Mutagenetix > Incidental Mutation

Incidental Mutation 'R5022:Dmxl1'

389306

Institutional Source

Beutler Lab

Gene Symbol

Dmxl1

Ensembl Gene

ENSMUSG00000037416

Gene Name

Dmx-like 1

Synonyms

C630007L23Rik

MMRRC Submission

042613-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.951) question?

Stock #

R5022 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

49832670-49965473 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 49895127 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Lysine at position 2206 (I2206K)

Ref Sequence

ENSEMBL: ENSMUSP00000045559 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041772] [ENSMUST00000180611]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000041772
AA Change: I2206K

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000045559
Gene: ENSMUSG00000037416
AA Change: I2206K

Domain	Start	End	E-Value	Type
WD40	100	136	8.22e1	SMART
WD40	156	195	2.88e-1	SMART
WD40	218	266	8.29e-1	SMART
low complexity region	367	378	N/A	INTRINSIC
WD40	464	505	1.53e2	SMART
Blast:WD40	719	772	1e-25	BLAST
WD40	957	999	1.1e1	SMART
Pfam:Rav1p_C	1102	1877	4.3e-84	PFAM
low complexity region	1922	1942	N/A	INTRINSIC
low complexity region	1966	1975	N/A	INTRINSIC
low complexity region	1993	2007	N/A	INTRINSIC
low complexity region	2147	2158	N/A	INTRINSIC
low complexity region	2371	2385	N/A	INTRINSIC
low complexity region	2397	2410	N/A	INTRINSIC
low complexity region	2449	2466	N/A	INTRINSIC
WD40	2735	2770	1.07e1	SMART
WD40	2773	2813	3.7e0	SMART
WD40	2825	2867	1.07e0	SMART
WD40	2873	2912	1.05e-2	SMART
WD40	2915	2954	4.51e-7	SMART
Blast:WD40	2957	3005	9e-26	BLAST

Predicted Effect

probably damaging
Transcript: ENSMUST00000180611
AA Change: I2206K

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000137871
Gene: ENSMUSG00000037416
AA Change: I2206K

Domain	Start	End	E-Value	Type
WD40	100	136	8.22e1	SMART
WD40	156	195	2.88e-1	SMART
WD40	218	266	8.29e-1	SMART
low complexity region	367	378	N/A	INTRINSIC
WD40	464	505	1.53e2	SMART
Blast:WD40	719	772	1e-25	BLAST
WD40	957	999	1.1e1	SMART
low complexity region	1195	1206	N/A	INTRINSIC
low complexity region	1258	1271	N/A	INTRINSIC
Pfam:Rav1p_C	1287	1876	9.4e-72	PFAM
low complexity region	1922	1942	N/A	INTRINSIC
low complexity region	1966	1975	N/A	INTRINSIC
low complexity region	1993	2007	N/A	INTRINSIC
low complexity region	2147	2158	N/A	INTRINSIC
low complexity region	2385	2398	N/A	INTRINSIC
low complexity region	2437	2454	N/A	INTRINSIC
WD40	2723	2758	1.07e1	SMART
WD40	2761	2801	3.7e0	SMART
WD40	2813	2855	1.07e0	SMART
WD40	2861	2900	1.05e-2	SMART
WD40	2903	2942	4.51e-7	SMART
Blast:WD40	2945	2993	9e-26	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000181907

Meta Mutation Damage Score

0.6250

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.4%
20x: 92.6%

Validation Efficiency

99% (110/111)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the WD repeat superfamily of proteins, which have regulatory functions. This gene is expressed in many tissue types including several types of eye tissue, and it has been associated with ocular phenotypes. In addition, it is upregulated in cultured cells that overexpress growth factor independence 1B, a transcription factor that is essential for hematopoietic cell development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]

