Mutagenetix > Incidental Mutation

Incidental Mutation 'R5160:Akap9'

396926

Institutional Source

Beutler Lab

Gene Symbol

Akap9

Ensembl Gene

ENSMUSG00000040407

Gene Name

A kinase (PRKA) anchor protein (yotiao) 9

Synonyms

AKAP450, G1-448-15, 5730481H23Rik, mei2-5, repro12

MMRRC Submission

042742-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.327) question?

Stock #

R5160 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

3928054-4081310 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 4030007 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 1920 (R1920G)

Ref Sequence

ENSEMBL: ENSMUSP00000046129 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044492]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000044492
AA Change: R1920G

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

SMART Domains

Protein: ENSMUSP00000046129
Gene: ENSMUSG00000040407
AA Change: R1920G

Domain	Start	End	E-Value	Type
low complexity region	9	18	N/A	INTRINSIC
low complexity region	33	44	N/A	INTRINSIC
low complexity region	98	115	N/A	INTRINSIC
Blast:HPT	126	197	6e-21	BLAST
low complexity region	237	249	N/A	INTRINSIC
low complexity region	297	315	N/A	INTRINSIC
coiled coil region	404	593	N/A	INTRINSIC
coiled coil region	622	756	N/A	INTRINSIC
coiled coil region	777	843	N/A	INTRINSIC
coiled coil region	888	958	N/A	INTRINSIC
low complexity region	982	997	N/A	INTRINSIC
coiled coil region	1037	1065	N/A	INTRINSIC
low complexity region	1233	1246	N/A	INTRINSIC
internal_repeat_2	1247	1312	7.75e-5	PROSPERO
internal_repeat_1	1377	1485	2.63e-5	PROSPERO
coiled coil region	1522	1589	N/A	INTRINSIC
coiled coil region	1789	2107	N/A	INTRINSIC
coiled coil region	2132	2318	N/A	INTRINSIC
internal_repeat_1	2322	2445	2.63e-5	PROSPERO
coiled coil region	2455	2494	N/A	INTRINSIC
low complexity region	2587	2598	N/A	INTRINSIC
low complexity region	2627	2640	N/A	INTRINSIC
internal_repeat_2	2934	2997	7.75e-5	PROSPERO
low complexity region	3000	3016	N/A	INTRINSIC
coiled coil region	3109	3307	N/A	INTRINSIC
coiled coil region	3455	3493	N/A	INTRINSIC
coiled coil region	3521	3556	N/A	INTRINSIC
Pfam:PACT_coil_coil	3576	3657	1.2e-27	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000196350

