Mutagenetix > Incidental Mutation

Incidental Mutation 'R5022:Celf2'

389214

Institutional Source

Beutler Lab

Gene Symbol

Celf2

Ensembl Gene

ENSMUSG00000002107

Gene Name

CUGBP, Elav-like family member 2

Synonyms

Napor-2, ETR-3, B230345P09Rik, Cugbp2

MMRRC Submission

042613-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.552) question?

Stock #

R5022 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

6539694-7509563 bp(-) (GRCm38)

Type of Mutation

intron

DNA Base Change (assembly)

C to T at 6607847 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000138974 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000002176] [ENSMUST00000100429] [ENSMUST00000114924] [ENSMUST00000114927] [ENSMUST00000114934] [ENSMUST00000142941] [ENSMUST00000150624] [ENSMUST00000170438] [ENSMUST00000182404] [ENSMUST00000182879] [ENSMUST00000182706] [ENSMUST00000183091] [ENSMUST00000183209] [ENSMUST00000182851] [ENSMUST00000183984]

AlphaFold

Q9Z0H4

Predicted Effect

probably benign
Transcript: ENSMUST00000002176

SMART Domains

Protein: ENSMUSP00000002176
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	17	95	1.29e-17	SMART
RRM	109	184	4.22e-22	SMART
low complexity region	194	223	N/A	INTRINSIC
low complexity region	252	279	N/A	INTRINSIC
low complexity region	281	293	N/A	INTRINSIC
low complexity region	326	355	N/A	INTRINSIC
low complexity region	379	392	N/A	INTRINSIC
RRM	400	473	3.2e-22	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000100429

SMART Domains

Protein: ENSMUSP00000097996
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	17	95	1.29e-17	SMART
RRM	109	184	4.22e-22	SMART
low complexity region	194	223	N/A	INTRINSIC
low complexity region	252	279	N/A	INTRINSIC
low complexity region	281	293	N/A	INTRINSIC
low complexity region	341	362	N/A	INTRINSIC
low complexity region	385	398	N/A	INTRINSIC
RRM	406	479	3.2e-22	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000114924

SMART Domains

Protein: ENSMUSP00000110574
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	59	137	1.29e-17	SMART
RRM	151	226	4.22e-22	SMART
low complexity region	236	265	N/A	INTRINSIC
low complexity region	294	321	N/A	INTRINSIC
low complexity region	323	335	N/A	INTRINSIC
low complexity region	368	397	N/A	INTRINSIC
low complexity region	421	434	N/A	INTRINSIC
RRM	442	515	3.2e-22	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000114927

SMART Domains

Protein: ENSMUSP00000110577
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	17	95	1.29e-17	SMART
RRM	109	184	4.22e-22	SMART
low complexity region	194	223	N/A	INTRINSIC
low complexity region	252	279	N/A	INTRINSIC
low complexity region	281	293	N/A	INTRINSIC
low complexity region	341	359	N/A	INTRINSIC
low complexity region	383	396	N/A	INTRINSIC
RRM	404	477	3.2e-22	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000114934

SMART Domains

Protein: ENSMUSP00000110584
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	59	137	1.29e-17	SMART
RRM	151	226	4.22e-22	SMART
low complexity region	236	265	N/A	INTRINSIC
low complexity region	294	321	N/A	INTRINSIC
low complexity region	323	335	N/A	INTRINSIC
low complexity region	368	397	N/A	INTRINSIC
low complexity region	421	434	N/A	INTRINSIC
RRM	442	515	3.2e-22	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000138347

SMART Domains

Protein: ENSMUSP00000114914
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	24	102	1.29e-17	SMART
RRM	116	184	1.64e-19	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000142941

