410,562 (GRCm39)	I128T	possibly damaging	Het
Arfgef2	T	G	2: 166,677,639 (GRCm39)	I88S	probably damaging	Het
Arfip2	A	G	7: 105,288,205 (GRCm39)		probably benign	Het
Atp5mf	A	T	5: 145,124,992 (GRCm39)		probably benign	Het
Atp7b	C	T	8: 22,518,188 (GRCm39)	E205K	possibly damaging	Het
Atp8b5	T	A	4: 43,369,715 (GRCm39)		probably null	Het
Cd22	A	G	7: 30,569,389 (GRCm39)	Y402H	possibly damaging	Het
Cd248	A	G	19: 5,119,990 (GRCm39)	T613A	probably benign	Het
Cdcp2	C	T	4: 106,963,904 (GRCm39)		probably benign	Het
Cenpc1	A	T	5: 86,194,405 (GRCm39)	D120E	probably benign	Het
Chd3	T	A	11: 69,250,656 (GRCm39)	H691L	probably damaging	Het
Colec12	C	T	18: 9,858,921 (GRCm39)	P568L	unknown	Het
Cped1	T	A	6: 22,121,038 (GRCm39)	Y373N	probably benign	Het
Cr2	A	T	1: 194,848,539 (GRCm39)	V328D	probably damaging	Het
Ctnnd2	A	T	15: 30,922,059 (GRCm39)	E895V	probably damaging	Het
D630045J12Rik	A	T	6: 38,126,706 (GRCm39)		probably benign	Het
Dcdc2a	A	T	13: 25,371,655 (GRCm39)		probably benign	Het
Dync1h1	C	A	12: 110,585,108 (GRCm39)	T837K	probably benign	Het
Eif2ak3	C	A	6: 70,858,716 (GRCm39)		probably benign	Het
Fat2	T	A	11: 55,142,944 (GRCm39)	M4302L	probably benign	Het
Flnb	T	C	14: 7,901,951 (GRCm38)	V938A	probably damaging	Het
Frmd4a	T	C	2: 4,608,903 (GRCm39)	Y928H	probably damaging	Het
Fyn	C	T	10: 39,387,978 (GRCm39)	T78M	probably benign	Het
Gdap2	A	G	3: 100,109,311 (GRCm39)	T443A	probably damaging	Het
Gde1	A	T	7: 118,294,283 (GRCm39)	F63L	probably benign	Het
Gjc3	A	G	5: 137,956,202 (GRCm39)	S28P	probably benign	Het
Gm10250	G	A	15: 5,150,473 (GRCm39)		probably null	Het
Hp1bp3	C	T	4: 137,964,520 (GRCm39)	S348F	probably damaging	Het
Klhl23	T	C	2: 69,664,310 (GRCm39)	V553A	probably damaging	Het
Lman2l	G	T	1: 36,463,945 (GRCm39)	S171*	probably null	Het
Lrp1b	T	C	2: 41,401,520 (GRCm39)	D378G	probably damaging	Het
Map3k11	T	C	19: 5,740,843 (GRCm39)	L190P	probably damaging	Het
Mki67	T	A	7: 135,298,188 (GRCm39)	Q2282L	probably damaging	Het
Mthfd2	T	A	6: 83,285,990 (GRCm39)	I272F	probably damaging	Het
Myom1	A	T	17: 71,352,750 (GRCm39)	D358V	probably damaging	Het
Nebl	T	C	2: 17,395,737 (GRCm39)		probably benign	Het
Nebl	T	A	2: 17,397,834 (GRCm39)	Q487H	possibly damaging	Het
Nlrp2	T	A	7: 5,325,417 (GRCm39)	N14Y	possibly damaging	Het
Or14a258	T	C	7: 86,035,514 (GRCm39)	Y118C	probably damaging	Het
Or1j11	T	A	2: 36,312,299 (GRCm39)	D296E	probably benign	Het
Or2z8	C	T	8: 72,812,244 (GRCm39)	T240M	probably damaging	Het
Or5ak22	T	A	2: 85,230,305 (GRCm39)	S191C	probably damaging	Het
Or8k40	T	C	2: 86,584,231 (GRCm39)	M284V	probably benign	Het
Pasd1	T	C	X: 70,983,161 (GRCm39)	C378R	possibly damaging	Het
Paxip1	C	T	5: 27,949,183 (GRCm39)		probably benign	Het
Pclo	A	G	5: 14,729,811 (GRCm39)		probably benign	Het
Pld2	T	G	11: 70,445,174 (GRCm39)	N591K	probably benign	Het
Plekha7	A	G	7: 115,769,939 (GRCm39)	M276T	probably damaging	Het
Prss39	T	A	1: 34,541,281 (GRCm39)		probably benign	Het
Prtg	A	G	9: 72,716,998 (GRCm39)	Y113C	probably damaging	Het
Rab38	T	A	7: 88,099,749 (GRCm39)	I88N	probably damaging	Het
Rbfox2	A	G	15: 76,976,057 (GRCm39)		probably benign	Het
Samd5	A	G	10: 9,550,683 (GRCm39)	W9R	probably damaging	Het
Sec14l1	A	T	11: 117,047,233 (GRCm39)	K637I	possibly damaging	Het
Sh2b1	A	T	7: 126,070,620 (GRCm39)	D360E	possibly damaging	Het
Sh3bp4	A	G	1: 89,073,036 (GRCm39)	N628S	possibly damaging	Het
Sim1	A	T	10: 50,784,057 (GRCm39)	I104F	probably damaging	Het
Smcp	T	A	3: 92,491,827 (GRCm39)	T7S	unknown	Het
Sp4	A	G	12: 118,264,551 (GRCm39)		probably benign	Het
Tectb	G	T	19: 55,170,393 (GRCm39)	K81N	probably damaging	Het
Thbs4	G	T	13: 92,890,918 (GRCm39)	H850N	probably benign	Het
Tiam1	T	C	16: 89,694,642 (GRCm39)	M272V	probably benign	Het
Trav13-3	T	A	14: 53,967,233 (GRCm39)		noncoding transcript	Het
Ubap2l	A	T	3: 89,928,680 (GRCm39)	S478T	possibly damaging	Het
Vmn2r85	A	G	10: 130,255,054 (GRCm39)		probably benign	Het

