Mutagenetix > Incidental Mutation

Incidental Mutation 'R6263:Efcab3'

506842

Institutional Source

Beutler Lab

Gene Symbol

Efcab3

Ensembl Gene

ENSMUSG00000020690

Gene Name

EF-hand calcium binding domain 3

Synonyms

Gm11639, Efcab13, 4921510J17Rik, Efcab15, Gm11639

MMRRC Submission

044437-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6263 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

104954418-105008363 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 104810312 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Asparagine at position 3150 (D3150N)

Ref Sequence

ENSEMBL: ENSMUSP00000148433 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000212287]

AlphaFold

Q80X60

Predicted Effect

unknown
Transcript: ENSMUST00000212287
AA Change: D3150N

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.4%
20x: 95.7%

Validation Efficiency

97% (66/68)

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahnak	A	G	19: 8,995,641 (GRCm39)	I5642V	probably benign	Het
Atp5f1a	A	G	18: 77,866,930 (GRCm39)		probably null	Het
Bltp1	T	A	3: 36,985,260 (GRCm39)	N863K	probably benign	Het
Bsn	A	T	9: 107,990,453 (GRCm39)	F1766L	probably damaging	Het
Ccdc141	T	C	2: 76,938,807 (GRCm39)	Q266R	probably damaging	Het
Cdh10	T	A	15: 18,964,154 (GRCm39)	D105E	possibly damaging	Het
Clca3a1	T	A	3: 144,455,539 (GRCm39)	D418V	probably damaging	Het
Cnnm2	C	A	19: 46,845,344 (GRCm39)	T612K	probably benign	Het
Col3a1	T	C	1: 45,360,735 (GRCm39)	V55A	unknown	Het
Cpd	A	C	11: 76,737,097 (GRCm39)	D232E	probably benign	Het
Csde1	A	G	3: 102,947,333 (GRCm39)	H95R	probably benign	Het
Ctcfl	T	A	2: 172,937,130 (GRCm39)	H596L	probably benign	Het
Cwc22	T	C	2: 77,726,515 (GRCm39)	R855G	possibly damaging	Het
Cwc25	A	G	11: 97,644,053 (GRCm39)	Y227H	probably damaging	Het
Cyp2c38	G	A	19: 39,380,659 (GRCm39)	P409S	probably damaging	Het
Ddx5	A	G	11: 106,679,139 (GRCm39)	S2P	possibly damaging	Het
Dnah2	C	A	11: 69,348,238 (GRCm39)	G2570W	probably damaging	Het
Dnajc10	T	A	2: 80,174,292 (GRCm39)	V528E	probably damaging	Het
Fmo1	A	G	1: 162,677,629 (GRCm39)		probably null	Het
Gpatch1	C	A	7: 35,002,848 (GRCm39)	D221Y	probably damaging	Het
Ino80	T	C	2: 119,213,895 (GRCm39)	Y1225C	probably damaging	Het
Itga7	T	A	10: 128,779,955 (GRCm39)	D501E	probably benign	Het
Lgr4	T	C	2: 109,842,243 (GRCm39)	S743P	possibly damaging	Het
Lilra5	A	T	7: 4,241,360 (GRCm39)	Y99F	probably damaging	Het
Lmna	A	G	3: 88,410,265 (GRCm39)	V49A	probably damaging	Het
Lrrc72	G	A	12: 36,258,603 (GRCm39)	R267*	probably null	Het
