Mutagenetix > Incidental Mutation

Incidental Mutation 'R5579:Mark2'

438345

Institutional Source

Beutler Lab

Gene Symbol

Mark2

Ensembl Gene

ENSMUSG00000024969

Gene Name

MAP/microtubule affinity regulating kinase 2

Synonyms

Emk, Par-1

MMRRC Submission

043267-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.917) question?

Stock #

R5579 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

7275396-7341860 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 7282816 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glycine at position 14 (V14G)

Ref Sequence

ENSEMBL: ENSMUSP00000132482 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025921] [ENSMUST00000032557] [ENSMUST00000051711] [ENSMUST00000164129] [ENSMUST00000164205] [ENSMUST00000165286] [ENSMUST00000165965] [ENSMUST00000166461] [ENSMUST00000167767] [ENSMUST00000168872] [ENSMUST00000171352] [ENSMUST00000169541] [ENSMUST00000171393]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000025921
AA Change: V439G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000025921
Gene: ENSMUSG00000024969
AA Change: V439G

Domain	Start	End	E-Value	Type
S_TKc	20	271	1.59e-108	SMART
UBA	292	329	7.69e-7	SMART
low complexity region	475	489	N/A	INTRINSIC
low complexity region	532	545	N/A	INTRINSIC
Pfam:KA1	697	743	2.5e-21	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000032557
AA Change: V472G

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000032557
Gene: ENSMUSG00000024969
AA Change: V472G

Domain	Start	End	E-Value	Type
S_TKc	53	304	1.59e-108	SMART
UBA	325	362	7.69e-7	SMART
low complexity region	511	524	N/A	INTRINSIC
Pfam:KA1	685	731	5.4e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000051711
AA Change: V472G

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

SMART Domains

Protein: ENSMUSP00000108969
Gene: ENSMUSG00000024969
AA Change: V472G

Domain	Start	End	E-Value	Type
S_TKc	53	304	1.59e-108	SMART
UBA	325	362	7.69e-7	SMART
low complexity region	508	522	N/A	INTRINSIC
low complexity region	565	578	N/A	INTRINSIC
Pfam:KA1	730	776	6.6e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000163345

SMART Domains

Protein: ENSMUSP00000125944
Gene: ENSMUSG00000024969

Domain	Start	End	E-Value	Type
low complexity region	3	15	N/A	INTRINSIC
low complexity region	58	71	N/A	INTRINSIC

Predicted Effect

silent
Transcript: ENSMUST00000164129

Predicted Effect

probably benign
Transcript: ENSMUST00000164205
AA Change: V472G

PolyPhen 2 Score 0.143 (Sensitivity: 0.92; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000127827
Gene: ENSMUSG00000024969
AA Change: V472G

Domain	Start	End	E-Value	Type
S_TKc	53	304	1.59e-108	SMART
UBA	325	362	7.69e-7	SMART
low complexity region	511	524	N/A	INTRINSIC
Pfam:KA1	676	722	5.4e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000165286
AA Change: V472G

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

SMART Domains

Protein: ENSMUSP00000126468
Gene: ENSMUSG00000024969
AA Change: V472G

Domain	Start	End	E-Value	Type
S_TKc	53	304	1.59e-108	SMART
UBA	325	362	7.69e-7	SMART
low complexity region	511	524	N/A	INTRINSIC
Pfam:KA1	670	716	6e-22	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000165881
AA Change: V51G

SMART Domains

Protein: ENSMUSP00000126753
Gene: ENSMUSG00000024969
AA Change: V51G

Domain	Start	End	E-Value	Type
low complexity region	88	102	N/A	INTRINSIC
low complexity region	145	158	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000165965
AA Change: V472G

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

SMART Domains

Protein: ENSMUSP00000131684
Gene: ENSMUSG00000024969
AA Change: V472G

Domain	Start	End	E-Value	Type
S_TKc	53	304	1.59e-108	SMART
UBA	325	362	7.69e-7	SMART
low complexity region	508	522	N/A	INTRINSIC
low complexity region	565	578	N/A	INTRINSIC
Pfam:KA1	732	776	7.2e-24	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000166461
AA Change: V9G

