Mutagenetix > Incidental Mutation

Incidental Mutation 'R2215:Akap8l'

241123

Institutional Source

Beutler Lab

Gene Symbol

Akap8l

Ensembl Gene

ENSMUSG00000002625

Gene Name

A kinase anchor protein 8-like

Synonyms

Nakap95

MMRRC Submission

040217-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.641) question?

Stock #

R2215 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

32540398-32569581 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 32540569 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 608 (E608G)

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

possibly damaging
Transcript: ENSMUST00000050214
AA Change: E608G

PolyPhen 2 Score 0.719 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000051389
Gene: ENSMUSG00000002625
AA Change: E608G

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

Meta Mutation Damage Score

0.0718

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.3%

Validation Efficiency

100% (68/68)

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acaca	T	A	11: 84,254,619 (GRCm39)	S1899T	probably damaging	Het
Accs	G	T	2: 93,672,243 (GRCm39)	N208K	probably benign	Het
Actn4	C	A	7: 28,618,178 (GRCm39)	V22L	possibly damaging	Het
Adam21	A	G	12: 81,607,064 (GRCm39)	S233P	probably damaging	Het
Adrm1b	G	A	3: 92,335,730 (GRCm39)	A324V	probably damaging	Het
Agmat	C	T	4: 141,476,899 (GRCm39)	R102C	probably benign	Het
Arap2	T	C	5: 62,834,519 (GRCm39)	I788V	probably damaging	Het
Arhgef12	G	T	9: 42,917,167 (GRCm39)	H391N	probably damaging	Het
Arhgef28	G	T	13: 98,187,529 (GRCm39)	H255Q	possibly damaging	Het
Baz1a	G	A	12: 55,022,154 (GRCm39)	R43*	probably null	Het
Bcas3	T	C	11: 85,692,769 (GRCm39)	S862P	probably damaging	Het
Blm	A	T	7: 80,149,595 (GRCm39)	H671Q	possibly damaging	Het
Bmp8a	C	T	4: 123,218,911 (GRCm39)	V166I	probably benign	Het
Cep120	G	T	18: 53,860,707 (GRCm39)	P241Q	probably damaging	Het
Col14a1	G	A	15: 55,244,238 (GRCm39)	G437E	unknown	Het
Cyp2a5	T	C	7: 26,539,900 (GRCm39)	L3S	probably damaging	Het
D16Ertd472e	T	C	16: 78,342,155 (GRCm39)	T242A	probably benign	Het
Dach1	A	G	14: 98,405,917 (GRCm39)		probably null	Het
Ddx20	A	T	3: 105,587,656 (GRCm39)		probably benign	Het
Eif4enif1	A	G	11: 3,177,476 (GRCm39)	S185G	probably damaging	Het
Ep400	A	T	5: 110,841,421 (GRCm39)		probably benign	Het
Fam117b	T	A	1: 60,008,219 (GRCm39)	I351K	probably damaging	Het
Fbxo31	T	C	8: 122,293,050 (GRCm39)	I112V	probably benign	Het
Galntl5	A	T	5: 25,403,476 (GRCm39)	N149I	probably damaging	Het
Gja8	A	T	3: 96,827,218 (GRCm39)	F148Y	probably damaging	Het
Gpatch1	A	T	7: 34,993,252 (GRCm39)	L531Q	possibly damaging	Het
Gprin1	G	A	13: 54,888,046 (GRCm39)	T76M	probably damaging	Het
Htr4	T	A	18: 62,546,787 (GRCm39)	C113*	probably null	Het
Igf1r	T	A	7: 67,814,982 (GRCm39)	D294E	probably benign	Het
Kdm6b	G	A	11: 69,295,870 (GRCm39)	P799L	unknown	Het
Lat	A	T	7: 125,967,137 (GRCm39)	V139E	probably damaging	Het
Lrrc34	G	A	3: 30,697,678 (GRCm39)	R51C	probably benign	Het
Map3k1	A	G	13: 111,892,322 (GRCm39)	S978P	probably benign	Het
Masp1	T	A	16: 23,271,271 (GRCm39)	D659V	possibly damaging	Het
Mcam	A	T	9: 44,051,250 (GRCm39)	R415*	probably null	Het
Mtmr10	A	G	7: 63,987,403 (GRCm39)	T648A	probably benign	Het
Myh2	T	C	11: 67,082,563 (GRCm39)	W1378R	probably benign	Het
Nipsnap2	A	G	5: 129,816,649 (GRCm39)	E64G	probably damaging	Het
Or4a68	T	C	2: 89,270,381 (GRCm39)	M81V	probably benign	Het
Or52n4b	T	C	7: 108,144,095 (GRCm39)	L119P	probably damaging	Het
Or6c3	A	T	10: 129,309,289 (GRCm39)	I243F	probably damaging	Het
Or9s27	G	A	1: 92,516,708 (GRCm39)	V219I	probably benign	Het
Pcdhb8	T	G	18: 37,490,127 (GRCm39)	S602A	probably damaging	Het
Peg10	A	T	6: 4,756,918 (GRCm39)		probably benign	Het
Pld1	A	T	3: 28,132,542 (GRCm39)	I577F	probably benign	Het
Plekhm1	A	T	11: 103,267,811 (GRCm39)	I720N	probably damaging	Het
Ppp2r1a	A	G	17: 21,182,005 (GRCm39)		probably null	Het
Retreg3	G	T	11: 101,010,459 (GRCm39)	Y49*	probably null	Het
Rrp36	T	C	17: 46,983,746 (GRCm39)	E22G	possibly damaging	Het
Sec14l2	C	A	11: 4,059,169 (GRCm39)	A167S	probably damaging	Het
Sema5b	A	G	16: 35,480,585 (GRCm39)	T751A	probably damaging	Het
Smarcc1	C	A	9: 110,066,907 (GRCm39)		probably benign	Het
Smox	T	C	2: 131,362,190 (GRCm39)		probably null	Het
Spats2l	A	T	1: 57,985,575 (GRCm39)	T543S	possibly damaging	Het
Sppl2a	G	T	2: 126,769,754 (GRCm39)	T34K	probably benign	Het
Svep1	T	C	4: 58,138,602 (GRCm39)		probably benign	Het
Tet2	T	A	3: 133,192,362 (GRCm39)	I691F	probably benign	Het
Tnxb	T	C	17: 34,923,114 (GRCm39)	Y2566H	possibly damaging	Het
Ttn	T	C	2: 76,570,853 (GRCm39)	E26680G	probably damaging	Het
Txlna	T	C	4: 129,533,111 (GRCm39)	E139G	possibly damaging	Het
Ubap2	T	C	4: 41,196,483 (GRCm39)		probably null	Het
Ubr3	A	T	2: 69,809,661 (GRCm39)		probably null	Het
Usp37	A	C	1: 74,483,685 (GRCm39)	F844V	probably damaging	Het
Usp6nl	A	G	2: 6,429,150 (GRCm39)	D204G	probably damaging	Het
Vmn1r230	T	C	17: 21,067,684 (GRCm39)	I291T	probably benign	Het
Zfp229	T	G	17: 21,965,258 (GRCm39)	V496G	possibly damaging	Het

