Mutagenetix > Incidental Mutation

Incidental Mutation 'R3739:Ankrd11'

270293

Institutional Source

Beutler Lab

Gene Symbol

Ankrd11

Ensembl Gene

ENSMUSG00000035569

Gene Name

ankyrin repeat domain 11

Synonyms

Yod, 3010027A04Rik, 2410104C19Rik, 9530048I21Rik

MMRRC Submission

040725-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R3739 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

123610561-123769016 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

A to G at 123623454 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000098333] [ENSMUST00000098334] [ENSMUST00000127664] [ENSMUST00000172906]

AlphaFold

E9Q4F7

Predicted Effect

probably benign
Transcript: ENSMUST00000098333

SMART Domains

Protein: ENSMUSP00000095938
Gene: ENSMUSG00000035569

Domain	Start	End	E-Value	Type
ANK	188	217	2.58e-3	SMART
ANK	221	250	1.31e-4	SMART
ANK	254	283	5.04e-6	SMART
low complexity region	311	324	N/A	INTRINSIC
low complexity region	366	377	N/A	INTRINSIC
low complexity region	429	440	N/A	INTRINSIC
low complexity region	470	487	N/A	INTRINSIC
low complexity region	499	521	N/A	INTRINSIC
low complexity region	534	549	N/A	INTRINSIC
low complexity region	596	609	N/A	INTRINSIC
low complexity region	649	669	N/A	INTRINSIC
coiled coil region	786	826	N/A	INTRINSIC
low complexity region	867	877	N/A	INTRINSIC
low complexity region	965	984	N/A	INTRINSIC
low complexity region	1040	1055	N/A	INTRINSIC
low complexity region	1058	1082	N/A	INTRINSIC
low complexity region	1187	1200	N/A	INTRINSIC
low complexity region	1204	1227	N/A	INTRINSIC
low complexity region	1268	1289	N/A	INTRINSIC
low complexity region	1294	1306	N/A	INTRINSIC
coiled coil region	1374	1406	N/A	INTRINSIC
low complexity region	1476	1496	N/A	INTRINSIC
low complexity region	1508	1523	N/A	INTRINSIC
low complexity region	1526	1547	N/A	INTRINSIC
coiled coil region	1598	1625	N/A	INTRINSIC
low complexity region	1770	1781	N/A	INTRINSIC
low complexity region	1874	1885	N/A	INTRINSIC
low complexity region	1913	1922	N/A	INTRINSIC
low complexity region	1969	1979	N/A	INTRINSIC
low complexity region	2035	2045	N/A	INTRINSIC
low complexity region	2057	2071	N/A	INTRINSIC
low complexity region	2162	2179	N/A	INTRINSIC
low complexity region	2191	2209	N/A	INTRINSIC
low complexity region	2224	2236	N/A	INTRINSIC
low complexity region	2250	2263	N/A	INTRINSIC
low complexity region	2294	2305	N/A	INTRINSIC
low complexity region	2391	2409	N/A	INTRINSIC
low complexity region	2445	2455	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000098334

