Mutagenetix > Incidental Mutation

Incidental Mutation 'R7671:Akap13'

592160

Institutional Source

Beutler Lab

Gene Symbol

Akap13

Ensembl Gene

ENSMUSG00000066406

Gene Name

A kinase (PRKA) anchor protein 13

Synonyms

AKAP-Lbc, 5730522G15Rik, 1700026G02Rik, PROTO-LBC, PROTO-LB, Ht31, 5830460E08Rik

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7671 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

75455534-75754609 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 75569900 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Lysine at position 17 (T17K)

Ref Sequence

ENSEMBL: ENSMUSP00000147237 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000166315] [ENSMUST00000207750]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000166315
AA Change: T17K

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

SMART Domains

Protein: ENSMUSP00000129784
Gene: ENSMUSG00000066406
AA Change: T17K

Domain	Start	End	E-Value	Type
low complexity region	174	184	N/A	INTRINSIC
low complexity region	773	789	N/A	INTRINSIC
low complexity region	896	908	N/A	INTRINSIC
low complexity region	1021	1032	N/A	INTRINSIC
low complexity region	1433	1448	N/A	INTRINSIC
low complexity region	1483	1505	N/A	INTRINSIC
low complexity region	1583	1594	N/A	INTRINSIC
low complexity region	1720	1750	N/A	INTRINSIC
C1	1755	1801	1.95e-4	SMART
low complexity region	1858	1869	N/A	INTRINSIC
RhoGEF	1961	2153	1.28e-61	SMART
PH	2195	2298	2.94e-11	SMART
coiled coil region	2308	2345	N/A	INTRINSIC
low complexity region	2393	2412	N/A	INTRINSIC
low complexity region	2444	2454	N/A	INTRINSIC
coiled coil region	2533	2646	N/A	INTRINSIC
low complexity region	2728	2734	N/A	INTRINSIC
low complexity region	2740	2753	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000207750
AA Change: T17K