PolyPhen 2 Score 0.065 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000128549
Gene: ENSMUSG00000024969
AA Change: V9G

Domain	Start	End	E-Value	Type
low complexity region	45	59	N/A	INTRINSIC
low complexity region	102	115	N/A	INTRINSIC
Pfam:KA1	261	307	1.9e-22	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000167767
AA Change: V14G

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000132482
Gene: ENSMUSG00000024969
AA Change: V14G

Domain	Start	End	E-Value	Type
low complexity region	53	66	N/A	INTRINSIC
PDB:3OSE\|A	220	264	1e-18	PDB

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000168852

Predicted Effect

probably benign
Transcript: ENSMUST00000168872
AA Change: V472G

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

SMART Domains

Protein: ENSMUSP00000128560
Gene: ENSMUSG00000024969
AA Change: V472G

Domain	Start	End	E-Value	Type
S_TKc	53	304	1.59e-108	SMART
UBA	325	362	7.69e-7	SMART
low complexity region	511	524	N/A	INTRINSIC
Pfam:KA1	661	707	5.9e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000171352
AA Change: V88G

PolyPhen 2 Score 0.165 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000129490
Gene: ENSMUSG00000024969
AA Change: V88G

Domain	Start	End	E-Value	Type
low complexity region	127	140	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000171721
AA Change: V462G

SMART Domains

Protein: ENSMUSP00000129506
Gene: ENSMUSG00000024969
AA Change: V462G

Domain	Start	End	E-Value	Type
S_TKc	44	295	1.59e-108	SMART
UBA	316	353	7.69e-7	SMART
low complexity region	499	513	N/A	INTRINSIC
low complexity region	556	569	N/A	INTRINSIC
Pfam:KA1	732	776	7.2e-24	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000170768

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000171044

Predicted Effect

probably benign
Transcript: ENSMUST00000169541

SMART Domains

Protein: ENSMUSP00000128779
Gene: ENSMUSG00000024969

Domain	Start	End	E-Value	Type
Pfam:Pkinase	53	110	1.7e-12	PFAM
Pfam:Pkinase_Tyr	53	110	7.2e-8	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000171393

