Mutagenetix > Incidental Mutation

Incidental Mutation 'R0724:Ank2'

262003

Institutional Source

Beutler Lab

Gene Symbol

Ank2

Ensembl Gene

ENSMUSG00000032826

Gene Name

ankyrin 2, brain

Synonyms

Ankyrin-B, Ank-2, Ankyrin-2, Gm4392, ankyrin B

MMRRC Submission

038906-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0724 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

126921612-127499350 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 126962337 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Histidine at position 1077 (R1077H)

Ref Sequence

ENSEMBL: ENSMUSP00000138251 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044443] [ENSMUST00000182064] [ENSMUST00000182078] [ENSMUST00000182711] [ENSMUST00000182959] [ENSMUST00000211813]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000044443
AA Change: R227H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000043765
Gene: ENSMUSG00000032826
AA Change: R227H

Domain	Start	End	E-Value	Type
low complexity region	9	22	N/A	INTRINSIC
low complexity region	57	69	N/A	INTRINSIC
ZU5	128	232	4.13e-61	SMART
Pfam:ZU5	289	374	2.8e-8	PFAM
low complexity region	587	597	N/A	INTRINSIC
DEATH	603	697	1.52e-27	SMART
low complexity region	732	748	N/A	INTRINSIC
low complexity region	860	873	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000182064
AA Change: R1098H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000138620
Gene: ENSMUSG00000032826
AA Change: R1098H

Domain	Start	End	E-Value	Type
ANK	9	38	1e1	SMART
ANK	42	71	8.9e-7	SMART
ANK	75	104	4.4e-9	SMART
ANK	108	137	2.8e-9	SMART
ANK	141	169	5.3e-1	SMART
ANK	170	199	7.3e-1	SMART
ANK	211	240	1.1e-7	SMART
ANK	244	273	4.4e-9	SMART
ANK	277	306	9.3e-8	SMART
ANK	310	339	2.1e-8	SMART
ANK	343	372	1.3e-7	SMART
ANK	376	405	6.2e-9	SMART
ANK	409	438	1.1e-7	SMART
ANK	442	471	2.9e-8	SMART
ANK	475	504	1.1e-5	SMART
ANK	508	537	6.5e-6	SMART
ANK	541	570	2.3e-7	SMART
ANK	574	603	2.4e-7	SMART
ANK	607	636	3.2e-9	SMART
ANK	640	669	5.5e-5	SMART
ANK	673	702	1.9e-8	SMART
ANK	706	735	3.3e-9	SMART
low complexity region	755	775	N/A	INTRINSIC
low complexity region	793	806	N/A	INTRINSIC
low complexity region	841	853	N/A	INTRINSIC
ZU5	912	1016	2e-63	SMART
low complexity region	1371	1381	N/A	INTRINSIC
low complexity region	1448	1463	N/A	INTRINSIC
low complexity region	1490	1503	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000182078
AA Change: R1011H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000138753
Gene: ENSMUSG00000032826
AA Change: R1011H

Domain	Start	End	E-Value	Type
low complexity region	7	18	N/A	INTRINSIC
low complexity region	114	125	N/A	INTRINSIC
low complexity region	191	209	N/A	INTRINSIC
low complexity region	304	312	N/A	INTRINSIC
low complexity region	478	493	N/A	INTRINSIC
low complexity region	527	544	N/A	INTRINSIC
DEATH	591	685	1e-29	SMART
low complexity region	720	736	N/A	INTRINSIC
low complexity region	848	861	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000182711
AA Change: R1093H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000138781
Gene: ENSMUSG00000032826
AA Change: R1093H