SMART Domains

Protein: ENSMUSP00000095939
Gene: ENSMUSG00000035569

Domain	Start	End	E-Value	Type
ANK	167	196	2.58e-3	SMART
ANK	200	229	1.31e-4	SMART
ANK	233	262	5.04e-6	SMART
low complexity region	290	303	N/A	INTRINSIC
low complexity region	345	356	N/A	INTRINSIC
low complexity region	408	419	N/A	INTRINSIC
low complexity region	449	466	N/A	INTRINSIC
low complexity region	478	500	N/A	INTRINSIC
low complexity region	513	528	N/A	INTRINSIC
low complexity region	575	588	N/A	INTRINSIC
low complexity region	628	648	N/A	INTRINSIC
coiled coil region	765	805	N/A	INTRINSIC
low complexity region	846	856	N/A	INTRINSIC
low complexity region	944	963	N/A	INTRINSIC
low complexity region	1019	1034	N/A	INTRINSIC
low complexity region	1037	1061	N/A	INTRINSIC
low complexity region	1166	1179	N/A	INTRINSIC
low complexity region	1183	1206	N/A	INTRINSIC
low complexity region	1247	1268	N/A	INTRINSIC
low complexity region	1273	1285	N/A	INTRINSIC
coiled coil region	1353	1385	N/A	INTRINSIC
low complexity region	1455	1475	N/A	INTRINSIC
low complexity region	1487	1502	N/A	INTRINSIC
low complexity region	1505	1526	N/A	INTRINSIC
coiled coil region	1577	1604	N/A	INTRINSIC
low complexity region	1749	1760	N/A	INTRINSIC
low complexity region	1853	1864	N/A	INTRINSIC
low complexity region	1892	1901	N/A	INTRINSIC
low complexity region	1948	1958	N/A	INTRINSIC
low complexity region	2014	2024	N/A	INTRINSIC
low complexity region	2036	2050	N/A	INTRINSIC
low complexity region	2141	2158	N/A	INTRINSIC
low complexity region	2170	2188	N/A	INTRINSIC
low complexity region	2203	2215	N/A	INTRINSIC
low complexity region	2229	2242	N/A	INTRINSIC
low complexity region	2273	2284	N/A	INTRINSIC
low complexity region	2370	2388	N/A	INTRINSIC
low complexity region	2424	2434	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000127664

SMART Domains

Protein: ENSMUSP00000118564
Gene: ENSMUSG00000092329

Domain	Start	End	E-Value	Type
Pfam:Glycos_transf_2	104	287	7.4e-31	PFAM
Pfam:Glyco_transf_7C	261	331	4.9e-8	PFAM
RICIN	406	531	9.28e-27	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000172906