SMART Domains

Protein: ENSMUSP00000129894
Gene: ENSMUSG00000024969

Domain	Start	End	E-Value	Type
Pfam:Pkinase	20	193	1.2e-59	PFAM
Pfam:Pkinase_Tyr	20	193	1.2e-35	PFAM
Pfam:RIO1	30	174	3e-7	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.8%
10x: 98.9%
20x: 97.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the Par-1 family of serine/threonine protein kinases. The protein is an important regulator of cell polarity in epithelial and neuronal cells, and also controls the stability of microtubules through phosphorylation and inactivation of several microtubule-associating proteins. The protein localizes to cell membranes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2009]
PHENOTYPE: Homozygotes for targeted null mutations exhibit proportionate dwarfism with smaller pituitaries and reduced growth hormone and prolactin secretion. Mutants develop autoimmunity and fail to breed when mated to each other. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 114 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca3	G	T	17: 24,376,729 (GRCm38)	C352F	probably damaging	Het
Abce1	A	T	8: 79,700,586 (GRCm38)	I237N	possibly damaging	Het
Acrbp	A	G	6: 125,061,099 (GRCm38)	D421G	probably benign	Het
Adam8	T	A	7: 139,988,984 (GRCm38)	Y201F	probably benign	Het
Adgrf1	T	A	17: 43,311,064 (GRCm38)	C731S	probably damaging	Het
Akap8l	A	T	17: 32,321,942 (GRCm38)	I529N	probably damaging	Het
Akap9	G	A	5: 4,064,714 (GRCm38)	G114D	possibly damaging	Het
Alox12b	T	A	11: 69,162,932 (GRCm38)	D158E	probably benign	Het
Ankrd11	A	G	8: 122,884,231 (GRCm38)	S2639P	probably damaging	Het
Ankrd42	T	C	7: 92,590,182 (GRCm38)	Y466C	possibly damaging	Het
Apobr	T	C	7: 126,587,675 (GRCm38)	I786T	probably benign	Het
Arhgef12	C	T	9: 43,010,193 (GRCm38)	G329R	probably benign	Het
Btnl1	T	C	17: 34,381,552 (GRCm38)		probably null	Het
Ccdc174	A	G	6: 91,881,350 (GRCm38)		probably null	Het
Ccdc183	T	C	2: 25,615,422 (GRCm38)	D177G	possibly damaging	Het
Cd14	A	G	18: 36,726,235 (GRCm38)	Y56H	probably benign	Het
Cep162	G	A	9: 87,203,671 (GRCm38)	A1200V	probably benign	Het
Clic3	T	C	2: 25,458,307 (GRCm38)	L128P	probably damaging	Het
Cntnap5b	A	T	1: 100,383,395 (GRCm38)	R538*	probably null	Het
Cntnap5b	A	T	1: 100,383,399 (GRCm38)	Q539L	probably benign	Het
Coq7	A	T	7: 118,517,335 (GRCm38)	N214K	unknown	Het
Cramp1	G	A	17: 24,973,113 (GRCm38)	H1018Y	possibly damaging	Het
Crtac1	T	A	19: 42,304,806 (GRCm38)	D288V	probably damaging	Het
Dab2ip	C	T	2: 35,715,327 (GRCm38)	R132*	probably null	Het
Dis3l	C	A	9: 64,330,835 (GRCm38)	C125F	probably benign	Het
Dnmt1	A	T	9: 20,920,205 (GRCm38)	V543D	probably damaging	Het
Dock9	A	T	14: 121,599,695 (GRCm38)	L67Q	probably damaging	Het