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 94.7%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a chemically induced allele exhibit male infertily with abnormal spermatogenesis and Sertoli maturation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aftph	G	A	11: 20,712,197 (GRCm38)	P681L	probably benign	Het
Ano9	G	A	7: 141,104,365 (GRCm38)	R495C	probably damaging	Het
Apoa5	A	G	9: 46,270,496 (GRCm38)	Y290C	probably damaging	Het
Apob	T	C	12: 8,012,126 (GRCm38)	I3536T	possibly damaging	Het
Arhgap42	T	G	9: 8,997,655 (GRCm38)	K823T	probably damaging	Het
Bicc1	T	C	10: 70,932,236 (GRCm38)	Y850C	probably damaging	Het
Cdh2	A	T	18: 16,629,587 (GRCm38)	D433E	probably damaging	Het
Cfap100	A	G	6: 90,413,710 (GRCm38)		probably null	Het
Col6a5	T	C	9: 105,931,009 (GRCm38)	N947D	unknown	Het
Col8a2	A	G	4: 126,310,412 (GRCm38)	K72E	possibly damaging	Het
Ddx18	A	G	1: 121,565,879 (GRCm38)		probably null	Het
Dna2	T	C	10: 62,947,154 (GRCm38)	V21A	probably benign	Het
Dnaja3	T	A	16: 4,684,288 (GRCm38)	M52K	probably benign	Het
Fnip2	G	A	3: 79,488,991 (GRCm38)	T504I	probably damaging	Het
Il18	G	A	9: 50,577,893 (GRCm38)		probably null	Het
Ina	T	A	19: 47,015,080 (GRCm38)	I109N	probably damaging	Het
Katnb1	G	T	8: 95,095,470 (GRCm38)	V275L	probably benign	Het
Kdm6b	C	A	11: 69,400,768 (GRCm38)		probably benign	Het
Kifc2	T	A	15: 76,662,977 (GRCm38)	L251Q	probably damaging	Het
Kmt2d	A	G	15: 98,840,224 (GRCm38)		probably benign	Het
Lcor	T	A	19: 41,555,614 (GRCm38)	V82E	probably damaging	Het
Limk2	A	C	11: 3,350,772 (GRCm38)	V190G	probably damaging	Het
Luc7l	A	G	17: 26,267,297 (GRCm38)	D150G	probably benign	Het
Magi3	T	A	3: 104,027,908 (GRCm38)	H903L	possibly damaging	Het
Mdh1b	C	T	1: 63,725,645 (GRCm38)	R33Q	probably null	Het
Myo9a	T	C	9: 59,871,802 (GRCm38)	F1614L	probably benign	Het
Ngly1	A	G	14: 16,281,751 (GRCm38)	T210A	probably damaging	Het
Oas1h	A	G	5: 120,871,082 (GRCm38)	Y285C	probably damaging	Het
Olfr1252	T	C	2: 89,721,419 (GRCm38)	R231G	probably damaging	Het
Olfr1382	T	C	11: 49,535,689 (GRCm38)	L168P	probably damaging	Het
Olfr1413	C	T	1: 92,573,822 (GRCm38)	T217I	probably benign	Het
Olfr209	C	T	16: 59,361,766 (GRCm38)	G151R	probably damaging	Het
Olfr364-ps1	T	A	2: 37,146,803 (GRCm38)	M197K	probably benign	Het
Olfr91	T	C	17: 37,093,724 (GRCm38)	D50G	possibly damaging	Het
Osbpl7	T	C	11: 97,054,556 (GRCm38)	S81P	probably damaging	Het
Pcdha3	T	C	18: 36,946,427 (GRCm38)	V74A	probably damaging	Het
Pi4ka	T	C	16: 17,323,053 (GRCm38)	D68G	probably benign	Het
Prkcz	A	T	4: 155,293,232 (GRCm38)	V79D	probably benign	Het
Ptpn12	T	A	5: 20,997,831 (GRCm38)	I650F	probably damaging	Het
Rb1	A	G	14: 73,264,455 (GRCm38)		silent	Het
Rnaseh2b	T	G	14: 62,353,531 (GRCm38)	Y56*	probably null	Het
Ryr3	A	T	2: 112,646,927 (GRCm38)	C4495S	probably damaging	Het
Tk1	A	G	11: 117,824,746 (GRCm38)	I45T	possibly damaging	Het
Ttc23l	G	T	15: 10,551,550 (GRCm38)	T30K	possibly damaging	Het
Upp1	T	C	11: 9,135,193 (GRCm38)	S227P	possibly damaging	Het
Vmn1r30	T	A	6: 58,435,383 (GRCm38)	N155Y	probably benign	Het
Wdr35	C	T	12: 9,008,487 (GRCm38)	A548V	probably damaging	Het
Zc3h3	A	T	15: 75,809,663 (GRCm38)	M523K	probably benign	Het
Zc3h4	T	C	7: 16,434,648 (GRCm38)	L894P	unknown	Het
Zfp790	C	T	7: 29,829,767 (GRCm38)	H626Y	probably benign	Het
Zfp873	C	T	10: 82,061,042 (GRCm38)	H536Y	possibly damaging	Het
Zmym4	A	T	4: 126,870,184 (GRCm38)	N1354K	probably damaging	Het
Zscan20	A	G	4: 128,592,482 (GRCm38)	S142P	possibly damaging	Het

