Mutagenetix > Incidental Mutation

Incidental Mutation 'R5893:Champ1'

457300

Institutional Source

Beutler Lab

Gene Symbol

Champ1

Ensembl Gene

ENSMUSG00000047710

Gene Name

chromosome alignment maintaining phosphoprotein 1

Synonyms

Zfp828, D8Ertd569e, D8Ertd457e

MMRRC Submission

044094-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.934) question?

Stock #

R5893 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

13919699-13931637 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 13928777 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Serine at position 312 (P312S)

Ref Sequence

ENSEMBL: ENSMUSP00000120117 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000051870] [ENSMUST00000128557]

AlphaFold

Q8K327

Predicted Effect

probably benign
Transcript: ENSMUST00000051870
AA Change: P312S

PolyPhen 2 Score 0.084 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000057270
Gene: ENSMUSG00000047710
AA Change: P312S

Domain	Start	End	E-Value	Type
ZnF_C2H2	14	37	1.62e0	SMART
ZnF_C2H2	62	85	2.29e1	SMART
internal_repeat_1	109	278	1.19e-9	PROSPERO
low complexity region	298	318	N/A	INTRINSIC
low complexity region	354	368	N/A	INTRINSIC
internal_repeat_1	373	534	1.19e-9	PROSPERO
low complexity region	602	613	N/A	INTRINSIC
low complexity region	677	690	N/A	INTRINSIC
ZnF_C2H2	699	722	2.68e1	SMART
ZnF_C2H2	728	750	1.79e-2	SMART
ZnF_C2H2	755	776	2.23e1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000083883

Predicted Effect

probably benign
Transcript: ENSMUST00000128557
AA Change: P312S

PolyPhen 2 Score 0.084 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000120117
Gene: ENSMUSG00000047710
AA Change: P312S

Domain	Start	End	E-Value	Type
ZnF_C2H2	14	37	1.62e0	SMART
ZnF_C2H2	62	85	2.29e1	SMART
internal_repeat_1	109	278	5.23e-7	PROSPERO
low complexity region	298	318	N/A	INTRINSIC
low complexity region	354	368	N/A	INTRINSIC
internal_repeat_1	373	534	5.23e-7	PROSPERO
low complexity region	602	613	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197610