Allele List at MGI

Other mutations in this stock

Total: 105 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca1	TCGACTGC	T	4: 53,041,570 (GRCm38)		probably null	Het
Abca15	T	C	7: 120,346,096 (GRCm38)	I465T	probably damaging	Het
Abca3	C	T	17: 24,374,300 (GRCm38)	R224C	probably damaging	Het
Abcb4	T	A	5: 8,909,054 (GRCm38)		probably null	Het
Acan	T	C	7: 79,092,808 (GRCm38)		probably null	Het
Aebp2	G	A	6: 140,637,730 (GRCm38)	R109Q	possibly damaging	Het
Agfg2	A	T	5: 137,660,160 (GRCm38)		probably null	Het
Ankib1	T	A	5: 3,734,011 (GRCm38)	I322F	possibly damaging	Het
AW551984	A	T	9: 39,597,965 (GRCm38)	N293K	probably benign	Het
BC028528	T	A	3: 95,888,823 (GRCm38)		probably benign	Het
Bicc1	A	G	10: 70,947,883 (GRCm38)	S393P	possibly damaging	Het
Birc6	A	G	17: 74,692,332 (GRCm38)	Y4656C	probably damaging	Het
Bmp3	A	G	5: 98,872,824 (GRCm38)	R369G	probably damaging	Het
C1d	T	A	11: 17,266,674 (GRCm38)	N135K	probably benign	Het
Ccdc148	G	A	2: 58,827,632 (GRCm38)	A453V	probably damaging	Het
Cd163	C	T	6: 124,325,288 (GRCm38)	T937I	probably damaging	Het
Celf2	C	T	2: 6,607,847 (GRCm38)		probably benign	Het
Chga	T	C	12: 102,562,837 (GRCm38)	W358R	probably damaging	Het
Clec4b2	A	T	6: 123,200,956 (GRCm38)	S77C	probably null	Het
Crim1	T	C	17: 78,280,129 (GRCm38)	V221A	possibly damaging	Het
D630003M21Rik	A	T	2: 158,217,633 (GRCm38)	S116T	probably damaging	Het
Dlg5	T	C	14: 24,136,622 (GRCm38)	E1847G	probably damaging	Het
Dusp7	T	A	9: 106,373,741 (GRCm38)	L355Q	probably damaging	Het
Eif1ad15	T	C	12: 88,321,301 (GRCm38)	I61V	probably benign	Het
Eif1ad16	A	T	12: 88,018,711 (GRCm38)	S21T	unknown	Het
Exd2	T	A	12: 80,496,790 (GRCm38)	N582K	probably damaging	Het
Fbln1	G	A	15: 85,237,626 (GRCm38)	S316N	probably damaging	Het
Fchsd1	A	G	18: 37,964,810 (GRCm38)	I340T	possibly damaging	Het
Fn1	T	C	1: 71,624,179 (GRCm38)	Y1050C	probably damaging	Het
Fsip2	A	G	2: 82,979,429 (GRCm38)	I2031V	probably benign	Het
Gm10803	A	C	2: 93,564,172 (GRCm38)	L96F	probably damaging	Het
Gm14569	T	C	X: 36,430,817 (GRCm38)	D1413G	probably benign	Het
Gm15455	T	C	1: 33,837,351 (GRCm38)		noncoding transcript	Het
Gm1818	G	C	12: 48,555,535 (GRCm38)		noncoding transcript	Het
Gm5420	A	T	10: 21,691,727 (GRCm38)		noncoding transcript	Het
Gm7104	A	T	12: 88,285,759 (GRCm38)		noncoding transcript	Het
Gp2	A	G	7: 119,449,114 (GRCm38)	I427T	probably damaging	Het
Gpc4	G	A	X: 52,074,563 (GRCm38)	R148C	probably damaging	Het
Gpr142	A	C	11: 114,804,388 (GRCm38)	S60R	probably benign	Het
Helz2	T	C	2: 181,240,569 (GRCm38)	R144G	probably benign	Het
Herc1	A	T	9: 66,470,326 (GRCm38)	K3458M	possibly damaging	Het
Hnf4g	G	T	3: 3,644,587 (GRCm38)	A144S	probably damaging	Het
Irs2	A	C	8: 10,987,012 (GRCm38)	*1322G	probably null	Het
Keg1	A	G	19: 12,719,157 (GRCm38)	N288S	probably damaging	Het
Kif19a	G	A	11: 114,767,227 (GRCm38)	M37I	probably benign	Het
Klhl1	G	A	14: 96,136,706 (GRCm38)	P635S	probably benign	Het
Klk14	G	A	7: 43,692,077 (GRCm38)	C51Y	probably damaging	Het
Lsm11	T	C	11: 45,944,839 (GRCm38)	D25G	probably damaging	Het
Manea	A	T	4: 26,336,630 (GRCm38)	Y215*	probably null	Het
Mdga2	C	T	12: 66,470,760 (GRCm38)	C100Y	possibly damaging	Het
Mthfd1	T	G	12: 76,294,374 (GRCm38)	V480G	probably damaging	Het
Mthfd1	T	A	12: 76,301,328 (GRCm38)	M582K	probably damaging	Het