Mapkbp1	T	C	2: 119,853,772 (GRCm39)	S1199P	probably damaging	Het
Mmp25	G	A	17: 23,849,768 (GRCm39)	A541V	possibly damaging	Het
Myh10	A	T	11: 68,701,058 (GRCm39)	N1756Y	probably damaging	Het
Nfe2	A	G	15: 103,159,378 (GRCm39)	I31T	probably damaging	Het
Nfe2l1	A	T	11: 96,708,570 (GRCm39)	F732I	probably benign	Het
Or4a39	C	G	2: 89,237,074 (GRCm39)	M116I	possibly damaging	Het
Or4c12b	T	A	2: 89,647,104 (GRCm39)	C145S	probably damaging	Het
Or52e19b	C	A	7: 103,032,403 (GRCm39)	V269F	possibly damaging	Het
Pax6	T	C	2: 105,523,199 (GRCm39)		probably null	Het
Phb1	A	G	11: 95,568,941 (GRCm39)	E192G	probably damaging	Het
Plekhn1	A	T	4: 156,309,650 (GRCm39)		probably null	Het
Plxnb2	A	T	15: 89,046,189 (GRCm39)	V942E	probably damaging	Het
Potegl	T	A	2: 23,156,745 (GRCm39)		probably benign	Het
Rsrc2	G	A	5: 123,877,751 (GRCm39)		probably benign	Het
Septin8	G	A	11: 53,439,210 (GRCm39)	C460Y	probably benign	Het
Slc13a2	CGTTATCTGT	CGT	11: 78,294,306 (GRCm39)		probably benign	Het
Slc16a7	A	G	10: 125,130,508 (GRCm39)	I59T	probably benign	Het
Slc35d1	A	T	4: 103,065,365 (GRCm39)	I172N	possibly damaging	Het
Smg5	A	T	3: 88,249,208 (GRCm39)	N40Y	possibly damaging	Het
Smurf1	A	G	5: 144,818,541 (GRCm39)	V633A	probably damaging	Het
Snx9	T	C	17: 5,937,324 (GRCm39)	V22A	probably damaging	Het
Sox6	A	T	7: 115,076,295 (GRCm39)	M741K	probably damaging	Het
Spata31d1d	T	C	13: 59,873,797 (GRCm39)	Q1246R	probably benign	Het
Sval1	A	G	6: 41,928,660 (GRCm39)	E24G	probably damaging	Het
Tas2r124	A	G	6: 132,731,867 (GRCm39)	I59V	probably benign	Het
Tmem151b	T	A	17: 45,857,992 (GRCm39)	T85S	probably benign	Het
Tpr	T	A	1: 150,317,996 (GRCm39)		probably null	Het
Trpm6	A	C	19: 18,831,472 (GRCm39)	T1446P	possibly damaging	Het
Tsc22d4	A	T	5: 137,766,441 (GRCm39)	K502N	possibly damaging	Het
Tssk3	C	T	4: 129,383,051 (GRCm39)	S207N	probably benign	Het
Ttbk1	G	T	17: 46,778,188 (GRCm39)	P618Q	probably damaging	Het
Ttll6	A	T	11: 96,047,371 (GRCm39)	M657L	probably benign	Het
Ubash3a	T	A	17: 31,434,069 (GRCm39)	I138N	probably benign	Het
Ush2a	A	G	1: 188,090,839 (GRCm39)	Y490C	probably damaging	Het
Vmn1r82	G	T	7: 12,039,461 (GRCm39)	V127F	probably damaging	Het
Vmn2r32	A	T	7: 7,479,691 (GRCm39)	S161T	possibly damaging	Het
Wdr49	T	C	3: 75,388,824 (GRCm39)	I58M	possibly damaging	Het
Wiz	A	T	17: 32,579,417 (GRCm39)		probably null	Het
Wrap53	A	T	11: 69,453,619 (GRCm39)	Y324*	probably null	Het
Zfp747	A	C	7: 126,975,138 (GRCm39)		probably benign	Het
Zfp827	A	G	8: 79,905,702 (GRCm39)	Y33C	probably damaging	Het

