Mutagenetix > Incidental Mutation

Incidental Mutation 'R1449:Camk4'

159178

Institutional Source

Beutler Lab

Gene Symbol

Camk4

Ensembl Gene

ENSMUSG00000038128

Gene Name

calcium/calmodulin-dependent protein kinase IV

Synonyms

A430110E23Rik, D18Bwg0362e, Ca2+/calmodulin-dependent protein kinase type IV/Gr, CaMKIV, CaMKIV/Gr

MMRRC Submission

039504-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.079) question?

Stock #

R1449 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

33067984-33324281 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 33072528 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 27 (D27G)

Ref Sequence

ENSEMBL: ENSMUSP00000046539 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042868]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000042868
AA Change: D27G

PolyPhen 2 Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000046539
Gene: ENSMUSG00000038128
AA Change: D27G

Domain	Start	End	E-Value	Type
low complexity region	4	21	N/A	INTRINSIC
S_TKc	42	296	8.7e-106	SMART
low complexity region	318	344	N/A	INTRINSIC
low complexity region	373	390	N/A	INTRINSIC
low complexity region	415	428	N/A	INTRINSIC
low complexity region	441	454	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000180941

Coding Region Coverage

1x: 98.8%
3x: 97.9%
10x: 94.7%
20x: 87.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene belongs to the serine/threonine protein kinase family, and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. This enzyme is a multifunctional serine/threonine protein kinase with limited tissue distribution, that has been implicated in transcriptional regulation in lymphocytes, neurons and male germ cells. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for different targeted mutations show variable phenotypes, including reduced viability, male and/or female sterility, and mild to severe neurological and spatial memory disorders. [provided by MGI curators]

Allele List at MGI

All alleles(4) : Targeted, knock-out(3) Targeted, other(1)