Other mutations in Akap9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00478:Akap9	APN	5	4,046,639 (GRCm38)	missense	probably damaging	0.97
IGL00642:Akap9	APN	5	3,960,842 (GRCm38)	missense	probably damaging	0.99
IGL00786:Akap9	APN	5	4,070,522 (GRCm38)	missense	probably damaging	1.00
IGL00788:Akap9	APN	5	4,060,480 (GRCm38)	missense	probably damaging	1.00
IGL00969:Akap9	APN	5	4,001,550 (GRCm38)	missense	probably benign
IGL01014:Akap9	APN	5	3,968,683 (GRCm38)	missense	probably benign	0.41
IGL01302:Akap9	APN	5	3,970,711 (GRCm38)	missense	probably benign	0.27
IGL01610:Akap9	APN	5	4,032,839 (GRCm38)	missense	possibly damaging	0.95
IGL01620:Akap9	APN	5	3,960,218 (GRCm38)	missense	probably benign	0.11
IGL01862:Akap9	APN	5	4,065,856 (GRCm38)	missense	probably damaging	0.99
IGL01862:Akap9	APN	5	3,951,705 (GRCm38)	missense	probably damaging	0.99
IGL02151:Akap9	APN	5	4,032,728 (GRCm38)	nonsense	probably null
IGL02635:Akap9	APN	5	4,070,500 (GRCm38)	missense	possibly damaging	0.59
IGL02858:Akap9	APN	5	4,069,130 (GRCm38)	missense	possibly damaging	0.88
IGL02967:Akap9	APN	5	3,976,164 (GRCm38)	missense	probably benign	0.07
IGL03064:Akap9	APN	5	3,968,755 (GRCm38)	missense	probably damaging	1.00
IGL03289:Akap9	APN	5	4,077,261 (GRCm38)	missense	probably damaging	1.00
Andy	UTSW	5	3,961,764 (GRCm38)	nonsense	probably null
blimey	UTSW	5	4,070,397 (GRCm38)	nonsense	probably null
hoarder	UTSW	5	4,069,089 (GRCm38)	missense	probably benign	0.00
marinarum	UTSW	5	4,013,875 (GRCm38)	nonsense	probably null
miser	UTSW	5	4,046,064 (GRCm38)	missense	probably benign	0.13
naviculus	UTSW	5	3,960,865 (GRCm38)	missense	probably damaging	0.98
thrifty	UTSW	5	3,976,209 (GRCm38)	missense	probably damaging	0.99
wee_one	UTSW	5	4,043,925 (GRCm38)	missense	probably damaging	1.00
FR4449:Akap9	UTSW	5	3,981,214 (GRCm38)	unclassified	probably benign
PIT1430001:Akap9	UTSW	5	4,029,849 (GRCm38)	missense	probably damaging	1.00
PIT4366001:Akap9	UTSW	5	4,046,221 (GRCm38)	missense	probably benign	0.24
R0088:Akap9	UTSW	5	3,961,946 (GRCm38)	missense	probably benign	0.22
R0309:Akap9	UTSW	5	4,069,038 (GRCm38)	missense	probably benign	0.01
R0387:Akap9	UTSW	5	3,951,678 (GRCm38)	splice site	probably benign
R0440:Akap9	UTSW	5	4,064,569 (GRCm38)	missense	probably damaging	0.99
R0441:Akap9	UTSW	5	3,961,714 (GRCm38)	missense	probably benign	0.15
R0491:Akap9	UTSW	5	3,972,851 (GRCm38)	unclassified	probably benign
R0501:Akap9	UTSW	5	3,970,685 (GRCm38)	missense	probably damaging	1.00
R0507:Akap9	UTSW	5	4,069,043 (GRCm38)	missense	probably benign	0.41
R0544:Akap9	UTSW	5	4,069,185 (GRCm38)	missense	probably benign	0.22
R0581:Akap9	UTSW	5	4,050,620 (GRCm38)	missense	probably benign	0.03
R0611:Akap9	UTSW	5	3,954,870 (GRCm38)	missense	probably benign	0.00