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.1%
20x: 94.4%

Validation Efficiency

95% (73/77)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a zinc finger protein that functions as a regulator of chromosome segregation in mitosis. The encoded protein is required for correct alignment of chromosomes on the metaphase plate, and plays a role in maintaining the attachment of sister kinetochores to microtubules from opposite spindle poles. Mutations in this gene are associated with autosomal dominant mental retardation-40. [provided by RefSeq, Oct 2016]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AAdacl4fm3	C	T	4: 144,429,766 (GRCm39)	V408I	probably benign	Het
Ablim1	T	A	19: 57,204,285 (GRCm39)	R35S	probably benign	Het
Acacb	A	T	5: 114,367,912 (GRCm39)	I1637F	probably benign	Het
Adamts18	A	T	8: 114,499,709 (GRCm39)	C402S	probably damaging	Het
Adra2b	T	A	2: 127,206,402 (GRCm39)	D306E	probably benign	Het
Ammecr1l	C	T	18: 31,911,973 (GRCm39)	T263I	probably damaging	Het
Antxr1	T	C	6: 87,114,241 (GRCm39)	I509V	probably benign	Het
Bahcc1	A	G	11: 120,176,256 (GRCm39)	E1967G	probably damaging	Het
Brap	T	A	5: 121,817,405 (GRCm39)	Y337*	probably null	Het
Brca2	T	C	5: 150,492,603 (GRCm39)	V3206A	probably benign	Het
Cacna1e	A	T	1: 154,313,069 (GRCm39)	F1486I	probably damaging	Het
Cbx4	A	G	11: 118,973,016 (GRCm39)	Y120H	probably damaging	Het
Ccar2	T	A	14: 70,388,800 (GRCm39)	Q137L	probably benign	Het
Ceacam12	A	G	7: 17,803,299 (GRCm39)	D235G	probably damaging	Het
Celsr1	A	G	15: 85,788,215 (GRCm39)	V2679A	probably benign	Het
Chst5	A	G	8: 112,616,828 (GRCm39)	L264S	probably damaging	Het
Cip2a	A	G	16: 48,817,863 (GRCm39)	S78G	probably benign	Het
Colec10	T	A	15: 54,274,185 (GRCm39)	F4L	probably benign	Het
Cyp2a4	G	A	7: 26,008,353 (GRCm39)	G165D	probably damaging	Het
Cyp2c29	G	C	19: 39,318,833 (GRCm39)	A438P	possibly damaging	Het
Dlat	A	G	9: 50,555,439 (GRCm39)		probably benign	Het
Dmxl2	A	G	9: 54,294,704 (GRCm39)	V2457A	possibly damaging	Het
Dnah7a	A	G	1: 53,496,944 (GRCm39)	M3104T	possibly damaging	Het
Dock8	C	T	19: 25,099,811 (GRCm39)	H645Y	probably damaging	Het
Ehbp1l1	T	C	19: 5,768,459 (GRCm39)	E948G	probably benign	Het
Eps8l2	C	T	7: 140,937,537 (GRCm39)	R384C	probably damaging	Het
Fam174a	A	T	1: 95,252,884 (GRCm39)	N162I	probably damaging	Het
Fbp2	T	A	13: 62,984,916 (GRCm39)	N335I	probably benign	Het
Foxred2	C	A	15: 77,831,344 (GRCm39)	G490C	probably damaging	Het
Fyttd1	T	G	16: 32,719,283 (GRCm39)	D200E	probably damaging	Het
Gdf15	A	T	8: 71,082,473 (GRCm39)	V211E	possibly damaging	Het
Gm6214	A	G	3: 140,545,107 (GRCm39)		noncoding transcript	Het
Havcr2	A	G	11: 46,347,143 (GRCm39)	Y40C	probably damaging	Het
Htra1	T	G	7: 130,563,321 (GRCm39)	V184G	probably damaging	Het
Hydin	A	T	8: 111,217,308 (GRCm39)	I1399F	probably benign	Het
Igtp	T	C	11: 58,097,474 (GRCm39)	L215P	probably damaging	Het
Kctd1	T	C	18: 15,102,745 (GRCm39)	E812G	possibly damaging	Het
Lap3	T	C	5: 45,668,621 (GRCm39)		probably benign	Het
Lgalsl2	A	T	7: 5,362,623 (GRCm39)	T85S	probably benign	Het
Lrp1b	C	A	2: 40,491,599 (GRCm39)	A223S	probably damaging	Het
Mtnr1b	A	T	9: 15,774,540 (GRCm39)	V173E	probably damaging	Het
Nat10	A	C	2: 103,552,184 (GRCm39)		probably benign	Het
Ndfip2	T	A	14: 105,532,291 (GRCm39)	V229E	probably damaging	Het
Nefh	G	A	11: 4,891,323 (GRCm39)	T432M	probably damaging	Het
Nfe2l3	A	G	6: 51,434,832 (GRCm39)	Y464C	probably damaging	Het
Nrip1	C	A	16: 76,090,841 (GRCm39)	A239S	probably damaging	Het
Olfml2b	A	G	1: 170,490,042 (GRCm39)	S221G	probably benign	Het
Orc4	G	T	2: 48,795,559 (GRCm39)	S389*	probably null	Het
P4hb	A	G	11: 120,462,476 (GRCm39)	S77P	probably damaging	Het
Pcyt2	T	C	11: 120,508,623 (GRCm39)		probably null	Het
Plagl1	T	C	10: 13,003,938 (GRCm39)		probably benign	Het
Poglut1	C	T	16: 38,349,957 (GRCm39)	R272Q	probably damaging	Het
Pramel26	T	A	4: 143,537,038 (GRCm39)	Y431F	probably damaging	Het
Rdh5	T	C	10: 128,750,090 (GRCm39)		probably null	Het
Rogdi	A	T	16: 4,831,258 (GRCm39)	L3*	probably null	Het
Skap1	T	C	11: 96,472,224 (GRCm39)	*166Q	probably null	Het
Slc38a4	A	G	15: 96,897,432 (GRCm39)	I461T	probably benign	Het
Snx31	A	C	15: 36,523,601 (GRCm39)	I360M	probably damaging	Het
Spata22	A	T	11: 73,227,073 (GRCm39)	K96*	probably null	Het
Strn3	A	T	12: 51,690,006 (GRCm39)		probably null	Het
Trip12	A	C	1: 84,736,884 (GRCm39)		probably benign	Het
Uggt1	A	T	1: 36,266,709 (GRCm39)		probably null	Het
Upk3a	A	C	15: 84,903,538 (GRCm39)	D79A	probably damaging	Het
Uts2r	A	T	11: 121,052,105 (GRCm39)	Y323F	probably benign	Het
Vmn2r1	A	T	3: 63,993,974 (GRCm39)	N107Y	probably damaging	Het
Vps13c	A	T	9: 67,810,121 (GRCm39)		probably null	Het
Wnt7b	A	G	15: 85,465,575 (GRCm39)		probably benign	Het
Zfp410	T	A	12: 84,384,385 (GRCm39)		probably null	Het