Other mutations in Efcab3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00897:Efcab3	APN	11	104,990,847 (GRCm39)	missense	probably damaging	1.00
IGL01308:Efcab3	APN	11	104,611,523 (GRCm39)	missense	probably benign	0.03
IGL01483:Efcab3	APN	11	104,630,173 (GRCm39)	missense	probably benign	0.03
IGL01695:Efcab3	APN	11	104,626,889 (GRCm39)	missense	probably damaging	1.00
IGL01860:Efcab3	APN	11	104,581,747 (GRCm39)	missense	probably benign	0.16
IGL01981:Efcab3	APN	11	104,612,258 (GRCm39)	intron	probably benign
IGL01984:Efcab3	APN	11	104,629,134 (GRCm39)	missense	probably benign	0.20
IGL02023:Efcab3	APN	11	104,612,258 (GRCm39)	intron	probably benign
IGL02252:Efcab3	APN	11	104,644,753 (GRCm39)	missense	possibly damaging	0.68
IGL02886:Efcab3	APN	11	104,986,700 (GRCm39)	missense	possibly damaging	0.95
IGL03116:Efcab3	APN	11	104,612,359 (GRCm39)	missense	probably benign	0.02
IGL03141:Efcab3	APN	11	104,986,696 (GRCm39)	missense	probably damaging	0.99
IGL03242:Efcab3	APN	11	104,997,230 (GRCm39)	missense	probably damaging	1.00
IGL03274:Efcab3	APN	11	104,611,919 (GRCm39)	missense	probably benign	0.03
IGL03408:Efcab3	APN	11	104,601,447 (GRCm39)	missense	probably benign	0.03
PIT4812001:Efcab3	UTSW	11	104,990,805 (GRCm39)	missense	probably null	0.00
R0018:Efcab3	UTSW	11	104,612,378 (GRCm39)	critical splice donor site	probably null
R0068:Efcab3	UTSW	11	104,611,648 (GRCm39)	missense	probably benign	0.29
R0350:Efcab3	UTSW	11	104,581,706 (GRCm39)	missense	probably benign	0.03
R0388:Efcab3	UTSW	11	105,000,227 (GRCm39)	missense	possibly damaging	0.61
R0646:Efcab3	UTSW	11	104,611,327 (GRCm39)	missense	probably benign	0.03
R0668:Efcab3	UTSW	11	104,611,318 (GRCm39)	missense	probably benign	0.16
R0715:Efcab3	UTSW	11	104,611,706 (GRCm39)	missense	possibly damaging	0.90
R0944:Efcab3	UTSW	11	104,601,556 (GRCm39)	splice site	probably null
R1330:Efcab3	UTSW	11	104,637,116 (GRCm39)	missense	possibly damaging	0.84
R1440:Efcab3	UTSW	11	104,999,581 (GRCm39)	splice site	probably benign
R1508:Efcab3	UTSW	11	104,601,503 (GRCm39)	missense	probably benign	0.03
R1540:Efcab3	UTSW	11	104,999,726 (GRCm39)	missense	probably benign	0.07
R1643:Efcab3	UTSW	11	104,589,804 (GRCm39)	missense	probably benign	0.16
R1651:Efcab3	UTSW	11	104,611,492 (GRCm39)	missense	probably benign	0.03
R1665:Efcab3	UTSW	11	104,611,940 (GRCm39)	missense	probably benign	0.07
R1702:Efcab3	UTSW	11	104,581,832 (GRCm39)	missense	probably benign	0.03
R1711:Efcab3	UTSW	11	104,611,514 (GRCm39)	missense	probably benign	0.07
R1779:Efcab3	UTSW	11	104,611,765 (GRCm39)	missense	probably benign	0.15
R1813:Efcab3	UTSW	11	104,611,514 (GRCm39)	missense	probably benign	0.07
R1818:Efcab3	UTSW	11	104,612,333 (GRCm39)	missense	probably benign	0.10
R1896:Efcab3	UTSW	11	104,611,514 (GRCm39)	missense	probably benign	0.07
R1969:Efcab3	UTSW	11	104,637,090 (GRCm39)	missense	probably damaging	1.00
R2029:Efcab3	UTSW	11	104,990,851 (GRCm39)	missense	probably damaging	0.99
