Mutagenetix > Incidental Mutations

Incidental Mutation 'R2136:Ankhd1'

235851

Institutional Source

Beutler Lab

Gene Symbol

Ankhd1

Ensembl Gene

ENSMUSG00000024483

Gene Name

ankyrin repeat and KH domain containing 1

Synonyms

MMRRC Submission

040139-MU

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2136 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

36559987-36665917 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 36647621 bp

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 1909 (T1909A)

Ref Sequence

ENSEMBL: ENSMUSP00000123270 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000006205] [ENSMUST00000142977] [ENSMUST00000155329]

Predicted Effect

probably benign
Transcript: ENSMUST00000006205
AA Change: T1909A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000006205
Gene: ENSMUSG00000024483
AA Change: T1909A

Domain	Start	End	E-Value	Type
low complexity region	20	38	N/A	INTRINSIC
low complexity region	48	78	N/A	INTRINSIC
low complexity region	91	109	N/A	INTRINSIC
ANK	207	236	2.11e2	SMART
ANK	240	269	3.31e-1	SMART
ANK	274	303	5.24e-4	SMART
ANK	307	336	7.64e-6	SMART
ANK	340	369	2.7e-6	SMART
ANK	374	403	3.23e-4	SMART
ANK	407	436	1.61e-4	SMART
ANK	440	469	5.16e-3	SMART
ANK	473	502	4.16e-7	SMART
ANK	507	536	1.68e-2	SMART
ANK	537	566	7.02e-5	SMART
ANK	570	599	7.95e-4	SMART
ANK	603	632	4.56e-4	SMART
ANK	637	666	9.64e-3	SMART
ANK	670	699	6.71e-2	SMART
coiled coil region	815	855	N/A	INTRINSIC
ANK	1057	1086	2.07e-2	SMART
ANK	1090	1119	2.48e-5	SMART
ANK	1124	1153	3.85e-2	SMART
ANK	1157	1186	1.61e-4	SMART
ANK	1192	1221	1.24e-5	SMART
ANK	1226	1255	1.59e-3	SMART
ANK	1259	1288	3.91e-3	SMART
ANK	1294	1323	5.93e-3	SMART
ANK	1327	1356	9.41e-6	SMART
ANK	1360	1393	3.8e-1	SMART
coiled coil region	1422	1486	N/A	INTRINSIC
low complexity region	1509	1526	N/A	INTRINSIC
low complexity region	1538	1557	N/A	INTRINSIC
low complexity region	1585	1604	N/A	INTRINSIC
KH	1693	1763	5.04e-13	SMART
low complexity region	1968	2001	N/A	INTRINSIC
low complexity region	2041	2057	N/A	INTRINSIC
low complexity region	2064	2081	N/A	INTRINSIC
low complexity region	2334	2346	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000037072
AA Change: T398A

SMART Domains

Protein: ENSMUSP00000040300
Gene: ENSMUSG00000024483
AA Change: T398A

Domain	Start	End	E-Value	Type
low complexity region	1	16	N/A	INTRINSIC
low complexity region	28	47	N/A	INTRINSIC
low complexity region	75	94	N/A	INTRINSIC
KH	183	253	5.04e-13	SMART
low complexity region	458	491	N/A	INTRINSIC
low complexity region	531	547	N/A	INTRINSIC
low complexity region	554	571	N/A	INTRINSIC
low complexity region	824	836	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000130035

SMART Domains

Protein: ENSMUSP00000117110
Gene: ENSMUSG00000024483

Domain	Start	End	E-Value	Type
ANK	2	26	5.35e2	SMART
ANK	30	59	9.41e-6	SMART
ANK	63	96	3.8e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000140061

SMART Domains

Protein: ENSMUSP00000121811
Gene: ENSMUSG00000024483

Domain	Start	End	E-Value	Type
low complexity region	54	70	N/A	INTRINSIC
low complexity region	77	94	N/A	INTRINSIC
low complexity region	355	375	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000142977
AA Change: T1909A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000120290
Gene: ENSMUSG00000024483
AA Change: T1909A