R0620:Akap9	UTSW	5	4,064,136 (GRCm38)	missense	probably damaging	0.98
R0639:Akap9	UTSW	5	4,060,318 (GRCm38)	missense	probably damaging	1.00
R0932:Akap9	UTSW	5	4,046,492 (GRCm38)	missense	possibly damaging	0.77
R0944:Akap9	UTSW	5	4,064,742 (GRCm38)	splice site	probably null
R1101:Akap9	UTSW	5	4,046,205 (GRCm38)	missense	probably benign	0.00
R1159:Akap9	UTSW	5	3,960,865 (GRCm38)	missense	probably damaging	0.98
R1170:Akap9	UTSW	5	4,055,671 (GRCm38)	missense	probably benign
R1185:Akap9	UTSW	5	3,948,783 (GRCm38)	missense	probably benign	0.13
R1185:Akap9	UTSW	5	3,948,783 (GRCm38)	missense	probably benign	0.13
R1185:Akap9	UTSW	5	3,948,783 (GRCm38)	missense	probably benign	0.13
R1453:Akap9	UTSW	5	3,975,614 (GRCm38)	splice site	probably null
R1551:Akap9	UTSW	5	4,069,174 (GRCm38)	missense	probably benign	0.02
R1608:Akap9	UTSW	5	3,961,783 (GRCm38)	missense	probably damaging	1.00
R1652:Akap9	UTSW	5	4,077,210 (GRCm38)	missense	probably damaging	1.00
R1659:Akap9	UTSW	5	4,064,633 (GRCm38)	missense	probably damaging	1.00
R1713:Akap9	UTSW	5	4,039,345 (GRCm38)	critical splice donor site	probably null
R1719:Akap9	UTSW	5	3,957,645 (GRCm38)	nonsense	probably null
R1720:Akap9	UTSW	5	3,972,791 (GRCm38)	missense	possibly damaging	0.63
R1757:Akap9	UTSW	5	4,001,667 (GRCm38)	missense	probably benign	0.41
R1872:Akap9	UTSW	5	4,001,406 (GRCm38)	missense	probably damaging	1.00
R1876:Akap9	UTSW	5	3,961,809 (GRCm38)	missense	probably benign	0.28
R1881:Akap9	UTSW	5	4,050,173 (GRCm38)	missense	probably benign
R1950:Akap9	UTSW	5	3,960,677 (GRCm38)	missense	probably damaging	1.00
R1980:Akap9	UTSW	5	3,972,771 (GRCm38)	missense	probably damaging	0.99
R1993:Akap9	UTSW	5	4,038,520 (GRCm38)	splice site	probably null
R2008:Akap9	UTSW	5	3,960,131 (GRCm38)	missense	possibly damaging	0.47
R2020:Akap9	UTSW	5	3,961,967 (GRCm38)	missense	probably damaging	1.00
R2051:Akap9	UTSW	5	3,975,685 (GRCm38)	nonsense	probably null
R2061:Akap9	UTSW	5	3,961,010 (GRCm38)	missense	probably damaging	1.00
R2109:Akap9	UTSW	5	4,044,847 (GRCm38)	missense	possibly damaging	0.47
R2135:Akap9	UTSW	5	4,064,509 (GRCm38)	missense	probably damaging	1.00
R2225:Akap9	UTSW	5	4,077,271 (GRCm38)	missense	probably damaging	0.96
R2232:Akap9	UTSW	5	4,046,603 (GRCm38)	missense	probably damaging	1.00
R2424:Akap9	UTSW	5	4,065,279 (GRCm38)	missense	probably damaging	0.97
R2483:Akap9	UTSW	5	3,976,235 (GRCm38)	missense	possibly damaging	0.65
R2879:Akap9	UTSW	5	3,976,353 (GRCm38)	intron	probably benign
R3622:Akap9	UTSW	5	3,976,235 (GRCm38)	missense	possibly damaging	0.65
R3623:Akap9	UTSW	5	3,976,235 (GRCm38)	missense	possibly damaging	0.65
R3624:Akap9	UTSW	5	3,976,235 (GRCm38)	missense	possibly damaging	0.65
R3722:Akap9	UTSW	5	4,070,351 (GRCm38)	missense	probably damaging	1.00
R3806:Akap9	UTSW	5	3,954,410 (GRCm38)	missense	probably benign	0.00