Ehbp1	A	T	11: 22,137,846 (GRCm38)	S413T	probably damaging	Het
Endov	A	G	11: 119,505,097 (GRCm38)	I158V	probably benign	Het
Epb41l4b	A	G	4: 57,064,802 (GRCm38)	V469A	possibly damaging	Het
Etf1	G	A	18: 34,913,601 (GRCm38)	P119S	probably damaging	Het
Fam135a	A	G	1: 24,029,727 (GRCm38)	L491P	possibly damaging	Het
Fancd2	A	T	6: 113,560,051 (GRCm38)		probably null	Het
Fank1	T	A	7: 133,869,329 (GRCm38)		probably null	Het
Fbh1	A	G	2: 11,748,993 (GRCm38)	I846T	probably damaging	Het
Gas2l3	T	C	10: 89,414,066 (GRCm38)	T397A	probably benign	Het
Gga1	T	C	15: 78,893,188 (GRCm38)	V513A	probably damaging	Het
Ggt1	T	C	10: 75,585,948 (GRCm38)	V543A	probably damaging	Het
Gm11596	A	T	11: 99,792,891 (GRCm38)	C134*	probably null	Het
Gnal	C	T	18: 67,088,771 (GRCm38)	R82C	unknown	Het
Hat1	T	C	2: 71,410,238 (GRCm38)	V92A	possibly damaging	Het
Icosl	C	T	10: 78,073,763 (GRCm38)	R181C	probably damaging	Het
Ift46	A	G	9: 44,786,863 (GRCm38)	M208V	possibly damaging	Het
Ighv1-26	T	C	12: 114,788,599 (GRCm38)	K42E	possibly damaging	Het
Ipo5	A	G	14: 120,938,613 (GRCm38)	K617E	probably benign	Het
Irx5	A	G	8: 92,359,913 (GRCm38)	D208G	probably benign	Het
Itgal	T	G	7: 127,306,929 (GRCm38)	V397G	probably benign	Het
Itpr2	G	A	6: 146,173,366 (GRCm38)	R2297*	probably null	Het
Itpr3	A	G	17: 27,113,519 (GRCm38)	D1779G	probably damaging	Het
Khdc4	T	C	3: 88,700,275 (GRCm38)	S345P	probably benign	Het
Krt4	T	A	15: 101,921,234 (GRCm38)	E286D	probably benign	Het
Loxl4	C	T	19: 42,604,290 (GRCm38)	G317E	probably damaging	Het
Mapk6	T	G	9: 75,388,062 (GRCm38)	H718P	possibly damaging	Het
Mbd5	A	G	2: 49,272,814 (GRCm38)	T1103A	possibly damaging	Het
Mcph1	A	G	8: 18,632,293 (GRCm38)	E482G	probably benign	Het
Mme	G	A	3: 63,348,645 (GRCm38)	E509K	probably damaging	Het
Mrgbp	A	G	2: 180,585,483 (GRCm38)	T204A	probably damaging	Het
Mycbp2	A	T	14: 103,291,333 (GRCm38)	F430I	probably damaging	Het
Myo6	A	G	9: 80,217,720 (GRCm38)	D27G	probably damaging	Het
Ncoa6	A	G	2: 155,406,677 (GRCm38)	L1569S	probably damaging	Het
Ndc1	T	A	4: 107,380,704 (GRCm38)	F235Y	possibly damaging	Het
Nmur2	A	T	11: 56,033,009 (GRCm38)	S240T	probably benign	Het
Or14c44	T	A	7: 86,412,726 (GRCm38)	Y121*	probably null	Het
Or52ae7	G	A	7: 103,470,914 (GRCm38)	V292M	probably damaging	Het
Or5d46	A	T	2: 88,340,413 (GRCm38)	I283F	possibly damaging	Het
Osbpl1a	G	T	18: 12,841,192 (GRCm38)	A62E	probably damaging	Het
Osbpl1a	A	C	18: 12,892,262 (GRCm38)	S333A	probably benign	Het
Otud4	C	T	8: 79,664,108 (GRCm38)	T417I	probably benign	Het
Pagr1a	T	C	7: 127,015,442 (GRCm38)	E197G	probably damaging	Het
Pcdh18	T	C	3: 49,744,977 (GRCm38)	Q1012R	probably damaging	Het