SMART Domains

Protein: ENSMUSP00000120459
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	17	95	1.29e-17	SMART
RRM	109	184	4.22e-22	SMART
low complexity region	194	223	N/A	INTRINSIC
low complexity region	252	279	N/A	INTRINSIC
low complexity region	281	293	N/A	INTRINSIC
low complexity region	341	362	N/A	INTRINSIC
low complexity region	385	398	N/A	INTRINSIC
RRM	406	479	3.2e-22	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000148321

Predicted Effect

probably benign
Transcript: ENSMUST00000150624

SMART Domains

Protein: ENSMUSP00000138297
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	17	95	1.29e-17	SMART
RRM	109	184	4.22e-22	SMART
low complexity region	194	223	N/A	INTRINSIC
low complexity region	252	279	N/A	INTRINSIC
low complexity region	281	293	N/A	INTRINSIC
low complexity region	341	359	N/A	INTRINSIC
low complexity region	383	396	N/A	INTRINSIC
RRM	404	477	3.2e-22	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000170438

SMART Domains

Protein: ENSMUSP00000130829
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	59	137	1.29e-17	SMART
RRM	151	226	4.22e-22	SMART
low complexity region	236	265	N/A	INTRINSIC
low complexity region	294	321	N/A	INTRINSIC
low complexity region	323	335	N/A	INTRINSIC
RRM	384	467	4.92e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182404

SMART Domains

Protein: ENSMUSP00000138769
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	22	97	4.22e-22	SMART
low complexity region	107	136	N/A	INTRINSIC
low complexity region	165	192	N/A	INTRINSIC
low complexity region	194	206	N/A	INTRINSIC
low complexity region	254	272	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183269

Predicted Effect

probably benign
Transcript: ENSMUST00000182879

SMART Domains

Protein: ENSMUSP00000138359
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	17	95	1.29e-17	SMART
RRM	109	184	4.22e-22	SMART
low complexity region	194	223	N/A	INTRINSIC
low complexity region	252	279	N/A	INTRINSIC
low complexity region	281	293	N/A	INTRINSIC
RRM	346	429	4.92e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182706

SMART Domains

Protein: ENSMUSP00000138764
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	53	131	1.29e-17	SMART
RRM	145	220	4.22e-22	SMART
low complexity region	230	259	N/A	INTRINSIC
low complexity region	288	315	N/A	INTRINSIC
low complexity region	317	329	N/A	INTRINSIC
low complexity region	362	391	N/A	INTRINSIC
low complexity region	415	428	N/A	INTRINSIC
RRM	436	509	3.2e-22	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000183091

SMART Domains

Protein: ENSMUSP00000138795
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	41	119	1.29e-17	SMART
RRM	133	208	4.22e-22	SMART
low complexity region	218	247	N/A	INTRINSIC
low complexity region	276	303	N/A	INTRINSIC
low complexity region	305	317	N/A	INTRINSIC
RRM	366	449	4.92e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000183209

SMART Domains

Protein: ENSMUSP00000138355
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	53	131	1.29e-17	SMART
RRM	145	220	4.22e-22	SMART
low complexity region	230	259	N/A	INTRINSIC
low complexity region	288	315	N/A	INTRINSIC
low complexity region	317	329	N/A	INTRINSIC
RRM	378	461	4.92e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182851

SMART Domains

Protein: ENSMUSP00000138363
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
RRM	41	119	1.29e-17	SMART
RRM	133	208	4.22e-22	SMART
low complexity region	218	247	N/A	INTRINSIC
low complexity region	276	303	N/A	INTRINSIC
low complexity region	305	317	N/A	INTRINSIC
low complexity region	350	379	N/A	INTRINSIC
low complexity region	403	416	N/A	INTRINSIC
RRM	424	497	3.2e-22	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000183984

SMART Domains

Protein: ENSMUSP00000138974
Gene: ENSMUSG00000002107

Domain	Start	End	E-Value	Type
low complexity region	2	54	N/A	INTRINSIC
RRM	104	182	1.29e-17	SMART
RRM	196	271	4.22e-22	SMART
low complexity region	281	310	N/A	INTRINSIC
low complexity region	339	366	N/A	INTRINSIC
low complexity region	368	380	N/A	INTRINSIC

