Mutagenetix > Incidental Mutation

Incidental Mutation 'R1640:Cerk'

173496

Institutional Source

Beutler Lab

Gene Symbol

Cerk

Ensembl Gene

ENSMUSG00000035891

Gene Name

ceramide kinase

Synonyms

D330016D08Rik

MMRRC Submission

039676-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.060) question?

Stock #

R1640 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

86023329-86070342 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 86033601 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 274 (V274A)

Ref Sequence

ENSEMBL: ENSMUSP00000038203 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044332] [ENSMUST00000156546]

AlphaFold

Q8K4Q7

Predicted Effect

probably damaging
Transcript: ENSMUST00000044332
AA Change: V274A

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000038203
Gene: ENSMUSG00000035891
AA Change: V274A

Domain	Start	End	E-Value	Type
Blast:PH	8	126	9e-39	BLAST
Pfam:DAGK_cat	132	274	1.1e-31	PFAM
low complexity region	356	367	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150767

Predicted Effect

probably benign
Transcript: ENSMUST00000156546

SMART Domains

Protein: ENSMUSP00000119472
Gene: ENSMUSG00000035891

Domain	Start	End	E-Value	Type
low complexity region	51	62	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000157732

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.1%
20x: 92.2%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] CERK converts ceramide to ceramide 1-phosphate (C1P), a sphingolipid metabolite. Both CERK and C1P have been implicated in various cellular processes, including proliferation, apoptosis, phagocytosis, and inflammation (Kim et al., 2006 [PubMed 16488390]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Mice homozygous for a null allele exhibit reduced body weight, increased susceptibility to infection and decreased neutrophil numbers. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810004N23Rik	C	A	8: 125,566,584 (GRCm39)	V279L	probably damaging	Het
Acot6	A	T	12: 84,147,900 (GRCm39)	Y52F	probably damaging	Het
Adam22	C	T	5: 8,195,689 (GRCm39)	V284I	probably damaging	Het
Agl	A	T	3: 116,545,739 (GRCm39)	H1352Q	probably benign	Het
Aldh18a1	G	A	19: 40,573,943 (GRCm39)	P27S	probably benign	Het
C1ra	A	G	6: 124,499,233 (GRCm39)	N473S	probably benign	Het
C87436	T	C	6: 86,423,233 (GRCm39)	L269P	probably damaging	Het
Calcrl	A	G	2: 84,164,021 (GRCm39)	V390A	probably damaging	Het
Ccp110	T	G	7: 118,314,751 (GRCm39)		probably null	Het
Chd1l	A	T	3: 97,488,307 (GRCm39)	S570T	probably benign	Het
Chst14	T	A	2: 118,757,379 (GRCm39)	W83R	probably damaging	Het
Chsy1	A	T	7: 65,821,262 (GRCm39)	D499V	probably benign	Het
Ckmt1	C	A	2: 121,190,198 (GRCm39)		probably null	Het
Cnot1	A	T	8: 96,496,460 (GRCm39)	V282D	probably damaging	Het
Cntn3	A	T	6: 102,218,974 (GRCm39)	S549T	possibly damaging	Het
Cntnap5c	A	T	17: 58,702,289 (GRCm39)	D1203V	probably benign	Het
Col4a4	A	G	1: 82,513,491 (GRCm39)	Y169H	unknown	Het
Cwc22	A	G	2: 77,745,874 (GRCm39)	F454S	possibly damaging	Het
Dab1	C	T	4: 104,588,948 (GRCm39)	A524V	probably benign	Het
Dhrs7	A	T	12: 72,699,089 (GRCm39)	W298R	possibly damaging	Het
Dock7	G	T	4: 98,833,483 (GRCm39)	T1906N	probably damaging	Het
Dpy19l3	T	C	7: 35,449,203 (GRCm39)	T67A	probably benign	Het
Drc1	A	G	5: 30,521,301 (GRCm39)	D654G	possibly damaging	Het
Ech1	A	T	7: 28,531,264 (GRCm39)	H284L	probably damaging	Het
Epc1	G	A	18: 6,441,175 (GRCm39)	Q8*	probably null	Het