Domain	Start	End	E-Value	Type
low complexity region	20	38	N/A	INTRINSIC
low complexity region	48	78	N/A	INTRINSIC
low complexity region	91	109	N/A	INTRINSIC
ANK	207	236	2.11e2	SMART
ANK	240	269	3.31e-1	SMART
ANK	274	303	5.24e-4	SMART
ANK	307	336	7.64e-6	SMART
ANK	340	369	2.7e-6	SMART
ANK	374	403	3.23e-4	SMART
ANK	407	436	1.61e-4	SMART
ANK	440	469	5.16e-3	SMART
ANK	473	502	4.16e-7	SMART
ANK	507	536	1.68e-2	SMART
ANK	537	566	7.02e-5	SMART
ANK	570	599	7.95e-4	SMART
ANK	603	632	4.56e-4	SMART
ANK	637	666	9.64e-3	SMART
ANK	670	699	6.71e-2	SMART
coiled coil region	815	855	N/A	INTRINSIC
ANK	1057	1086	2.07e-2	SMART
ANK	1090	1119	2.48e-5	SMART
ANK	1124	1153	3.85e-2	SMART
ANK	1157	1186	1.61e-4	SMART
ANK	1192	1221	1.24e-5	SMART
ANK	1226	1255	1.59e-3	SMART
ANK	1259	1288	3.91e-3	SMART
ANK	1294	1323	5.93e-3	SMART
ANK	1327	1356	9.41e-6	SMART
ANK	1360	1393	3.8e-1	SMART
coiled coil region	1422	1486	N/A	INTRINSIC
low complexity region	1509	1526	N/A	INTRINSIC
low complexity region	1538	1557	N/A	INTRINSIC
low complexity region	1585	1604	N/A	INTRINSIC
KH	1693	1763	5.04e-13	SMART
low complexity region	1968	2001	N/A	INTRINSIC
low complexity region	2041	2057	N/A	INTRINSIC
low complexity region	2064	2081	N/A	INTRINSIC
low complexity region	2334	2346	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152940

Predicted Effect

probably benign
Transcript: ENSMUST00000153612

SMART Domains

Protein: ENSMUSP00000116462
Gene: ENSMUSG00000024483

Domain	Start	End	E-Value	Type
ANK	10	39	9.41e-6	SMART
ANK	43	76	3.8e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000155329
AA Change: T1909A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000123270
Gene: ENSMUSG00000024483
AA Change: T1909A