Other mutations in Akap8l

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00590:Akap8l	APN	17	32,552,071 (GRCm39)	missense	possibly damaging	0.82
IGL01603:Akap8l	APN	17	32,564,327 (GRCm39)	missense	probably damaging	1.00
IGL02028:Akap8l	APN	17	32,557,495 (GRCm39)	splice site	probably null
IGL02033:Akap8l	APN	17	32,557,246 (GRCm39)	missense	probably damaging	1.00
IGL02301:Akap8l	APN	17	32,551,900 (GRCm39)	splice site	probably benign
R1136:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1137:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1192:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1277:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1279:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1703:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1705:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1706:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1727:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1763:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1774:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1796:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R1954:Akap8l	UTSW	17	32,555,710 (GRCm39)	missense	possibly damaging	0.74
R2072:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R2073:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R2074:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R2107:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R2108:Akap8l	UTSW	17	32,551,457 (GRCm39)	missense	probably damaging	1.00
R2214:Akap8l	UTSW	17	32,557,799 (GRCm39)	critical splice acceptor site	probably null
R2219:Akap8l	UTSW	17	32,553,605 (GRCm39)	missense	probably benign	0.23
R2234:Akap8l	UTSW	17	32,557,777 (GRCm39)	missense	probably damaging	1.00
R2871:Akap8l	UTSW	17	32,557,416 (GRCm39)	missense	possibly damaging	0.84
R2871:Akap8l	UTSW	17	32,557,416 (GRCm39)	missense	possibly damaging	0.84
R4273:Akap8l	UTSW	17	32,540,905 (GRCm39)	nonsense	probably null
R4379:Akap8l	UTSW	17	32,540,488 (GRCm39)	unclassified	probably benign
R5061:Akap8l	UTSW	17	32,551,868 (GRCm39)	missense	probably damaging	1.00
R5337:Akap8l	UTSW	17	32,555,368 (GRCm39)	missense	possibly damaging	0.71
R5377:Akap8l	UTSW	17	32,540,485 (GRCm39)	unclassified	probably benign
R5579:Akap8l	UTSW	17	32,540,916 (GRCm39)	missense	probably damaging	1.00
R5609:Akap8l	UTSW	17	32,557,374 (GRCm39)	missense	probably damaging	1.00
R5667:Akap8l	UTSW	17	32,557,266 (GRCm39)	missense	probably damaging	1.00
R5671:Akap8l	UTSW	17	32,557,266 (GRCm39)	missense	probably damaging	1.00
R5747:Akap8l	UTSW	17	32,564,352 (GRCm39)	missense	probably damaging	0.97
R6186:Akap8l	UTSW	17	32,552,018 (GRCm39)	missense	probably benign	0.02
R6400:Akap8l	UTSW	17	32,555,294 (GRCm39)	missense	probably damaging	0.99
R6482:Akap8l	UTSW	17	32,564,370 (GRCm39)	missense	possibly damaging	0.94
R6712:Akap8l	UTSW	17	32,551,862 (GRCm39)	missense	probably damaging	1.00
R7165:Akap8l	UTSW	17	32,557,386 (GRCm39)	missense	probably damaging	0.99
R7485:Akap8l	UTSW	17	32,554,545 (GRCm39)	missense	probably benign	0.03
R7729:Akap8l	UTSW	17	32,552,068 (GRCm39)	missense	probably damaging	1.00
R9437:Akap8l	UTSW	17	32,553,608 (GRCm39)	missense	probably benign	0.24
R9651:Akap8l	UTSW	17	32,557,783 (GRCm39)	missense	probably damaging	1.00
R9652:Akap8l	UTSW	17	32,557,783 (GRCm39)	missense	probably damaging	1.00
V5088:Akap8l	UTSW	17	32,555,713 (GRCm39)	critical splice acceptor site	probably null

Predicted Primers

PCR Primer
(F):5'- AGCGGTTCTAGCGCGTTTAC -3'
(R):5'- TTCACTGACAACCCAGAGGAG -3'

Sequencing Primer
(F):5'- AGGCGCACTTCTAGGGG -3'
(R):5'- CTGACAACCCAGAGGAGGAAAAG -3'

Posted On

2014-10-15