Domain	Start	End	E-Value	Type
ANK	26	55	1e1	SMART
ANK	59	88	8.9e-7	SMART
ANK	92	121	4.4e-9	SMART
ANK	125	154	2.8e-9	SMART
ANK	158	186	5.3e-1	SMART
ANK	187	216	7.3e-1	SMART
ANK	228	257	1.1e-7	SMART
ANK	261	290	4.4e-9	SMART
ANK	294	323	9.3e-8	SMART
ANK	327	356	2.1e-8	SMART
ANK	360	389	1.3e-7	SMART
ANK	393	422	6.2e-9	SMART
ANK	426	455	1.1e-7	SMART
ANK	459	488	2.9e-8	SMART
ANK	492	521	1.1e-5	SMART
ANK	525	554	6.5e-6	SMART
ANK	558	587	2.3e-7	SMART
ANK	591	620	5.3e-7	SMART
ANK	624	653	2.4e-7	SMART
ANK	657	686	3.2e-9	SMART
ANK	690	719	5.5e-5	SMART
ANK	723	752	1.9e-8	SMART
ANK	756	785	3.3e-9	SMART
low complexity region	805	825	N/A	INTRINSIC
low complexity region	843	856	N/A	INTRINSIC
ZU5	961	1098	1.1e-50	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000182959
AA Change: R1077H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000138251
Gene: ENSMUSG00000032826
AA Change: R1077H

Domain	Start	End	E-Value	Type
ANK	9	38	1.63e3	SMART
ANK	42	71	1.4e-4	SMART
ANK	75	104	6.76e-7	SMART
ANK	108	137	4.46e-7	SMART
ANK	141	169	8.36e1	SMART
ANK	170	199	1.17e2	SMART
ANK	211	240	1.76e-5	SMART
ANK	244	273	6.76e-7	SMART
ANK	277	306	1.43e-5	SMART
ANK	310	339	3.33e-6	SMART
ANK	343	372	2.02e-5	SMART
ANK	376	405	9.55e-7	SMART
ANK	409	438	1.76e-5	SMART
ANK	442	471	4.71e-6	SMART
ANK	475	504	1.7e-3	SMART
ANK	508	537	1.05e-3	SMART
ANK	541	570	3.51e-5	SMART
ANK	574	603	8.65e-5	SMART
ANK	607	636	3.76e-5	SMART
ANK	640	669	5.12e-7	SMART
ANK	673	702	8.39e-3	SMART
ANK	706	735	2.9e-6	SMART
ANK	739	768	5.12e-7	SMART
low complexity region	788	808	N/A	INTRINSIC
low complexity region	826	839	N/A	INTRINSIC
low complexity region	874	886	N/A	INTRINSIC
Pfam:ZU5	945	1028	1.5e-30	PFAM
Pfam:ZU5	1021	1082	4.4e-21	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183075

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000196018

Predicted Effect

probably benign
Transcript: ENSMUST00000211813

Meta Mutation Damage Score

0.2740

Coding Region Coverage

1x: 99.3%
3x: 98.9%
10x: 97.5%
20x: 95.2%

Validation Efficiency

100% (62/62)