R2139:Efcab3	UTSW	11	104,642,737 (GRCm39)	missense	possibly damaging	0.53
R2165:Efcab3	UTSW	11	104,642,688 (GRCm39)	missense	possibly damaging	0.93
R2359:Efcab3	UTSW	11	104,630,106 (GRCm39)	missense	possibly damaging	0.80
R2394:Efcab3	UTSW	11	104,629,121 (GRCm39)	missense	probably benign	0.17
R2401:Efcab3	UTSW	11	104,963,144 (GRCm39)	critical splice donor site	probably null
R2406:Efcab3	UTSW	11	104,611,457 (GRCm39)	missense	probably benign	0.03
R2570:Efcab3	UTSW	11	104,624,490 (GRCm39)	missense	probably damaging	1.00
R3795:Efcab3	UTSW	11	104,624,501 (GRCm39)	missense	possibly damaging	0.94
R3901:Efcab3	UTSW	11	104,974,713 (GRCm39)	missense	possibly damaging	0.68
R4244:Efcab3	UTSW	11	105,002,629 (GRCm39)	missense	probably damaging	1.00
R4352:Efcab3	UTSW	11	104,630,140 (GRCm39)	missense	probably null	0.25
R4359:Efcab3	UTSW	11	104,624,547 (GRCm39)	splice site	probably null
R4424:Efcab3	UTSW	11	104,626,940 (GRCm39)	critical splice donor site	probably null
R4895:Efcab3	UTSW	11	105,008,227 (GRCm39)	unclassified	probably benign
R4895:Efcab3	UTSW	11	104,640,496 (GRCm39)	missense	probably damaging	1.00
R4895:Efcab3	UTSW	11	104,611,112 (GRCm39)	missense	probably benign	0.16
R5006:Efcab3	UTSW	11	104,620,503 (GRCm39)	splice site	probably null
R5066:Efcab3	UTSW	11	104,611,490 (GRCm39)	missense	probably benign	0.03
R5316:Efcab3	UTSW	11	104,967,286 (GRCm39)	missense	possibly damaging	0.80
R5329:Efcab3	UTSW	11	104,644,632 (GRCm39)	splice site	probably null
R5405:Efcab3	UTSW	11	104,612,018 (GRCm39)	missense	probably benign	0.07
R5814:Efcab3	UTSW	11	104,626,940 (GRCm39)	critical splice donor site	probably benign
R5888:Efcab3	UTSW	11	104,612,227 (GRCm39)	splice site	probably benign
R5910:Efcab3	UTSW	11	104,581,760 (GRCm39)	missense	probably benign	0.01
R5975:Efcab3	UTSW	11	104,578,375 (GRCm39)	start gained	probably benign
R6019:Efcab3	UTSW	11	104,933,728 (GRCm39)	critical splice donor site	probably null
R6028:Efcab3	UTSW	11	104,660,481 (GRCm39)	critical splice donor site	probably null
R6048:Efcab3	UTSW	11	104,835,259 (GRCm39)	missense	unknown
R6059:Efcab3	UTSW	11	104,927,595 (GRCm39)	missense	probably benign	0.03
R6147:Efcab3	UTSW	11	104,858,566 (GRCm39)	missense	unknown
R6176:Efcab3	UTSW	11	104,683,383 (GRCm39)	missense	probably benign	0.16
R6181:Efcab3	UTSW	11	104,722,159 (GRCm39)	missense	probably benign	0.25
R6196:Efcab3	UTSW	11	104,746,386 (GRCm39)	missense	probably benign	0.07
R6245:Efcab3	UTSW	11	104,675,834 (GRCm39)	missense	probably benign	0.03
R6262:Efcab3	UTSW	11	104,784,579 (GRCm39)	missense	probably benign	0.24
R6277:Efcab3	UTSW	11	104,901,148 (GRCm39)	missense	possibly damaging	0.49
R6338:Efcab3	UTSW	11	104,734,034 (GRCm39)	nonsense	probably null
R6355:Efcab3	UTSW	11	104,896,511 (GRCm39)	missense	probably benign	0.29
R6356:Efcab3	UTSW	11	104,784,533 (GRCm39)	missense	probably benign	0.19
R6365:Efcab3	UTSW	11	104,815,412 (GRCm39)	missense	unknown