Domain	Start	End	E-Value	Type
low complexity region	20	38	N/A	INTRINSIC
low complexity region	48	78	N/A	INTRINSIC
low complexity region	91	109	N/A	INTRINSIC
ANK	207	236	2.11e2	SMART
ANK	240	269	3.31e-1	SMART
ANK	274	303	5.24e-4	SMART
ANK	307	336	7.64e-6	SMART
ANK	340	369	2.7e-6	SMART
ANK	374	403	3.23e-4	SMART
ANK	407	436	1.61e-4	SMART
ANK	440	469	5.16e-3	SMART
ANK	473	502	4.16e-7	SMART
ANK	507	536	1.68e-2	SMART
ANK	537	566	7.02e-5	SMART
ANK	570	599	7.95e-4	SMART
ANK	603	632	4.56e-4	SMART
ANK	637	666	9.64e-3	SMART
ANK	670	699	6.71e-2	SMART
coiled coil region	815	855	N/A	INTRINSIC
ANK	1057	1086	2.07e-2	SMART
ANK	1090	1119	2.48e-5	SMART
ANK	1124	1153	3.85e-2	SMART
ANK	1157	1186	1.61e-4	SMART
ANK	1192	1221	1.24e-5	SMART
ANK	1226	1255	1.59e-3	SMART
ANK	1259	1288	3.91e-3	SMART
ANK	1294	1323	5.93e-3	SMART
ANK	1327	1356	9.41e-6	SMART
ANK	1360	1393	3.8e-1	SMART
coiled coil region	1422	1486	N/A	INTRINSIC
low complexity region	1509	1526	N/A	INTRINSIC
low complexity region	1538	1557	N/A	INTRINSIC
low complexity region	1585	1604	N/A	INTRINSIC
KH	1693	1763	5.04e-13	SMART
low complexity region	1968	2001	N/A	INTRINSIC
low complexity region	2041	2057	N/A	INTRINSIC
low complexity region	2064	2081	N/A	INTRINSIC
low complexity region	2342	2362	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.6%
20x: 95.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210010C04Rik	A	G	6: 41,035,462	F6S	probably benign	Het
2810474O19Rik	T	A	6: 149,328,822	I1122K	probably benign	Het
A930003A15Rik	T	G	16: 19,883,780		noncoding transcript	Het
Abca5	T	C	11: 110,319,832	T174A	probably benign	Het
Abcg3	G	A	5: 104,966,814	S279L	probably benign	Het
Acap3	T	C	4: 155,896,912	L85P	probably damaging	Het
Adgrl3	A	G	5: 81,512,254	K290R	probably damaging	Het
Asap1	T	C	15: 64,110,959	D832G	probably damaging	Het
Atp6v0a2	T	A	5: 124,718,488	L702Q	possibly damaging	Het
Bsn	A	G	9: 108,113,231	V1774A	probably damaging	Het
Cd209e	T	C	8: 3,853,248	E48G	probably benign	Het
Cdadc1	T	C	14: 59,568,044		probably null	Het
Cfap65	C	CA	1: 74,917,273		probably null	Het
Cln3	A	C	7: 126,582,799	S30R	probably benign	Het
Cluap1	C	T	16: 3,933,772	R332W	probably damaging	Het
Crb1	A	T	1: 139,337,425	V85E	probably benign	Het
Crocc	G	A	4: 141,032,954	R789W	probably damaging	Het
Cwh43	A	G	5: 73,415,054	I212V	probably benign	Het
Cyp2t4	C	A	7: 27,158,160	F391L	probably benign	Het
Dhx35	G	T	2: 158,831,861	R404L	probably damaging	Het
Disp1	A	G	1: 183,088,378	L826S	probably damaging	Het
Dync2h1	T	A	9: 7,122,772	E2061D	probably damaging	Het
Ep300	T	A	15: 81,640,447	Y1393N	unknown	Het
Fap	C	T	2: 62,524,207	G446D	possibly damaging	Het
Fat3	A	G	9: 16,377,051	I392T	probably benign	Het