MGI Phenotype

PHENOTYPE: Homozygous mutation of this gene results in death by postnatal day 8, although some animals survive to P20. Mutant animals display reduced body size, impaired balance and locomotion, brain structure dysmorphologies, abnormal lens, and optic nerve degeneration. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700018F24Rik	A	G	5: 145,044,763 (GRCm38)	E136G	probably benign	Het
Adgre4	T	A	17: 55,852,281 (GRCm38)	S655R	probably benign	Het
Ak7	T	A	12: 105,710,254 (GRCm38)	V71E	probably benign	Het
Anxa3	A	G	5: 96,828,748 (GRCm38)	T198A	possibly damaging	Het
Atp1a1	A	T	3: 101,592,439 (GRCm38)	I109N	possibly damaging	Het
Camta1	A	G	4: 151,077,892 (GRCm38)	I119T	probably damaging	Het
Carm1	A	G	9: 21,587,374 (GRCm38)	Y504C	probably damaging	Het
Casp1	C	T	9: 5,303,077 (GRCm38)	P177L	probably benign	Het
Ccdc122	C	A	14: 77,092,077 (GRCm38)		probably benign	Het
Ces1a	A	G	8: 93,039,513 (GRCm38)	S158P	probably damaging	Het
Ces3a	T	A	8: 105,050,195 (GRCm38)	D103E	possibly damaging	Het
Clstn1	A	C	4: 149,643,624 (GRCm38)	D583A	possibly damaging	Het
Corin	A	G	5: 72,332,795 (GRCm38)		probably benign	Het
Cryba1	T	C	11: 77,719,457 (GRCm38)	D144G	probably damaging	Het
Cwf19l2	G	T	9: 3,421,377 (GRCm38)		probably null	Het
Dis3l	T	C	9: 64,307,126 (GRCm38)	T1027A	possibly damaging	Het
Dopey2	A	G	16: 93,762,325 (GRCm38)	E653G	probably benign	Het
Dst	A	G	1: 34,188,677 (GRCm38)	I1459V	probably benign	Het
Dyrk3	T	C	1: 131,130,140 (GRCm38)	T64A	probably benign	Het
Emp2	C	T	16: 10,284,615 (GRCm38)	C111Y	probably benign	Het
Enam	A	G	5: 88,501,994 (GRCm38)	Y454C	probably damaging	Het
Fbn1	A	T	2: 125,352,064 (GRCm38)	C1328S	probably benign	Het
Gata3	T	C	2: 9,874,575 (GRCm38)	T197A	probably benign	Het
Gm1043	A	G	5: 37,187,229 (GRCm38)	T212A	probably damaging	Het
Gm15448	T	C	7: 3,816,872 (GRCm38)	N564S	possibly damaging	Het
H2-Eb1	T	C	17: 34,315,032 (GRCm38)		probably benign	Het
Hand1	T	C	11: 57,831,680 (GRCm38)	H36R	probably damaging	Het
Hmgcs2	C	A	3: 98,297,001 (GRCm38)	Y239*	probably null	Het
Hoxc12	A	G	15: 102,937,055 (GRCm38)	Y68C	probably damaging	Het
Inpp5a	A	G	7: 139,516,663 (GRCm38)	I143V	probably benign	Het
Klhdc2	C	A	12: 69,297,048 (GRCm38)	F18L	probably benign	Het
Kpnb1	T	C	11: 97,178,304 (GRCm38)	Y251C	probably damaging	Het
Lrch4	A	T	5: 137,637,308 (GRCm38)	N315I	probably damaging	Het
Map3k10	A	C	7: 27,668,355 (GRCm38)	V286G	probably damaging	Het
Myo7b	G	A	18: 32,005,549 (GRCm38)		probably benign	Het
Nlrp2	G	T	7: 5,319,222 (GRCm38)	L809I	probably damaging	Het
Oacyl	T	C	18: 65,737,825 (GRCm38)		probably benign	Het
Olfr735	A	G	14: 50,345,917 (GRCm38)	V175A	possibly damaging	Het
Paxbp1	T	A	16: 91,036,536 (GRCm38)	D270V	probably damaging	Het
Pdia3	G	A	2: 121,432,377 (GRCm38)	G275S	probably damaging	Het
Plcb3	G	A	19: 6,963,392 (GRCm38)	R359C	probably damaging	Het
Plcxd3	G	A	15: 4,516,868 (GRCm38)	S118N	probably damaging	Het
Ptpn14	T	C	1: 189,850,947 (GRCm38)	S664P	possibly damaging	Het
Sirt1	T	C	10: 63,323,973 (GRCm38)	I443V	possibly damaging	Het
Slc7a8	G	A	14: 54,735,186 (GRCm38)		probably benign	Het
Smim14	A	G	5: 65,453,339 (GRCm38)		probably benign	Het
Sost	C	T	11: 101,966,918 (GRCm38)	C19Y	probably benign	Het
Tcaf1	G	T	6: 42,675,367 (GRCm38)	A727E	probably damaging	Het
Thoc1	T	C	18: 9,963,829 (GRCm38)	L144P	probably damaging	Het
Tmem132b	A	T	5: 125,783,421 (GRCm38)	T577S	possibly damaging	Het
Tnfrsf21	C	T	17: 43,038,213 (GRCm38)	H239Y	probably benign	Het
Tshr	T	C	12: 91,538,286 (GRCm38)	F666S	probably damaging	Het
Wdr1	A	G	5: 38,540,862 (GRCm38)	V192A	possibly damaging	Het
Zfp697	T	C	3: 98,428,166 (GRCm38)	W416R	probably damaging	Het