R6378:Efcab3	UTSW	11	104,999,620 (GRCm39)	missense	possibly damaging	0.83
R6391:Efcab3	UTSW	11	104,885,143 (GRCm39)	missense	possibly damaging	0.92
R6494:Efcab3	UTSW	11	104,990,845 (GRCm39)	missense	possibly damaging	0.93
R6556:Efcab3	UTSW	11	104,899,077 (GRCm39)	missense	probably null	0.03
R6573:Efcab3	UTSW	11	104,971,461 (GRCm39)	missense	possibly damaging	0.91
R6604:Efcab3	UTSW	11	104,589,772 (GRCm39)	nonsense	probably null
R6605:Efcab3	UTSW	11	104,890,107 (GRCm39)	splice site	probably null
R6634:Efcab3	UTSW	11	104,784,609 (GRCm39)	missense	probably benign	0.17
R6723:Efcab3	UTSW	11	105,007,906 (GRCm39)	missense	possibly damaging	0.95
R6851:Efcab3	UTSW	11	104,896,521 (GRCm39)	missense	probably benign	0.03
R6862:Efcab3	UTSW	11	104,612,284 (GRCm39)	nonsense	probably null
R6949:Efcab3	UTSW	11	104,799,896 (GRCm39)	missense	probably damaging	1.00
R6970:Efcab3	UTSW	11	104,667,182 (GRCm39)	missense	probably benign	0.03
R7014:Efcab3	UTSW	11	104,584,248 (GRCm39)	missense	probably benign	0.03
R7097:Efcab3	UTSW	11	104,899,787 (GRCm39)	missense	possibly damaging	0.68
R7122:Efcab3	UTSW	11	104,899,787 (GRCm39)	missense	possibly damaging	0.68
R7124:Efcab3	UTSW	11	104,629,100 (GRCm39)	missense	probably benign	0.17
R7146:Efcab3	UTSW	11	104,913,764 (GRCm39)	missense	probably benign	0.03
R7146:Efcab3	UTSW	11	104,858,578 (GRCm39)	missense	unknown
R7154:Efcab3	UTSW	11	104,589,966 (GRCm39)	splice site	probably null
R7175:Efcab3	UTSW	11	104,838,237 (GRCm39)	missense	unknown
R7189:Efcab3	UTSW	11	104,986,690 (GRCm39)	missense	probably benign
R7198:Efcab3	UTSW	11	104,642,711 (GRCm39)	missense	probably benign	0.15
R7211:Efcab3	UTSW	11	104,615,435 (GRCm39)	critical splice donor site	probably null
R7211:Efcab3	UTSW	11	104,601,539 (GRCm39)	missense	probably benign	0.01
R7216:Efcab3	UTSW	11	104,771,375 (GRCm39)	missense	possibly damaging	0.49
R7221:Efcab3	UTSW	11	104,791,432 (GRCm39)	missense	probably benign	0.36
R7233:Efcab3	UTSW	11	104,730,669 (GRCm39)	missense	possibly damaging	0.69
R7236:Efcab3	UTSW	11	104,790,093 (GRCm39)	missense	probably benign	0.10
R7262:Efcab3	UTSW	11	104,745,432 (GRCm39)	critical splice donor site	probably null
R7289:Efcab3	UTSW	11	104,929,184 (GRCm39)	missense	probably benign	0.24
R7323:Efcab3	UTSW	11	104,920,837 (GRCm39)	missense	probably benign	0.07
R7378:Efcab3	UTSW	11	104,605,528 (GRCm39)	missense	probably benign	0.03
R7388:Efcab3	UTSW	11	104,611,871 (GRCm39)	missense	probably damaging	0.97
R7390:Efcab3	UTSW	11	104,615,411 (GRCm39)	missense	possibly damaging	0.46
R7411:Efcab3	UTSW	11	104,890,549 (GRCm39)	missense	probably benign	0.10
R7468:Efcab3	UTSW	11	104,640,526 (GRCm39)	missense	probably benign	0.17
R7483:Efcab3	UTSW	11	105,000,112 (GRCm39)	missense	probably benign	0.39
R7497:Efcab3	UTSW	11	104,653,516 (GRCm39)	critical splice donor site	probably null
R7612:Efcab3	UTSW	11	104,999,647 (GRCm39)	missense	possibly damaging	0.80
R7620:Efcab3	UTSW	11	104,722,969 (GRCm39)	missense	possibly damaging	0.95