R3919:Akap9	UTSW	5	3,961,764 (GRCm38)	nonsense	probably null
R4023:Akap9	UTSW	5	3,992,077 (GRCm38)	missense	possibly damaging	0.66
R4093:Akap9	UTSW	5	4,043,996 (GRCm38)	missense	probably damaging	0.99
R4434:Akap9	UTSW	5	4,032,708 (GRCm38)	missense	probably damaging	0.99
R4529:Akap9	UTSW	5	4,043,948 (GRCm38)	missense	probably damaging	1.00
R4530:Akap9	UTSW	5	4,043,948 (GRCm38)	missense	probably damaging	1.00
R4532:Akap9	UTSW	5	4,043,948 (GRCm38)	missense	probably damaging	1.00
R4533:Akap9	UTSW	5	4,043,948 (GRCm38)	missense	probably damaging	1.00
R4585:Akap9	UTSW	5	3,976,151 (GRCm38)	missense	probably benign	0.00
R4586:Akap9	UTSW	5	3,976,151 (GRCm38)	missense	probably benign	0.00
R4655:Akap9	UTSW	5	4,046,403 (GRCm38)	missense	probably benign	0.14
R4676:Akap9	UTSW	5	4,064,515 (GRCm38)	nonsense	probably null
R4676:Akap9	UTSW	5	4,032,774 (GRCm38)	missense	probably damaging	1.00
R4724:Akap9	UTSW	5	4,055,339 (GRCm38)	missense	probably benign
R4731:Akap9	UTSW	5	3,962,266 (GRCm38)	missense	possibly damaging	0.54
R4732:Akap9	UTSW	5	4,013,901 (GRCm38)	missense	probably damaging	0.98
R4733:Akap9	UTSW	5	4,013,901 (GRCm38)	missense	probably damaging	0.98
R4743:Akap9	UTSW	5	3,961,013 (GRCm38)	missense	probably damaging	1.00
R4749:Akap9	UTSW	5	3,968,737 (GRCm38)	missense	probably benign	0.41
R4756:Akap9	UTSW	5	4,001,418 (GRCm38)	missense	probably damaging	0.99
R4757:Akap9	UTSW	5	4,008,382 (GRCm38)	missense	probably damaging	1.00
R4860:Akap9	UTSW	5	4,034,916 (GRCm38)	intron	probably benign
R4937:Akap9	UTSW	5	4,050,145 (GRCm38)	splice site	probably null
R4960:Akap9	UTSW	5	3,957,664 (GRCm38)	missense	probably benign	0.15
R4974:Akap9	UTSW	5	3,961,466 (GRCm38)	missense	possibly damaging	0.81
R5101:Akap9	UTSW	5	4,001,748 (GRCm38)	missense	probably damaging	0.96
R5200:Akap9	UTSW	5	3,960,734 (GRCm38)	missense	probably benign	0.00
R5245:Akap9	UTSW	5	3,976,209 (GRCm38)	missense	probably damaging	0.99
R5293:Akap9	UTSW	5	3,948,687 (GRCm38)	missense	probably damaging	0.99
R5408:Akap9	UTSW	5	4,058,458 (GRCm38)	missense	possibly damaging	0.84
R5507:Akap9	UTSW	5	3,968,683 (GRCm38)	missense	probably benign	0.41
R5517:Akap9	UTSW	5	4,001,665 (GRCm38)	missense	possibly damaging	0.76
R5579:Akap9	UTSW	5	4,064,714 (GRCm38)	missense	possibly damaging	0.93
R5619:Akap9	UTSW	5	3,954,760 (GRCm38)	intron	probably benign
R5645:Akap9	UTSW	5	4,050,590 (GRCm38)	missense	probably benign	0.09
R5669:Akap9	UTSW	5	4,050,540 (GRCm38)	nonsense	probably null
R5686:Akap9	UTSW	5	3,971,926 (GRCm38)	missense	probably benign	0.00
R5697:Akap9	UTSW	5	3,960,170 (GRCm38)	missense	possibly damaging	0.92
R5821:Akap9	UTSW	5	4,046,064 (GRCm38)	missense	probably benign	0.13
R5875:Akap9	UTSW	5	4,077,285 (GRCm38)	missense	probably benign	0.01