Other mutations in Ank2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01298:Ank2	APN	3	126,959,720 (GRCm38)	missense	possibly damaging	0.80
IGL01652:Ank2	APN	3	126,933,041 (GRCm38)	missense	probably benign	0.00
IGL01969:Ank2	APN	3	126,953,223 (GRCm38)	missense	possibly damaging	0.47
IGL02122:Ank2	APN	3	126,937,874 (GRCm38)	splice site	probably benign
IGL02537:Ank2	APN	3	126,955,916 (GRCm38)	missense	probably damaging	1.00
IGL02858:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL02981:Ank2	APN	3	126,934,562 (GRCm38)	missense	possibly damaging	0.58
IGL02981:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03024:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03074:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03111:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03129:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03174:Ank2	APN	3	126,940,095 (GRCm38)	missense	probably damaging	0.98
IGL03177:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03185:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03188:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03242:Ank2	APN	3	126,928,805 (GRCm38)	missense	possibly damaging	0.90
IGL03244:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03248:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03285:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03304:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03358:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03380:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03389:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03400:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
IGL03409:Ank2	APN	3	126,955,870 (GRCm38)	missense	probably damaging	1.00
ballast	UTSW	3	126,943,133 (GRCm38)	missense	unknown
Chain	UTSW	3	126,946,938 (GRCm38)	intron	probably benign
Deadman	UTSW	3	126,929,822 (GRCm38)	missense	probably benign	0.19
drag	UTSW	3	127,003,982 (GRCm38)	missense	probably damaging	1.00
mooring	UTSW	3	126,934,577 (GRCm38)	missense	possibly damaging	0.73
Treasure	UTSW	3	126,946,749 (GRCm38)	missense	unknown
Windlass	UTSW	3	126,946,149 (GRCm38)	missense	probably benign
R0033:Ank2	UTSW	3	127,104,748 (GRCm38)	splice site	probably benign
R0042:Ank2	UTSW	3	126,936,631 (GRCm38)	missense	probably damaging	0.99
R0042:Ank2	UTSW	3	126,936,631 (GRCm38)	missense	probably damaging	0.99
R0079:Ank2	UTSW	3	126,934,615 (GRCm38)	missense	probably benign	0.01
R0423:Ank2	UTSW	3	126,929,860 (GRCm38)	nonsense	probably null
R0699:Ank2	UTSW	3	126,929,829 (GRCm38)	missense	probably benign	0.00
R0990:Ank2	UTSW	3	126,934,666 (GRCm38)	missense	possibly damaging	0.64
R1450:Ank2	UTSW	3	126,957,302 (GRCm38)	missense	possibly damaging	0.94
R1500:Ank2	UTSW	3	126,932,982 (GRCm38)	missense	probably benign
R1702:Ank2	UTSW	3	126,955,899 (GRCm38)	missense	probably benign	0.00
R1703:Ank2	UTSW	3	126,929,766 (GRCm38)	missense	probably damaging	1.00