Pcdhgb5	A	C	18: 37,731,637 (GRCm38)	I162L	probably benign	Het
Pdpr	T	A	8: 111,123,816 (GRCm38)	Y462N	probably damaging	Het
Pkhd1	A	T	1: 20,523,142 (GRCm38)	H1582Q	probably damaging	Het
Polr1b	A	G	2: 129,110,108 (GRCm38)	K352R	probably damaging	Het
Poteg	G	A	8: 27,448,037 (GRCm38)	V12M	probably damaging	Het
Pou2f1	A	C	1: 165,915,162 (GRCm38)	V54G	probably damaging	Het
Ppme1	A	G	7: 100,344,975 (GRCm38)	L177P	probably damaging	Het
Prkce	A	G	17: 86,619,948 (GRCm38)	D550G	probably damaging	Het
Prrc2c	A	G	1: 162,680,758 (GRCm38)		probably null	Het
Ptpn22	A	G	3: 103,882,139 (GRCm38)		probably null	Het
Rabif	G	A	1: 134,506,205 (GRCm38)	V86M	probably damaging	Het
Rbm25	T	A	12: 83,668,507 (GRCm38)	M484K	probably benign	Het
Rcn2	G	A	9: 56,057,429 (GRCm38)	A224T	probably benign	Het
Rexo5	T	A	7: 119,834,403 (GRCm38)		probably null	Het
Rnase1	A	T	14: 51,145,762 (GRCm38)	I45N	probably benign	Het
Rnmt	T	A	18: 68,306,115 (GRCm38)	D98E	possibly damaging	Het
Rprd2	A	G	3: 95,785,059 (GRCm38)	F188L	probably damaging	Het
Scube2	G	A	7: 109,810,737 (GRCm38)	T643M	probably damaging	Het
Skic3	T	C	13: 76,185,200 (GRCm38)	W25R	probably damaging	Het
Slc7a15	T	C	12: 8,539,344 (GRCm38)	I68V	probably benign	Het
Slco1a5	A	T	6: 142,242,125 (GRCm38)	V496D	possibly damaging	Het
Slitrk6	T	G	14: 110,751,217 (GRCm38)	S353R	possibly damaging	Het
Smpd5	T	A	15: 76,295,125 (GRCm38)	I53K	possibly damaging	Het
Tas2r108	T	C	6: 40,494,087 (GRCm38)	S166P	probably benign	Het
Tcstv7a	T	A	13: 119,828,415 (GRCm38)	M82L	probably benign	Het
Tecpr1	C	A	5: 144,214,344 (GRCm38)	V245L	possibly damaging	Het
Tenm3	G	T	8: 48,236,764 (GRCm38)	N1929K	probably damaging	Het
Tigd5	T	G	15: 75,911,025 (GRCm38)	F412C	probably damaging	Het
Timm17a	A	T	1: 135,306,188 (GRCm38)	S74T	possibly damaging	Het
Tle1	A	T	4: 72,139,808 (GRCm38)	L60Q	probably damaging	Het
Tmem132d	T	C	5: 127,796,000 (GRCm38)	E515G	possibly damaging	Het
Tmem65	T	C	15: 58,794,397 (GRCm38)	N115S	probably benign	Het
Trmt5	C	A	12: 73,281,652 (GRCm38)	R259L	possibly damaging	Het
Trmt9b	T	C	8: 36,512,041 (GRCm38)	V266A	probably benign	Het
Vmn2r50	A	T	7: 10,050,089 (GRCm38)	W153R	probably benign	Het
Vwa3a	T	G	7: 120,768,173 (GRCm38)	S184A	probably benign	Het
Zbtb25	A	G	12: 76,349,164 (GRCm38)	L428P	possibly damaging	Het
Zbtb49	C	T	5: 38,200,816 (GRCm38)	D698N	probably damaging	Het
Zbtb8os	T	G	4: 129,340,735 (GRCm38)	D35E	probably damaging	Het
Zfp316	T	C	5: 143,264,491 (GRCm38)	T56A	unknown	Het
Zfp334	A	T	2: 165,380,487 (GRCm38)	C545*	probably null	Het
Zmiz1	C	A	14: 25,644,856 (GRCm38)	S247R	probably damaging	Het
Zscan18	A	G	7: 12,775,381 (GRCm38)		probably benign	Het
Zzef1	T	C	11: 72,900,637 (GRCm38)	V2189A	probably damaging	Het