Myh7b	G	C	2: 155,632,373 (GRCm38)	R1669S	possibly damaging	Het
Nanos1	T	C	19: 60,756,980 (GRCm38)	Y239H	probably damaging	Het
Nat8	G	A	6: 85,830,857 (GRCm38)	T98I	possibly damaging	Het
Ndufs3	C	A	2: 90,898,660 (GRCm38)	A161S	probably benign	Het
Nexmif	A	T	X: 104,087,350 (GRCm38)	N320K	probably damaging	Het
Or10h1	T	C	17: 33,199,777 (GRCm38)	F239S	probably damaging	Het
Or2m12	A	T	16: 19,286,059 (GRCm38)	V228D	probably damaging	Het
Or2r3	A	T	6: 42,471,287 (GRCm38)	V297E	possibly damaging	Het
Or4c111	A	G	2: 89,014,043 (GRCm38)	V7A	probably damaging	Het
Or4c122	C	T	2: 89,249,417 (GRCm38)	M92I	probably benign	Het
Or4k15	T	C	14: 50,127,012 (GRCm38)	V145A	possibly damaging	Het
Or52e2	G	A	7: 103,155,735 (GRCm38)	P4L	probably benign	Het
Or6c69c	T	C	10: 130,074,593 (GRCm38)	L61P	probably damaging	Het
Pcdhb14	T	A	18: 37,450,170 (GRCm38)	N776K	probably benign	Het
Pip5k1c	G	A	10: 81,310,889 (GRCm38)		probably null	Het
Plk4	G	A	3: 40,802,077 (GRCm38)		probably null	Het
Prmt8	A	G	6: 127,711,163 (GRCm38)	Y231H	possibly damaging	Het
Prpf4b	T	C	13: 34,883,599 (GRCm38)		probably benign	Het
Ptpn21	G	A	12: 98,679,407 (GRCm38)	R1091C	probably damaging	Het
Pwwp2b	C	T	7: 139,255,578 (GRCm38)	P312S	possibly damaging	Het
Rad21	A	T	15: 51,966,706 (GRCm38)	I503K	probably benign	Het
Rai14	A	G	15: 10,574,506 (GRCm38)	S789P	probably damaging	Het
Rbm26	C	T	14: 105,144,252 (GRCm38)	D486N	probably damaging	Het
Rnf20	A	G	4: 49,642,016 (GRCm38)		probably benign	Het
Ros1	A	G	10: 52,124,075 (GRCm38)	V1118A	possibly damaging	Het
Sema3d	A	C	5: 12,584,956 (GRCm38)	Y663S	probably damaging	Het
Serpina6	A	G	12: 103,651,712 (GRCm38)	W281R	probably damaging	Het
Slc8a3	A	G	12: 81,199,558 (GRCm38)	V900A	probably damaging	Het
Spats2l	G	T	1: 57,879,556 (GRCm38)	V30L	probably damaging	Het
Spg21	A	G	9: 65,475,949 (GRCm38)	D139G	probably damaging	Het
Sun3	T	C	11: 9,038,314 (GRCm38)	T3A	probably damaging	Het
Tep1	A	G	14: 50,828,999 (GRCm38)	Y2335H	probably benign	Het
Tesl1	G	A	X: 23,907,241 (GRCm38)	G327E	probably damaging	Het
Timd5	T	A	11: 46,528,532 (GRCm38)	D58E	probably damaging	Het
Timm21	C	A	18: 84,949,414 (GRCm38)	V112L	possibly damaging	Het
Tlk1	A	T	2: 70,742,065 (GRCm38)	N386K	probably benign	Het
Trappc10	G	T	10: 78,217,160 (GRCm38)	F260L	possibly damaging	Het
Trgv1	T	A	13: 19,340,231 (GRCm38)	S42T	probably benign	Het
Trmt112	T	C	19: 6,910,753 (GRCm38)	V91A	probably benign	Het
Ucp2	A	T	7: 100,498,372 (GRCm38)	N186I	possibly damaging	Het
Vmn1r119	A	G	7: 21,012,320 (GRCm38)	S46P	probably benign	Het
Vmn2r101	A	T	17: 19,611,387 (GRCm38)		probably null	Het
Vmn2r105	T	A	17: 20,208,414 (GRCm38)	H800L	probably damaging	Het
Vmn2r69	T	C	7: 85,411,159 (GRCm38)	M406V	possibly damaging	Het
Vmn2r84	A	G	10: 130,386,548 (GRCm38)	L601P	probably damaging	Het
Vps16	A	G	2: 130,439,452 (GRCm38)	S235G	probably benign	Het
Wap	T	C	11: 6,637,339 (GRCm38)		probably benign	Het
Wdr11	A	G	7: 129,624,711 (GRCm38)	I744M	probably benign	Het
Xiap	T	C	X: 42,094,465 (GRCm38)	F23L	probably benign	Het
Xkr7	A	G	2: 153,054,380 (GRCm38)	T385A	probably benign	Het
Zfp524	A	T	7: 5,018,417 (GRCm38)	I315F	probably benign	Het
Zfp62	T	A	11: 49,215,729 (GRCm38)	S216T	probably damaging	Het
Znfx1	T	C	2: 167,039,826 (GRCm38)	Y217C	probably damaging	Het