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.4%
20x: 92.6%

Validation Efficiency

99% (110/111)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 105 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca1	TCGACTGC	T	4: 53,041,570 (GRCm38)		probably null	Het
Abca15	T	C	7: 120,346,096 (GRCm38)	I465T	probably damaging	Het
Abca3	C	T	17: 24,374,300 (GRCm38)	R224C	probably damaging	Het
Abcb4	T	A	5: 8,909,054 (GRCm38)		probably null	Het
Acan	T	C	7: 79,092,808 (GRCm38)		probably null	Het
Aebp2	G	A	6: 140,637,730 (GRCm38)	R109Q	possibly damaging	Het
Agfg2	A	T	5: 137,660,160 (GRCm38)		probably null	Het
Ankib1	T	A	5: 3,734,011 (GRCm38)	I322F	possibly damaging	Het
AW551984	A	T	9: 39,597,965 (GRCm38)	N293K	probably benign	Het
BC028528	T	A	3: 95,888,823 (GRCm38)		probably benign	Het
Bicc1	A	G	10: 70,947,883 (GRCm38)	S393P	possibly damaging	Het
Birc6	A	G	17: 74,692,332 (GRCm38)	Y4656C	probably damaging	Het
Bmp3	A	G	5: 98,872,824 (GRCm38)	R369G	probably damaging	Het
C1d	T	A	11: 17,266,674 (GRCm38)	N135K	probably benign	Het
Ccdc148	G	A	2: 58,827,632 (GRCm38)	A453V	probably damaging	Het
Cd163	C	T	6: 124,325,288 (GRCm38)	T937I	probably damaging	Het
Chga	T	C	12: 102,562,837 (GRCm38)	W358R	probably damaging	Het
Clec4b2	A	T	6: 123,200,956 (GRCm38)	S77C	probably null	Het
Crim1	T	C	17: 78,280,129 (GRCm38)	V221A	possibly damaging	Het
D630003M21Rik	A	T	2: 158,217,633 (GRCm38)	S116T	probably damaging	Het
Dlg5	T	C	14: 24,136,622 (GRCm38)	E1847G	probably damaging	Het
Dmxl1	T	A	18: 49,895,127 (GRCm38)	I2206K	probably damaging	Het
Dusp7	T	A	9: 106,373,741 (GRCm38)	L355Q	probably damaging	Het
Exd2	T	A	12: 80,496,790 (GRCm38)	N582K	probably damaging	Het
Fbln1	G	A	15: 85,237,626 (GRCm38)	S316N	probably damaging	Het
Fchsd1	A	G	18: 37,964,810 (GRCm38)	I340T	possibly damaging	Het
Fn1	T	C	1: 71,624,179 (GRCm38)	Y1050C	probably damaging	Het
Fsip2	A	G	2: 82,979,429 (GRCm38)	I2031V	probably benign	Het
Gm10803	A	C	2: 93,564,172 (GRCm38)	L96F	probably damaging	Het
Gm12169	T	A	11: 46,528,532 (GRCm38)	D58E	probably damaging	Het
Gm14569	T	C	X: 36,430,817 (GRCm38)	D1413G	probably benign	Het
Gm15455	T	C	1: 33,837,351 (GRCm38)		noncoding transcript	Het
Gm1818	G	C	12: 48,555,535 (GRCm38)		noncoding transcript	Het
