Mutagenetix > Incidental Mutation

Incidental Mutation 'R5579:Akap8l'

438333

Institutional Source

Beutler Lab

Gene Symbol

Akap8l

Ensembl Gene

ENSMUSG00000002625

Gene Name

A kinase (PRKA) anchor protein 8-like

Synonyms

Nakap95

MMRRC Submission

043267-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.694) question?

Stock #

R5579 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

32321425-32350581 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 32321942 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 529 (I529N)

Ref Sequence

ENSEMBL: ENSMUSP00000051389 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000002699] [ENSMUST00000050214]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000002699

SMART Domains

Protein: ENSMUSP00000002699
Gene: ENSMUSG00000024045

Domain	Start	End	E-Value	Type
SCOP:d1a0tp_	12	108	3e-19	SMART
low complexity region	183	198	N/A	INTRINSIC
low complexity region	257	270	N/A	INTRINSIC
low complexity region	354	384	N/A	INTRINSIC
ZnF_C2H2	387	411	9.46e0	SMART
Blast:ZnF_C2H2	476	501	9e-9	BLAST
low complexity region	551	582	N/A	INTRINSIC
low complexity region	642	651	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000050214
AA Change: I529N

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

SMART Domains

Protein: ENSMUSP00000051389
Gene: ENSMUSG00000002625
AA Change: I529N

Domain	Start	End	E-Value	Type
low complexity region	37	62	N/A	INTRINSIC
low complexity region	78	93	N/A	INTRINSIC
low complexity region	112	120	N/A	INTRINSIC
low complexity region	236	257	N/A	INTRINSIC
low complexity region	296	306	N/A	INTRINSIC
low complexity region	307	324	N/A	INTRINSIC
low complexity region	330	350	N/A	INTRINSIC
coiled coil region	356	383	N/A	INTRINSIC
ZnF_C2H2	389	413	1.05e1	SMART
SCOP:d1jvr__	538	613	7e-5	SMART
low complexity region	628	640	N/A	INTRINSIC