Fpr-rs4	CAGGAA	CA	17: 18,022,334		probably null	Het
Glipr1l1	T	C	10: 112,060,476	V56A	probably damaging	Het
Grsf1	A	G	5: 88,672,658	V7A	probably benign	Het
Hmcn1	G	A	1: 150,633,659	A3646V	probably damaging	Het
Ipo9	A	T	1: 135,394,285	I569N	probably damaging	Het
Irs1	G	T	1: 82,290,042	P151Q	probably damaging	Het
Kalrn	T	C	16: 34,307,724	D491G	possibly damaging	Het
Kctd7	T	C	5: 130,152,366	L210P	probably damaging	Het
Lifr	C	A	15: 7,181,857	D625E	possibly damaging	Het
Lrguk	T	C	6: 34,043,519	V201A	probably benign	Het
Mark1	A	G	1: 184,919,573	V135A	probably damaging	Het
Mical2	T	A	7: 112,271,515	D70E	possibly damaging	Het
Mrc1	T	C	2: 14,270,189	Y434H	probably damaging	Het
Myh10	C	A	11: 68,804,714	Q1556K	probably damaging	Het
Nav1	G	A	1: 135,454,436	T1400I	probably null	Het
Olfr1173	T	C	2: 88,274,240	K270E	probably damaging	Het
Olfr1178	T	A	2: 88,391,319	I24N	probably benign	Het
Olfr1289	T	C	2: 111,483,616	V62A	probably damaging	Het
Olfr13	A	G	6: 43,174,501	K172E	probably benign	Het
Olfr142	A	C	2: 90,252,253	V245G	probably damaging	Het
Olfr339	A	G	2: 36,421,938	D180G	probably damaging	Het
Olfr513	G	A	7: 108,755,223	M122I	possibly damaging	Het
Osmr	T	A	15: 6,852,462	Q67L	probably damaging	Het
Pan2	T	G	10: 128,313,637	V522G	possibly damaging	Het
Pard3	T	G	8: 127,376,885		probably null	Het
Pcdhgc5	G	T	18: 37,820,113	A147S	possibly damaging	Het
Pcsk9	T	C	4: 106,446,770	I506V	probably benign	Het
Polr3d	GCCCCC	GCCCC	14: 70,443,047		probably null	Het
Prdm4	G	A	10: 85,893,351	R731*	probably null	Het
Prdx6b	T	A	2: 80,293,163	D105E	probably damaging	Het
Rab42	A	G	4: 132,302,479	L144P	probably damaging	Het
Ralbp1	T	A	17: 65,864,666	K104M	probably damaging	Het
Rrp12	A	G	19: 41,892,599	V131A	probably damaging	Het
Sbno1	C	T	5: 124,387,534		probably null	Het
Sbno2	A	T	10: 80,062,693	I645N	probably damaging	Het
Scfd2	T	C	5: 74,206,367	K624R	probably benign	Het
Sgk2	C	A	2: 162,999,179		probably null	Het
Sirt4	A	G	5: 115,479,701	S299P	probably benign	Het
Slit2	C	T	5: 48,304,225	A1521V	probably benign	Het
Socs7	T	G	11: 97,373,107	V275G	possibly damaging	Het
Spink11	G	A	18: 44,190,487	P102S	probably benign	Het
Tacc3	A	G	5: 33,671,404	N534D	probably damaging	Het
Tas2r115	T	C	6: 132,737,346	Y214C	probably damaging	Het
Tcaf1	A	T	6: 42,673,520	M875K	probably benign	Het
Ttc22	T	A	4: 106,622,672	L41Q	possibly damaging	Het
Ttc37	T	C	13: 76,173,354	S1322P	possibly damaging	Het
Vasn	T	A	16: 4,649,795	C535*	probably null	Het
Vcan	T	A	13: 89,689,737	I2563F	probably damaging	Het
Vmn2r63	T	G	7: 42,926,873	Q505H	probably damaging	Het
Vmn2r65	T	G	7: 84,943,573	Q475H	probably damaging	Het
Zbtb43	T	C	2: 33,454,520	Y231C	probably damaging	Het
Zfp292	A	G	4: 34,810,266	V931A	probably benign	Het