Other mutations in Dmxl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00163:Dmxl1	APN	18	49,851,467 (GRCm38)	missense	probably damaging	1.00
IGL00668:Dmxl1	APN	18	49,939,553 (GRCm38)	missense	possibly damaging	0.64
IGL00740:Dmxl1	APN	18	49,917,668 (GRCm38)	missense	probably benign	0.00
IGL00969:Dmxl1	APN	18	49,912,725 (GRCm38)	missense	probably benign	0.02
IGL01113:Dmxl1	APN	18	49,912,751 (GRCm38)	missense	probably benign	0.01
IGL01384:Dmxl1	APN	18	49,857,334 (GRCm38)	missense	probably benign
IGL01475:Dmxl1	APN	18	49,871,714 (GRCm38)	missense	probably damaging	1.00
IGL01559:Dmxl1	APN	18	49,920,938 (GRCm38)	missense	probably damaging	0.99
IGL01578:Dmxl1	APN	18	49,962,205 (GRCm38)	missense	probably damaging	1.00
IGL01632:Dmxl1	APN	18	49,863,025 (GRCm38)	missense	probably damaging	0.99
IGL01814:Dmxl1	APN	18	49,864,868 (GRCm38)	missense	probably damaging	1.00
IGL01843:Dmxl1	APN	18	49,878,382 (GRCm38)	nonsense	probably null
IGL01933:Dmxl1	APN	18	49,877,785 (GRCm38)	missense	probably benign	0.17
IGL01952:Dmxl1	APN	18	49,890,654 (GRCm38)	missense	probably benign	0.11
IGL02120:Dmxl1	APN	18	49,894,178 (GRCm38)	missense	possibly damaging	0.83
IGL02162:Dmxl1	APN	18	49,961,163 (GRCm38)	missense	probably benign	0.00
IGL02213:Dmxl1	APN	18	49,877,674 (GRCm38)	splice site	probably benign
IGL02261:Dmxl1	APN	18	49,840,499 (GRCm38)	missense	possibly damaging	0.85
IGL02689:Dmxl1	APN	18	49,864,895 (GRCm38)	missense	probably damaging	1.00
IGL02892:Dmxl1	APN	18	49,859,120 (GRCm38)	missense	probably damaging	0.96
IGL03232:Dmxl1	APN	18	49,878,180 (GRCm38)	missense	probably benign	0.01
IGL03258:Dmxl1	APN	18	49,920,893 (GRCm38)	missense	probably damaging	1.00
IGL03298:Dmxl1	APN	18	49,864,818 (GRCm38)	missense	probably benign
capture	UTSW	18	49,962,261 (GRCm38)	missense	probably damaging	1.00
carnivora	UTSW	18	49,864,383 (GRCm38)	missense	probably damaging	0.99
digestion	UTSW	18	49,878,259 (GRCm38)	missense	probably damaging	1.00
drowning	UTSW	18	49,878,225 (GRCm38)	missense	possibly damaging	0.55
hibiscus	UTSW	18	49,889,467 (GRCm38)	missense	probably damaging	1.00
impound	UTSW	18	49,893,249 (GRCm38)	missense	probably benign
pitcher	UTSW	18	49,864,148 (GRCm38)	missense	probably damaging	1.00
PIT4810001:Dmxl1	UTSW	18	49,931,963 (GRCm38)	missense	probably damaging	1.00
R0001:Dmxl1	UTSW	18	49,888,897 (GRCm38)	splice site	probably benign
R0027:Dmxl1	UTSW	18	49,957,295 (GRCm38)	splice site	probably benign
R0042:Dmxl1	UTSW	18	49,864,035 (GRCm38)	missense	probably benign	0.03
R0042:Dmxl1	UTSW	18	49,864,035 (GRCm38)	missense	probably benign	0.03
R0046:Dmxl1	UTSW	18	49,878,082 (GRCm38)	missense	probably benign	0.22
R0046:Dmxl1	UTSW	18	49,878,082 (GRCm38)	missense	probably benign	0.22
R0257:Dmxl1	UTSW	18	49,955,803 (GRCm38)	splice site	probably benign
R0349:Dmxl1	UTSW	18	49,879,282 (GRCm38)	missense	probably damaging	0.99
R0390:Dmxl1	UTSW	18	49,879,362 (GRCm38)	missense	probably benign	0.14
