Mutagenetix > Incidental Mutation

Incidental Mutation 'R5061:Akap8l'

386649

Institutional Source

Beutler Lab

Gene Symbol

Akap8l

Ensembl Gene

ENSMUSG00000002625

Gene Name

A kinase anchor protein 8-like

Synonyms

Nakap95

MMRRC Submission

042651-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.567) question?

Stock #

R5061 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

32540398-32569581 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 32551868 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Threonine at position 441 (K441T)

Ref Sequence

ENSEMBL: ENSMUSP00000051389 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000050214
AA Change: K441T

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000051389
Gene: ENSMUSG00000002625
AA Change: K441T

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

0.6995

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 93.7%

Validation Efficiency

100% (71/71)

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700009N14Rik	A	G	4: 39,450,953 (GRCm39)	H53R	probably benign	Het
Abcg1	A	G	17: 31,311,366 (GRCm39)	K124E	probably damaging	Het
Acot4	G	T	12: 84,085,475 (GRCm39)	R64L	probably benign	Het
Adam22	G	C	5: 8,230,238 (GRCm39)		probably benign	Het
Add2	G	A	6: 86,064,029 (GRCm39)		probably null	Het
Adgrb3	G	A	1: 25,107,209 (GRCm39)		probably benign	Het
Aspn	T	A	13: 49,720,080 (GRCm39)	S365R	probably damaging	Het
Atxn1	T	G	13: 45,710,569 (GRCm39)	K788Q	probably damaging	Het
Atxn2l	G	T	7: 126,099,375 (GRCm39)	H135N	probably damaging	Het
Borcs8	T	G	8: 70,593,008 (GRCm39)		probably null	Het
Col5a1	G	A	2: 27,842,390 (GRCm39)	D422N	unknown	Het
Cstad	A	T	2: 30,498,275 (GRCm39)	T37S	unknown	Het
Dgkq	A	T	5: 108,801,989 (GRCm39)	D455E	probably benign	Het
Dop1a	T	C	9: 86,385,161 (GRCm39)		probably benign	Het
Ebf3	T	C	7: 136,915,288 (GRCm39)	I84V	possibly damaging	Het
Ehmt2	C	T	17: 35,118,067 (GRCm39)	R40*	probably null	Het
Eif3e	A	T	15: 43,115,657 (GRCm39)	W370R	probably damaging	Het
Eya3	T	A	4: 132,431,689 (GRCm39)	D323E	probably damaging	Het
F5	T	C	1: 164,021,749 (GRCm39)	L1408P	probably benign	Het
Fam110d	T	C	4: 133,979,041 (GRCm39)	T146A	probably benign	Het
Gfod1	C	T	13: 43,353,992 (GRCm39)	G328S	probably benign	Het
Gja1	T	A	10: 56,263,752 (GRCm39)	L37Q	probably damaging	Het
Gm10650	T	A	3: 127,833,666 (GRCm39)		noncoding transcript	Het
Gm14226	T	A	2: 154,867,106 (GRCm39)	H354Q	probably benign	Het
Gm15056	T	C	8: 21,390,758 (GRCm39)	T60A	probably benign	Het
Hsd11b1	A	T	1: 192,924,553 (GRCm39)	N6K	probably benign	Het
Ighv1-36	T	C	12: 114,843,742 (GRCm39)	I39M	probably benign	Het
Igkv4-80	A	C	6: 68,993,649 (GRCm39)	S81A	probably benign	Het
Kdm7a	G	A	6: 39,128,386 (GRCm39)	P482S	possibly damaging	Het
Lama5	C	A	2: 179,840,579 (GRCm39)	E607*	probably null	Het