R1710:Ank2	UTSW	3	126,933,060 (GRCm38)	nonsense	probably null
R1743:Ank2	UTSW	3	126,928,675 (GRCm38)	missense	probably damaging	0.99
R1775:Ank2	UTSW	3	126,934,547 (GRCm38)	missense	probably benign	0.00
R1852:Ank2	UTSW	3	126,997,851 (GRCm38)	critical splice donor site	probably null
R2198:Ank2	UTSW	3	126,934,577 (GRCm38)	missense	possibly damaging	0.73
R2892:Ank2	UTSW	3	127,248,243 (GRCm38)	splice site	probably null
R2893:Ank2	UTSW	3	127,248,243 (GRCm38)	splice site	probably null
R2894:Ank2	UTSW	3	127,248,243 (GRCm38)	splice site	probably null
R3148:Ank2	UTSW	3	126,933,075 (GRCm38)	missense	probably benign	0.00
R3776:Ank2	UTSW	3	126,942,262 (GRCm38)	intron	probably benign
R3784:Ank2	UTSW	3	126,953,193 (GRCm38)	missense	probably damaging	1.00
R3856:Ank2	UTSW	3	126,929,844 (GRCm38)	missense	probably benign	0.00
R3906:Ank2	UTSW	3	127,016,898 (GRCm38)	missense	probably damaging	1.00
R3907:Ank2	UTSW	3	127,016,898 (GRCm38)	missense	probably damaging	1.00
R3953:Ank2	UTSW	3	126,988,160 (GRCm38)	missense	probably damaging	1.00
R3963:Ank2	UTSW	3	126,934,596 (GRCm38)	missense	probably benign
R4367:Ank2	UTSW	3	126,946,149 (GRCm38)	missense	probably benign
R4414:Ank2	UTSW	3	127,225,762 (GRCm38)	critical splice donor site	probably null
R4432:Ank2	UTSW	3	126,947,806 (GRCm38)	intron	probably benign
R4433:Ank2	UTSW	3	126,947,806 (GRCm38)	intron	probably benign
R4579:Ank2	UTSW	3	126,958,963 (GRCm38)	missense	probably damaging	1.00
R4597:Ank2	UTSW	3	126,988,151 (GRCm38)	missense	probably damaging	1.00
R4603:Ank2	UTSW	3	127,032,016 (GRCm38)	missense	probably benign	0.00
R4729:Ank2	UTSW	3	126,976,896 (GRCm38)	nonsense	probably null
R4815:Ank2	UTSW	3	126,936,761 (GRCm38)	missense	probably benign
R4826:Ank2	UTSW	3	126,956,001 (GRCm38)	missense	probably benign	0.35
R4871:Ank2	UTSW	3	126,959,795 (GRCm38)	missense	probably damaging	1.00
R4880:Ank2	UTSW	3	127,046,826 (GRCm38)	splice site	probably null
R4915:Ank2	UTSW	3	126,942,671 (GRCm38)	intron	probably benign
R4935:Ank2	UTSW	3	126,956,064 (GRCm38)	missense	probably damaging	1.00
R4936:Ank2	UTSW	3	126,955,039 (GRCm38)	missense	possibly damaging	0.94
R4937:Ank2	UTSW	3	126,962,401 (GRCm38)	missense	probably damaging	1.00
R4946:Ank2	UTSW	3	126,941,940 (GRCm38)	intron	probably benign
R4963:Ank2	UTSW	3	127,032,096 (GRCm38)	missense	probably benign	0.01
R4989:Ank2	UTSW	3	126,963,445 (GRCm38)	missense	possibly damaging	0.94
R5023:Ank2	UTSW	3	126,941,871 (GRCm38)	intron	probably benign
R5060:Ank2	UTSW	3	126,945,921 (GRCm38)	intron	probably benign
R5078:Ank2	UTSW	3	126,942,353 (GRCm38)	intron	probably benign
R5086:Ank2	UTSW	3	126,947,348 (GRCm38)	intron	probably benign
R5134:Ank2	UTSW	3	126,963,445 (GRCm38)	missense	possibly damaging	0.94
R5148:Ank2	UTSW	3	127,025,636 (GRCm38)	splice site	probably null
R5175:Ank2	UTSW	3	127,004,024 (GRCm38)	missense	probably damaging	1.00
R5275:Ank2	UTSW	3	127,032,183 (GRCm38)	missense	probably damaging	1.00