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211940

Predicted Effect

probably benign
Transcript: ENSMUST00000212050

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000212337

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000212728

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.0%

Validation Efficiency

98% (49/50)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This locus encodes an ankryin repeat domain-containing protein. The encoded protein inhibits ligand-dependent activation of transcription. Mutations in this gene have been associated with KBG syndrome, which is characterized by macrodontia, distinctive craniofacial features, short stature, skeletal anomalies, global developmental delay, seizures and intellectual disability. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 2 and X. [provided by RefSeq, Jan 2012]
PHENOTYPE: Mice homozygous for a spontaneous allele die by E9.5, are small and fail to turn. Mice heterozygous for a spontaneous allele exhibit craniofacial abnormalities, decreased weight, osteoporosis and osteopenia. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 48 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9930111J21Rik2	A	T	11: 48,910,108 (GRCm39)	L775*	probably null	Het
Abcb8	A	G	5: 24,605,619 (GRCm39)	S168G	probably benign	Het
Ahnak2	T	C	12: 112,740,992 (GRCm39)	I1027V	probably benign	Het
Alox12e	A	G	11: 70,210,668 (GRCm39)	L318P	probably damaging	Het
Anks1b	T	A	10: 89,869,078 (GRCm39)	I46N	probably damaging	Het
Apoa5	G	C	9: 46,180,415 (GRCm39)	W7S	probably damaging	Het
Arnt2	T	C	7: 83,993,009 (GRCm39)	H177R	probably null	Het
Cacna1c	T	C	6: 118,718,913 (GRCm39)	D220G	probably benign	Het
Dst	C	T	1: 34,307,975 (GRCm39)		probably benign	Het
Eml6	C	A	11: 29,753,137 (GRCm39)	V925L	probably benign	Het
Fbll1	G	A	11: 35,688,505 (GRCm39)	H253Y	possibly damaging	Het
Galnt1	A	G	18: 24,404,712 (GRCm39)	T350A	probably benign	Het
Gbp10	T	A	5: 105,372,324 (GRCm39)	E145D	possibly damaging	Het
Gfm1	T	C	3: 67,364,033 (GRCm39)	I503T	probably damaging	Het
Hmcn2	A	T	2: 31,226,624 (GRCm39)	K200*	probably null	Het
Ifi203	T	A	1: 173,757,040 (GRCm39)		probably benign	Het
Itgbl1	T	C	14: 124,204,090 (GRCm39)	F394L	probably damaging	Het
Itpkc	T	A	7: 26,927,029 (GRCm39)	D295V	possibly damaging	Het
Klra17	T	A	6: 129,850,328 (GRCm39)	I41F	probably benign	Het
Lcorl	A	T	5: 45,891,383 (GRCm39)	N323K	possibly damaging	Het
Ltbp2	A	T	12: 84,851,248 (GRCm39)	C836S	probably damaging	Het
Mfsd2b	A	G	12: 4,920,578 (GRCm39)	S80P	probably damaging	Het
Ms4a18	A	T	19: 10,988,863 (GRCm39)	H164Q	probably damaging	Het
Mybbp1a	A	G	11: 72,339,563 (GRCm39)	H882R	possibly damaging	Het
Myh9	G	A	15: 77,651,012 (GRCm39)	R1612C	probably damaging	Het
Myo18a	A	G	11: 77,736,441 (GRCm39)	D1514G	probably damaging	Het
Nsun2	T	C	13: 69,777,757 (GRCm39)	I441T	probably benign	Het
Ntng1	A	T	3: 109,842,007 (GRCm39)	D255E	probably damaging	Het
Or2y1	A	G	11: 49,386,287 (GRCm39)	D309G	possibly damaging	Het
Osbpl2	G	A	2: 179,803,353 (GRCm39)	R475H	probably damaging	Het
Pclo	A	C	5: 14,730,913 (GRCm39)	K3138N	unknown	Het
Pcsk7	A	G	9: 45,838,057 (GRCm39)	T572A	possibly damaging	Het
Pex11a	C	T	7: 79,389,918 (GRCm39)	R56H	possibly damaging	Het
Pnma8b	C	T	7: 16,680,521 (GRCm39)	H502Y	probably benign	Het
Saa4	T	A	7: 46,379,053 (GRCm39)	N96Y	possibly damaging	Het
Serpinb6d	T	A	13: 33,851,663 (GRCm39)	V140E	probably damaging	Het
Srsf4	C	T	4: 131,627,413 (GRCm39)		probably benign	Het
St18	G	A	1: 6,925,697 (GRCm39)		probably null	Het
Taf3	T	C	2: 9,956,469 (GRCm39)	E566G	possibly damaging	Het
Tnr	T	C	1: 159,750,983 (GRCm39)	S1315P	possibly damaging	Het
Trappc11	T	C	8: 47,967,138 (GRCm39)	E412G	probably damaging	Het
Trpc2	G	A	7: 101,733,711 (GRCm39)	S220N	probably damaging	Het
Trpm7	A	G	2: 126,693,441 (GRCm39)	V48A	probably damaging	Het
Tubb6	A	G	18: 67,535,121 (GRCm39)	Y340C	probably damaging	Het
Vmn1r197	C	A	13: 22,512,746 (GRCm39)	Y222*	probably null	Het
Vmn2r97	T	C	17: 19,148,413 (GRCm39)	S103P	probably damaging	Het
Zfp362	C	G	4: 128,680,682 (GRCm39)		probably benign	Het
Zfp423	A	G	8: 88,507,972 (GRCm39)	C666R	probably damaging	Het