Gm4907	G	A	X: 23,907,241 (GRCm38)	G327E	probably damaging	Het
Gm5039	T	C	12: 88,321,301 (GRCm38)	I61V	probably benign	Het
Gm5420	A	T	10: 21,691,727 (GRCm38)		noncoding transcript	Het
Gm6803	A	T	12: 88,018,711 (GRCm38)	S21T	unknown	Het
Gm7104	A	T	12: 88,285,759 (GRCm38)		noncoding transcript	Het
Gp2	A	G	7: 119,449,114 (GRCm38)	I427T	probably damaging	Het
Gpc4	G	A	X: 52,074,563 (GRCm38)	R148C	probably damaging	Het
Gpr142	A	C	11: 114,804,388 (GRCm38)	S60R	probably benign	Het
Helz2	T	C	2: 181,240,569 (GRCm38)	R144G	probably benign	Het
Herc1	A	T	9: 66,470,326 (GRCm38)	K3458M	possibly damaging	Het
Hnf4g	G	T	3: 3,644,587 (GRCm38)	A144S	probably damaging	Het
Irs2	A	C	8: 10,987,012 (GRCm38)	*1322G	probably null	Het
Keg1	A	G	19: 12,719,157 (GRCm38)	N288S	probably damaging	Het
Kif19a	G	A	11: 114,767,227 (GRCm38)	M37I	probably benign	Het
Klhl1	G	A	14: 96,136,706 (GRCm38)	P635S	probably benign	Het
Klk14	G	A	7: 43,692,077 (GRCm38)	C51Y	probably damaging	Het
Lsm11	T	C	11: 45,944,839 (GRCm38)	D25G	probably damaging	Het
Manea	A	T	4: 26,336,630 (GRCm38)	Y215*	probably null	Het
Mdga2	C	T	12: 66,470,760 (GRCm38)	C100Y	possibly damaging	Het
Mthfd1	T	G	12: 76,294,374 (GRCm38)	V480G	probably damaging	Het
Mthfd1	T	A	12: 76,301,328 (GRCm38)	M582K	probably damaging	Het
Myh7b	G	C	2: 155,632,373 (GRCm38)	R1669S	possibly damaging	Het
Nanos1	T	C	19: 60,756,980 (GRCm38)	Y239H	probably damaging	Het
Nat8	G	A	6: 85,830,857 (GRCm38)	T98I	possibly damaging	Het
Ndufs3	C	A	2: 90,898,660 (GRCm38)	A161S	probably benign	Het
Nexmif	A	T	X: 104,087,350 (GRCm38)	N320K	probably damaging	Het
Olfr1216	A	G	2: 89,014,043 (GRCm38)	V7A	probably damaging	Het
Olfr1228	C	T	2: 89,249,417 (GRCm38)	M92I	probably benign	Het
Olfr164	A	T	16: 19,286,059 (GRCm38)	V228D	probably damaging	Het
Olfr239	T	C	17: 33,199,777 (GRCm38)	F239S	probably damaging	Het
Olfr457	A	T	6: 42,471,287 (GRCm38)	V297E	possibly damaging	Het
Olfr589	G	A	7: 103,155,735 (GRCm38)	P4L	probably benign	Het
Olfr727	T	C	14: 50,127,012 (GRCm38)	V145A	possibly damaging	Het
Olfr822	T	C	10: 130,074,593 (GRCm38)	L61P	probably damaging	Het
Pcdhb14	T	A	18: 37,450,170 (GRCm38)	N776K	probably benign	Het
Pip5k1c	G	A	10: 81,310,889 (GRCm38)		probably null	Het