Lao1	T	A	4: 118,824,673 (GRCm39)	S252T	probably benign	Het
Lrp12	A	G	15: 39,741,650 (GRCm39)	F355S	probably damaging	Het
Mlycd	T	C	8: 120,137,043 (GRCm39)	F421S	probably damaging	Het
Nectin3	T	C	16: 46,268,812 (GRCm39)	E530G	probably benign	Het
Nifk	T	C	1: 118,260,669 (GRCm39)	*270R	probably null	Het
Ocln	T	C	13: 100,676,106 (GRCm39)	Y129C	probably damaging	Het
Or10ag60	C	T	2: 87,438,176 (GRCm39)	T148I	probably benign	Het
Or4f54	T	A	2: 111,122,832 (GRCm39)	L73H	probably damaging	Het
Or52l1	T	A	7: 104,829,864 (GRCm39)	I219F	possibly damaging	Het
Or5b117	A	T	19: 13,431,349 (GRCm39)	C177*	probably null	Het
Otx1	C	A	11: 21,947,037 (GRCm39)	A91S	probably damaging	Het
Pcdhb22	G	T	18: 37,652,179 (GRCm39)	G216C	probably damaging	Het
Ppcs	T	C	4: 119,276,412 (GRCm39)	K58E	probably damaging	Het
Prss38	T	C	11: 59,265,196 (GRCm39)	T123A	probably damaging	Het
Rap1gap	T	A	4: 137,447,744 (GRCm39)		probably null	Het
Rbm18	A	G	2: 36,017,217 (GRCm39)	F54L	possibly damaging	Het
Rwdd3	G	A	3: 120,953,432 (GRCm39)		probably benign	Het
Ryr2	T	C	13: 11,650,422 (GRCm39)	K138E	possibly damaging	Het
Sec24a	T	C	11: 51,604,359 (GRCm39)		probably null	Het
Serpinb10	A	G	1: 107,468,701 (GRCm39)	T115A	probably benign	Het
Slco1a8	T	A	6: 141,954,414 (GRCm39)	M20L	probably benign	Het
Slx4ip	T	G	2: 136,885,930 (GRCm39)	F83L	probably damaging	Het
St3gal1	A	T	15: 66,980,078 (GRCm39)	S274T	probably benign	Het
Stab1	A	C	14: 30,885,056 (GRCm39)	C121W	probably damaging	Het
Stab2	A	G	10: 86,743,249 (GRCm39)	L1149P	probably damaging	Het
Svil	T	G	18: 5,048,954 (GRCm39)	I77R	probably benign	Het
Tbk1	T	G	10: 121,412,241 (GRCm39)	E47A	possibly damaging	Het
Tert	C	T	13: 73,782,397 (GRCm39)	T557I	probably damaging	Het
Tfap2c	A	G	2: 172,393,947 (GRCm39)	D252G	probably damaging	Het
Tll1	C	A	8: 64,506,983 (GRCm39)	C586F	probably damaging	Het
Tln2	T	G	9: 67,261,750 (GRCm39)	N663T	probably benign	Het
Tmem245	T	A	4: 56,946,945 (GRCm39)	Y156F	possibly damaging	Het
Uhrf1	G	T	17: 56,627,542 (GRCm39)		probably null	Het
Unc79	T	A	12: 103,134,700 (GRCm39)	M2417K	possibly damaging	Het
Ush2a	T	C	1: 188,689,471 (GRCm39)	V5011A	probably benign	Het
Virma	T	C	4: 11,494,840 (GRCm39)	V47A	possibly damaging	Het
Vmn2r53	A	C	7: 12,315,741 (GRCm39)	S693A	probably benign	Het
Vps54	G	A	11: 21,269,881 (GRCm39)		probably benign	Het
Znfx1	T	C	2: 166,907,318 (GRCm39)		probably benign	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
R2215:Akap8l	UTSW	17	32,540,569 (GRCm39)	missense	possibly damaging	0.72
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
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'- TCTACACGAGCCTGAGACTG -3'
(R):5'- ATGGGTAGCCACCTTGACAG -3'

Sequencing Primer
(F):5'- CGAGCCTGAGACTGGTGAAC -3'
(R):5'- TTGACAGCAAGTTCCACAAGG -3'

Posted On

2016-06-06