Other mutations in Ankhd1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00088:Ankhd1	APN	18	36665459	unclassified	probably benign
IGL00927:Ankhd1	APN	18	36632072	missense	probably benign	0.01
IGL01367:Ankhd1	APN	18	36578643	missense	probably benign	0.16
IGL01624:Ankhd1	APN	18	36658013	missense	probably damaging	1.00
IGL01725:Ankhd1	APN	18	36648153	missense	probably benign	0.04
IGL01767:Ankhd1	APN	18	36648374	missense	probably damaging	1.00
IGL02005:Ankhd1	APN	18	36648426	missense	probably damaging	1.00
IGL02009:Ankhd1	APN	18	36624661	missense	probably damaging	1.00
IGL02246:Ankhd1	APN	18	36656726	missense	probably damaging	1.00
IGL02336:Ankhd1	APN	18	36594814	missense	probably damaging	0.97
IGL02628:Ankhd1	APN	18	36647703	missense	probably benign	0.00
IGL02644:Ankhd1	APN	18	36578775	critical splice donor site	probably null
IGL02735:Ankhd1	APN	18	36648546	missense	probably benign	0.00
IGL02877:Ankhd1	APN	18	36594823	missense	probably damaging	1.00
IGL03129:Ankhd1	APN	18	36658008	nonsense	probably null
IGL03163:Ankhd1	APN	18	36647628	missense	probably damaging	0.97
IGL03182:Ankhd1	APN	18	36578774	missense	probably benign	0.06
IGL03184:Ankhd1	APN	18	36647777	missense	probably damaging	1.00
IGL03398:Ankhd1	APN	18	36656837	splice site	probably benign
FR4304:Ankhd1	UTSW	18	36560924	small insertion	probably benign
R0051:Ankhd1	UTSW	18	36647188	unclassified	probably benign
R0089:Ankhd1	UTSW	18	36640356	missense	probably damaging	0.99
R0105:Ankhd1	UTSW	18	36646766	missense	probably damaging	1.00
R0149:Ankhd1	UTSW	18	36647214	missense	probably damaging	1.00
R0243:Ankhd1	UTSW	18	36634734	missense	probably damaging	1.00
R0322:Ankhd1	UTSW	18	36658008	nonsense	probably null
R0361:Ankhd1	UTSW	18	36647214	missense	probably damaging	1.00
R0389:Ankhd1	UTSW	18	36644599	missense	possibly damaging	0.48
R0418:Ankhd1	UTSW	18	36634300	missense	probably damaging	1.00
R0443:Ankhd1	UTSW	18	36644599	missense	possibly damaging	0.48
R0540:Ankhd1	UTSW	18	36640280	missense	probably damaging	1.00
R0607:Ankhd1	UTSW	18	36640280	missense	probably damaging	1.00
R0738:Ankhd1	UTSW	18	36645249	splice site	probably benign
R1127:Ankhd1	UTSW	18	36634346	missense	probably damaging	1.00
R1434:Ankhd1	UTSW	18	36625159	missense	probably benign	0.09
R1742:Ankhd1	UTSW	18	36625265	missense	probably damaging	1.00
R1776:Ankhd1	UTSW	18	36647308	missense	probably benign	0.17
R1856:Ankhd1	UTSW	18	36644527	missense	probably benign	0.00
R1923:Ankhd1	UTSW	18	36648030	missense	probably benign	0.08
R2044:Ankhd1	UTSW	18	36645113	missense	probably benign	0.31
R2112:Ankhd1	UTSW	18	36641626	missense	probably damaging	1.00
R2115:Ankhd1	UTSW	18	36634308	missense	probably damaging	1.00
R2196:Ankhd1	UTSW	18	36648379	missense	probably damaging	1.00
R2291:Ankhd1	UTSW	18	36644333	missense	probably benign	0.31
R2305:Ankhd1	UTSW	18	36642926	missense	possibly damaging	0.59
R2309:Ankhd1	UTSW	18	36624765	missense	probably damaging	1.00
R2519:Ankhd1	UTSW	18	36578543	intron	probably null
R2958:Ankhd1	UTSW	18	36634729	missense	probably damaging	1.00
R3978:Ankhd1	UTSW	18	36647613	missense	probably damaging	0.96
R3980:Ankhd1	UTSW	18	36647613	missense	probably damaging	0.96
R4159:Ankhd1	UTSW	18	36589540	missense	possibly damaging	0.91
R4199:Ankhd1	UTSW	18	36661048	unclassified	probably benign
R4323:Ankhd1	UTSW	18	36578633	missense	probably damaging	1.00
R4356:Ankhd1	UTSW	18	36643043	nonsense	probably null
R4496:Ankhd1	UTSW	18	36560786	missense	probably damaging	0.98
R4551:Ankhd1	UTSW	18	36655507	unclassified	probably null
R4590:Ankhd1	UTSW	18	36583644	missense	probably damaging	1.00
R4667:Ankhd1	UTSW	18	36648021	missense	possibly damaging	0.77
R4889:Ankhd1	UTSW	18	36578734	missense	probably null	0.00
