Mutagenetix > Incidental Mutation

Incidental Mutation 'R4082:Cdc123'

316913

Institutional Source

Beutler Lab

Gene Symbol

Cdc123

Ensembl Gene

ENSMUSG00000039128

Gene Name

cell division cycle 123

Synonyms

G431001I09Rik

MMRRC Submission

041624-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4082 (G1)

Quality Score

220

Status

Validated

Chromosome

Chromosomal Location

5799105-5849975 bp(-) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

G to A at 5815566 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000043864]

AlphaFold

Q8CII2

Predicted Effect

probably benign
Transcript: ENSMUST00000043864

SMART Domains

Protein: ENSMUSP00000043033
Gene: ENSMUSG00000039128

Domain	Start	End	E-Value	Type
Pfam:D123	14	314	3e-107	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000124287

Predicted Effect

probably benign
Transcript: ENSMUST00000128467

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000138312

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152519

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.4%

Validation Efficiency

99% (73/74)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700021P04Rik	T	G	19: 24,043,366 (GRCm39)		noncoding transcript	Het
a	A	T	2: 154,887,678 (GRCm39)	D46V	probably damaging	Het
Aass	A	T	6: 23,109,497 (GRCm39)	D324E	possibly damaging	Het
Abca12	G	T	1: 71,306,622 (GRCm39)	T2028K	possibly damaging	Het
Abt1	T	C	13: 23,606,316 (GRCm39)	T213A	probably benign	Het
Adcy1	A	C	11: 7,014,117 (GRCm39)	Y173S	probably damaging	Het
Aim2	T	C	1: 173,287,417 (GRCm39)		probably null	Het
Akr1d1	G	A	6: 37,534,424 (GRCm39)	V193M	probably damaging	Het
Cars1	C	T	7: 143,123,234 (GRCm39)	E461K	probably damaging	Het
Ccdc80	T	C	16: 44,943,290 (GRCm39)	L800P	probably damaging	Het
Ccl22	A	G	8: 95,473,536 (GRCm39)	Y27C	probably damaging	Het
Cldn11	A	T	3: 31,217,278 (GRCm39)	I149F	probably benign	Het
Col14a1	T	C	15: 55,300,429 (GRCm39)	Y986H	unknown	Het
Col6a3	G	A	1: 90,749,605 (GRCm39)	L410F	probably damaging	Het
Crocc	T	C	4: 140,761,282 (GRCm39)		probably null	Het
Cubn	A	G	2: 13,433,374 (GRCm39)		probably benign	Het
Cwc25	G	T	11: 97,644,744 (GRCm39)	Q205K	probably benign	Het
Cyp2e1	T	C	7: 140,350,991 (GRCm39)	I321T	possibly damaging	Het
Eps8l1	T	A	7: 4,473,797 (GRCm39)		probably null	Het
Fasl	C	T	1: 161,609,420 (GRCm39)	V189M	probably damaging	Het
Fbxw5	T	C	2: 25,394,643 (GRCm39)		probably null	Het
Flg2	A	C	3: 93,110,828 (GRCm39)	E952A	unknown	Het
Gpd1l	A	T	9: 114,746,146 (GRCm39)	L90Q	probably damaging	Het
Grik4	G	T	9: 42,509,180 (GRCm39)	F414L	probably benign	Het
Kcnh8	GAGACCAACGAGCAGCTGATGCTTCAGA	GAGA	17: 53,032,934 (GRCm39)	74	probably benign	Het
Klhl3	C	T	13: 58,166,611 (GRCm39)	G407S	probably null	Het
Lmbr1	T	C	5: 29,463,753 (GRCm39)	E157G	probably damaging	Het
Lrp2	T	A	2: 69,343,617 (GRCm39)	H914L	probably damaging	Het
Mrpl20	A	T	4: 155,892,970 (GRCm39)	D67V	probably damaging	Het
Myo15a	A	G	11: 60,378,022 (GRCm39)	T1346A	possibly damaging	Het
Naip5	A	T	13: 100,382,338 (GRCm39)	C124S	probably damaging	Het
Or10ag2	T	A	2: 87,248,801 (GRCm39)	Y134*	probably null	Het
Or13n4	T	C	7: 106,423,245 (GRCm39)	T163A	possibly damaging	Het
Or52u1	T	A	7: 104,237,830 (GRCm39)	V290D	probably damaging	Het
Osbp	A	G	19: 11,956,030 (GRCm39)	D385G	probably benign	Het
Paip1	G	A	13: 119,593,540 (GRCm39)	D460N	probably damaging	Het
Pde3b	T	C	7: 114,093,823 (GRCm39)	S356P	probably benign	Het
Pms2	A	G	5: 143,867,837 (GRCm39)	M814V	probably damaging	Het
Polg	C	A	7: 79,114,576 (GRCm39)	K128N	probably damaging	Het
Polk	G	T	13: 96,620,181 (GRCm39)	T694K	probably benign	Het
Pom121	T	C	5: 135,417,491 (GRCm39)	K342R	unknown	Het
Pou5f2	T	C	13: 78,174,024 (GRCm39)	L322P	probably damaging	Het
Prorp	G	T	12: 55,351,398 (GRCm39)	V236F	possibly damaging	Het
Ptpn6	T	C	6: 124,705,382 (GRCm39)	D183G	probably damaging	Het
Pygb	G	A	2: 150,668,391 (GRCm39)		probably null	Het
Ralgds	C	T	2: 28,442,283 (GRCm39)		probably benign	Het
Ret	T	C	6: 118,130,927 (GRCm39)	T1079A	possibly damaging	Het
Rspo2	A	C	15: 42,885,933 (GRCm39)	V241G	probably benign	Het
Smg1	T	A	7: 117,759,469 (GRCm39)		probably benign	Het
Snph	T	C	2: 151,435,722 (GRCm39)	D402G	probably damaging	Het
Spta1	A	G	1: 174,041,632 (GRCm39)	D1334G	probably benign	Het
Stard13	C	A	5: 151,016,294 (GRCm39)		probably null	Het
Sufu	A	G	19: 46,413,541 (GRCm39)	M141V	probably damaging	Het
Sytl2	T	A	7: 90,057,635 (GRCm39)	V831D	possibly damaging	Het
Tc2n	T	C	12: 101,617,414 (GRCm39)	E335G	possibly damaging	Het
Tex11	C	A	X: 99,977,021 (GRCm39)	A487S	possibly damaging	Het
Tmcc1	T	A	6: 116,020,441 (GRCm39)	H118L	probably damaging	Het
Tulp4	C	T	17: 6,282,055 (GRCm39)	H695Y	probably damaging	Het
Vmn1r209	A	C	13: 22,989,785 (GRCm39)	L302V	probably null	Het
Vmn2r117	C	T	17: 23,679,080 (GRCm39)	V715I	probably benign	Het
Vopp1	A	T	6: 57,766,964 (GRCm39)	Y37*	probably null	Het
Xrn1	A	G	9: 95,863,973 (GRCm39)	T528A	probably benign	Het
Zfhx2	T	C	14: 55,302,662 (GRCm39)	D1774G	probably benign	Het
Zfp955b	T	A	17: 33,521,129 (GRCm39)	D199E	probably benign	Het
Zp2	T	C	7: 119,734,475 (GRCm39)	S525G	probably benign	Het