Other mutations in Ankrd11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00949:Ankrd11	APN	8	123,635,467 (GRCm39)	missense	possibly damaging	0.59
IGL00971:Ankrd11	APN	8	123,622,092 (GRCm39)	missense	probably damaging	1.00
IGL01017:Ankrd11	APN	8	123,621,467 (GRCm39)	missense	probably damaging	1.00
IGL01137:Ankrd11	APN	8	123,611,075 (GRCm39)	missense	probably damaging	0.99
IGL01659:Ankrd11	APN	8	123,622,110 (GRCm39)	missense	probably damaging	1.00
IGL01920:Ankrd11	APN	8	123,642,636 (GRCm39)	splice site	probably benign
IGL01964:Ankrd11	APN	8	123,616,475 (GRCm39)	missense	probably damaging	0.97
IGL02131:Ankrd11	APN	8	123,621,149 (GRCm39)	missense	probably damaging	1.00
IGL02226:Ankrd11	APN	8	123,618,984 (GRCm39)	missense	probably damaging	1.00
IGL02549:Ankrd11	APN	8	123,618,032 (GRCm39)	missense	probably damaging	1.00
IGL02642:Ankrd11	APN	8	123,617,390 (GRCm39)	missense	probably damaging	1.00
IGL02643:Ankrd11	APN	8	123,619,061 (GRCm39)	missense	probably damaging	0.98
IGL02861:Ankrd11	APN	8	123,622,566 (GRCm39)	missense	probably damaging	0.99
IGL03086:Ankrd11	APN	8	123,621,249 (GRCm39)	missense	probably damaging	1.00
IGL03336:Ankrd11	APN	8	123,618,582 (GRCm39)	missense	probably benign	0.00
anchors	UTSW	8	123,622,509 (GRCm39)	missense	probably damaging	0.99
away	UTSW	8	123,618,692 (GRCm39)	missense	probably damaging	1.00
bluebell	UTSW	8	123,618,524 (GRCm39)	missense	probably damaging	0.97
Navy	UTSW	8	123,635,473 (GRCm39)	nonsense	probably null
BB001:Ankrd11	UTSW	8	123,622,641 (GRCm39)	missense	possibly damaging	0.95
BB011:Ankrd11	UTSW	8	123,622,641 (GRCm39)	missense	possibly damaging	0.95
R0051:Ankrd11	UTSW	8	123,616,481 (GRCm39)	missense	probably damaging	1.00
R0051:Ankrd11	UTSW	8	123,616,481 (GRCm39)	missense	probably damaging	1.00
R0110:Ankrd11	UTSW	8	123,618,914 (GRCm39)	missense	possibly damaging	0.95
R0281:Ankrd11	UTSW	8	123,622,307 (GRCm39)	missense	probably benign	0.01
R0450:Ankrd11	UTSW	8	123,618,914 (GRCm39)	missense	possibly damaging	0.95
R0481:Ankrd11	UTSW	8	123,626,775 (GRCm39)	missense	probably damaging	1.00
R0542:Ankrd11	UTSW	8	123,622,509 (GRCm39)	missense	probably damaging	0.99
R0606:Ankrd11	UTSW	8	123,619,571 (GRCm39)	missense	probably benign	0.04
R0702:Ankrd11	UTSW	8	123,616,505 (GRCm39)	missense	probably damaging	1.00
R0730:Ankrd11	UTSW	8	123,618,692 (GRCm39)	missense	probably damaging	1.00
R0737:Ankrd11	UTSW	8	123,622,575 (GRCm39)	missense	probably damaging	0.99
R1401:Ankrd11	UTSW	8	123,619,789 (GRCm39)	missense	probably benign	0.23
R1464:Ankrd11	UTSW	8	123,619,463 (GRCm39)	missense	probably damaging	1.00
R1464:Ankrd11	UTSW	8	123,619,463 (GRCm39)	missense	probably damaging	1.00
R1470:Ankrd11	UTSW	8	123,626,463 (GRCm39)	missense	probably damaging	0.98
R1470:Ankrd11	UTSW	8	123,626,463 (GRCm39)	missense	probably damaging	0.98
R1641:Ankrd11	UTSW	8	123,618,485 (GRCm39)	missense	probably benign	0.03
R1950:Ankrd11	UTSW	8	123,616,608 (GRCm39)	missense	probably damaging	1.00
