Mutagenetix > Incidental Mutation

Incidental Mutation 'R7808:Camk1g'

600910

Institutional Source

Beutler Lab

Gene Symbol

Camk1g

Ensembl Gene

ENSMUSG00000016179

Gene Name

calcium/calmodulin-dependent protein kinase I gamma

Synonyms

CLICK-III, CaMKIgamma

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.104) question?

Stock #

R7808 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

193346346-193370298 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 193350285 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 273 (R273G)

Ref Sequence

ENSEMBL: ENSMUSP00000016323 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000016323] [ENSMUST00000169907]

AlphaFold

Q91VB2

Predicted Effect

possibly damaging
Transcript: ENSMUST00000016323
AA Change: R273G

PolyPhen 2 Score 0.514 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000016323
Gene: ENSMUSG00000016179
AA Change: R273G

Domain	Start	End	E-Value	Type
S_TKc	23	277	9.53e-112	SMART
low complexity region	376	389	N/A	INTRINSIC

Predicted Effect

SMART Domains

Protein: ENSMUSP00000131451
Gene: ENSMUSG00000016179
AA Change: R233G

Domain	Start	End	E-Value	Type
S_TKc	2	238	5.19e-72	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000169907
AA Change: R273G

PolyPhen 2 Score 0.525 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000128143
Gene: ENSMUSG00000016179
AA Change: R273G

Domain	Start	End	E-Value	Type
S_TKc	23	277	9.53e-112	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