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700013G24Rik	A	G	4: 137,182,666 (GRCm39)	N274D	possibly damaging	Het
6430571L13Rik	T	A	9: 107,219,689 (GRCm39)	N47K	probably damaging	Het
Aasdh	C	T	5: 77,034,136 (GRCm39)	A472T	probably benign	Het
Abca13	A	G	11: 9,248,580 (GRCm39)	T2776A	probably damaging	Het
Adamts10	T	A	17: 33,764,613 (GRCm39)	V711D	probably damaging	Het
Adrb3	G	A	8: 27,717,415 (GRCm39)	R345C	probably damaging	Het
Ak7	T	C	12: 105,708,520 (GRCm39)	V325A	possibly damaging	Het
Armc6	G	A	8: 70,677,943 (GRCm39)	L129F	probably benign	Het
Bend6	T	C	1: 33,917,424 (GRCm39)	N10S	probably benign	Het
Bmpr1b	T	C	3: 141,577,134 (GRCm39)	E59G	possibly damaging	Het
Brd3	A	G	2: 27,340,263 (GRCm39)		probably null	Het
Brd3	A	G	2: 27,347,028 (GRCm39)	Y369H	probably damaging	Het
Cacna1e	C	T	1: 154,361,408 (GRCm39)		probably null	Het
Camkk1	T	G	11: 72,924,710 (GRCm39)	S308A	probably damaging	Het
Catsperb	A	G	12: 101,554,456 (GRCm39)	T717A	probably benign	Het
Cdh23	A	T	10: 60,212,730 (GRCm39)	S1563R	probably damaging	Het
Cep44	A	T	8: 56,993,985 (GRCm39)	S197R	probably benign	Het
Col3a1	T	A	1: 45,360,771 (GRCm39)	I67N	unknown	Het
Dcaf12l1	T	C	X: 43,878,304 (GRCm39)	T165A	probably benign	Het
Dicer1	T	C	12: 104,695,502 (GRCm39)	Y143C	possibly damaging	Het
Dlg5	A	G	14: 24,185,711 (GRCm39)	I1898T	possibly damaging	Het
Dnah1	T	C	14: 30,985,908 (GRCm39)	N3762D	probably damaging	Het
Dscaml1	A	T	9: 45,653,521 (GRCm39)	T1382S	possibly damaging	Het
Entpd3	A	T	9: 120,395,555 (GRCm39)	R513W	probably damaging	Het
Foxred1	A	G	9: 35,120,738 (GRCm39)	S132P	probably damaging	Het
Ftsj3	T	C	11: 106,143,826 (GRCm39)	I273V	probably benign	Het
Hsd17b7	C	T	1: 169,787,251 (GRCm39)		probably null	Het
Iars1	T	A	13: 49,887,186 (GRCm39)	V1253D	probably damaging	Het
Iqsec1	T	A	6: 90,667,790 (GRCm39)	K216*	probably null	Het
Itga7	A	G	10: 128,789,370 (GRCm39)	D971G	probably benign	Het
Kcnk2	G	A	1: 189,072,223 (GRCm39)	S35L	probably benign	Het
Kif13a	T	C	13: 46,966,212 (GRCm39)	Y402C	probably damaging	Het
Lamc1	A	G	1: 153,126,241 (GRCm39)	S484P	probably benign	Het
Lap3	T	C	5: 45,666,861 (GRCm39)		probably null	Het
Lhx8	G	T	3: 154,033,742 (GRCm39)	S46*	probably null	Het
Lin7a	T	C	10: 107,159,813 (GRCm39)	S42P	probably damaging	Het
Lrba	G	A	3: 86,261,585 (GRCm39)	R1513Q	probably damaging	Het
Maml2	C	A	9: 13,531,980 (GRCm39)	P398Q	possibly damaging	Het
Mast2	T	C	4: 116,166,210 (GRCm39)	I1201V	probably damaging	Het
Mmp20	A	T	9: 7,642,769 (GRCm39)	D201V	probably damaging	Het
Morn5	T	A	2: 35,947,092 (GRCm39)	C123*	probably null	Het
Mrpl4	A	G	9: 20,918,807 (GRCm39)	K175E	possibly damaging	Het
Nav3	A	T	10: 109,689,372 (GRCm39)	S302T	probably benign	Het
Ndrg2	T	C	14: 52,145,591 (GRCm39)	Y217C	probably damaging	Het
Nfx1	A	G	4: 40,976,803 (GRCm39)	D159G	probably damaging	Het
Nlrp9b	A	T	7: 19,757,089 (GRCm39)	T109S	possibly damaging	Het
Npepps	A	G	11: 97,097,980 (GRCm39)	Y909H	probably benign	Het
Or10g1	A	G	14: 52,648,024 (GRCm39)	C102R	probably damaging	Het
Or11g7	A	G	14: 50,691,378 (GRCm39)	N290D	probably damaging	Het
Or51a25	A	T	7: 102,373,397 (GRCm39)	F100Y	probably damaging	Het
Or6c211	T	A	10: 129,506,238 (GRCm39)	D50V	probably damaging	Het
Or6c69b	A	C	10: 129,626,723 (GRCm39)	V245G	probably damaging	Het
Pcdh1	T	C	18: 38,322,929 (GRCm39)	H968R	probably damaging	Het
Pde1b	T	A	15: 103,433,470 (GRCm39)	I296N	probably damaging	Het
Phldb1	T	A	9: 44,627,930 (GRCm39)	T172S	probably benign	Het
Plxdc2	T	C	2: 16,665,592 (GRCm39)	V215A	possibly damaging	Het
Poln	A	G	5: 34,171,682 (GRCm39)	I695T	probably damaging	Het
Pou6f2	G	T	13: 18,347,000 (GRCm39)	Q31K	probably damaging	Het
Psd	T	A	19: 46,313,250 (GRCm39)	Y40F	probably damaging	Het
Rnf126	T	C	10: 79,597,448 (GRCm39)	N155D	probably benign	Het
Rpl36-ps3	C	A	12: 12,962,032 (GRCm39)		noncoding transcript	Het
Rrp15	C	A	1: 186,468,465 (GRCm39)	V184F	possibly damaging	Het
Rslcan18	G	T	13: 67,250,164 (GRCm39)	L24M	possibly damaging	Het
Sall1	A	G	8: 89,759,111 (GRCm39)	I331T	probably benign	Het
Slamf7	A	T	1: 171,468,606 (GRCm39)	N95K	possibly damaging	Het
Slc1a6	T	C	10: 78,635,951 (GRCm39)	Y339H	probably damaging	Het
Slc39a8	A	G	3: 135,532,446 (GRCm39)	N72D	probably benign	Het
Slf1	A	G	13: 77,231,568 (GRCm39)	S604P	probably damaging	Het
Slfn4	C	T	11: 83,079,819 (GRCm39)	T110M	probably benign	Het
Tnpo1	T	C	13: 99,015,220 (GRCm39)	T116A	probably damaging	Het
Tor1b	T	C	2: 30,845,893 (GRCm39)	I190T	probably damaging	Het
Ttn	C	A	2: 76,800,138 (GRCm39)	E357*	probably null	Het
Tubg2	G	T	11: 101,047,699 (GRCm39)	E95*	probably null	Het
Ubap2	A	G	4: 41,209,351 (GRCm39)		probably null	Het
Ube2i	T	C	17: 25,487,538 (GRCm39)	D67G	possibly damaging	Het
Ubxn11	A	G	4: 133,852,203 (GRCm39)	E50G	probably damaging	Het
Wnk1	A	G	6: 119,929,779 (GRCm39)	V1246A	probably damaging	Het
Zcchc7	A	G	4: 44,929,124 (GRCm39)	T38A	possibly damaging	Het
Zfp236	A	G	18: 82,664,130 (GRCm39)	S552P	probably damaging	Het