R7638:Efcab3	UTSW	11	104,927,625 (GRCm39)	missense	probably benign	0.03
R7661:Efcab3	UTSW	11	104,617,503 (GRCm39)	missense	probably benign	0.03
R7667:Efcab3	UTSW	11	104,642,737 (GRCm39)	missense	possibly damaging	0.53
R7682:Efcab3	UTSW	11	104,855,174 (GRCm39)	splice site	probably null
R7708:Efcab3	UTSW	11	104,855,397 (GRCm39)	missense	unknown
R7719:Efcab3	UTSW	11	105,002,674 (GRCm39)	missense	probably benign	0.14
R7721:Efcab3	UTSW	11	104,615,366 (GRCm39)	nonsense	probably null
R7735:Efcab3	UTSW	11	104,962,465 (GRCm39)	missense	probably benign
R7747:Efcab3	UTSW	11	104,733,429 (GRCm39)	missense	probably damaging	0.96
R7840:Efcab3	UTSW	11	104,624,539 (GRCm39)	missense	probably benign	0.07
R7846:Efcab3	UTSW	11	104,605,571 (GRCm39)	critical splice donor site	probably null
R7893:Efcab3	UTSW	11	104,870,186 (GRCm39)	missense	unknown
R7895:Efcab3	UTSW	11	105,008,150 (GRCm39)	missense	probably benign	0.29
R7897:Efcab3	UTSW	11	104,889,061 (GRCm39)	missense	probably benign	0.24
R7936:Efcab3	UTSW	11	104,890,524 (GRCm39)	missense	possibly damaging	0.89
R7936:Efcab3	UTSW	11	104,937,385 (GRCm39)	critical splice donor site	probably null
R7959:Efcab3	UTSW	11	104,933,627 (GRCm39)	missense	probably damaging	0.96
R8031:Efcab3	UTSW	11	104,772,295 (GRCm39)	missense	possibly damaging	0.49
R8041:Efcab3	UTSW	11	104,810,305 (GRCm39)	missense	unknown
R8054:Efcab3	UTSW	11	104,621,226 (GRCm39)	missense	probably benign	0.07
R8056:Efcab3	UTSW	11	104,799,896 (GRCm39)	missense	probably damaging	0.98
R8061:Efcab3	UTSW	11	104,997,275 (GRCm39)	missense	probably benign	0.00
R8088:Efcab3	UTSW	11	104,889,072 (GRCm39)	missense	probably benign	0.10
R8112:Efcab3	UTSW	11	104,841,026 (GRCm39)	missense	unknown
R8116:Efcab3	UTSW	11	105,002,677 (GRCm39)	missense	possibly damaging	0.65
R8340:Efcab3	UTSW	11	104,876,856 (GRCm39)	missense	unknown
R8405:Efcab3	UTSW	11	104,612,024 (GRCm39)	missense	probably benign	0.02
R8413:Efcab3	UTSW	11	104,811,135 (GRCm39)	missense	unknown
R8472:Efcab3	UTSW	11	104,709,463 (GRCm39)	missense	probably benign	0.07
R8549:Efcab3	UTSW	11	104,890,521 (GRCm39)	missense	probably damaging	0.99
R8699:Efcab3	UTSW	11	104,672,072 (GRCm39)	missense	probably benign	0.03
R8711:Efcab3	UTSW	11	104,743,371 (GRCm39)	missense	probably benign	0.03
R8732:Efcab3	UTSW	11	104,695,100 (GRCm39)	missense	probably benign	0.03
R8745:Efcab3	UTSW	11	104,749,304 (GRCm39)	missense	possibly damaging	0.57
R8806:Efcab3	UTSW	11	104,928,695 (GRCm39)	missense	probably benign	0.07
R8810:Efcab3	UTSW	11	104,805,721 (GRCm39)	missense	unknown
R8845:Efcab3	UTSW	11	104,899,787 (GRCm39)	missense	possibly damaging	0.68
R8870:Efcab3	UTSW	11	104,791,500 (GRCm39)	missense	probably benign	0.07
R8872:Efcab3	UTSW	11	104,760,880 (GRCm39)	missense	probably benign	0.19
R8879:Efcab3	UTSW	11	104,581,781 (GRCm39)	missense	probably benign	0.03
R8924:Efcab3	UTSW	11	104,806,253 (GRCm39)	frame shift	probably null
R8954:Efcab3	UTSW	11	104,909,525 (GRCm39)	critical splice donor site	probably null