Plk4	G	A	3: 40,802,077 (GRCm38)		probably null	Het
Prmt8	A	G	6: 127,711,163 (GRCm38)	Y231H	possibly damaging	Het
Prpf4b	T	C	13: 34,883,599 (GRCm38)		probably benign	Het
Ptpn21	G	A	12: 98,679,407 (GRCm38)	R1091C	probably damaging	Het
Pwwp2b	C	T	7: 139,255,578 (GRCm38)	P312S	possibly damaging	Het
Rad21	A	T	15: 51,966,706 (GRCm38)	I503K	probably benign	Het
Rai14	A	G	15: 10,574,506 (GRCm38)	S789P	probably damaging	Het
Rbm26	C	T	14: 105,144,252 (GRCm38)	D486N	probably damaging	Het
Rnf20	A	G	4: 49,642,016 (GRCm38)		probably benign	Het
Ros1	A	G	10: 52,124,075 (GRCm38)	V1118A	possibly damaging	Het
Sema3d	A	C	5: 12,584,956 (GRCm38)	Y663S	probably damaging	Het
Serpina6	A	G	12: 103,651,712 (GRCm38)	W281R	probably damaging	Het
Slc8a3	A	G	12: 81,199,558 (GRCm38)	V900A	probably damaging	Het
Spats2l	G	T	1: 57,879,556 (GRCm38)	V30L	probably damaging	Het
Spg21	A	G	9: 65,475,949 (GRCm38)	D139G	probably damaging	Het
Sun3	T	C	11: 9,038,314 (GRCm38)	T3A	probably damaging	Het
Tcrg-V1	T	A	13: 19,340,231 (GRCm38)	S42T	probably benign	Het
Tep1	A	G	14: 50,828,999 (GRCm38)	Y2335H	probably benign	Het
Timm21	C	A	18: 84,949,414 (GRCm38)	V112L	possibly damaging	Het
Tlk1	A	T	2: 70,742,065 (GRCm38)	N386K	probably benign	Het
Trappc10	G	T	10: 78,217,160 (GRCm38)	F260L	possibly damaging	Het
Trmt112	T	C	19: 6,910,753 (GRCm38)	V91A	probably benign	Het
Ucp2	A	T	7: 100,498,372 (GRCm38)	N186I	possibly damaging	Het
Vmn1r119	A	G	7: 21,012,320 (GRCm38)	S46P	probably benign	Het
Vmn2r101	A	T	17: 19,611,387 (GRCm38)		probably null	Het
Vmn2r105	T	A	17: 20,208,414 (GRCm38)	H800L	probably damaging	Het
Vmn2r69	T	C	7: 85,411,159 (GRCm38)	M406V	possibly damaging	Het
Vmn2r84	A	G	10: 130,386,548 (GRCm38)	L601P	probably damaging	Het
Vps16	A	G	2: 130,439,452 (GRCm38)	S235G	probably benign	Het
Wap	T	C	11: 6,637,339 (GRCm38)		probably benign	Het
Wdr11	A	G	7: 129,624,711 (GRCm38)	I744M	probably benign	Het
Xiap	T	C	X: 42,094,465 (GRCm38)	F23L	probably benign	Het
Xkr7	A	G	2: 153,054,380 (GRCm38)	T385A	probably benign	Het
Zfp524	A	T	7: 5,018,417 (GRCm38)	I315F	probably benign	Het
Zfp62	T	A	11: 49,215,729 (GRCm38)	S216T	probably damaging	Het
Znfx1	T	C	2: 167,039,826 (GRCm38)	Y217C	probably damaging	Het