Other mutations in Camk4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
7510:Camk4	UTSW	18	33,289,892 (GRCm39)	missense	probably null	0.99
R0244:Camk4	UTSW	18	33,312,678 (GRCm39)	critical splice donor site	probably null
R0408:Camk4	UTSW	18	33,262,845 (GRCm39)	missense	probably damaging	1.00
R0744:Camk4	UTSW	18	33,072,507 (GRCm39)	missense	unknown
R0836:Camk4	UTSW	18	33,072,507 (GRCm39)	missense	unknown
R0903:Camk4	UTSW	18	33,315,383 (GRCm39)	missense	probably benign	0.08
R1456:Camk4	UTSW	18	33,262,896 (GRCm39)	splice site	probably benign
R1677:Camk4	UTSW	18	33,309,275 (GRCm39)	missense	probably damaging	1.00
R1733:Camk4	UTSW	18	33,211,074 (GRCm39)	missense	possibly damaging	0.54
R1909:Camk4	UTSW	18	33,291,869 (GRCm39)	splice site	probably null
R2186:Camk4	UTSW	18	33,315,394 (GRCm39)	missense	probably damaging	0.99
R2291:Camk4	UTSW	18	33,240,996 (GRCm39)	critical splice donor site	probably null
R3874:Camk4	UTSW	18	33,291,907 (GRCm39)	missense	possibly damaging	0.70
R3968:Camk4	UTSW	18	33,312,634 (GRCm39)	missense	possibly damaging	0.94
R3969:Camk4	UTSW	18	33,312,634 (GRCm39)	missense	possibly damaging	0.94
R3970:Camk4	UTSW	18	33,312,634 (GRCm39)	missense	possibly damaging	0.94
R4858:Camk4	UTSW	18	33,309,266 (GRCm39)	missense	probably damaging	0.98
R5251:Camk4	UTSW	18	33,317,932 (GRCm39)	missense	probably benign	0.31
R5343:Camk4	UTSW	18	33,211,122 (GRCm39)	missense	probably damaging	0.99
R5972:Camk4	UTSW	18	33,240,979 (GRCm39)	missense	probably damaging	1.00
R6155:Camk4	UTSW	18	33,072,500 (GRCm39)	missense	unknown
R6728:Camk4	UTSW	18	33,317,992 (GRCm39)	missense	probably benign
R7088:Camk4	UTSW	18	33,072,584 (GRCm39)	missense	probably benign	0.02
R7135:Camk4	UTSW	18	33,240,996 (GRCm39)	critical splice donor site	probably null
R7372:Camk4	UTSW	18	33,318,178 (GRCm39)	missense	probably benign	0.34
R7490:Camk4	UTSW	18	33,072,598 (GRCm39)	critical splice donor site	probably null
R7525:Camk4	UTSW	18	33,318,085 (GRCm39)	missense	probably benign	0.04
R7890:Camk4	UTSW	18	33,318,058 (GRCm39)	missense	probably benign	0.01
R8446:Camk4	UTSW	18	33,289,810 (GRCm39)	missense	probably damaging	0.99
R9038:Camk4	UTSW	18	33,291,953 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- CTAGTGGCTTCCCCAGGCAAATG -3'
(R):5'- GTGTCGCAGCTAGAGGGACAAC -3'

Sequencing Primer
(F):5'- ggaagggagagcacaggg -3'
(R):5'- CTAGAGGGACAACTAGCGTG -3'

Posted On

2014-03-14