Other mutations in Mark2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00567:Mark2	APN	19	7,341,184 (GRCm38)	missense	possibly damaging	0.53
IGL01522:Mark2	APN	19	7,281,238 (GRCm38)	missense	probably benign	0.06
IGL02368:Mark2	APN	19	7,284,490 (GRCm38)	missense	probably damaging	1.00
IGL02836:Mark2	APN	19	7,278,040 (GRCm38)	critical splice donor site	probably null
IGL03233:Mark2	APN	19	7,284,726 (GRCm38)	missense	possibly damaging	0.89
Unprintable	UTSW	19	7,285,902 (GRCm38)	missense	probably damaging	1.00
R0015:Mark2	UTSW	19	7,285,777 (GRCm38)	nonsense	probably null
R0025:Mark2	UTSW	19	7,285,922 (GRCm38)	missense	probably damaging	1.00
R0025:Mark2	UTSW	19	7,285,922 (GRCm38)	missense	probably damaging	1.00
R0035:Mark2	UTSW	19	7,284,652 (GRCm38)	splice site	probably benign
R0035:Mark2	UTSW	19	7,284,652 (GRCm38)	splice site	probably benign
R0047:Mark2	UTSW	19	7,283,577 (GRCm38)	splice site	probably benign
R0047:Mark2	UTSW	19	7,283,577 (GRCm38)	splice site	probably benign
R0335:Mark2	UTSW	19	7,281,828 (GRCm38)	missense	probably benign	0.27
R0627:Mark2	UTSW	19	7,281,960 (GRCm38)	critical splice acceptor site	probably null
R0734:Mark2	UTSW	19	7,285,981 (GRCm38)	splice site	probably benign
R0744:Mark2	UTSW	19	7,285,824 (GRCm38)	missense	probably damaging	1.00
R0836:Mark2	UTSW	19	7,285,824 (GRCm38)	missense	probably damaging	1.00
R1099:Mark2	UTSW	19	7,277,425 (GRCm38)	missense	probably benign	0.41
R1861:Mark2	UTSW	19	7,290,763 (GRCm38)	missense	possibly damaging	0.73
R1873:Mark2	UTSW	19	7,284,515 (GRCm38)	missense	probably damaging	1.00
R2160:Mark2	UTSW	19	7,282,747 (GRCm38)	missense	probably damaging	1.00
R2161:Mark2	UTSW	19	7,282,747 (GRCm38)	missense	probably damaging	1.00
R2162:Mark2	UTSW	19	7,282,747 (GRCm38)	missense	probably damaging	1.00
R2308:Mark2	UTSW	19	7,281,934 (GRCm38)	missense	probably damaging	1.00
R2844:Mark2	UTSW	19	7,286,862 (GRCm38)	missense	probably damaging	1.00
R2845:Mark2	UTSW	19	7,286,862 (GRCm38)	missense	probably damaging	1.00
R2846:Mark2	UTSW	19	7,286,862 (GRCm38)	missense	probably damaging	1.00
R2902:Mark2	UTSW	19	7,283,448 (GRCm38)	missense	probably benign	0.00
R2935:Mark2	UTSW	19	7,285,889 (GRCm38)	missense	probably benign	0.09
R3853:Mark2	UTSW	19	7,277,290 (GRCm38)	missense	probably damaging	1.00
R4377:Mark2	UTSW	19	7,290,689 (GRCm38)	missense	possibly damaging	0.66
R4522:Mark2	UTSW	19	7,285,948 (GRCm38)	missense	probably damaging	1.00
R4737:Mark2	UTSW	19	7,281,232 (GRCm38)	missense	probably damaging	0.96
R5103:Mark2	UTSW	19	7,284,503 (GRCm38)	missense	probably damaging	1.00
R5154:Mark2	UTSW	19	7,283,074 (GRCm38)	missense	probably damaging	0.99
R6163:Mark2	UTSW	19	7,290,761 (GRCm38)	missense	probably benign	0.00
R6186:Mark2	UTSW	19	7,283,202 (GRCm38)	missense	probably benign	0.01
R6387:Mark2	UTSW	19	7,285,902 (GRCm38)	missense	probably damaging	1.00
R7032:Mark2	UTSW	19	7,287,333 (GRCm38)	missense	probably damaging	1.00
R7949:Mark2	UTSW	19	7,284,716 (GRCm38)	missense	probably benign	0.12
R8792:Mark2	UTSW	19	7,281,215 (GRCm38)	missense	probably benign	0.00
R8825:Mark2	UTSW	19	7,341,206 (GRCm38)	missense	probably benign	0.00
R8854:Mark2	UTSW	19	7,281,004 (GRCm38)	missense	probably benign	0.01
R9374:Mark2	UTSW	19	7,285,898 (GRCm38)	missense	possibly damaging	0.60
R9551:Mark2	UTSW	19	7,285,898 (GRCm38)	missense	possibly damaging	0.60
R9552:Mark2	UTSW	19	7,285,898 (GRCm38)	missense	possibly damaging	0.60

Predicted Primers

PCR Primer
(F):5'- GGTGGATGGCTAGACTGAAC -3'
(R):5'- ATCTTCCTTGCTGAAGCCTGG -3'

Sequencing Primer
(F):5'- ACTCCAGGGACATTGCTCTG -3'
(R):5'- GCCCTTGGCTGTACCTGAG -3'

Posted On

2016-10-26