R4923:Ankhd1	UTSW	18	36589452	missense	probably damaging	1.00
R5091:Ankhd1	UTSW	18	36625027	missense	possibly damaging	0.68
R5254:Ankhd1	UTSW	18	36656715	missense	probably benign	0.05
R5314:Ankhd1	UTSW	18	36561058	splice site	probably null
R5336:Ankhd1	UTSW	18	36646716	missense	probably damaging	1.00
R5367:Ankhd1	UTSW	18	36589408	missense	probably damaging	1.00
R5384:Ankhd1	UTSW	18	36591495	missense	probably damaging	1.00
R5385:Ankhd1	UTSW	18	36591495	missense	probably damaging	1.00
R5387:Ankhd1	UTSW	18	36634644	missense	probably damaging	1.00
R5458:Ankhd1	UTSW	18	36648485	missense	probably benign	0.01
R5599:Ankhd1	UTSW	18	36560807	missense	probably damaging	0.98
R5659:Ankhd1	UTSW	18	36561050	missense	probably damaging	1.00
R5750:Ankhd1	UTSW	18	36624902	missense	probably benign	0.00
R5874:Ankhd1	UTSW	18	36640269	missense	possibly damaging	0.92
R5894:Ankhd1	UTSW	18	36647524	missense	probably damaging	0.99
R5969:Ankhd1	UTSW	18	36600834	missense	probably damaging	1.00
R6133:Ankhd1	UTSW	18	36625126	missense	possibly damaging	0.77
R6190:Ankhd1	UTSW	18	36611809	missense	possibly damaging	0.84
R6247:Ankhd1	UTSW	18	36654146	missense	probably benign	0.00
R6512:Ankhd1	UTSW	18	36591456	missense	probably damaging	1.00
R6649:Ankhd1	UTSW	18	36600783	unclassified	probably null
R6653:Ankhd1	UTSW	18	36600783	unclassified	probably null
R6763:Ankhd1	UTSW	18	36642969	missense	probably benign	0.31
R6976:Ankhd1	UTSW	18	36648254	missense	probably benign	0.00
R7075:Ankhd1	UTSW	18	36559989	missense
R7208:Ankhd1	UTSW	18	36625028	missense	probably benign
R7305:Ankhd1	UTSW	18	36632205	missense
R7615:Ankhd1	UTSW	18	36656773	missense
R7654:Ankhd1	UTSW	18	36594101	missense	probably damaging	1.00
R7781:Ankhd1	UTSW	18	36625205	missense	probably damaging	1.00
RF001:Ankhd1	UTSW	18	36560921	small insertion	probably benign
RF004:Ankhd1	UTSW	18	36560910	small insertion	probably benign
RF007:Ankhd1	UTSW	18	36560909	small insertion	probably benign
RF008:Ankhd1	UTSW	18	36560924	small insertion	probably benign
RF009:Ankhd1	UTSW	18	36560922	small insertion	probably benign
RF013:Ankhd1	UTSW	18	36560926	small insertion	probably benign
RF016:Ankhd1	UTSW	18	36560909	small insertion	probably benign
RF016:Ankhd1	UTSW	18	36560910	small insertion	probably benign
RF017:Ankhd1	UTSW	18	36560909	small insertion	probably benign
RF018:Ankhd1	UTSW	18	36560912	small insertion	probably benign
RF026:Ankhd1	UTSW	18	36560912	small insertion	probably benign
RF030:Ankhd1	UTSW	18	36560913	small insertion	probably benign
RF030:Ankhd1	UTSW	18	36560927	small insertion	probably benign
RF039:Ankhd1	UTSW	18	36560918	small insertion	probably benign
RF043:Ankhd1	UTSW	18	36560917	small insertion	probably benign
RF046:Ankhd1	UTSW	18	36560926	small insertion	probably benign
RF047:Ankhd1	UTSW	18	36560917	small insertion	probably benign
RF047:Ankhd1	UTSW	18	36560923	small insertion	probably benign
RF049:Ankhd1	UTSW	18	36560923	small insertion	probably benign
RF050:Ankhd1	UTSW	18	36560927	small insertion	probably benign
RF054:Ankhd1	UTSW	18	36560929	small insertion	probably benign
RF057:Ankhd1	UTSW	18	36560929	small insertion	probably benign
RF060:Ankhd1	UTSW	18	36560922	small insertion	probably benign
RF061:Ankhd1	UTSW	18	36560921	small insertion	probably benign
RF062:Ankhd1	UTSW	18	36560918	small insertion	probably benign
X0027:Ankhd1	UTSW	18	36624832	missense	probably damaging	1.00
X0065:Ankhd1	UTSW	18	36578764	nonsense	probably null
X0066:Ankhd1	UTSW	18	36646704	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCCAACAAATGTACGCTCTC -3'
(R):5'- GGTCTTAGGCACACAAGCAAAC -3'

Sequencing Primer
(F):5'- GCCAACAAATGTACGCTCTCCTTTC -3'
(R):5'- CAACTGCTTTCTGACGGATGAAG -3'

Posted On

2014-10-01