R5897:Akap9	UTSW	5	4,077,904 (GRCm38)	missense	probably benign	0.23
R5999:Akap9	UTSW	5	4,043,925 (GRCm38)	missense	probably damaging	1.00
R6025:Akap9	UTSW	5	4,032,801 (GRCm38)	missense	probably damaging	1.00
R6078:Akap9	UTSW	5	4,067,924 (GRCm38)	critical splice donor site	probably null
R6138:Akap9	UTSW	5	4,067,924 (GRCm38)	critical splice donor site	probably null
R6225:Akap9	UTSW	5	3,962,105 (GRCm38)	missense	probably damaging	1.00
R6243:Akap9	UTSW	5	4,065,000 (GRCm38)	splice site	probably null
R6326:Akap9	UTSW	5	3,962,061 (GRCm38)	missense	probably damaging	1.00
R6564:Akap9	UTSW	5	4,028,491 (GRCm38)	missense	probably damaging	0.98
R6617:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R6625:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R6632:Akap9	UTSW	5	4,013,842 (GRCm38)	splice site	probably null
R6677:Akap9	UTSW	5	4,029,869 (GRCm38)	missense	probably benign	0.21
R6717:Akap9	UTSW	5	4,064,086 (GRCm38)	missense	probably damaging	1.00
R6893:Akap9	UTSW	5	3,961,709 (GRCm38)	missense	probably benign	0.32
R6915:Akap9	UTSW	5	3,960,551 (GRCm38)	missense	probably benign	0.03
R6938:Akap9	UTSW	5	4,046,628 (GRCm38)	missense	possibly damaging	0.91
R6972:Akap9	UTSW	5	4,046,699 (GRCm38)	missense	possibly damaging	0.62
R6973:Akap9	UTSW	5	4,046,699 (GRCm38)	missense	possibly damaging	0.62
R6993:Akap9	UTSW	5	4,065,866 (GRCm38)	missense	possibly damaging	0.65
R7032:Akap9	UTSW	5	3,954,896 (GRCm38)	missense	probably benign
R7164:Akap9	UTSW	5	4,060,364 (GRCm38)	missense	probably damaging	0.96
R7170:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R7192:Akap9	UTSW	5	4,005,723 (GRCm38)	splice site	probably null
R7284:Akap9	UTSW	5	3,956,246 (GRCm38)	missense	probably damaging	1.00
R7299:Akap9	UTSW	5	4,032,696 (GRCm38)	missense	probably damaging	1.00
R7313:Akap9	UTSW	5	4,004,933 (GRCm38)	missense	probably damaging	1.00
R7326:Akap9	UTSW	5	4,045,930 (GRCm38)	missense	possibly damaging	0.47
R7343:Akap9	UTSW	5	4,046,364 (GRCm38)	missense	probably damaging	0.99
R7455:Akap9	UTSW	5	3,972,792 (GRCm38)	missense	probably benign	0.03
R7482:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R7489:Akap9	UTSW	5	4,004,933 (GRCm38)	missense	probably damaging	1.00
R7525:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R7528:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R7576:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R7577:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R7578:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R7610:Akap9	UTSW	5	3,957,677 (GRCm38)	missense	possibly damaging	0.95
R7658:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R7754:Akap9	UTSW	5	4,046,736 (GRCm38)	missense	probably benign	0.03
R7818:Akap9	UTSW	5	4,013,875 (GRCm38)	nonsense	probably null