Other mutations in Epb41l5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01103:Epb41l5	APN	1	119,495,577 (GRCm39)	missense	probably benign	0.03
IGL01983:Epb41l5	APN	1	119,506,814 (GRCm39)	splice site	probably benign
IGL02085:Epb41l5	APN	1	119,500,586 (GRCm39)	missense	probably benign
IGL02834:Epb41l5	APN	1	119,551,685 (GRCm39)	missense	probably benign	0.22
IGL02975:Epb41l5	APN	1	119,506,811 (GRCm39)	splice site	probably benign
IGL03001:Epb41l5	APN	1	119,545,374 (GRCm39)	missense	probably damaging	1.00
IGL03331:Epb41l5	APN	1	119,545,149 (GRCm39)	missense	probably damaging	1.00
R0096:Epb41l5	UTSW	1	119,551,641 (GRCm39)	splice site	probably benign
R0124:Epb41l5	UTSW	1	119,561,370 (GRCm39)	nonsense	probably null
R0128:Epb41l5	UTSW	1	119,477,632 (GRCm39)	missense	possibly damaging	0.81
R0241:Epb41l5	UTSW	1	119,495,509 (GRCm39)	splice site	probably null
R0357:Epb41l5	UTSW	1	119,536,934 (GRCm39)	missense	probably damaging	1.00
R0624:Epb41l5	UTSW	1	119,551,688 (GRCm39)	missense	probably damaging	1.00
R0711:Epb41l5	UTSW	1	119,551,641 (GRCm39)	splice site	probably benign
R0848:Epb41l5	UTSW	1	119,477,684 (GRCm39)	missense	probably benign	0.01
R1340:Epb41l5	UTSW	1	119,476,861 (GRCm39)	makesense	probably null
R1401:Epb41l5	UTSW	1	119,506,634 (GRCm39)	splice site	probably benign
R1416:Epb41l5	UTSW	1	119,477,606 (GRCm39)	splice site	probably benign
R1452:Epb41l5	UTSW	1	119,476,896 (GRCm39)	missense	probably damaging	1.00
R1646:Epb41l5	UTSW	1	119,477,752 (GRCm39)	splice site	probably benign
R1889:Epb41l5	UTSW	1	119,476,902 (GRCm39)	missense	possibly damaging	0.82
R1895:Epb41l5	UTSW	1	119,476,902 (GRCm39)	missense	possibly damaging	0.82
R3082:Epb41l5	UTSW	1	119,536,992 (GRCm39)	missense	probably damaging	1.00
R3742:Epb41l5	UTSW	1	119,532,973 (GRCm39)	missense	probably benign
R4194:Epb41l5	UTSW	1	119,535,823 (GRCm39)	missense	probably damaging	1.00
R4787:Epb41l5	UTSW	1	119,523,725 (GRCm39)	missense	probably benign	0.00
R4983:Epb41l5	UTSW	1	119,482,801 (GRCm39)	missense	probably benign	0.00
R6825:Epb41l5	UTSW	1	119,547,931 (GRCm39)	missense	possibly damaging	0.54
R6943:Epb41l5	UTSW	1	119,536,859 (GRCm39)	missense	probably damaging	1.00
R6944:Epb41l5	UTSW	1	119,536,859 (GRCm39)	missense	probably damaging	1.00
R7334:Epb41l5	UTSW	1	119,551,679 (GRCm39)	missense	probably damaging	1.00
R8553:Epb41l5	UTSW	1	119,477,671 (GRCm39)	missense	possibly damaging	0.88
R8904:Epb41l5	UTSW	1	119,547,936 (GRCm39)	missense	probably damaging	1.00
R8955:Epb41l5	UTSW	1	119,570,292 (GRCm39)	missense	probably damaging	1.00
R9147:Epb41l5	UTSW	1	119,570,319 (GRCm39)	missense	probably damaging	1.00
R9258:Epb41l5	UTSW	1	119,506,701 (GRCm39)	missense	probably benign
R9351:Epb41l5	UTSW	1	119,477,639 (GRCm39)	missense	probably benign	0.01
R9366:Epb41l5	UTSW	1	119,548,448 (GRCm39)	missense	probably damaging	1.00
R9370:Epb41l5	UTSW	1	119,561,312 (GRCm39)	missense	probably damaging	1.00
R9680:Epb41l5	UTSW	1	119,535,804 (GRCm39)	missense	probably damaging	1.00
R9779:Epb41l5	UTSW	1	119,545,093 (GRCm39)	critical splice donor site	probably null
Z1177:Epb41l5	UTSW	1	119,536,941 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TGGTGAGGAGATTTTAGGCTGACCC -3'
(R):5'- AGTGACACTGATGTGAAGCTGCAAG -3'

Sequencing Primer
(F):5'- GAGATTTTAGGCTGACCCCCAAG -3'
(R):5'- AAGCTGCAAGGTTGTTATCTGAC -3'

Posted On

2013-06-12