R5295:Ank2	UTSW	3	127,032,183 (GRCm38)	missense	probably damaging	1.00
R5303:Ank2	UTSW	3	126,945,804 (GRCm38)	intron	probably benign
R5309:Ank2	UTSW	3	126,959,768 (GRCm38)	missense	probably damaging	0.99
R5312:Ank2	UTSW	3	126,959,768 (GRCm38)	missense	probably damaging	0.99
R5352:Ank2	UTSW	3	127,498,991 (GRCm38)	utr 5 prime	probably benign
R5355:Ank2	UTSW	3	126,944,049 (GRCm38)	intron	probably benign
R5386:Ank2	UTSW	3	126,981,933 (GRCm38)	missense	probably benign	0.01
R5396:Ank2	UTSW	3	126,953,226 (GRCm38)	missense	probably damaging	1.00
R5518:Ank2	UTSW	3	126,959,699 (GRCm38)	missense	probably damaging	0.98
R5534:Ank2	UTSW	3	126,947,298 (GRCm38)	intron	probably benign
R5554:Ank2	UTSW	3	126,998,973 (GRCm38)	missense	possibly damaging	0.78
R5582:Ank2	UTSW	3	126,946,305 (GRCm38)	intron	probably benign
R5747:Ank2	UTSW	3	126,941,751 (GRCm38)	intron	probably benign
R5794:Ank2	UTSW	3	126,930,020 (GRCm38)	missense	probably benign	0.00
R5831:Ank2	UTSW	3	127,339,159 (GRCm38)	start gained	probably benign
R5925:Ank2	UTSW	3	126,932,963 (GRCm38)	missense	probably benign	0.18
R5954:Ank2	UTSW	3	126,997,861 (GRCm38)	missense	probably benign	0.34
R5956:Ank2	UTSW	3	126,942,688 (GRCm38)	intron	probably benign
R5986:Ank2	UTSW	3	127,012,686 (GRCm38)	missense	possibly damaging	0.94
R5992:Ank2	UTSW	3	126,959,651 (GRCm38)	critical splice donor site	probably null
R6020:Ank2	UTSW	3	126,946,821 (GRCm38)	intron	probably benign
R6027:Ank2	UTSW	3	126,997,879 (GRCm38)	missense	possibly damaging	0.92
R6049:Ank2	UTSW	3	126,943,020 (GRCm38)	missense	possibly damaging	0.95
R6060:Ank2	UTSW	3	126,955,952 (GRCm38)	missense	probably damaging	1.00
R6114:Ank2	UTSW	3	127,011,051 (GRCm38)	missense	probably damaging	1.00
R6124:Ank2	UTSW	3	127,248,151 (GRCm38)	missense	probably benign	0.31
R6156:Ank2	UTSW	3	126,944,237 (GRCm38)	missense	probably damaging	1.00
R6173:Ank2	UTSW	3	127,052,746 (GRCm38)	missense	probably damaging	1.00
R6176:Ank2	UTSW	3	126,945,471 (GRCm38)	missense	probably benign	0.05
R6184:Ank2	UTSW	3	126,962,398 (GRCm38)	missense	probably damaging	1.00
R6199:Ank2	UTSW	3	127,004,006 (GRCm38)	missense	probably damaging	1.00
R6241:Ank2	UTSW	3	127,052,748 (GRCm38)	missense	probably damaging	1.00
R6254:Ank2	UTSW	3	126,941,804 (GRCm38)	intron	probably benign
R6259:Ank2	UTSW	3	127,016,986 (GRCm38)	missense	probably benign	0.28
R6260:Ank2	UTSW	3	126,943,557 (GRCm38)	missense	probably benign
R6321:Ank2	UTSW	3	126,946,938 (GRCm38)	intron	probably benign
R6393:Ank2	UTSW	3	126,929,757 (GRCm38)	missense	probably damaging	1.00
R6406:Ank2	UTSW	3	127,032,225 (GRCm38)	missense	probably damaging	1.00
R6544:Ank2	UTSW	3	126,933,222 (GRCm38)	missense	probably damaging	0.99
R6583:Ank2	UTSW	3	127,016,964 (GRCm38)	missense	probably damaging	1.00
R6739:Ank2	UTSW	3	127,079,994 (GRCm38)	missense	probably damaging	1.00
R6754:Ank2	UTSW	3	127,096,839 (GRCm38)	intron	probably benign