Coding Region Coverage

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

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 114 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810403A07Rik	T	C	3: 88,700,275	S345P	probably benign	Het
6430573F11Rik	T	C	8: 36,512,041	V266A	probably benign	Het
Abca3	G	T	17: 24,376,729	C352F	probably damaging	Het
Abce1	A	T	8: 79,700,586	I237N	possibly damaging	Het
Acrbp	A	G	6: 125,061,099	D421G	probably benign	Het
Adam8	T	A	7: 139,988,984	Y201F	probably benign	Het
Adgrf1	T	A	17: 43,311,064	C731S	probably damaging	Het
AF067063	T	A	13: 119,828,415	M82L	probably benign	Het
Akap9	G	A	5: 4,064,714	G114D	possibly damaging	Het
Alox12b	T	A	11: 69,162,932	D158E	probably benign	Het
Ankrd11	A	G	8: 122,884,231	S2639P	probably damaging	Het
Ankrd42	T	C	7: 92,590,182	Y466C	possibly damaging	Het
Apobr	T	C	7: 126,587,675	I786T	probably benign	Het
Arhgef12	C	T	9: 43,010,193	G329R	probably benign	Het
Btnl1	T	C	17: 34,381,552		probably null	Het
Ccdc174	A	G	6: 91,881,350		probably null	Het
Ccdc183	T	C	2: 25,615,422	D177G	possibly damaging	Het
Cd14	A	G	18: 36,726,235	Y56H	probably benign	Het
Cep162	G	A	9: 87,203,671	A1200V	probably benign	Het
Clic3	T	C	2: 25,458,307	L128P	probably damaging	Het
Cntnap5b	A	T	1: 100,383,399	Q539L	probably benign	Het
Cntnap5b	A	T	1: 100,383,395	R538*	probably null	Het
Coq7	A	T	7: 118,517,335	N214K	unknown	Het
Cramp1l	G	A	17: 24,973,113	H1018Y	possibly damaging	Het
Crtac1	T	A	19: 42,304,806	D288V	probably damaging	Het
Dab2ip	C	T	2: 35,715,327	R132*	probably null	Het
Dis3l	C	A	9: 64,330,835	C125F	probably benign	Het
Dnmt1	A	T	9: 20,920,205	V543D	probably damaging	Het
Dock9	A	T	14: 121,599,695	L67Q	probably damaging	Het
Ehbp1	A	T	11: 22,137,846	S413T	probably damaging	Het
Endov	A	G	11: 119,505,097	I158V	probably benign	Het
Epb41l4b	A	G	4: 57,064,802	V469A	possibly damaging	Het
Etf1	G	A	18: 34,913,601	P119S	probably damaging	Het
Fam135a	A	G	1: 24,029,727	L491P	possibly damaging	Het
Fancd2	A	T	6: 113,560,051		probably null	Het
Fank1	T	A	7: 133,869,329		probably null	Het
Fbxo18	A	G	2: 11,748,993	I846T	probably damaging	Het
Gas2l3	T	C	10: 89,414,066	T397A	probably benign	Het
Gga1	T	C	15: 78,893,188	V513A	probably damaging	Het
Ggt1	T	C	10: 75,585,948	V543A	probably damaging	Het
Gm11596	A	T	11: 99,792,891	C134*	probably null	Het
Gnal	C	T	18: 67,088,771	R82C	unknown	Het
Hat1	T	C	2: 71,410,238	V92A	possibly damaging	Het
Icosl	C	T	10: 78,073,763	R181C	probably damaging	Het
Ift46	A	G	9: 44,786,863	M208V	possibly damaging	Het
Ighv1-26	T	C	12: 114,788,599	K42E	possibly damaging	Het
Ipo5	A	G	14: 120,938,613	K617E	probably benign	Het
Irx5	A	G	8: 92,359,913	D208G	probably benign	Het
Itgal	T	G	7: 127,306,929	V397G	probably benign	Het
Itpr2	G	A	6: 146,173,366	R2297*	probably null	Het
Itpr3	A	G	17: 27,113,519	D1779G	probably damaging	Het
Krt4	T	A	15: 101,921,234	E286D	probably benign	Het
Loxl4	C	T	19: 42,604,290	G317E	probably damaging	Het
Mapk6	T	G	9: 75,388,062	H718P	possibly damaging	Het
Mark2	A	C	19: 7,282,816	V14G	probably damaging	Het
Mbd5	A	G	2: 49,272,814	T1103A	possibly damaging	Het
Mcph1	A	G	8: 18,632,293	E482G	probably benign	Het
Mme	G	A	3: 63,348,645	E509K	probably damaging	Het
Mrgbp	A	G	2: 180,585,483	T204A	probably damaging	Het
Mycbp2	A	T	14: 103,291,333	F430I	probably damaging	Het
Myo6	A	G	9: 80,217,720	D27G	probably damaging	Het
Ncoa6	A	G	2: 155,406,677	L1569S	probably damaging	Het
Ndc1	T	A	4: 107,380,704	F235Y	possibly damaging	Het
Nmur2	A	T	11: 56,033,009	S240T	probably benign	Het
Olfr1176	A	T	2: 88,340,413	I283F	possibly damaging	Het
Olfr301	T	A	7: 86,412,726	Y121*	probably null	Het
Olfr608	G	A	7: 103,470,914	V292M	probably damaging	Het
Osbpl1a	G	T	18: 12,841,192	A62E	probably damaging	Het
Osbpl1a	A	C	18: 12,892,262	S333A	probably benign	Het
Otud4	C	T	8: 79,664,108	T417I	probably benign	Het
Pagr1a	T	C	7: 127,015,442	E197G	probably damaging	Het
Pcdh18	T	C	3: 49,744,977	Q1012R	probably damaging	Het
Pcdhgb5	A	C	18: 37,731,637	I162L	probably benign	Het
Pdpr	T	A	8: 111,123,816	Y462N	probably damaging	Het
Pkhd1	A	T	1: 20,523,142	H1582Q	probably damaging	Het
Polr1b	A	G	2: 129,110,108	K352R	probably damaging	Het
Poteg	G	A	8: 27,448,037	V12M	probably damaging	Het
Pou2f1	A	C	1: 165,915,162	V54G	probably damaging	Het
Ppme1	A	G	7: 100,344,975	L177P	probably damaging	Het
Prkce	A	G	17: 86,619,948	D550G	probably damaging	Het
Prrc2c	A	G	1: 162,680,758		probably null	Het
Ptpn22	A	G	3: 103,882,139		probably null	Het
Rabif	G	A	1: 134,506,205	V86M	probably damaging	Het
Rbm25	T	A	12: 83,668,507	M484K	probably benign	Het
Rcn2	G	A	9: 56,057,429	A224T	probably benign	Het
Rexo5	T	A	7: 119,834,403		probably null	Het
Rnase1	A	T	14: 51,145,762	I45N	probably benign	Het
Rnmt	T	A	18: 68,306,115	D98E	possibly damaging	Het
Rprd2	A	G	3: 95,785,059	F188L	probably damaging	Het
Scube2	G	A	7: 109,810,737	T643M	probably damaging	Het
Slc7a15	T	C	12: 8,539,344	I68V	probably benign	Het
Slco1a5	A	T	6: 142,242,125	V496D	possibly damaging	Het
Slitrk6	T	G	14: 110,751,217	S353R	possibly damaging	Het
Smpd5	T	A	15: 76,295,125	I53K	possibly damaging	Het
Tas2r108	T	C	6: 40,494,087	S166P	probably benign	Het
Tecpr1	C	A	5: 144,214,344	V245L	possibly damaging	Het
Tenm3	G	T	8: 48,236,764	N1929K	probably damaging	Het
Tigd5	T	G	15: 75,911,025	F412C	probably damaging	Het
Timm17a	A	T	1: 135,306,188	S74T	possibly damaging	Het
Tle1	A	T	4: 72,139,808	L60Q	probably damaging	Het
Tmem132d	T	C	5: 127,796,000	E515G	possibly damaging	Het
Tmem65	T	C	15: 58,794,397	N115S	probably benign	Het
Trmt5	C	A	12: 73,281,652	R259L	possibly damaging	Het
Ttc37	T	C	13: 76,185,200	W25R	probably damaging	Het
Vmn2r50	A	T	7: 10,050,089	W153R	probably benign	Het
Vwa3a	T	G	7: 120,768,173	S184A	probably benign	Het
Zbtb25	A	G	12: 76,349,164	L428P	possibly damaging	Het
Zbtb49	C	T	5: 38,200,816	D698N	probably damaging	Het
Zbtb8os	T	G	4: 129,340,735	D35E	probably damaging	Het
Zfp316	T	C	5: 143,264,491	T56A	unknown	Het
Zfp334	A	T	2: 165,380,487	C545*	probably null	Het
Zmiz1	C	A	14: 25,644,856	S247R	probably damaging	Het
Zscan18	A	G	7: 12,775,381		probably benign	Het
Zzef1	T	C	11: 72,900,637	V2189A	probably damaging	Het