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

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms containing c-terminal dbl oncogene homology (DH) and pleckstrin homology (PH) domains. The DH domain is associated with guanine nucleotide exchange activation for the Rho/Rac family of small GTP binding proteins, resulting in the conversion of the inactive GTPase to the active form capable of transducing signals. The PH domain has multiple functions. Therefore, these isoforms function as scaffolding proteins to coordinate a Rho signaling pathway, function as protein kinase A-anchoring proteins and, in addition, enhance ligand-dependent activity of estrogen receptors alpha and beta. [provided by RefSeq, Jul 2012]
PHENOTYPE: Mice homozygous for a null allele exhibit embryonic lethality during organogenesis, arrested heart development, and forebrain hypoplasia. Heterozygous mice exhibit small spleen, impaired lymphocyte response to osmotic stress, decreased response to glucocorticoid, osteoporosis and impared osteogenesis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610009O20Rik	T	A	18: 38,259,925 (GRCm38)	I394N	probably damaging	Het
4930435E12Rik	C	T	16: 38,828,091 (GRCm38)	D219N	possibly damaging	Het
4932438A13Rik	T	C	3: 36,943,231 (GRCm38)	F1146L	probably damaging	Het
4933406M09Rik	T	C	1: 134,390,062 (GRCm38)	C191R	probably benign	Het
Ankrd29	T	A	18: 12,260,986 (GRCm38)	K257I	probably damaging	Het
Bicc1	A	G	10: 70,957,167 (GRCm38)	L219P	probably benign	Het
Boc	C	T	16: 44,491,849 (GRCm38)	V617M		Het
Ccl8	A	G	11: 82,115,207 (GRCm38)		probably benign	Het
Col18a1	A	G	10: 77,085,383 (GRCm38)	L261P	unknown	Het
Col5a3	T	A	9: 20,775,086 (GRCm38)		probably null	Het
Cryba4	A	C	5: 112,248,173 (GRCm38)		probably null	Het
Csf2rb	A	G	15: 78,338,930 (GRCm38)	Y114C	probably damaging	Het
Ctif	T	C	18: 75,472,016 (GRCm38)	D484G	probably damaging	Het
Ctnnal1	A	G	4: 56,837,848 (GRCm38)	F261L	probably damaging	Het
Defb22	A	T	2: 152,486,030 (GRCm38)	N78K	unknown	Het
Efr3a	G	A	15: 65,837,434 (GRCm38)		probably null	Het
Elp4	G	T	2: 105,904,481 (GRCm38)	A3E	probably damaging	Het
Emilin2	A	G	17: 71,273,910 (GRCm38)	V607A	probably benign	Het
Epsti1	A	G	14: 77,904,490 (GRCm38)	Y2C	probably damaging	Het
Fam81b	G	T	13: 76,271,294 (GRCm38)	L46I	possibly damaging	Het
Fam81b	A	C	13: 76,271,293 (GRCm38)	L46R	probably damaging	Het
Fbxo15	T	A	18: 84,964,153 (GRCm38)	H288Q	probably damaging	Het
Gabrg1	T	A	5: 70,815,980 (GRCm38)	N77I	probably damaging	Het
Ganab	A	G	19: 8,912,852 (GRCm38)	Y715C	possibly damaging	Het
Hist3h2ba	T	C	11: 58,949,276 (GRCm38)	S113P	possibly damaging	Het
Iqgap2	T	C	13: 95,628,119 (GRCm38)	D1539G	probably damaging	Het
Kcp	T	C	6: 29,496,517 (GRCm38)	N633S	probably benign	Het
Krt6a	C	A	15: 101,690,543 (GRCm38)	S529I	unknown	Het
Leo1	A	G	9: 75,445,562 (GRCm38)	H129R	probably benign	Het
Lmf1	G	A	17: 25,579,349 (GRCm38)	V55M	possibly damaging	Het
Mcm9	A	G	10: 53,537,569 (GRCm38)	S472P	probably benign	Het
Med27	T	A	2: 29,377,938 (GRCm38)	V33D		Het
Mup15	C	T	4: 61,438,289 (GRCm38)	E80K	probably benign	Het
Myo18a	G	A	11: 77,859,420 (GRCm38)	R199H		Het
Nebl	T	A	2: 17,390,916 (GRCm38)	R558*	probably null	Het
Olfr1121	A	G	2: 87,372,269 (GRCm38)	T246A	probably damaging	Het
Olfr1252	A	T	2: 89,721,259 (GRCm38)	I284K	probably damaging	Het
Olfr1329	A	T	4: 118,916,986 (GRCm38)	H160Q	probably benign	Het
Olfr506	T	C	7: 108,612,991 (GRCm38)	I228T	probably damaging	Het
Olfr740	G	T	14: 50,453,885 (GRCm38)	V278L	probably benign	Het
Olfr815	T	C	10: 129,902,353 (GRCm38)	D119G	probably damaging	Het
Olfr890	A	T	9: 38,143,440 (GRCm38)	M97L	probably benign	Het
Pde11a	A	T	2: 76,215,353 (GRCm38)	F376I	possibly damaging	Het
Prima1	A	T	12: 103,235,661 (GRCm38)	C52S	probably damaging	Het
Pxn	G	A	5: 115,548,547 (GRCm38)	R366H	not run	Het
Sgce	T	C	6: 4,691,564 (GRCm38)	Y337C	probably damaging	Het
Slc25a10	T	A	11: 120,495,460 (GRCm38)	M130K	probably benign	Het
Slc29a2	A	T	19: 5,024,262 (GRCm38)	N5I	probably benign	Het
Slc35a1	A	T	4: 34,673,875 (GRCm38)	H150Q		Het
Slc5a4a	T	A	10: 76,147,550 (GRCm38)	V7D	unknown	Het
Stk17b	T	A	1: 53,766,000 (GRCm38)	D134V	probably damaging	Het
Thbs3	T	A	3: 89,216,707 (GRCm38)	S36T	probably benign	Het
Thsd4	A	G	9: 60,428,174 (GRCm38)	S152P	probably benign	Het
Tmem67	G	T	4: 12,063,698 (GRCm38)	H422N	probably benign	Het
Tram1	C	A	1: 13,589,644 (GRCm38)	V27F	probably damaging	Het
Trim14	A	G	4: 46,507,238 (GRCm38)	V326A	possibly damaging	Het