Other mutations in Cdc123

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00159:Cdc123	APN	2	5,809,746 (GRCm39)	missense	probably benign	0.01
IGL00422:Cdc123	APN	2	5,803,260 (GRCm39)	missense	probably benign	0.07
IGL01860:Cdc123	APN	2	5,808,752 (GRCm39)	splice site	probably benign
IGL03002:Cdc123	APN	2	5,803,166 (GRCm39)	splice site	probably benign
Sinking	UTSW	2	5,803,174 (GRCm39)	missense	possibly damaging	0.82
R0563:Cdc123	UTSW	2	5,803,212 (GRCm39)	missense	probably benign
R1412:Cdc123	UTSW	2	5,808,776 (GRCm39)	missense	possibly damaging	0.80
R1584:Cdc123	UTSW	2	5,808,788 (GRCm39)	critical splice acceptor site	probably null
R1838:Cdc123	UTSW	2	5,799,702 (GRCm39)	splice site	probably null
R2064:Cdc123	UTSW	2	5,800,354 (GRCm39)	splice site	probably benign
R2144:Cdc123	UTSW	2	5,815,617 (GRCm39)	missense	probably benign	0.19
R4679:Cdc123	UTSW	2	5,849,703 (GRCm39)	missense	probably damaging	1.00
R4970:Cdc123	UTSW	2	5,809,748 (GRCm39)	missense	possibly damaging	0.59
R5089:Cdc123	UTSW	2	5,809,811 (GRCm39)	missense	probably benign	0.00
R5112:Cdc123	UTSW	2	5,809,748 (GRCm39)	missense	possibly damaging	0.59
R5691:Cdc123	UTSW	2	5,827,986 (GRCm39)	missense	probably benign	0.00
R5914:Cdc123	UTSW	2	5,803,174 (GRCm39)	missense	possibly damaging	0.82
R7860:Cdc123	UTSW	2	5,808,775 (GRCm39)	missense	probably benign	0.00
R8695:Cdc123	UTSW	2	5,826,174 (GRCm39)	missense	possibly damaging	0.69
R8865:Cdc123	UTSW	2	5,800,235 (GRCm39)	intron	probably benign
R9018:Cdc123	UTSW	2	5,849,683 (GRCm39)	missense	probably benign	0.00
R9265:Cdc123	UTSW	2	5,808,765 (GRCm39)	missense	possibly damaging	0.50
Z1176:Cdc123	UTSW	2	5,809,796 (GRCm39)	missense	probably damaging	0.97

Predicted Primers

PCR Primer
(F):5'- AGACTGTGTATATTCTCTGTGTACAGT -3'
(R):5'- TGCTTCATGGGATCAAAGCT -3'

Sequencing Primer
(F):5'- GGATGGAGACCTCTTTCTAGCAC -3'
(R):5'- GCTTCATGGGATCAAAGCTCATATTG -3'

Posted On

2015-05-15