Mutagenetix > Incidental Mutations

Incidental Mutation 'R7466:Cep44'

578780

Institutional Source

Beutler Lab

Gene Symbol

Cep44

Ensembl Gene

ENSMUSG00000038215

Gene Name

centrosomal protein 44

Synonyms

4933440G23Rik, BC088983

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably essential (E-score: 0.811) question?

Stock #

R7466 (G1)

Quality Score

217.468

Status

Validated

Chromosome

Chromosomal Location

56531522-56551047 bp(-) (GRCm38)

Type of Mutation

frame shift

DNA Base Change (assembly)

AACGC to A at 56540983 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000042586 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040330] [ENSMUST00000130930] [ENSMUST00000134162] [ENSMUST00000135337] [ENSMUST00000140107]

Predicted Effect

probably null
Transcript: ENSMUST00000040330

SMART Domains

Protein: ENSMUSP00000042586
Gene: ENSMUSG00000038215

Domain	Start	End	E-Value	Type
Pfam:CEP44	5	131	2.5e-52	PFAM
coiled coil region	232	263	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000123493

SMART Domains

Protein: ENSMUSP00000116884
Gene: ENSMUSG00000038215

Domain	Start	End	E-Value	Type
Pfam:CEP44	1	73	3.3e-31	PFAM
coiled coil region	173	204	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000130930

SMART Domains

Protein: ENSMUSP00000118959
Gene: ENSMUSG00000038215

Domain	Start	End	E-Value	Type
Pfam:CEP44	5	63	3.2e-19	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000134162

SMART Domains

Protein: ENSMUSP00000117526
Gene: ENSMUSG00000038215

Domain	Start	End	E-Value	Type
Pfam:CEP44	5	102	9.1e-42	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000135337

SMART Domains

Protein: ENSMUSP00000122835
Gene: ENSMUSG00000038215

Domain	Start	End	E-Value	Type
Pfam:CEP44	5	80	1e-28	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000140107

SMART Domains

Protein: ENSMUSP00000114502
Gene: ENSMUSG00000038215

Domain	Start	End	E-Value	Type
Pfam:CEP44	5	136	1.7e-53	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

99% (83/84)

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AI182371	T	A	2: 35,088,741	K203*	probably null	Het
Akr1c13	T	C	13: 4,192,437		probably benign	Het
Amer3	A	G	1: 34,587,993	S438G	probably damaging	Het
Aqp9	T	A	9: 71,163,261		probably null	Het
Art4	G	T	6: 136,854,850	H98N	probably damaging	Het
Bdh1	T	C	16: 31,447,604	S70P	probably benign	Het
Ccdc61	A	C	7: 18,891,105	Y503D	probably damaging	Het
Cd163l1	T	C	7: 140,220,706		probably null	Het
Cd180	A	T	13: 102,704,995	N183I	probably damaging	Het
Cd200r2	C	T	16: 44,909,174	A64V	probably damaging	Het
Ceacam9	A	C	7: 16,723,855	K98Q	probably benign	Het
Cfap77	G	T	2: 28,955,613	D247E	probably benign	Het
Cftr	T	C	6: 18,227,973	M388T	probably benign	Het
Chrnb1	G	A	11: 69,784,650	H493Y	probably damaging	Het
Ckap2	A	C	8: 22,177,386	M153R	probably benign	Het
Cnot6l	A	G	5: 96,131,128	V77A	probably benign	Het
Col12a1	C	T	9: 79,655,407	E1798K	possibly damaging	Het
Cth	T	A	3: 157,924,885	D49V	probably benign	Het
Ctnnb1	T	C	9: 120,955,416	S425P	probably damaging	Het
Ctnnd1	T	C	2: 84,610,785	N690S	probably benign	Het
Cyhr1	C	T	15: 76,648,186	D241N	probably benign	Het
Dennd4c	A	G	4: 86,774,331	D26G	probably damaging	Het
Dlg5	G	A	14: 24,245,212	P80L	probably damaging	Het
Eef2k	A	G	7: 120,903,484		probably null	Het
Ephb2	C	T	4: 136,659,065	R791H	probably damaging	Het
Erh	T	C	12: 80,640,983	Y22C	probably benign	Het
F5	C	T	1: 164,193,328	T1124I	possibly damaging	Het
Fam220a	T	A	5: 143,563,471	C213S	possibly damaging	Het
Fat2	G	T	11: 55,310,432	N605K	probably damaging	Het
Ganab	C	A	19: 8,914,569	S780*	probably null	Het
Gbgt1	C	T	2: 28,502,207	P67S	probably damaging	Het
Gm17190	G	T	13: 96,082,779	G208*	probably null	Het
Grhl2	A	G	15: 37,291,616	Y316C	probably damaging	Het
H2-T10	T	C	17: 36,120,849	T38A	probably benign	Het
Ins1	A	G	19: 52,264,420		probably benign	Het
Ippk	T	C	13: 49,432,467		probably null	Het
Klc4	T	A	17: 46,639,910	I258F	probably benign	Het
Manba	C	A	3: 135,542,393	L348I	probably benign	Het
Mgam	A	G	6: 40,744,789	N347S	probably benign	Het
Myo18b	T	C	5: 112,723,892	T2108A	probably benign	Het
Naip5	A	T	13: 100,221,986	L914*	probably null	Het
Nsa2	C	T	13: 97,131,220	A242T	probably benign	Het
Nsd2	G	A	5: 33,882,147	W834*	probably null	Het
Olfr1134	T	C	2: 87,656,396	N175S	possibly damaging	Het
Olfr1419	T	A	19: 11,870,316	D300V	possibly damaging	Het
Olfr285	T	C	15: 98,313,380	M57V	probably damaging	Het
Olfr469	A	T	7: 107,822,922	C182*	probably null	Het
Pam	A	T	1: 97,842,247	D599E	probably damaging	Het
Phf20l1	A	G	15: 66,636,884	K864R	probably damaging	Het
Plcl2	A	G	17: 50,608,468	D835G	probably damaging	Het
Ppm1m	C	A	9: 106,196,157	A329S	probably damaging	Het
Prep	T	C	10: 45,150,438	V486A	probably benign	Het
Prkcb	A	T	7: 122,516,844	N182I	probably damaging	Het
Prkcz	A	G	4: 155,271,602	F355S	probably damaging	Het
Psg20	C	T	7: 18,684,467	S125N	probably benign	Het
Psmd12	A	G	11: 107,492,057	D234G	probably benign	Het
Pvrig	A	T	5: 138,342,008	M14L	probably benign	Het
Rabgap1l	C	T	1: 160,226,484		probably null	Het
Rfc1	A	T	5: 65,275,426	C764S	probably damaging	Het
Ryr3	T	C	2: 112,926,957	D351G	probably benign	Het
Serpinb9g	T	C	13: 33,495,167	F340S	probably benign	Het
Sirpb1c	C	A	3: 15,832,266	L315F	probably damaging	Het
Slc24a1	C	G	9: 64,928,404	E814Q	unknown	Het
Slc26a11	A	T	11: 119,374,502	Q355L	probably damaging	Het
Sp100	C	T	1: 85,707,239	L483F	possibly damaging	Het
St5	A	G	7: 109,525,346	L1096P	probably damaging	Het
Ston1	T	A	17: 88,635,901	M245K	probably benign	Het
Swap70	T	A	7: 110,274,772	D442E	probably benign	Het
Syne2	T	A	12: 76,046,186	V450D	possibly damaging	Het
Tbck	T	A	3: 132,752,563	N651K	probably damaging	Het
Timd4	A	T	11: 46,817,758	T204S	probably benign	Het
Tmem102	A	G	11: 69,804,885	L87P	probably damaging	Het
Tmem55a	T	A	4: 14,912,477	Y195*	probably null	Het
Tmprss11e	T	A	5: 86,709,480	T325S	probably benign	Het
Trpm1	G	A	7: 64,240,582	V978M	probably damaging	Het
Wdr12	A	T	1: 60,094,511	D19E	probably benign	Het
Wdr35	G	A	12: 9,005,773	V482I	probably benign	Het
Wdr63	T	C	3: 146,055,618	D661G	probably benign	Het
Zer1	T	C	2: 30,101,484		probably null	Het
Zfp503	T	C	14: 21,986,011	D279G	probably benign	Het
Zfp870	A	T	17: 32,883,762	C198S	possibly damaging	Het
Zfyve26	C	T	12: 79,287,807	E146K	probably benign	Het
Zkscan6	T	C	11: 65,828,531	V459A	probably damaging	Het