Other mutations in Akap13

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00161:Akap13	APN	7	75,725,971 (GRCm38)	missense	probably damaging	0.99
IGL00332:Akap13	APN	7	75,728,919 (GRCm38)	missense	probably damaging	1.00
IGL00481:Akap13	APN	7	75,723,895 (GRCm38)	missense	probably damaging	1.00
IGL00590:Akap13	APN	7	75,610,669 (GRCm38)	missense	probably benign	0.01
IGL00655:Akap13	APN	7	75,704,398 (GRCm38)	missense	probably damaging	0.99
IGL00766:Akap13	APN	7	75,704,512 (GRCm38)	missense	probably damaging	0.96
IGL00818:Akap13	APN	7	75,609,727 (GRCm38)	missense	probably benign	0.00
IGL00826:Akap13	APN	7	75,677,447 (GRCm38)	missense	probably damaging	1.00
IGL01014:Akap13	APN	7	75,750,633 (GRCm38)	utr 3 prime	probably benign
IGL01090:Akap13	APN	7	75,666,531 (GRCm38)	missense	probably benign	0.44
IGL01155:Akap13	APN	7	75,569,936 (GRCm38)	missense	probably damaging	1.00
IGL01326:Akap13	APN	7	75,725,348 (GRCm38)	missense	probably benign	0.30
IGL01456:Akap13	APN	7	75,602,847 (GRCm38)	missense	probably damaging	0.98
IGL01460:Akap13	APN	7	75,747,846 (GRCm38)	missense	probably benign	0.29
IGL01568:Akap13	APN	7	75,608,522 (GRCm38)	nonsense	probably null	0.00
IGL01610:Akap13	APN	7	75,747,605 (GRCm38)	missense	probably damaging	1.00
IGL01610:Akap13	APN	7	75,720,180 (GRCm38)	missense	possibly damaging	0.71
IGL01615:Akap13	APN	7	75,697,393 (GRCm38)	missense	probably damaging	1.00
IGL01667:Akap13	APN	7	75,570,019 (GRCm38)	missense	probably damaging	1.00
IGL01705:Akap13	APN	7	75,746,767 (GRCm38)	missense	possibly damaging	0.86
IGL02070:Akap13	APN	7	75,666,545 (GRCm38)	missense	probably benign	0.27
IGL02269:Akap13	APN	7	75,602,911 (GRCm38)	missense	probably benign
IGL02421:Akap13	APN	7	75,717,806 (GRCm38)	missense	possibly damaging	0.66
IGL02870:Akap13	APN	7	75,609,188 (GRCm38)	missense	probably damaging	0.96
IGL02944:Akap13	APN	7	75,608,657 (GRCm38)	missense	probably benign
IGL03051:Akap13	APN	7	75,610,485 (GRCm38)	nonsense	probably null
IGL03160:Akap13	APN	7	75,730,417 (GRCm38)	missense	probably damaging	1.00
IGL03245:Akap13	APN	7	75,609,752 (GRCm38)	missense	probably damaging	0.99
R0254:Akap13	UTSW	7	75,736,604 (GRCm38)	splice site	probably benign
R0310:Akap13	UTSW	7	75,614,930 (GRCm38)	missense	probably damaging	0.99
R0373:Akap13	UTSW	7	75,730,500 (GRCm38)	missense	probably damaging	1.00
R0373:Akap13	UTSW	7	75,609,929 (GRCm38)	missense	probably benign	0.00
R0408:Akap13	UTSW	7	75,746,796 (GRCm38)	missense	probably damaging	1.00
R0631:Akap13	UTSW	7	75,614,996 (GRCm38)	missense	probably damaging	0.99
R0646:Akap13	UTSW	7	75,747,746 (GRCm38)	missense	probably damaging	1.00
R0781:Akap13	UTSW	7	75,611,377 (GRCm38)	missense	possibly damaging	0.56
R0845:Akap13	UTSW	7	75,725,380 (GRCm38)	missense	probably damaging	1.00
R1004:Akap13	UTSW	7	75,687,286 (GRCm38)	missense	probably damaging	0.99
R1024:Akap13	UTSW	7	75,677,409 (GRCm38)	missense	probably damaging	1.00
R1110:Akap13	UTSW	7	75,611,377 (GRCm38)	missense	possibly damaging	0.56
R1346:Akap13	UTSW	7	75,609,592 (GRCm38)	missense	possibly damaging	0.67
