Mutagenetix > Incidental Mutation

Incidental Mutation 'R4059:Epb41l4b'

314376

Institutional Source

Beutler Lab

Gene Symbol

Epb41l4b

Ensembl Gene

ENSMUSG00000028434

Gene Name

erythrocyte membrane protein band 4.1 like 4b

Synonyms

Ehm2, 6430543G08Rik, Epb4.1l4b, Lulu2, D4Ertd346e

MMRRC Submission

040970-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4059 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

56991972-57143437 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (1 bp from exon)

DNA Base Change (assembly)

C to T at 57024337 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000092687 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044022] [ENSMUST00000095076]

AlphaFold

Q9JMC8

Predicted Effect

probably null
Transcript: ENSMUST00000044022

SMART Domains

Protein: ENSMUSP00000037625
Gene: ENSMUSG00000028434

Domain	Start	End	E-Value	Type
low complexity region	71	83	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000095076

SMART Domains

Protein: ENSMUSP00000092687
Gene: ENSMUSG00000028434

Domain	Start	End	E-Value	Type
low complexity region	18	57	N/A	INTRINSIC
low complexity region	60	72	N/A	INTRINSIC
B41	81	277	4.09e-69	SMART
FERM_C	281	373	1.76e-35	SMART
FA	378	422	2.86e-12	SMART
low complexity region	504	513	N/A	INTRINSIC
low complexity region	692	704	N/A	INTRINSIC

Meta Mutation Damage Score

0.9478

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.1%
20x: 94.6%

Validation Efficiency

98% (54/55)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930453N24Rik	A	G	16: 64,586,821 (GRCm39)	V301A	probably benign	Het
Agbl3	T	C	6: 34,823,834 (GRCm39)	L833P	probably damaging	Het
Amph	T	C	13: 19,326,168 (GRCm39)	S633P	probably damaging	Het
Aspscr1	T	C	11: 120,577,505 (GRCm39)	V60A	probably benign	Het
Atp13a3	C	A	16: 30,173,064 (GRCm39)	C271F	possibly damaging	Het
B4galt3	C	A	1: 171,101,613 (GRCm39)	H196N	probably damaging	Het
BC051019	C	T	7: 109,317,202 (GRCm39)	W163*	probably null	Het
Capza1	T	C	3: 104,732,427 (GRCm39)	E245G	probably damaging	Het
Cd81	G	T	7: 142,619,030 (GRCm39)	C18F	probably damaging	Het
Cfap45	G	T	1: 172,366,056 (GRCm39)	R303L	probably benign	Het
Commd9	T	C	2: 101,725,499 (GRCm39)	V24A	possibly damaging	Het
Dennd4a	A	G	9: 64,819,174 (GRCm39)	N1742D	possibly damaging	Het
Dgat1	G	T	15: 76,388,371 (GRCm39)	A182D	possibly damaging	Het
Dlg4	T	C	11: 69,917,909 (GRCm39)	L64P	probably benign	Het
Dna2	A	G	10: 62,792,768 (GRCm39)	D261G	probably damaging	Het
Fam13c	T	C	10: 70,390,338 (GRCm39)	L533P	probably damaging	Het
Fjx1	T	C	2: 102,281,066 (GRCm39)	T290A	possibly damaging	Het
Hid1	C	T	11: 115,247,565 (GRCm39)	E278K	probably damaging	Het
Hsd3b7	T	C	7: 127,400,717 (GRCm39)	I57T	probably damaging	Het
Igfn1	A	G	1: 135,897,494 (GRCm39)	V1024A	probably benign	Het
Itgae	A	G	11: 73,002,960 (GRCm39)	K175E	probably benign	Het
Klhl32	T	C	4: 24,792,781 (GRCm39)	T14A	probably damaging	Het
Krt23	T	C	11: 99,376,614 (GRCm39)	T181A	probably benign	Het
Lmo2	T	C	2: 103,811,407 (GRCm39)	Y147H	probably damaging	Het
Lrrc36	A	G	8: 106,154,428 (GRCm39)	E33G	probably damaging	Het
Mettl13	G	T	1: 162,373,755 (GRCm39)	H165Q	probably damaging	Het
Mocos	G	A	18: 24,812,447 (GRCm39)	G447D	probably damaging	Het
Ngef	T	A	1: 87,413,953 (GRCm39)	K399N	probably damaging	Het
Ntrk1	A	G	3: 87,688,786 (GRCm39)	L589P	probably damaging	Het
Or4c104	C	T	2: 88,586,795 (GRCm39)	V75I	probably benign	Het
Pcdha2	A	G	18: 37,072,935 (GRCm39)	S189G	probably benign	Het
Peg10	T	G	6: 4,756,427 (GRCm39)		probably benign	Het
Pkhd1l1	C	T	15: 44,414,156 (GRCm39)	H2808Y	probably benign	Het
Plekhg1	A	G	10: 3,907,087 (GRCm39)	D668G	probably damaging	Het
Ptcd2	A	G	13: 99,481,084 (GRCm39)	C32R	probably damaging	Het
Rgs8	A	G	1: 153,566,742 (GRCm39)	T98A	probably null	Het
Rhoh	G	A	5: 66,049,931 (GRCm39)	S67N	probably benign	Het
Rnd3	A	G	2: 51,038,760 (GRCm39)	F43L	probably damaging	Het
Runx1	A	G	16: 92,441,134 (GRCm39)	V225A	probably benign	Het
Runx1t1	T	C	4: 13,889,769 (GRCm39)	V566A	probably benign	Het
Sall2	A	G	14: 52,552,028 (GRCm39)	I387T	probably damaging	Het
Sec14l1	T	A	11: 117,040,024 (GRCm39)	V384D	possibly damaging	Het
Sh3rf3	T	C	10: 58,919,355 (GRCm39)	C491R	probably damaging	Het
Slc22a27	T	A	19: 7,856,973 (GRCm39)		probably benign	Het
Spire1	A	G	18: 67,678,783 (GRCm39)	S53P	probably damaging	Het
Tmco3	A	G	8: 13,370,848 (GRCm39)	R671G	probably benign	Het
Tmpo	A	G	10: 90,998,123 (GRCm39)	S555P	probably benign	Het
Tnip1	A	G	11: 54,802,395 (GRCm39)	S638P	probably benign	Het
Tspan8	C	T	10: 115,671,187 (GRCm39)	R115*	probably null	Het
Txnrd1	A	G	10: 82,721,114 (GRCm39)	E510G	probably benign	Het
Ucp3	T	C	7: 100,131,871 (GRCm39)	Y241H	probably damaging	Het
Vmn2r96	A	G	17: 18,818,339 (GRCm39)	I831V	probably benign	Het
Zan	T	C	5: 137,435,082 (GRCm39)	I2104V	unknown	Het
Zfp619	A	C	7: 39,184,823 (GRCm39)	R284S	probably benign	Het
Zfp715	T	C	7: 42,951,155 (GRCm39)	M48V	probably benign	Het