R2004:Ankrd11	UTSW	8	123,629,161 (GRCm39)	critical splice donor site	probably null
R2401:Ankrd11	UTSW	8	123,635,473 (GRCm39)	nonsense	probably null
R2425:Ankrd11	UTSW	8	123,619,902 (GRCm39)	missense	possibly damaging	0.86
R2830:Ankrd11	UTSW	8	123,618,935 (GRCm39)	missense	probably damaging	1.00
R2910:Ankrd11	UTSW	8	123,635,537 (GRCm39)	missense	probably damaging	1.00
R2911:Ankrd11	UTSW	8	123,635,537 (GRCm39)	missense	probably damaging	1.00
R3736:Ankrd11	UTSW	8	123,618,524 (GRCm39)	missense	probably damaging	0.97
R3738:Ankrd11	UTSW	8	123,623,454 (GRCm39)	unclassified	probably benign
R3813:Ankrd11	UTSW	8	123,618,117 (GRCm39)	missense	probably benign
R4012:Ankrd11	UTSW	8	123,619,156 (GRCm39)	missense	probably damaging	0.98
R4183:Ankrd11	UTSW	8	123,626,415 (GRCm39)	missense	possibly damaging	0.88
R4213:Ankrd11	UTSW	8	123,617,765 (GRCm39)	missense	probably benign	0.00
R4469:Ankrd11	UTSW	8	123,623,326 (GRCm39)	missense	probably damaging	1.00
R4482:Ankrd11	UTSW	8	123,620,228 (GRCm39)	missense	probably damaging	1.00
R4935:Ankrd11	UTSW	8	123,626,922 (GRCm39)	missense	probably benign	0.02
R4940:Ankrd11	UTSW	8	123,616,560 (GRCm39)	missense	probably damaging	1.00
R5145:Ankrd11	UTSW	8	123,617,943 (GRCm39)	utr 3 prime	probably benign
R5154:Ankrd11	UTSW	8	123,619,878 (GRCm39)	missense	probably damaging	1.00
R5230:Ankrd11	UTSW	8	123,617,216 (GRCm39)	missense	probably benign	0.11
R5283:Ankrd11	UTSW	8	123,610,921 (GRCm39)	missense	probably damaging	1.00
R5377:Ankrd11	UTSW	8	123,620,453 (GRCm39)	splice site	probably null
R5513:Ankrd11	UTSW	8	123,619,259 (GRCm39)	missense	probably benign	0.38
R5518:Ankrd11	UTSW	8	123,617,733 (GRCm39)	missense	possibly damaging	0.93
R5549:Ankrd11	UTSW	8	123,617,117 (GRCm39)	missense	probably benign	0.02
R5579:Ankrd11	UTSW	8	123,610,970 (GRCm39)	missense	probably damaging	0.97
R5595:Ankrd11	UTSW	8	123,621,043 (GRCm39)	nonsense	probably null
R5650:Ankrd11	UTSW	8	123,614,136 (GRCm39)	missense	probably damaging	0.99
R5717:Ankrd11	UTSW	8	123,619,377 (GRCm39)	missense	possibly damaging	0.92
R5753:Ankrd11	UTSW	8	123,622,043 (GRCm39)	missense	possibly damaging	0.90
R5782:Ankrd11	UTSW	8	123,626,756 (GRCm39)	missense	probably damaging	1.00
R5812:Ankrd11	UTSW	8	123,620,544 (GRCm39)	splice site	probably null
R5823:Ankrd11	UTSW	8	123,622,529 (GRCm39)	missense	probably benign	0.12
R5900:Ankrd11	UTSW	8	123,617,805 (GRCm39)	missense	probably benign	0.00
R5975:Ankrd11	UTSW	8	123,616,488 (GRCm39)	missense	possibly damaging	0.93
R5979:Ankrd11	UTSW	8	123,619,139 (GRCm39)	missense	probably damaging	1.00
R6000:Ankrd11	UTSW	8	123,617,934 (GRCm39)	missense	possibly damaging	0.73
R6145:Ankrd11	UTSW	8	123,619,400 (GRCm39)	missense	probably damaging	1.00
R6252:Ankrd11	UTSW	8	123,620,561 (GRCm39)	missense	possibly damaging	0.87
R6302:Ankrd11	UTSW	8	123,616,728 (GRCm39)	missense	probably benign
R6457:Ankrd11	UTSW	8	123,635,503 (GRCm39)	missense	probably damaging	1.00
R6513:Ankrd11	UTSW	8	123,616,919 (GRCm39)	missense	probably benign	0.02