R6786:Ank2	UTSW	3	126,958,932 (GRCm38)	missense	probably damaging	0.99
R6798:Ank2	UTSW	3	126,944,264 (GRCm38)	intron	probably benign
R6882:Ank2	UTSW	3	126,945,757 (GRCm38)	intron	probably benign
R6940:Ank2	UTSW	3	126,941,972 (GRCm38)	intron	probably benign
R6949:Ank2	UTSW	3	127,010,884 (GRCm38)	missense	probably benign	0.00
R7001:Ank2	UTSW	3	127,077,581 (GRCm38)	missense	probably damaging	1.00
R7033:Ank2	UTSW	3	126,944,850 (GRCm38)	nonsense	probably null
R7036:Ank2	UTSW	3	126,946,392 (GRCm38)	intron	probably benign
R7045:Ank2	UTSW	3	127,012,744 (GRCm38)	missense	probably damaging	1.00
R7048:Ank2	UTSW	3	127,025,618 (GRCm38)	missense	probably benign	0.03
R7054:Ank2	UTSW	3	126,943,303 (GRCm38)	intron	probably benign
R7069:Ank2	UTSW	3	126,946,298 (GRCm38)	intron	probably benign
R7091:Ank2	UTSW	3	127,023,351 (GRCm38)	missense	probably damaging	0.98
R7107:Ank2	UTSW	3	127,003,982 (GRCm38)	missense	probably damaging	1.00
R7175:Ank2	UTSW	3	126,946,941 (GRCm38)	missense	unknown
R7191:Ank2	UTSW	3	126,946,392 (GRCm38)	missense	unknown
R7272:Ank2	UTSW	3	126,943,133 (GRCm38)	missense	unknown
R7381:Ank2	UTSW	3	126,936,628 (GRCm38)	missense	possibly damaging	0.46
R7394:Ank2	UTSW	3	126,936,653 (GRCm38)	missense	possibly damaging	0.77
R7462:Ank2	UTSW	3	126,943,034 (GRCm38)	missense	unknown
R7490:Ank2	UTSW	3	126,958,889 (GRCm38)	missense	probably damaging	0.99
R7514:Ank2	UTSW	3	127,025,603 (GRCm38)	missense	probably benign	0.06
R7534:Ank2	UTSW	3	126,934,333 (GRCm38)	splice site	probably null
R7540:Ank2	UTSW	3	126,988,159 (GRCm38)	missense	possibly damaging	0.94
R7547:Ank2	UTSW	3	126,945,203 (GRCm38)	missense	unknown
R7579:Ank2	UTSW	3	126,946,398 (GRCm38)	missense	unknown
R7584:Ank2	UTSW	3	126,946,128 (GRCm38)	nonsense	probably null
R7625:Ank2	UTSW	3	127,052,800 (GRCm38)	missense	probably damaging	1.00
R7698:Ank2	UTSW	3	127,032,211 (GRCm38)	missense	probably benign	0.35
R7716:Ank2	UTSW	3	126,943,166 (GRCm38)	missense	unknown
R7718:Ank2	UTSW	3	126,965,013 (GRCm38)	missense	possibly damaging	0.88
R7722:Ank2	UTSW	3	127,029,302 (GRCm38)	missense	probably benign	0.01
R7738:Ank2	UTSW	3	126,947,622 (GRCm38)	missense
R7977:Ank2	UTSW	3	126,945,707 (GRCm38)	missense	unknown
R7987:Ank2	UTSW	3	126,945,707 (GRCm38)	missense	unknown
R8007:Ank2	UTSW	3	126,936,447 (GRCm38)	intron	probably benign
R8150:Ank2	UTSW	3	126,947,513 (GRCm38)	missense
R8161:Ank2	UTSW	3	127,032,129 (GRCm38)	missense
R8196:Ank2	UTSW	3	126,929,883 (GRCm38)	missense	probably damaging	0.99
R8248:Ank2	UTSW	3	126,937,785 (GRCm38)	missense	possibly damaging	0.78
R8255:Ank2	UTSW	3	126,946,749 (GRCm38)	missense	unknown
R8279:Ank2	UTSW	3	126,933,171 (GRCm38)	missense	probably benign	0.04
R8300:Ank2	UTSW	3	127,010,906 (GRCm38)	missense
R8716:Ank2	UTSW	3	126,942,839 (GRCm38)	nonsense	probably null
R8724:Ank2	UTSW	3	126,943,756 (GRCm38)	missense	unknown
R8765:Ank2	UTSW	3	127,057,082 (GRCm38)	missense	possibly damaging	0.94