Other mutations in Cep44

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00545:Cep44	APN	8	56547400	missense	probably damaging	1.00
IGL02932:Cep44	APN	8	56547424	missense	probably damaging	1.00
R0347:Cep44	UTSW	8	56545475	missense	probably damaging	1.00
R0609:Cep44	UTSW	8	56544152	missense	possibly damaging	0.79
R0669:Cep44	UTSW	8	56540973	missense	possibly damaging	0.74
R1449:Cep44	UTSW	8	56540950	missense	probably benign	0.01
R1493:Cep44	UTSW	8	56532835	missense	probably damaging	1.00
R4114:Cep44	UTSW	8	56545422	missense	probably benign	0.25
R4422:Cep44	UTSW	8	56538617	missense	probably benign	0.00
R4423:Cep44	UTSW	8	56538617	missense	probably benign	0.00
R4425:Cep44	UTSW	8	56538617	missense	probably benign	0.00
R4621:Cep44	UTSW	8	56542916	missense	probably damaging	0.99
R5017:Cep44	UTSW	8	56544207	missense	possibly damaging	0.86
R5190:Cep44	UTSW	8	56532796	missense	probably benign	0.05
R5898:Cep44	UTSW	8	56541021	missense	probably damaging	1.00
R5938:Cep44	UTSW	8	56547422	missense	possibly damaging	0.93
R6080:Cep44	UTSW	8	56539841	missense	possibly damaging	0.50
R6150:Cep44	UTSW	8	56539805	missense	probably benign	0.39
R7016:Cep44	UTSW	8	56544199	missense	possibly damaging	0.89
R7141:Cep44	UTSW	8	56539851	missense	probably damaging	1.00
R7753:Cep44	UTSW	8	56532807	missense	probably benign	0.16
R7841:Cep44	UTSW	8	56540983	frame shift	probably null
Z1176:Cep44	UTSW	8	56544128	missense	possibly damaging	0.63

Predicted Primers

PCR Primer
(F):5'- CACTGACTCCTATTCAGAAAGACTG -3'
(R):5'- AGTTGAACTATGTCTCCCAAGC -3'

Sequencing Primer
(F):5'- CATTCGTAAGTAATAACATAGGTGCC -3'
(R):5'- GAATCGTGGCAGTAAACCA -3'

Posted On

2019-10-07