R0511:Dmxl1	UTSW	18	49,891,467 (GRCm38)	nonsense	probably null
R0539:Dmxl1	UTSW	18	49,857,430 (GRCm38)	splice site	probably benign
R0542:Dmxl1	UTSW	18	49,893,694 (GRCm38)	missense	probably benign	0.05
R0587:Dmxl1	UTSW	18	49,935,307 (GRCm38)	missense	probably benign	0.39
R0635:Dmxl1	UTSW	18	49,851,423 (GRCm38)	splice site	probably benign
R0744:Dmxl1	UTSW	18	49,833,148 (GRCm38)	missense	probably damaging	1.00
R0836:Dmxl1	UTSW	18	49,833,148 (GRCm38)	missense	probably damaging	1.00
R0845:Dmxl1	UTSW	18	49,893,402 (GRCm38)	missense	probably damaging	1.00
R1218:Dmxl1	UTSW	18	49,893,611 (GRCm38)	missense	probably damaging	1.00
R1278:Dmxl1	UTSW	18	49,893,225 (GRCm38)	missense	probably benign
R1313:Dmxl1	UTSW	18	49,878,483 (GRCm38)	missense	probably damaging	1.00
R1313:Dmxl1	UTSW	18	49,878,483 (GRCm38)	missense	probably damaging	1.00
R1349:Dmxl1	UTSW	18	49,888,853 (GRCm38)	missense	probably damaging	1.00
R1453:Dmxl1	UTSW	18	49,857,249 (GRCm38)	missense	probably benign	0.05
R1522:Dmxl1	UTSW	18	49,852,367 (GRCm38)	missense	probably benign	0.05
R1629:Dmxl1	UTSW	18	49,859,286 (GRCm38)	critical splice donor site	probably null
R1638:Dmxl1	UTSW	18	49,890,767 (GRCm38)	nonsense	probably null
R1646:Dmxl1	UTSW	18	49,962,261 (GRCm38)	missense	probably damaging	1.00
R1719:Dmxl1	UTSW	18	49,934,637 (GRCm38)	missense	probably damaging	1.00
R1732:Dmxl1	UTSW	18	49,902,988 (GRCm38)	missense	probably benign
R1732:Dmxl1	UTSW	18	49,893,444 (GRCm38)	nonsense	probably null
R1886:Dmxl1	UTSW	18	49,859,135 (GRCm38)	missense	probably benign	0.09
R1887:Dmxl1	UTSW	18	49,859,135 (GRCm38)	missense	probably benign	0.09
R1895:Dmxl1	UTSW	18	49,955,914 (GRCm38)	splice site	probably null
R1911:Dmxl1	UTSW	18	49,878,163 (GRCm38)	missense	probably benign	0.00
R2020:Dmxl1	UTSW	18	49,889,558 (GRCm38)	nonsense	probably null
R2116:Dmxl1	UTSW	18	49,878,817 (GRCm38)	missense	probably damaging	1.00
R2196:Dmxl1	UTSW	18	49,917,631 (GRCm38)	missense	probably benign	0.00
R2206:Dmxl1	UTSW	18	49,894,094 (GRCm38)	missense	probably benign	0.12
R2216:Dmxl1	UTSW	18	49,893,923 (GRCm38)	missense	probably benign	0.00
R2255:Dmxl1	UTSW	18	49,846,639 (GRCm38)	missense	probably benign	0.34
R2333:Dmxl1	UTSW	18	49,919,976 (GRCm38)	splice site	probably null
R2343:Dmxl1	UTSW	18	49,890,678 (GRCm38)	missense	probably damaging	1.00
R2496:Dmxl1	UTSW	18	49,880,791 (GRCm38)	missense	possibly damaging	0.51
R3757:Dmxl1	UTSW	18	49,935,317 (GRCm38)	missense	probably damaging	0.98
R3758:Dmxl1	UTSW	18	49,935,317 (GRCm38)	missense	probably damaging	0.98
R3783:Dmxl1	UTSW	18	49,865,122 (GRCm38)	missense	probably damaging	1.00
R3786:Dmxl1	UTSW	18	49,865,122 (GRCm38)	missense	probably damaging	1.00
R3787:Dmxl1	UTSW	18	49,865,122 (GRCm38)	missense	probably damaging	1.00
R3885:Dmxl1	UTSW	18	49,878,259 (GRCm38)	missense	probably damaging	1.00
R3886:Dmxl1	UTSW	18	49,878,259 (GRCm38)	missense	probably damaging	1.00
R3887:Dmxl1	UTSW	18	49,878,259 (GRCm38)	missense	probably damaging	1.00