R1349:Akap13	UTSW	7	75,609,592 (GRCm38)	missense	possibly damaging	0.67
R1372:Akap13	UTSW	7	75,609,592 (GRCm38)	missense	possibly damaging	0.67
R1387:Akap13	UTSW	7	75,586,193 (GRCm38)	missense	probably damaging	0.97
R1442:Akap13	UTSW	7	75,735,778 (GRCm38)	missense	probably damaging	0.99
R1466:Akap13	UTSW	7	75,729,049 (GRCm38)	missense	possibly damaging	0.79
R1466:Akap13	UTSW	7	75,729,049 (GRCm38)	missense	possibly damaging	0.79
R1584:Akap13	UTSW	7	75,729,049 (GRCm38)	missense	possibly damaging	0.79
R1696:Akap13	UTSW	7	75,609,592 (GRCm38)	missense	possibly damaging	0.67
R1738:Akap13	UTSW	7	75,677,194 (GRCm38)	missense	probably damaging	1.00
R1773:Akap13	UTSW	7	75,683,451 (GRCm38)	missense	possibly damaging	0.80
R1785:Akap13	UTSW	7	75,611,434 (GRCm38)	missense	probably benign	0.16
R1786:Akap13	UTSW	7	75,611,434 (GRCm38)	missense	probably benign	0.16
R1791:Akap13	UTSW	7	75,611,035 (GRCm38)	missense	probably benign	0.00
R1819:Akap13	UTSW	7	75,608,705 (GRCm38)	missense	probably benign	0.04
R1879:Akap13	UTSW	7	75,610,727 (GRCm38)	missense	probably benign	0.01
R1989:Akap13	UTSW	7	75,704,516 (GRCm38)	missense	probably benign	0.01
R2016:Akap13	UTSW	7	75,704,531 (GRCm38)	missense	probably damaging	0.99
R2092:Akap13	UTSW	7	75,610,570 (GRCm38)	missense	probably benign	0.05
R2126:Akap13	UTSW	7	75,725,304 (GRCm38)	missense	possibly damaging	0.95
R2131:Akap13	UTSW	7	75,611,434 (GRCm38)	missense	probably benign	0.16
R2132:Akap13	UTSW	7	75,611,434 (GRCm38)	missense	probably benign	0.16
R2133:Akap13	UTSW	7	75,611,434 (GRCm38)	missense	probably benign	0.16
R2251:Akap13	UTSW	7	75,739,477 (GRCm38)	missense	possibly damaging	0.50
R3704:Akap13	UTSW	7	75,666,550 (GRCm38)	missense	probably damaging	1.00
R3713:Akap13	UTSW	7	75,586,181 (GRCm38)	missense	probably damaging	0.98
R3731:Akap13	UTSW	7	75,611,377 (GRCm38)	missense	probably benign	0.39
R3765:Akap13	UTSW	7	75,608,837 (GRCm38)	missense	probably benign	0.04
R3788:Akap13	UTSW	7	75,702,153 (GRCm38)	critical splice donor site	probably null
R3793:Akap13	UTSW	7	75,610,141 (GRCm38)	missense	probably benign	0.00
R3970:Akap13	UTSW	7	75,569,951 (GRCm38)	nonsense	probably null
R4205:Akap13	UTSW	7	75,610,919 (GRCm38)	missense	probably benign	0.05
R4257:Akap13	UTSW	7	75,611,285 (GRCm38)	missense	probably damaging	0.98
R4374:Akap13	UTSW	7	75,608,984 (GRCm38)	missense	probably damaging	0.96
R4448:Akap13	UTSW	7	75,742,760 (GRCm38)	missense	probably damaging	1.00
R4450:Akap13	UTSW	7	75,742,760 (GRCm38)	missense	probably damaging	1.00
R4457:Akap13	UTSW	7	75,739,465 (GRCm38)	missense	probably damaging	0.99
R4458:Akap13	UTSW	7	75,739,465 (GRCm38)	missense	probably damaging	0.99
R4466:Akap13	UTSW	7	75,602,773 (GRCm38)	splice site	probably null
R4632:Akap13	UTSW	7	75,666,553 (GRCm38)	missense	possibly damaging	0.91
R4667:Akap13	UTSW	7	75,729,094 (GRCm38)	missense	probably damaging	1.00
R4669:Akap13	UTSW	7	75,729,094 (GRCm38)	missense	probably damaging	1.00
R4671:Akap13	UTSW	7	75,579,564 (GRCm38)	nonsense	probably null