R6582:Ankrd11	UTSW	8	123,618,368 (GRCm39)	missense	probably benign	0.00
R6738:Ankrd11	UTSW	8	123,618,660 (GRCm39)	missense	probably damaging	0.99
R6865:Ankrd11	UTSW	8	123,621,683 (GRCm39)	missense	probably benign	0.41
R6913:Ankrd11	UTSW	8	123,621,650 (GRCm39)	missense	probably benign	0.01
R7101:Ankrd11	UTSW	8	123,622,194 (GRCm39)	missense	probably benign	0.35
R7116:Ankrd11	UTSW	8	123,622,869 (GRCm39)	missense	probably damaging	1.00
R7477:Ankrd11	UTSW	8	123,621,124 (GRCm39)	missense	possibly damaging	0.91
R7534:Ankrd11	UTSW	8	123,621,149 (GRCm39)	missense	probably damaging	1.00
R7555:Ankrd11	UTSW	8	123,614,145 (GRCm39)	missense	probably damaging	0.99
R7627:Ankrd11	UTSW	8	123,617,690 (GRCm39)	missense	possibly damaging	0.63
R7658:Ankrd11	UTSW	8	123,620,403 (GRCm39)	missense	probably benign
R7721:Ankrd11	UTSW	8	123,621,498 (GRCm39)	missense	probably damaging	1.00
R7731:Ankrd11	UTSW	8	123,622,172 (GRCm39)	missense	probably benign	0.12
R7792:Ankrd11	UTSW	8	123,610,970 (GRCm39)	missense	probably damaging	0.97
R7924:Ankrd11	UTSW	8	123,622,641 (GRCm39)	missense	possibly damaging	0.95
R7939:Ankrd11	UTSW	8	123,617,812 (GRCm39)	missense	probably damaging	1.00
R8022:Ankrd11	UTSW	8	123,614,332 (GRCm39)	missense	probably damaging	1.00
R8222:Ankrd11	UTSW	8	123,622,347 (GRCm39)	missense	probably damaging	0.98
R8362:Ankrd11	UTSW	8	123,618,797 (GRCm39)	missense	probably damaging	0.96
R8430:Ankrd11	UTSW	8	123,620,105 (GRCm39)	missense	probably benign	0.01
R8511:Ankrd11	UTSW	8	123,626,468 (GRCm39)	missense
R8726:Ankrd11	UTSW	8	123,620,765 (GRCm39)	missense	possibly damaging	0.90
R8888:Ankrd11	UTSW	8	123,621,014 (GRCm39)	missense	possibly damaging	0.87
R8895:Ankrd11	UTSW	8	123,621,014 (GRCm39)	missense	possibly damaging	0.87
R8928:Ankrd11	UTSW	8	123,622,718 (GRCm39)	missense	probably damaging	0.99
R8930:Ankrd11	UTSW	8	123,622,718 (GRCm39)	missense	probably damaging	0.99
R8931:Ankrd11	UTSW	8	123,622,718 (GRCm39)	missense	probably damaging	0.99
R8936:Ankrd11	UTSW	8	123,621,840 (GRCm39)	missense	possibly damaging	0.69
R9018:Ankrd11	UTSW	8	123,622,251 (GRCm39)	missense	probably damaging	1.00
R9113:Ankrd11	UTSW	8	123,614,072 (GRCm39)	missense	possibly damaging	0.60
R9399:Ankrd11	UTSW	8	123,618,179 (GRCm39)	missense	probably benign
R9644:Ankrd11	UTSW	8	123,617,682 (GRCm39)	missense	probably benign	0.00
R9645:Ankrd11	UTSW	8	123,617,682 (GRCm39)	missense	probably benign	0.00
R9647:Ankrd11	UTSW	8	123,617,682 (GRCm39)	missense	probably benign	0.00
R9683:Ankrd11	UTSW	8	123,617,682 (GRCm39)	missense	probably benign	0.00
RF019:Ankrd11	UTSW	8	123,623,373 (GRCm39)	missense	probably damaging	1.00
Z1176:Ankrd11	UTSW	8	123,622,542 (GRCm39)	missense	possibly damaging	0.68
Z1177:Ankrd11	UTSW	8	123,626,881 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TATGTAGACACTGCACGGTGC -3'
(R):5'- CGTGACCTGCTTGTCAAAGG -3'

Sequencing Primer
(F):5'- GGCCAGGCAGCACAGAG -3'
(R):5'- TGCTTGTCAAAGGGACCC -3'

Posted On

2015-03-18