Etv5	A	T	16: 22,254,664 (GRCm39)	D65E	probably damaging	Het
F2rl3	A	G	8: 73,489,534 (GRCm39)	R254G	probably benign	Het
Fabp5	T	G	3: 10,080,170 (GRCm39)	F73L	probably benign	Het
Fbrs	T	C	7: 127,086,483 (GRCm39)	I611T	probably damaging	Het
Flnc	T	C	6: 29,433,806 (GRCm39)	S117P	possibly damaging	Het
Frmd4b	A	C	6: 97,285,634 (GRCm39)	S291A	possibly damaging	Het
Galnt13	A	G	2: 54,950,558 (GRCm39)	Y413C	probably damaging	Het
Gfer	A	G	17: 24,914,337 (GRCm39)	Y109H	possibly damaging	Het
Gli2	T	C	1: 118,764,254 (GRCm39)	H1299R	possibly damaging	Het
Gm10110	T	C	14: 90,135,679 (GRCm39)		noncoding transcript	Het
Gprc5a	T	G	6: 135,055,652 (GRCm39)	L33W	probably damaging	Het
Grin3a	T	C	4: 49,844,721 (GRCm39)	T121A	probably benign	Het
Grk3	A	G	5: 113,163,248 (GRCm39)	V33A	probably benign	Het
Hc	A	T	2: 34,947,336 (GRCm39)	Y59*	probably null	Het
Hrnr	A	G	3: 93,239,823 (GRCm39)	I3354V	unknown	Het
Hyou1	C	G	9: 44,300,703 (GRCm39)	T924S	probably benign	Het
Ifi209	T	G	1: 173,464,931 (GRCm39)	H20Q	probably damaging	Het
Ifi44	A	G	3: 151,438,171 (GRCm39)	V372A	probably benign	Het
Igdcc4	T	A	9: 65,030,077 (GRCm39)	L328H	probably damaging	Het
Jkampl	A	G	6: 73,445,869 (GRCm39)	Y227H	probably benign	Het
Kif18a	A	G	2: 109,120,161 (GRCm39)	T155A	probably benign	Het
Kmt2d	A	G	15: 98,742,938 (GRCm39)		probably benign	Het
Kri1	T	C	9: 21,191,753 (GRCm39)	D281G	possibly damaging	Het
Larp1b	T	A	3: 40,988,507 (GRCm39)	M1K	probably null	Het
Loxhd1	A	G	18: 77,490,259 (GRCm39)	D1225G	probably damaging	Het
Mzf1	A	G	7: 12,777,197 (GRCm39)	*736Q	probably null	Het
Naip2	C	T	13: 100,298,489 (GRCm39)	A516T	possibly damaging	Het
Ncf2	T	A	1: 152,683,784 (GRCm39)	M1K	probably null	Het
Or5t15	T	A	2: 86,681,571 (GRCm39)	H157L	probably benign	Het
Or8h10	A	C	2: 86,808,963 (GRCm39)	M59R	probably damaging	Het
Parp12	T	C	6: 39,073,574 (GRCm39)	D417G	probably benign	Het
Parp12	T	C	6: 39,088,612 (GRCm39)	H208R	probably damaging	Het
Pcif1	T	C	2: 164,727,603 (GRCm39)	I132T	probably benign	Het
Pck2	A	G	14: 55,786,041 (GRCm39)	D610G	possibly damaging	Het
Plbd1	T	C	6: 136,617,123 (GRCm39)	K185E	probably benign	Het
Ppp2r5a	T	C	1: 191,086,126 (GRCm39)	M425V	probably damaging	Het
Rapgef6	T	A	11: 54,548,231 (GRCm39)	V805D	probably damaging	Het
Rprd2	C	T	3: 95,671,059 (GRCm39)		probably benign	Het
Ryr3	A	G	2: 112,731,178 (GRCm39)	S711P	probably damaging	Het
Slc17a3	T	A	13: 24,036,340 (GRCm39)	L212*	probably null	Het
Slc4a8	A	G	15: 100,681,668 (GRCm39)	D41G	probably benign	Het
Slc9a3	T	A	13: 74,306,937 (GRCm39)	V354E	probably damaging	Het
Spen	A	G	4: 141,196,254 (GRCm39)	I3632T	probably damaging	Het
Tesc	A	G	5: 118,192,914 (GRCm39)	S77G	probably benign	Het
Tet3	A	T	6: 83,346,297 (GRCm39)	V1245D	probably benign	Het
Tox4	T	A	14: 52,530,000 (GRCm39)	D553E	possibly damaging	Het
Tpmt	A	T	13: 47,180,759 (GRCm39)	Y193*	probably null	Het
Trio	T	C	15: 27,833,130 (GRCm39)	Y1169C	probably damaging	Het
Urb1	G	A	16: 90,569,514 (GRCm39)	T1404I	probably benign	Het
Usp47	T	C	7: 111,682,334 (GRCm39)	S540P	probably damaging	Het
Vmn1r178	A	T	7: 23,593,548 (GRCm39)	M126L	possibly damaging	Het
Vmn1r223	T	C	13: 23,434,348 (GRCm39)	F314S	probably damaging	Het
Vmn2r112	A	T	17: 22,824,097 (GRCm39)	I451L	probably benign	Het
Zfc3h1	A	G	10: 115,242,806 (GRCm39)		probably null	Het
Zfp503	A	T	14: 22,034,969 (GRCm39)	L649Q	probably damaging	Het
Zfp977	A	C	7: 42,229,530 (GRCm39)	C332G	probably damaging	Het