R4821:Akap13	UTSW	7	75,677,507 (GRCm38)	intron	probably benign
R4868:Akap13	UTSW	7	75,743,504 (GRCm38)	missense	probably damaging	1.00
R4894:Akap13	UTSW	7	75,725,320 (GRCm38)	missense	possibly damaging	0.76
R4943:Akap13	UTSW	7	75,749,240 (GRCm38)	missense	probably benign	0.22
R4962:Akap13	UTSW	7	75,749,430 (GRCm38)	missense	probably damaging	0.98
R4988:Akap13	UTSW	7	75,730,528 (GRCm38)	missense	probably damaging	1.00
R5119:Akap13	UTSW	7	75,687,252 (GRCm38)	missense	probably damaging	0.98
R5141:Akap13	UTSW	7	75,609,614 (GRCm38)	missense	probably benign	0.18
R5419:Akap13	UTSW	7	75,610,243 (GRCm38)	missense	probably benign	0.01
R5427:Akap13	UTSW	7	75,728,869 (GRCm38)	missense	possibly damaging	0.89
R5429:Akap13	UTSW	7	75,602,904 (GRCm38)	missense	possibly damaging	0.70
R5432:Akap13	UTSW	7	75,602,830 (GRCm38)	missense	probably damaging	1.00
R5458:Akap13	UTSW	7	75,586,301 (GRCm38)	missense	probably damaging	1.00
R5636:Akap13	UTSW	7	75,704,372 (GRCm38)	missense	probably damaging	0.96
R5643:Akap13	UTSW	7	75,702,154 (GRCm38)	critical splice donor site	probably null
R5898:Akap13	UTSW	7	75,729,146 (GRCm38)	missense	probably damaging	1.00
R5932:Akap13	UTSW	7	75,610,184 (GRCm38)	missense	probably damaging	1.00
R6135:Akap13	UTSW	7	75,609,908 (GRCm38)	missense	possibly damaging	0.94
R6137:Akap13	UTSW	7	75,677,416 (GRCm38)	missense	probably damaging	1.00
R6182:Akap13	UTSW	7	75,586,280 (GRCm38)	missense	probably benign	0.45
R6310:Akap13	UTSW	7	75,749,193 (GRCm38)	missense	probably damaging	0.99
R6346:Akap13	UTSW	7	75,685,254 (GRCm38)	missense	probably damaging	1.00
R6466:Akap13	UTSW	7	75,727,044 (GRCm38)	missense	probably benign	0.01
R6605:Akap13	UTSW	7	75,579,768 (GRCm38)	missense	probably damaging	0.98
R6617:Akap13	UTSW	7	75,730,363 (GRCm38)	missense	possibly damaging	0.95
R6621:Akap13	UTSW	7	75,569,981 (GRCm38)	missense	probably damaging	1.00
R6703:Akap13	UTSW	7	75,602,898 (GRCm38)	missense	probably damaging	1.00
R6750:Akap13	UTSW	7	75,739,458 (GRCm38)	missense	probably benign	0.03
R7069:Akap13	UTSW	7	75,610,262 (GRCm38)	missense	probably benign	0.29
R7116:Akap13	UTSW	7	75,720,195 (GRCm38)	missense	probably benign	0.00
R7158:Akap13	UTSW	7	75,579,594 (GRCm38)	missense	probably damaging	0.97
R7159:Akap13	UTSW	7	75,730,579 (GRCm38)	missense	possibly damaging	0.72
R7467:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R7468:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R7471:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R7472:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R7477:Akap13	UTSW	7	75,749,247 (GRCm38)	missense	probably benign
R7636:Akap13	UTSW	7	75,609,873 (GRCm38)	missense	probably benign	0.04
R7650:Akap13	UTSW	7	75,643,454 (GRCm38)	missense	probably benign	0.20
R7681:Akap13	UTSW	7	75,728,796 (GRCm38)	missense	possibly damaging	0.91
R7752:Akap13	UTSW	7	75,677,258 (GRCm38)	missense	possibly damaging	0.74
R7784:Akap13	UTSW	7	75,610,328 (GRCm38)	missense	probably benign	0.00