R3888:Dmxl1	UTSW	18	49,878,259 (GRCm38)	missense	probably damaging	1.00
R3889:Dmxl1	UTSW	18	49,878,259 (GRCm38)	missense	probably damaging	1.00
R4014:Dmxl1	UTSW	18	49,863,962 (GRCm38)	missense	probably benign
R4033:Dmxl1	UTSW	18	49,851,431 (GRCm38)	missense	possibly damaging	0.95
R4096:Dmxl1	UTSW	18	49,961,197 (GRCm38)	missense	probably damaging	1.00
R4366:Dmxl1	UTSW	18	49,878,017 (GRCm38)	nonsense	probably null
R4406:Dmxl1	UTSW	18	49,889,553 (GRCm38)	missense	probably damaging	1.00
R4412:Dmxl1	UTSW	18	49,848,761 (GRCm38)	missense	probably benign
R4454:Dmxl1	UTSW	18	49,893,332 (GRCm38)	missense	probably benign	0.01
R4459:Dmxl1	UTSW	18	49,961,216 (GRCm38)	missense	possibly damaging	0.80
R4569:Dmxl1	UTSW	18	49,852,360 (GRCm38)	missense	probably damaging	1.00
R4570:Dmxl1	UTSW	18	49,852,360 (GRCm38)	missense	probably damaging	1.00
R4606:Dmxl1	UTSW	18	49,962,181 (GRCm38)	missense	probably damaging	0.98
R4649:Dmxl1	UTSW	18	49,878,631 (GRCm38)	missense	probably damaging	0.99
R4683:Dmxl1	UTSW	18	49,878,021 (GRCm38)	missense	probably damaging	1.00
R4782:Dmxl1	UTSW	18	49,862,992 (GRCm38)	missense	probably damaging	1.00
R4878:Dmxl1	UTSW	18	49,851,476 (GRCm38)	missense	probably damaging	1.00
R4879:Dmxl1	UTSW	18	49,889,467 (GRCm38)	missense	probably damaging	1.00
R4881:Dmxl1	UTSW	18	49,957,281 (GRCm38)	intron	probably benign
R4885:Dmxl1	UTSW	18	49,878,795 (GRCm38)	missense	probably damaging	0.99
R4916:Dmxl1	UTSW	18	49,877,697 (GRCm38)	missense	probably damaging	1.00
R5056:Dmxl1	UTSW	18	49,870,923 (GRCm38)	missense	probably benign	0.00
R5177:Dmxl1	UTSW	18	49,893,584 (GRCm38)	missense	probably damaging	0.99
R5342:Dmxl1	UTSW	18	49,951,235 (GRCm38)	missense	probably damaging	0.96
R5421:Dmxl1	UTSW	18	49,863,119 (GRCm38)	critical splice donor site	probably null
R5433:Dmxl1	UTSW	18	49,867,899 (GRCm38)	splice site	probably null
R5484:Dmxl1	UTSW	18	49,889,464 (GRCm38)	missense	probably damaging	1.00
R5598:Dmxl1	UTSW	18	49,864,478 (GRCm38)	missense	probably benign	0.04
R5633:Dmxl1	UTSW	18	49,877,697 (GRCm38)	missense	probably damaging	1.00
R5638:Dmxl1	UTSW	18	49,891,626 (GRCm38)	missense	possibly damaging	0.95
R5694:Dmxl1	UTSW	18	49,894,257 (GRCm38)	missense	probably damaging	1.00
R5696:Dmxl1	UTSW	18	49,931,941 (GRCm38)	nonsense	probably null
R5706:Dmxl1	UTSW	18	49,957,395 (GRCm38)	critical splice donor site	probably null
R5745:Dmxl1	UTSW	18	49,846,586 (GRCm38)	missense	probably benign
R5876:Dmxl1	UTSW	18	49,870,984 (GRCm38)	missense	possibly damaging	0.70
R6054:Dmxl1	UTSW	18	49,857,386 (GRCm38)	missense	probably benign	0.00
R6145:Dmxl1	UTSW	18	49,912,766 (GRCm38)	missense	possibly damaging	0.90
R6189:Dmxl1	UTSW	18	49,893,335 (GRCm38)	missense	probably benign	0.33
R6213:Dmxl1	UTSW	18	49,863,015 (GRCm38)	missense	possibly damaging	0.93
R6219:Dmxl1	UTSW	18	49,902,367 (GRCm38)	missense	probably damaging	0.99
R6221:Dmxl1	UTSW	18	49,871,732 (GRCm38)	missense	probably damaging	0.96