Other mutations in Epb41l4b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02141:Epb41l4b	APN	4	57,103,422 (GRCm39)	critical splice donor site	probably null
IGL02311:Epb41l4b	APN	4	57,076,456 (GRCm39)	missense	probably damaging	1.00
Episode	UTSW	4	57,142,866 (GRCm39)	missense	probably benign	0.00
R0456:Epb41l4b	UTSW	4	57,142,843 (GRCm39)	splice site	probably null
R0799:Epb41l4b	UTSW	4	57,086,003 (GRCm39)	missense	probably damaging	1.00
R0905:Epb41l4b	UTSW	4	57,103,528 (GRCm39)	missense	probably damaging	1.00
R1208:Epb41l4b	UTSW	4	57,077,252 (GRCm39)	critical splice acceptor site	probably null
R1208:Epb41l4b	UTSW	4	57,077,252 (GRCm39)	critical splice acceptor site	probably null
R1506:Epb41l4b	UTSW	4	57,088,824 (GRCm39)	missense	probably damaging	1.00
R1618:Epb41l4b	UTSW	4	57,032,204 (GRCm39)	missense	probably benign	0.00
R1919:Epb41l4b	UTSW	4	57,040,993 (GRCm39)	missense	probably damaging	0.99
R1956:Epb41l4b	UTSW	4	57,038,553 (GRCm39)	missense	possibly damaging	0.94
R2041:Epb41l4b	UTSW	4	57,084,070 (GRCm39)	missense	probably damaging	0.98
R2048:Epb41l4b	UTSW	4	57,142,866 (GRCm39)	missense	probably benign	0.00
R3434:Epb41l4b	UTSW	4	57,040,865 (GRCm39)	missense	probably benign	0.41
R4175:Epb41l4b	UTSW	4	57,076,556 (GRCm39)	missense	probably damaging	1.00
R4694:Epb41l4b	UTSW	4	57,019,875 (GRCm39)	missense	probably benign	0.01
R4817:Epb41l4b	UTSW	4	57,103,428 (GRCm39)	missense	probably damaging	1.00
R5076:Epb41l4b	UTSW	4	57,040,984 (GRCm39)	missense	probably damaging	1.00
R5179:Epb41l4b	UTSW	4	57,063,181 (GRCm39)	missense	probably benign	0.01
R5246:Epb41l4b	UTSW	4	57,040,989 (GRCm39)	missense	probably damaging	0.99
R5530:Epb41l4b	UTSW	4	57,086,003 (GRCm39)	missense	probably damaging	1.00
R5579:Epb41l4b	UTSW	4	57,064,802 (GRCm39)	missense	possibly damaging	0.62
R5784:Epb41l4b	UTSW	4	57,086,003 (GRCm39)	missense	probably damaging	1.00
R6772:Epb41l4b	UTSW	4	57,063,140 (GRCm39)	missense	probably benign
R6965:Epb41l4b	UTSW	4	57,040,915 (GRCm39)	missense	probably damaging	1.00
R7045:Epb41l4b	UTSW	4	57,103,522 (GRCm39)	missense	possibly damaging	0.94
R7316:Epb41l4b	UTSW	4	57,019,867 (GRCm39)	missense	probably benign	0.01
R7750:Epb41l4b	UTSW	4	57,076,913 (GRCm39)	critical splice donor site	probably null
R7954:Epb41l4b	UTSW	4	57,088,034 (GRCm39)	missense	probably damaging	1.00
R9032:Epb41l4b	UTSW	4	57,041,064 (GRCm39)	splice site	probably null
R9085:Epb41l4b	UTSW	4	57,041,064 (GRCm39)	splice site	probably null
R9130:Epb41l4b	UTSW	4	57,103,447 (GRCm39)	missense	possibly damaging	0.82
R9386:Epb41l4b	UTSW	4	57,076,553 (GRCm39)	missense	probably damaging	1.00
Z1177:Epb41l4b	UTSW	4	57,063,191 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- GAGAGGTTATGCCAGACTCC -3'
(R):5'- AAGCTGAATATCACCTGAGAAGCC -3'

Sequencing Primer
(F):5'- GAGAGGTTATGCCAGACTCCCAATC -3'
(R):5'- TGAGAAGCCTAATACAAGAGCATTAC -3'

Posted On

2015-04-30