Other mutations in Cerk

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01414:Cerk	APN	15	86,043,343 (GRCm39)	missense	probably benign	0.02
IGL01653:Cerk	APN	15	86,033,552 (GRCm39)	nonsense	probably null
IGL01732:Cerk	APN	15	86,030,517 (GRCm39)	missense	possibly damaging	0.68
IGL03107:Cerk	APN	15	86,027,014 (GRCm39)	missense	probably benign	0.00
resnick	UTSW	15	86,040,869 (GRCm39)	splice site	probably null
BB007:Cerk	UTSW	15	86,028,920 (GRCm39)	missense	possibly damaging	0.83
BB017:Cerk	UTSW	15	86,028,920 (GRCm39)	missense	possibly damaging	0.83
IGL02837:Cerk	UTSW	15	86,028,896 (GRCm39)	nonsense	probably null
R0318:Cerk	UTSW	15	86,035,766 (GRCm39)	missense	possibly damaging	0.89
R0517:Cerk	UTSW	15	86,040,849 (GRCm39)	missense	probably damaging	1.00
R1052:Cerk	UTSW	15	86,033,565 (GRCm39)	missense	possibly damaging	0.95
R2049:Cerk	UTSW	15	86,027,009 (GRCm39)	missense	probably benign
R2885:Cerk	UTSW	15	86,027,084 (GRCm39)	missense	probably damaging	1.00
R3887:Cerk	UTSW	15	86,033,532 (GRCm39)	missense	possibly damaging	0.95
R3931:Cerk	UTSW	15	86,039,311 (GRCm39)	nonsense	probably null
R4033:Cerk	UTSW	15	86,039,228 (GRCm39)	missense	possibly damaging	0.47
R4234:Cerk	UTSW	15	86,026,989 (GRCm39)	missense	probably benign	0.00
R4945:Cerk	UTSW	15	86,040,802 (GRCm39)	missense	probably benign	0.44
R5742:Cerk	UTSW	15	86,025,773 (GRCm39)	missense	probably damaging	1.00
R6160:Cerk	UTSW	15	86,026,974 (GRCm39)	missense	probably benign	0.43
R6309:Cerk	UTSW	15	86,040,869 (GRCm39)	splice site	probably null
R7002:Cerk	UTSW	15	86,040,795 (GRCm39)	missense	possibly damaging	0.56
R7360:Cerk	UTSW	15	86,043,327 (GRCm39)	missense	probably damaging	1.00
R7930:Cerk	UTSW	15	86,028,920 (GRCm39)	missense	possibly damaging	0.83
R9406:Cerk	UTSW	15	86,028,787 (GRCm39)	missense	possibly damaging	0.80
R9698:Cerk	UTSW	15	86,026,995 (GRCm39)	missense	probably benign	0.30
R9744:Cerk	UTSW	15	86,033,491 (GRCm39)	missense	probably damaging	1.00
X0067:Cerk	UTSW	15	86,030,547 (GRCm39)	missense	possibly damaging	0.62

Predicted Primers

PCR Primer
(F):5'- CTGGGTCACACTAGCCAGATTCAAG -3'
(R):5'- ACTCCAATTGCCACACTGAGCG -3'

Sequencing Primer
(F):5'- GAGCACCTTGTCAGCATCTG -3'
(R):5'- GCGTGCTCTGTTTCTGC -3'

Posted On

2014-04-24