R7816:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R7817:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R7834:Akap13	UTSW	7	75,742,642 (GRCm38)	missense	possibly damaging	0.85
R7880:Akap13	UTSW	7	75,586,216 (GRCm38)	missense	probably damaging	0.97
R7942:Akap13	UTSW	7	75,611,470 (GRCm38)	missense	possibly damaging	0.50
R8006:Akap13	UTSW	7	75,579,696 (GRCm38)	missense	probably damaging	1.00
R8009:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R8011:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R8012:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R8013:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R8016:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R8089:Akap13	UTSW	7	75,610,592 (GRCm38)	missense	possibly damaging	0.94
R8138:Akap13	UTSW	7	75,702,231 (GRCm38)	splice site	probably null
R8174:Akap13	UTSW	7	75,728,869 (GRCm38)	missense	possibly damaging	0.89
R8298:Akap13	UTSW	7	75,747,804 (GRCm38)	missense	probably damaging	1.00
R8444:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R8445:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R8465:Akap13	UTSW	7	75,727,038 (GRCm38)	missense	probably benign	0.11
R8512:Akap13	UTSW	7	75,611,086 (GRCm38)	missense	probably damaging	0.99
R8523:Akap13	UTSW	7	75,730,465 (GRCm38)	missense	probably damaging	1.00
R8793:Akap13	UTSW	7	75,725,328 (GRCm38)	missense	probably benign	0.35
R8907:Akap13	UTSW	7	75,610,708 (GRCm38)	missense	probably damaging	0.99
R8907:Akap13	UTSW	7	75,610,696 (GRCm38)	missense	probably benign	0.08
R8928:Akap13	UTSW	7	75,609,858 (GRCm38)	missense	probably benign	0.00
R8929:Akap13	UTSW	7	75,609,004 (GRCm38)	missense	probably benign	0.00
R8937:Akap13	UTSW	7	75,534,853 (GRCm38)	critical splice donor site	probably null
R8967:Akap13	UTSW	7	75,729,134 (GRCm38)	missense	possibly damaging	0.80
R8986:Akap13	UTSW	7	75,609,326 (GRCm38)	missense	probably benign
R9152:Akap13	UTSW	7	75,611,285 (GRCm38)	missense	probably damaging	0.98
R9153:Akap13	UTSW	7	75,609,481 (GRCm38)	missense	probably benign	0.00
R9160:Akap13	UTSW	7	75,735,778 (GRCm38)	missense	possibly damaging	0.88
R9192:Akap13	UTSW	7	75,704,501 (GRCm38)	missense	probably benign	0.06
R9319:Akap13	UTSW	7	75,609,088 (GRCm38)	missense	probably benign	0.01
R9513:Akap13	UTSW	7	75,704,527 (GRCm38)	missense	probably benign	0.01
R9515:Akap13	UTSW	7	75,704,527 (GRCm38)	missense	probably benign	0.01
R9516:Akap13	UTSW	7	75,704,527 (GRCm38)	missense	probably benign	0.01
R9523:Akap13	UTSW	7	75,643,445 (GRCm38)	missense
R9564:Akap13	UTSW	7	75,609,413 (GRCm38)	missense	probably benign
R9621:Akap13	UTSW	7	75,736,342 (GRCm38)	missense	probably benign	0.09
R9686:Akap13	UTSW	7	75,586,336 (GRCm38)	missense	probably damaging	1.00
Z1176:Akap13	UTSW	7	75,730,552 (GRCm38)	missense	probably damaging	0.99
Z1177:Akap13	UTSW	7	75,615,005 (GRCm38)	missense	probably benign	0.17

Predicted Primers

PCR Primer
(F):5'- GGAGTTTGAATGCACACGTTACC -3'
(R):5'- ATATGTGTGCGTGTGTCCCC -3'

Sequencing Primer
(F):5'- TGCACACGTTACCATTTCAAAG -3'
(R):5'- CAGAGTTTCACGCCCAGGTTTAG -3'

Posted On

2019-11-12