R8960:Efcab3	UTSW	11	104,820,772 (GRCm39)	splice site	probably benign
R8975:Efcab3	UTSW	11	104,954,415 (GRCm39)	missense	probably benign	0.17
R8988:Efcab3	UTSW	11	104,911,352 (GRCm39)	missense	probably benign	0.07
R8998:Efcab3	UTSW	11	104,640,477 (GRCm39)	missense	probably benign	0.09
R8999:Efcab3	UTSW	11	104,640,477 (GRCm39)	missense	probably benign	0.09
R9002:Efcab3	UTSW	11	104,920,822 (GRCm39)	missense	probably damaging	0.99
R9012:Efcab3	UTSW	11	104,711,347 (GRCm39)	critical splice donor site	probably null
R9036:Efcab3	UTSW	11	104,927,601 (GRCm39)	missense	probably benign	0.03
R9037:Efcab3	UTSW	11	104,803,791 (GRCm39)	missense	unknown
R9059:Efcab3	UTSW	11	104,642,689 (GRCm39)	missense	possibly damaging	0.73
R9066:Efcab3	UTSW	11	104,631,688 (GRCm39)	intron	probably benign
R9122:Efcab3	UTSW	11	104,856,605 (GRCm39)	missense	unknown
R9125:Efcab3	UTSW	11	104,736,360 (GRCm39)	missense	probably damaging	1.00
R9127:Efcab3	UTSW	11	104,741,407 (GRCm39)	missense	probably benign	0.07
R9171:Efcab3	UTSW	11	104,800,708 (GRCm39)	missense	probably benign	0.36
R9219:Efcab3	UTSW	11	104,836,691 (GRCm39)	missense	unknown
R9224:Efcab3	UTSW	11	104,661,801 (GRCm39)	missense	probably benign	0.07
R9235:Efcab3	UTSW	11	104,907,987 (GRCm39)	missense	probably benign	0.19
R9294:Efcab3	UTSW	11	104,722,126 (GRCm39)	missense	probably benign	0.24
R9318:Efcab3	UTSW	11	104,856,648 (GRCm39)	critical splice donor site	probably null
R9322:Efcab3	UTSW	11	104,765,199 (GRCm39)	missense	probably benign	0.36
R9361:Efcab3	UTSW	11	104,896,524 (GRCm39)	missense	probably benign	0.03
R9408:Efcab3	UTSW	11	104,621,255 (GRCm39)	critical splice donor site	probably null
R9434:Efcab3	UTSW	11	104,899,863 (GRCm39)	missense	probably benign	0.24
R9477:Efcab3	UTSW	11	104,836,698 (GRCm39)	missense	unknown
R9658:Efcab3	UTSW	11	104,611,120 (GRCm39)	missense	probably benign	0.03
R9719:Efcab3	UTSW	11	104,867,912 (GRCm39)	missense	unknown
R9751:Efcab3	UTSW	11	104,783,911 (GRCm39)	missense	probably benign	0.19
R9763:Efcab3	UTSW	11	104,890,485 (GRCm39)	missense	possibly damaging	0.89
X0026:Efcab3	UTSW	11	105,007,937 (GRCm39)	missense	probably benign	0.03
X0026:Efcab3	UTSW	11	104,611,801 (GRCm39)	missense	probably benign	0.07
Z1088:Efcab3	UTSW	11	104,642,728 (GRCm39)	missense	probably damaging	0.96
Z1176:Efcab3	UTSW	11	104,990,872 (GRCm39)	missense	probably damaging	1.00
Z1176:Efcab3	UTSW	11	104,892,793 (GRCm39)	missense	probably benign	0.29
Z1176:Efcab3	UTSW	11	104,999,598 (GRCm39)	nonsense	probably null
Z1177:Efcab3	UTSW	11	104,711,344 (GRCm39)	missense	probably benign	0.03
Z1177:Efcab3	UTSW	11	104,630,164 (GRCm39)	nonsense	probably null
Z1177:Efcab3	UTSW	11	104,814,845 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- CAAACTTTATATGCCCCAGTACAGG -3'
(R):5'- AACACAAAAGCCTGTCTCTAGATG -3'

Sequencing Primer
(F):5'- CCAGTACAGGGGAACGCCAG -3'
(R):5'- AAAAGCCTGTCTCTAGATGTTGCC -3'

Posted On

2018-03-15