R6276:Dmxl1	UTSW	18	49,846,586 (GRCm38)	missense	probably benign
R6319:Dmxl1	UTSW	18	49,852,300 (GRCm38)	missense	probably benign	0.00
R6426:Dmxl1	UTSW	18	49,864,578 (GRCm38)	missense	probably damaging	0.99
R6567:Dmxl1	UTSW	18	49,859,179 (GRCm38)	missense	probably damaging	0.99
R6739:Dmxl1	UTSW	18	49,878,246 (GRCm38)	missense	probably benign	0.03
R6743:Dmxl1	UTSW	18	49,880,780 (GRCm38)	missense	possibly damaging	0.95
R6776:Dmxl1	UTSW	18	49,893,974 (GRCm38)	missense	probably damaging	1.00
R6827:Dmxl1	UTSW	18	49,921,024 (GRCm38)	missense	probably damaging	1.00
R6828:Dmxl1	UTSW	18	49,921,024 (GRCm38)	missense	probably damaging	1.00
R6829:Dmxl1	UTSW	18	49,921,024 (GRCm38)	missense	probably damaging	1.00
R6830:Dmxl1	UTSW	18	49,921,024 (GRCm38)	missense	probably damaging	1.00
R6833:Dmxl1	UTSW	18	49,955,823 (GRCm38)	missense	probably damaging	0.99
R6834:Dmxl1	UTSW	18	49,955,823 (GRCm38)	missense	probably damaging	0.99
R6856:Dmxl1	UTSW	18	49,852,288 (GRCm38)	nonsense	probably null
R6857:Dmxl1	UTSW	18	49,864,835 (GRCm38)	missense	probably damaging	0.99
R6881:Dmxl1	UTSW	18	49,935,305 (GRCm38)	missense	probably benign	0.00
R6882:Dmxl1	UTSW	18	49,843,784 (GRCm38)	critical splice acceptor site	probably null
R6892:Dmxl1	UTSW	18	49,920,902 (GRCm38)	missense	probably damaging	0.98
R6897:Dmxl1	UTSW	18	49,863,057 (GRCm38)	missense	possibly damaging	0.51
R6897:Dmxl1	UTSW	18	49,851,495 (GRCm38)	missense	probably null	0.99
R6917:Dmxl1	UTSW	18	49,864,148 (GRCm38)	missense	probably damaging	1.00
R7192:Dmxl1	UTSW	18	49,955,853 (GRCm38)	missense	probably damaging	0.99
R7447:Dmxl1	UTSW	18	49,864,614 (GRCm38)	missense	probably damaging	0.99
R7460:Dmxl1	UTSW	18	49,878,612 (GRCm38)	missense	probably benign	0.00
R7570:Dmxl1	UTSW	18	49,893,957 (GRCm38)	missense	possibly damaging	0.82
R7626:Dmxl1	UTSW	18	49,902,794 (GRCm38)	missense	probably benign
R7629:Dmxl1	UTSW	18	49,859,270 (GRCm38)	missense	probably damaging	1.00
R7644:Dmxl1	UTSW	18	49,893,552 (GRCm38)	missense	probably benign
R7688:Dmxl1	UTSW	18	49,955,871 (GRCm38)	missense	probably benign	0.03
R7689:Dmxl1	UTSW	18	49,846,618 (GRCm38)	missense	probably benign	0.00
R7712:Dmxl1	UTSW	18	49,893,461 (GRCm38)	missense	probably damaging	0.99
R7808:Dmxl1	UTSW	18	49,878,315 (GRCm38)	missense	probably benign	0.00
R7834:Dmxl1	UTSW	18	49,920,977 (GRCm38)	missense	probably damaging	1.00
R7848:Dmxl1	UTSW	18	49,840,490 (GRCm38)	missense	possibly damaging	0.88
R7849:Dmxl1	UTSW	18	49,961,147 (GRCm38)	missense	probably benign	0.00
R7881:Dmxl1	UTSW	18	49,864,383 (GRCm38)	missense	probably damaging	0.99
R7884:Dmxl1	UTSW	18	49,893,407 (GRCm38)	missense	possibly damaging	0.65
R8073:Dmxl1	UTSW	18	49,878,433 (GRCm38)	missense	probably damaging	1.00
R8089:Dmxl1	UTSW	18	49,888,830 (GRCm38)	missense	probably damaging	0.99
R8266:Dmxl1	UTSW	18	49,843,811 (GRCm38)	missense	probably benign	0.17
R8371:Dmxl1	UTSW	18	49,898,714 (GRCm38)	missense	probably benign	0.08