R7979:Akap9	UTSW	5	4,050,381 (GRCm38)	missense	probably benign
R7991:Akap9	UTSW	5	4,064,949 (GRCm38)	splice site	probably null
R8036:Akap9	UTSW	5	4,070,397 (GRCm38)	nonsense	probably null
R8054:Akap9	UTSW	5	4,038,707 (GRCm38)	critical splice donor site	probably null
R8116:Akap9	UTSW	5	4,061,183 (GRCm38)	missense	probably benign	0.04
R8150:Akap9	UTSW	5	3,961,982 (GRCm38)	missense	probably damaging	1.00
R8234:Akap9	UTSW	5	4,044,845 (GRCm38)	missense	probably benign	0.18
R8348:Akap9	UTSW	5	3,948,897 (GRCm38)	critical splice donor site	probably null
R8365:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R8366:Akap9	UTSW	5	3,968,745 (GRCm38)	missense	probably benign	0.04
R8448:Akap9	UTSW	5	3,948,897 (GRCm38)	critical splice donor site	probably null
R8466:Akap9	UTSW	5	4,038,659 (GRCm38)	missense	probably damaging	1.00
R8772:Akap9	UTSW	5	4,046,255 (GRCm38)	missense	probably damaging	1.00
R8881:Akap9	UTSW	5	3,961,279 (GRCm38)	missense
R8937:Akap9	UTSW	5	4,044,048 (GRCm38)	missense	possibly damaging	0.78
R8956:Akap9	UTSW	5	3,948,805 (GRCm38)	missense	possibly damaging	0.79
R9000:Akap9	UTSW	5	4,055,650 (GRCm38)	missense	probably benign
R9049:Akap9	UTSW	5	4,064,597 (GRCm38)	missense
R9074:Akap9	UTSW	5	4,077,959 (GRCm38)	missense	probably benign	0.40
R9124:Akap9	UTSW	5	4,061,284 (GRCm38)	missense	probably damaging	0.99
R9129:Akap9	UTSW	5	4,069,089 (GRCm38)	missense	probably benign	0.00
R9371:Akap9	UTSW	5	3,961,852 (GRCm38)	missense	possibly damaging	0.83
R9424:Akap9	UTSW	5	3,962,224 (GRCm38)	nonsense	probably null
R9424:Akap9	UTSW	5	3,962,223 (GRCm38)	nonsense	probably null
R9509:Akap9	UTSW	5	4,046,349 (GRCm38)	missense	probably benign
R9515:Akap9	UTSW	5	4,055,709 (GRCm38)	missense	probably damaging	1.00
R9567:Akap9	UTSW	5	4,077,311 (GRCm38)	missense	possibly damaging	0.89
R9587:Akap9	UTSW	5	4,069,149 (GRCm38)	missense	probably damaging	1.00
R9619:Akap9	UTSW	5	4,044,833 (GRCm38)	missense	probably damaging	1.00
R9635:Akap9	UTSW	5	4,050,545 (GRCm38)	missense	probably benign	0.20
R9680:Akap9	UTSW	5	3,961,587 (GRCm38)	missense	probably benign	0.03
R9691:Akap9	UTSW	5	3,960,491 (GRCm38)	missense	probably damaging	1.00
R9726:Akap9	UTSW	5	4,003,757 (GRCm38)	missense	probably benign	0.39
U15987:Akap9	UTSW	5	4,067,924 (GRCm38)	critical splice donor site	probably null
X0026:Akap9	UTSW	5	4,014,039 (GRCm38)	missense	probably damaging	1.00
X0057:Akap9	UTSW	5	3,975,598 (GRCm38)	critical splice acceptor site	probably null
Z1176:Akap9	UTSW	5	3,962,251 (GRCm38)	missense	probably damaging	0.96
Z1177:Akap9	UTSW	5	4,046,189 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GAGACAACTCCATTTTCTTCCATTG -3'
(R):5'- ACAGATGTTTCAGCACCAGTAATC -3'

Sequencing Primer
(F):5'- CTTCCATTGTGTCTTATAGGTGTC -3'
(R):5'- GGCTACTAACAATTTGCCTTTAAAG -3'

Posted On

2016-06-21