Other mutations in Akap8l

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00590:Akap8l	APN	17	32333097	missense	possibly damaging	0.82
IGL01603:Akap8l	APN	17	32345353	missense	probably damaging	1.00
IGL02028:Akap8l	APN	17	32338521	splice site	probably null
IGL02033:Akap8l	APN	17	32338272	missense	probably damaging	1.00
IGL02301:Akap8l	APN	17	32332926	splice site	probably benign
R1136:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1137:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1192:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1277:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1279:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1703:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1705:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1706:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1727:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1763:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1774:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1796:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R1954:Akap8l	UTSW	17	32336736	missense	possibly damaging	0.74
R2072:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R2073:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R2074:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R2107:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R2108:Akap8l	UTSW	17	32332483	missense	probably damaging	1.00
R2214:Akap8l	UTSW	17	32338825	critical splice acceptor site	probably null
R2215:Akap8l	UTSW	17	32321595	missense	possibly damaging	0.72
R2219:Akap8l	UTSW	17	32334631	missense	probably benign	0.23
R2234:Akap8l	UTSW	17	32338803	missense	probably damaging	1.00
R2871:Akap8l	UTSW	17	32338442	missense	possibly damaging	0.84
R2871:Akap8l	UTSW	17	32338442	missense	possibly damaging	0.84
R4273:Akap8l	UTSW	17	32321931	nonsense	probably null
R4379:Akap8l	UTSW	17	32321514	unclassified	probably benign
R5061:Akap8l	UTSW	17	32332894	missense	probably damaging	1.00
R5337:Akap8l	UTSW	17	32336394	missense	possibly damaging	0.71
R5377:Akap8l	UTSW	17	32321511	unclassified	probably benign
R5609:Akap8l	UTSW	17	32338400	missense	probably damaging	1.00
R5667:Akap8l	UTSW	17	32338292	missense	probably damaging	1.00
R5671:Akap8l	UTSW	17	32338292	missense	probably damaging	1.00
R5747:Akap8l	UTSW	17	32345378	missense	probably damaging	0.97
R6186:Akap8l	UTSW	17	32333044	missense	probably benign	0.02
R6400:Akap8l	UTSW	17	32336320	missense	probably damaging	0.99
R6482:Akap8l	UTSW	17	32345396	missense	possibly damaging	0.94
R6712:Akap8l	UTSW	17	32332888	missense	probably damaging	1.00
R7165:Akap8l	UTSW	17	32338412	missense	probably damaging	0.99
R7485:Akap8l	UTSW	17	32335571	missense	probably benign	0.03
R7729:Akap8l	UTSW	17	32333094	missense	probably damaging	1.00
R9437:Akap8l	UTSW	17	32334634	missense	probably benign	0.24
R9651:Akap8l	UTSW	17	32338809	missense	probably damaging	1.00
R9652:Akap8l	UTSW	17	32338809	missense	probably damaging	1.00
V5088:Akap8l	UTSW	17	32336739	critical splice acceptor site	probably null

Predicted Primers

PCR Primer
(F):5'- TCCTCTGGGTTGTCAGTGAAAG -3'
(R):5'- GTGGGTGATCAGATCGAATCC -3'

Sequencing Primer
(F):5'- TCAGTGAAAGGATTCTCGCC -3'
(R):5'- GGTGATCAGATCGAATCCTAGTTCC -3'

Posted On

2016-10-26