Other mutations in Celf2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00925:Celf2	APN	2	6,721,577 (GRCm38)	missense	probably benign	0.00
IGL01974:Celf2	APN	2	6,604,031 (GRCm38)	missense	probably damaging	1.00
IGL02159:Celf2	APN	2	6,604,177 (GRCm38)	nonsense	probably null
LCD18:Celf2	UTSW	2	6,779,076 (GRCm38)	intron	probably benign
R0113:Celf2	UTSW	2	6,624,714 (GRCm38)	missense	probably damaging	1.00
R0511:Celf2	UTSW	2	6,604,176 (GRCm38)	missense	probably damaging	1.00
R0711:Celf2	UTSW	2	6,721,415 (GRCm38)	critical splice donor site	probably null
R1755:Celf2	UTSW	2	6,884,958 (GRCm38)	start codon destroyed	probably benign	0.01
R1802:Celf2	UTSW	2	6,549,933 (GRCm38)	missense	probably damaging	1.00
R1898:Celf2	UTSW	2	6,604,164 (GRCm38)	missense	probably damaging	1.00
R1912:Celf2	UTSW	2	6,615,753 (GRCm38)	missense	probably damaging	1.00
R2422:Celf2	UTSW	2	6,553,889 (GRCm38)	missense	probably damaging	1.00
R2848:Celf2	UTSW	2	6,604,125 (GRCm38)	missense	probably damaging	0.96
R2849:Celf2	UTSW	2	6,604,125 (GRCm38)	missense	probably damaging	0.96
R3708:Celf2	UTSW	2	6,624,678 (GRCm38)	missense	probably damaging	1.00
R4295:Celf2	UTSW	2	6,604,064 (GRCm38)	missense	probably benign	0.10
R4601:Celf2	UTSW	2	6,586,020 (GRCm38)	missense	possibly damaging	0.87
R4602:Celf2	UTSW	2	6,586,020 (GRCm38)	missense	possibly damaging	0.87
R4610:Celf2	UTSW	2	6,586,020 (GRCm38)	missense	possibly damaging	0.87
R4611:Celf2	UTSW	2	6,586,020 (GRCm38)	missense	possibly damaging	0.87
R4667:Celf2	UTSW	2	6,721,528 (GRCm38)	missense	probably benign	0.44
R4668:Celf2	UTSW	2	6,721,528 (GRCm38)	missense	probably benign	0.44
R4669:Celf2	UTSW	2	6,721,528 (GRCm38)	missense	probably benign	0.44
R4790:Celf2	UTSW	2	6,549,903 (GRCm38)	missense	probably damaging	1.00
R5369:Celf2	UTSW	2	7,081,081 (GRCm38)	intron	probably benign
R5540:Celf2	UTSW	2	6,553,932 (GRCm38)	missense	probably benign	0.43
R5805:Celf2	UTSW	2	6,553,787 (GRCm38)	missense	probably damaging	1.00
R5913:Celf2	UTSW	2	7,081,158 (GRCm38)	start codon destroyed	probably null	0.02
R6330:Celf2	UTSW	2	6,884,955 (GRCm38)	missense	probably benign	0.05
R7505:Celf2	UTSW	2	6,624,700 (GRCm38)	missense	probably damaging	1.00
R7662:Celf2	UTSW	2	6,553,917 (GRCm38)	missense	probably damaging	1.00
R8316:Celf2	UTSW	2	6,547,103 (GRCm38)	missense	probably benign	0.03
R8437:Celf2	UTSW	2	6,547,145 (GRCm38)	missense	probably damaging	1.00
R8860:Celf2	UTSW	2	6,560,657 (GRCm38)	critical splice donor site	probably null
R9170:Celf2	UTSW	2	6,549,835 (GRCm38)	missense	possibly damaging	0.75
R9373:Celf2	UTSW	2	6,547,104 (GRCm38)	missense	probably benign	0.24
R9374:Celf2	UTSW	2	6,586,075 (GRCm38)	missense	possibly damaging	0.95
R9382:Celf2	UTSW	2	6,721,593 (GRCm38)	missense	probably damaging	1.00
R9623:Celf2	UTSW	2	6,615,711 (GRCm38)	missense	probably damaging	1.00
R9626:Celf2	UTSW	2	6,586,024 (GRCm38)	missense	probably benign	0.33
R9718:Celf2	UTSW	2	6,721,538 (GRCm38)	missense	probably damaging	1.00
X0018:Celf2	UTSW	2	6,553,913 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CAGGTGGAAGGTCTCACTAAAG -3'
(R):5'- ACAAGCGTCCAACCCTTTTG -3'

Sequencing Primer
(F):5'- AGTACATTTCCAGTCATGAGGG -3'
(R):5'- AAGCGTCCAACCCTTTTGTCTTG -3'

Posted On

2016-06-06