Validation Efficiency

99% (86/87)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein similar to calcium/calmodulin dependent protein kinase, however, its exact function is not known. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit impaired dendritogenesis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 88 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110051M20Rik	T	C	2: 91,444,594		probably benign	Het
1700113H08Rik	T	C	10: 87,121,435	V11A	probably benign	Het
Abca12	A	T	1: 71,274,634		probably null	Het
Abcc12	T	A	8: 86,507,939	M1232L	probably benign	Het
Adamts1	T	C	16: 85,800,229	Y314C	probably damaging	Het
Adgb	A	G	10: 10,378,659		probably null	Het
Ankrd12	T	A	17: 65,985,653	K928N	possibly damaging	Het
Ano5	A	T	7: 51,587,795	K789I	possibly damaging	Het
Cacna1d	G	T	14: 30,111,069	N938K	probably damaging	Het
Caprin2	C	A	6: 148,843,030	V966F	probably damaging	Het
Card6	T	C	15: 5,099,472	H814R	probably benign	Het
Ccdc84	T	C	9: 44,412,918	Q228R	probably null	Het
Cflar	A	G	1: 58,711,581		probably benign	Het
Cftr	T	A	6: 18,204,205	N66K	probably benign	Het
Clasrp	C	T	7: 19,588,746		probably null	Het
Clec4a4	T	C	6: 122,990,380	I5T	probably damaging	Het
Cmtr2	T	C	8: 110,221,619	I187T	possibly damaging	Het
Cnga1	A	T	5: 72,604,273	F633I	possibly damaging	Het
Col16a1	C	T	4: 130,073,264	P909S	unknown	Het
Csf1	C	A	3: 107,760,045	A7S	possibly damaging	Het
Dhx30	A	T	9: 110,086,202	V833D	probably benign	Het
Dlg2	T	G	7: 92,431,055	I712M	probably benign	Het
Dmxl1	T	A	18: 49,878,315	F1180I	probably benign	Het
Dnah9	T	A	11: 66,005,805	K2398*	probably null	Het
Dus1l	C	T	11: 120,789,436	G471D	possibly damaging	Het
Dync1h1	A	T	12: 110,655,459	N3412I	possibly damaging	Het
Dync1i2	T	A	2: 71,250,834		probably null	Het
Dysf	T	C	6: 84,070,929	S333P	possibly damaging	Het
Eed	A	T	7: 89,956,333	N349K	probably benign	Het
Eipr1	A	T	12: 28,766,770		probably null	Het
Fam160a2	G	A	7: 105,384,525	R509C	probably damaging	Het
Fbxw16	A	C	9: 109,448,154	V40G	probably damaging	Het
Fgfr4	A	C	13: 55,161,156	R363S	possibly damaging	Het
Fgl2	A	T	5: 21,373,231	N172I	possibly damaging	Het
Gabbr2	T	A	4: 46,875,744	H126L	possibly damaging	Het
Gcnt2	A	T	13: 40,860,862	N170Y	possibly damaging	Het
Gpt	A	G	15: 76,698,893		probably null	Het
Igsf10	A	G	3: 59,328,068	I1564T	probably benign	Het
Il22ra1	C	A	4: 135,750,796	Q393K	possibly damaging	Het
Inpp5d	A	T	1: 87,683,845	K340*	probably null	Het
Jcad	A	G	18: 4,673,113	K292E	probably damaging	Het
Krt5	T	A	15: 101,709,018	T427S	probably benign	Het
Krt76	T	C	15: 101,890,494	D252G	probably damaging	Het
Krtap26-1	A	G	16: 88,647,310	V141A	not run	Het
Lce6a	A	T	3: 92,620,335	V55D	probably benign	Het
Lpxn	C	T	19: 12,824,821	S170F	possibly damaging	Het
Magi2	T	C	5: 20,465,840	V394A	probably benign	Het
Mbnl1	G	A	3: 60,614,821		probably null	Het
Med16	T	A	10: 79,898,418	K554M	probably damaging	Het
Mettl14	T	C	3: 123,372,585	D276G	possibly damaging	Het
Mphosph9	T	C	5: 124,260,946	D1002G	probably damaging	Het
Mroh9	T	C	1: 163,039,109	E686G	probably damaging	Het
Nav1	T	C	1: 135,452,248	Y1512C	unknown	Het
Neb	T	C	2: 52,192,023	Y5712C	probably damaging	Het
Nek7	T	A	1: 138,561,771		probably benign	Het
Nptx1	T	A	11: 119,544,636	I285F	probably damaging	Het
Oas1d	G	T	5: 120,914,971	E30*	probably null	Het
Olfr404-ps1	A	T	11: 74,239,899	I112F	probably damaging	Het
Olfr429	C	A	1: 174,089,851	Y270*	probably null	Het
Olfr577	A	G	7: 102,973,110	V294A	possibly damaging	Het
Parp4	T	G	14: 56,635,748	S1150A	possibly damaging	Het
Pinx1	A	T	14: 63,919,292	K223*	probably null	Het
Plekha5	T	C	6: 140,583,914	L1034S	probably damaging	Het
Ppp4r3a	A	G	12: 101,053,496	V400A	possibly damaging	Het
Prtg	A	T	9: 72,842,697	I128F	possibly damaging	Het
Rars	T	C	11: 35,828,707	E96G	probably benign	Het
Rhpn1	T	A	15: 75,713,450	S551T	probably benign	Het
Selenow	C	T	7: 15,922,251		probably null	Het
Serpina9	A	T	12: 104,001,225		probably null	Het
Shank3	A	T	15: 89,548,880	D1276V	probably damaging	Het
Slc17a2	A	C	13: 23,819,334	H285P	probably damaging	Het
Slc27a6	A	G	18: 58,609,195	T494A	probably damaging	Het
Slc6a21	A	C	7: 45,282,936	T54P		Het
Syne2	A	G	12: 75,983,727		probably null	Het
Tal1	T	C	4: 115,068,292	V186A	probably benign	Het
Tarsl2	A	G	7: 65,652,261	K178E	probably benign	Het
Tex10	T	A	4: 48,459,984	I456L	probably benign	Het
Tfcp2	A	G	15: 100,522,429	F175S	probably damaging	Het
Timp2	C	T	11: 118,303,800	A188T	probably damaging	Het
Tmc5	T	A	7: 118,669,217	I836N	probably damaging	Het
Tmem100	T	A	11: 90,035,476	M43K	probably benign	Het
Ulk2	A	G	11: 61,854,552	Y9H	probably damaging	Het
Usp7	T	C	16: 8,705,163	K311E	probably damaging	Het
Vmn1r238	G	A	18: 3,123,033	T127I	probably benign	Het
Vmn2r28	T	C	7: 5,493,679	Y58C	probably damaging	Het
Wdr55	G	A	18: 36,760,416	G44S	probably benign	Het
Zfp677	C	A	17: 21,397,385	H235N	probably damaging	Het
Zfp869	T	A	8: 69,706,986	R312S	probably damaging	Het