Other mutations in Champ1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00530:Champ1	APN	8	13,929,522 (GRCm39)	missense	possibly damaging	0.68
IGL00775:Champ1	APN	8	13,929,509 (GRCm39)	missense	probably damaging	1.00
IGL02451:Champ1	APN	8	13,928,739 (GRCm39)	missense	probably damaging	1.00
IGL03283:Champ1	APN	8	13,928,786 (GRCm39)	missense	probably benign	0.04
PIT4810001:Champ1	UTSW	8	13,929,234 (GRCm39)	missense	probably benign	0.37
R0664:Champ1	UTSW	8	13,929,485 (GRCm39)	missense	probably damaging	0.96
R2219:Champ1	UTSW	8	13,930,017 (GRCm39)	missense	probably damaging	1.00
R3077:Champ1	UTSW	8	13,928,832 (GRCm39)	missense	probably benign
R3735:Champ1	UTSW	8	13,928,735 (GRCm39)	missense	probably damaging	1.00
R3838:Champ1	UTSW	8	13,929,939 (GRCm39)	missense	probably damaging	1.00
R4714:Champ1	UTSW	8	13,928,063 (GRCm39)	missense	probably damaging	1.00
R4933:Champ1	UTSW	8	13,929,137 (GRCm39)	missense	probably benign	0.14
R5294:Champ1	UTSW	8	13,928,981 (GRCm39)	missense	probably damaging	1.00
R6548:Champ1	UTSW	8	13,930,002 (GRCm39)	missense	probably damaging	1.00
R7261:Champ1	UTSW	8	13,928,517 (GRCm39)	missense	possibly damaging	0.90
R7467:Champ1	UTSW	8	13,928,579 (GRCm39)	missense	possibly damaging	0.89
R7747:Champ1	UTSW	8	13,929,990 (GRCm39)	missense	probably damaging	1.00
R9328:Champ1	UTSW	8	13,929,392 (GRCm39)	missense	probably damaging	1.00
R9464:Champ1	UTSW	8	13,929,114 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGTCTCCAGAGTCACCAGTAC -3'
(R):5'- TTCCAGGAACCAGATGAGACTG -3'

Sequencing Primer
(F):5'- CAGTGCATCTCCAGAGTCTCG -3'
(R):5'- ACTGAAGACTTCCAGGATGC -3'

Posted On

2017-02-15