R8402:Dmxl1	UTSW	18	49,878,342 (GRCm38)	missense	probably benign
R8402:Dmxl1	UTSW	18	49,878,326 (GRCm38)	nonsense	probably null
R8402:Dmxl1	UTSW	18	49,878,327 (GRCm38)	missense	probably benign	0.09
R8423:Dmxl1	UTSW	18	49,865,116 (GRCm38)	missense	probably damaging	1.00
R8678:Dmxl1	UTSW	18	49,871,692 (GRCm38)	nonsense	probably null
R8702:Dmxl1	UTSW	18	49,859,135 (GRCm38)	missense	probably benign	0.09
R8749:Dmxl1	UTSW	18	49,955,870 (GRCm38)	missense	probably damaging	1.00
R8813:Dmxl1	UTSW	18	49,957,339 (GRCm38)	missense	probably damaging	0.99
R8877:Dmxl1	UTSW	18	49,878,225 (GRCm38)	missense	possibly damaging	0.55
R8945:Dmxl1	UTSW	18	49,939,572 (GRCm38)	missense	probably damaging	1.00
R8971:Dmxl1	UTSW	18	49,893,674 (GRCm38)	missense	probably damaging	1.00
R8971:Dmxl1	UTSW	18	49,864,508 (GRCm38)	missense	possibly damaging	0.96
R8978:Dmxl1	UTSW	18	49,922,612 (GRCm38)	missense	probably benign	0.37
R8987:Dmxl1	UTSW	18	49,893,852 (GRCm38)	missense
R9011:Dmxl1	UTSW	18	49,864,173 (GRCm38)	missense	probably damaging	1.00
R9124:Dmxl1	UTSW	18	49,939,572 (GRCm38)	missense	probably damaging	1.00
R9131:Dmxl1	UTSW	18	49,939,572 (GRCm38)	missense	probably damaging	1.00
R9132:Dmxl1	UTSW	18	49,939,572 (GRCm38)	missense	probably damaging	1.00
R9156:Dmxl1	UTSW	18	49,939,572 (GRCm38)	missense	probably damaging	1.00
R9165:Dmxl1	UTSW	18	49,878,925 (GRCm38)	missense	probably damaging	1.00
R9244:Dmxl1	UTSW	18	49,893,249 (GRCm38)	missense	probably benign
R9254:Dmxl1	UTSW	18	49,891,500 (GRCm38)	missense	possibly damaging	0.67
R9262:Dmxl1	UTSW	18	49,843,852 (GRCm38)	missense	probably benign	0.03
R9335:Dmxl1	UTSW	18	49,859,120 (GRCm38)	missense	probably damaging	0.96
R9375:Dmxl1	UTSW	18	49,958,410 (GRCm38)	missense	probably damaging	1.00
R9379:Dmxl1	UTSW	18	49,891,500 (GRCm38)	missense	possibly damaging	0.67
R9434:Dmxl1	UTSW	18	49,877,721 (GRCm38)	missense	probably damaging	0.98
R9470:Dmxl1	UTSW	18	49,893,710 (GRCm38)	missense	possibly damaging	0.69
R9500:Dmxl1	UTSW	18	49,878,204 (GRCm38)	missense	probably damaging	1.00
R9507:Dmxl1	UTSW	18	49,891,500 (GRCm38)	missense	possibly damaging	0.94
R9617:Dmxl1	UTSW	18	49,865,161 (GRCm38)	missense	probably damaging	1.00
R9642:Dmxl1	UTSW	18	49,880,758 (GRCm38)	missense	probably damaging	1.00
RF009:Dmxl1	UTSW	18	49,893,394 (GRCm38)	missense	probably damaging	0.96
X0025:Dmxl1	UTSW	18	49,864,368 (GRCm38)	missense	probably damaging	0.98
X0066:Dmxl1	UTSW	18	49,919,899 (GRCm38)	missense	probably damaging	1.00
Z1088:Dmxl1	UTSW	18	49,920,965 (GRCm38)	missense	probably benign
Z1188:Dmxl1	UTSW	18	49,868,003 (GRCm38)	missense	probably damaging	0.96
Z1189:Dmxl1	UTSW	18	49,868,003 (GRCm38)	missense	probably damaging	0.96

Predicted Primers

PCR Primer
(F):5'- AGCATTTTCCTCCTCAGATCATAAC -3'
(R):5'- ACAAGTAGAGCAGGGATCTCAC -3'

Sequencing Primer
(F):5'- TTTGAACACTTTTGAAAGTTACTCTG -3'
(R):5'- GGATCTCACAGAAGGTAGATGTG -3'

Posted On

2016-06-06