R8779:Ank2	UTSW	3	126,965,102 (GRCm38)	missense	probably damaging	0.99
R8783:Ank2	UTSW	3	127,052,806 (GRCm38)	missense	probably damaging	1.00
R8785:Ank2	UTSW	3	126,997,921 (GRCm38)	missense	probably damaging	1.00
R8826:Ank2	UTSW	3	126,947,302 (GRCm38)	missense	unknown
R8872:Ank2	UTSW	3	126,997,876 (GRCm38)	missense	possibly damaging	0.88
R8903:Ank2	UTSW	3	127,046,782 (GRCm38)	missense	probably damaging	1.00
R8906:Ank2	UTSW	3	126,933,071 (GRCm38)	missense	probably benign	0.00
R8918:Ank2	UTSW	3	126,943,731 (GRCm38)	missense	unknown
R8947:Ank2	UTSW	3	126,942,747 (GRCm38)	intron	probably benign
R8977:Ank2	UTSW	3	126,944,926 (GRCm38)	missense	unknown
R8990:Ank2	UTSW	3	127,048,180 (GRCm38)	critical splice donor site	probably null
R8994:Ank2	UTSW	3	126,929,822 (GRCm38)	missense	probably benign	0.19
R9009:Ank2	UTSW	3	126,934,376 (GRCm38)	unclassified	probably benign
R9123:Ank2	UTSW	3	126,940,095 (GRCm38)	missense	probably damaging	1.00
R9125:Ank2	UTSW	3	126,940,095 (GRCm38)	missense	probably damaging	1.00
R9130:Ank2	UTSW	3	127,016,916 (GRCm38)	missense
R9175:Ank2	UTSW	3	126,928,753 (GRCm38)	missense	possibly damaging	0.52
R9220:Ank2	UTSW	3	126,943,437 (GRCm38)	missense	unknown
R9225:Ank2	UTSW	3	126,942,462 (GRCm38)	missense	unknown
R9286:Ank2	UTSW	3	127,052,732 (GRCm38)	missense	probably damaging	0.99
R9325:Ank2	UTSW	3	126,981,855 (GRCm38)	missense	probably damaging	0.98
R9367:Ank2	UTSW	3	126,945,029 (GRCm38)	missense	unknown
R9385:Ank2	UTSW	3	126,959,717 (GRCm38)	missense	probably benign	0.00
R9391:Ank2	UTSW	3	126,937,745 (GRCm38)	missense	probably damaging	0.99
R9422:Ank2	UTSW	3	127,096,856 (GRCm38)	missense	unknown
R9536:Ank2	UTSW	3	126,942,382 (GRCm38)	missense	unknown
R9647:Ank2	UTSW	3	126,998,974 (GRCm38)	missense	possibly damaging	0.93
R9650:Ank2	UTSW	3	126,942,180 (GRCm38)	missense	unknown
R9666:Ank2	UTSW	3	126,933,189 (GRCm38)	nonsense	probably null
R9686:Ank2	UTSW	3	126,946,901 (GRCm38)	missense	unknown
R9730:Ank2	UTSW	3	127,225,844 (GRCm38)	missense
R9738:Ank2	UTSW	3	126,943,472 (GRCm38)	missense	unknown
R9743:Ank2	UTSW	3	126,940,145 (GRCm38)	missense	possibly damaging	0.81
R9747:Ank2	UTSW	3	126,959,018 (GRCm38)	missense	probably damaging	1.00
R9800:Ank2	UTSW	3	126,946,500 (GRCm38)	missense	unknown
R9803:Ank2	UTSW	3	126,959,077 (GRCm38)	missense	possibly damaging	0.64
RF020:Ank2	UTSW	3	126,945,476 (GRCm38)	missense	unknown
Z1088:Ank2	UTSW	3	127,029,509 (GRCm38)	missense	possibly damaging	0.45
Z1177:Ank2	UTSW	3	126,944,357 (GRCm38)	missense	unknown
Z1187:Ank2	UTSW	3	126,955,952 (GRCm38)	missense	probably damaging	1.00
Z1190:Ank2	UTSW	3	126,955,952 (GRCm38)	missense	probably damaging	1.00
Z1192:Ank2	UTSW	3	126,955,952 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGCAGTGCCTTATCCACATGCC -3'
(R):5'- TCAAAGGAGACGTTCCAGAATGCC -3'

Sequencing Primer
(F):5'- ATCCACATGCCTCTGCCTTAG -3'
(R):5'- CCACAGGGAAATATCATTTGGC -3'

Posted On

2015-02-04