Other mutations in Camk1g

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00433:Camk1g	APN	1	193347349	unclassified	probably benign
IGL02637:Camk1g	APN	1	193348388	missense	probably benign	0.38
G1patch:Camk1g	UTSW	1	193350320	missense	possibly damaging	0.80
I2288:Camk1g	UTSW	1	193351106	splice site	probably benign
R0375:Camk1g	UTSW	1	193356401	splice site	probably benign
R0433:Camk1g	UTSW	1	193354058	missense	probably damaging	0.99
R0967:Camk1g	UTSW	1	193350296	missense	probably damaging	1.00
R1161:Camk1g	UTSW	1	193348354	missense	probably benign
R1227:Camk1g	UTSW	1	193347433	missense	possibly damaging	0.73
R1469:Camk1g	UTSW	1	193362091	missense	possibly damaging	0.89
R1469:Camk1g	UTSW	1	193362091	missense	possibly damaging	0.89
R1641:Camk1g	UTSW	1	193356357	missense	probably benign	0.25
R3109:Camk1g	UTSW	1	193354993	missense	probably damaging	1.00
R3160:Camk1g	UTSW	1	193359807	missense	possibly damaging	0.66
R3161:Camk1g	UTSW	1	193359807	missense	possibly damaging	0.66
R3162:Camk1g	UTSW	1	193359807	missense	possibly damaging	0.66
R3162:Camk1g	UTSW	1	193359807	missense	possibly damaging	0.66
R4638:Camk1g	UTSW	1	193356359	missense	probably damaging	1.00
R4642:Camk1g	UTSW	1	193356359	missense	probably damaging	1.00
R4644:Camk1g	UTSW	1	193356359	missense	probably damaging	1.00
R4756:Camk1g	UTSW	1	193362085	missense	probably benign	0.03
R4781:Camk1g	UTSW	1	193356344	missense	probably benign	0.00
R4987:Camk1g	UTSW	1	193348475	missense	probably damaging	0.99
R5224:Camk1g	UTSW	1	193355034	missense	probably damaging	1.00
R5407:Camk1g	UTSW	1	193347372	splice site	probably null
R5932:Camk1g	UTSW	1	193354039	missense	probably benign	0.25
R6725:Camk1g	UTSW	1	193350320	missense	possibly damaging	0.80
R7071:Camk1g	UTSW	1	193359809	missense	probably benign	0.10
R7908:Camk1g	UTSW	1	193359774	missense	probably damaging	1.00
R8135:Camk1g	UTSW	1	193354027	missense	possibly damaging	0.79
R8355:Camk1g	UTSW	1	193351047	missense	probably damaging	1.00
R8737:Camk1g	UTSW	1	193348486	critical splice acceptor site	probably null
R8811:Camk1g	UTSW	1	193362100	missense	probably damaging	1.00
R9506:Camk1g	UTSW	1	193348055	critical splice donor site	probably null
R9680:Camk1g	UTSW	1	193348175	missense	probably benign	0.00
R9688:Camk1g	UTSW	1	193348721	missense	probably damaging	1.00
Z1176:Camk1g	UTSW	1	193362100	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCTTGGCCTTTGCTTTTAGAAG -3'
(R):5'- AGAGCTCTCTTCTTGGTGGC -3'

Sequencing Primer
(F):5'- TTTAGAAGTGGTTAGAGCACGTAGC -3'
(R):5'- AGAGCTCTCTTCTTGGTGGCTTATG -3'

Posted On

2019-11-26