Mutagenetix > Incidental Mutations

Incidental Mutation 'R6904:Cdcp1'

538689

Institutional Source

Beutler Lab

Gene Symbol

Cdcp1

Ensembl Gene

ENSMUSG00000035498

Gene Name

CUB domain containing protein 1

Synonyms

MMRRC Submission

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6904 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

123170824-123216038 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 123173915 bp

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 697 (D697G)

Ref Sequence

ENSEMBL: ENSMUSP00000042057 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039229]

Predicted Effect

probably benign
Transcript: ENSMUST00000039229
AA Change: D697G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000042057
Gene: ENSMUSG00000035498
AA Change: D697G

Domain	Start	End	E-Value	Type
signal peptide	1	29	N/A	INTRINSIC
internal_repeat_1	56	267	1.33e-11	PROSPERO
internal_repeat_1	374	591	1.33e-11	PROSPERO
transmembrane domain	668	690	N/A	INTRINSIC
low complexity region	770	782	N/A	INTRINSIC
low complexity region	792	802	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.2%
20x: 97.2%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a transmembrane protein which contains three extracellular CUB domains and acts as a substrate for Src family kinases. The protein plays a role in the tyrosine phosphorylation-dependent regulation of cellular events that are involved in tumor invasion and metastasis. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]
PHENOTYPE: Mice homozygous for a knock-out allele are viable and fertile. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610021A01Rik	T	A	7: 41,626,092	Y406*	probably null	Het
9530053A07Rik	C	T	7: 28,137,213	R186C	probably damaging	Het
Acadvl	T	C	11: 70,014,333	D109G	probably benign	Het
Adam24	G	A	8: 40,681,503	G670E	probably damaging	Het
Angpt1	T	C	15: 42,459,740	M378V	probably benign	Het
Ankrd33	G	A	15: 101,117,112		probably null	Het
Apol7b	G	A	15: 77,423,425	T290I	probably benign	Het
Atg4a-ps	A	G	3: 103,645,864	W54R	probably damaging	Het
B3glct	A	G	5: 149,739,604		probably null	Het
Bmp7	A	G	2: 172,872,913	S368P	probably damaging	Het
Boc	A	G	16: 44,491,791	V636A	probably damaging	Het
Cacna1i	G	A	15: 80,374,801	R1237H	probably damaging	Het
Cep85l	T	C	10: 53,349,098	T132A	probably benign	Het
Ces1b	T	A	8: 93,060,410	Y447F	probably damaging	Het
Cntn4	A	T	6: 106,697,583	T1015S	probably benign	Het
Eea1	T	G	10: 96,002,879		probably null	Het
Gm12800	G	A	4: 101,910,094	C180Y	possibly damaging	Het
Gm4788	T	G	1: 139,731,653	N642H	possibly damaging	Het
Hipk1	A	T	3: 103,777,512	N262K	possibly damaging	Het
Jmjd8	G	A	17: 25,829,052	R41H	possibly damaging	Het
Klhl3	T	A	13: 58,030,445	T344S	probably damaging	Het
Krt39	T	C	11: 99,519,821	D175G	probably damaging	Het
Map4k1	A	G	7: 28,986,802	Y81C	probably damaging	Het
Mpdu1	T	A	11: 69,658,585	T95S	probably benign	Het
Myl12b	A	T	17: 70,977,140	I31N	probably damaging	Het
Ndufaf5	T	A	2: 140,188,780	Y195*	probably null	Het
Olfr1141	A	G	2: 87,753,879	V38A	probably benign	Het
Olfr1224-ps1	G	A	2: 89,156,813	R121C	possibly damaging	Het
Olfr617	T	A	7: 103,584,520	I166N	possibly damaging	Het
Olfr621-ps1	A	T	7: 103,629,583	F126I	probably benign	Het
Olfr984	T	C	9: 40,101,356	I45V	probably benign	Het
Oxgr1	T	A	14: 120,022,019	I259F	possibly damaging	Het
Pcdhb9	T	A	18: 37,401,917	D321E	probably benign	Het
Pi4kb	G	T	3: 94,993,150	R392L	probably damaging	Het
Prss41	T	C	17: 23,837,648	K151R	probably benign	Het
Rev3l	T	A	10: 39,821,481	V658D	probably benign	Het
Snx4	A	G	16: 33,294,738	I430V	probably damaging	Het
Tanc2	C	T	11: 105,835,230	H407Y	possibly damaging	Het
Tcf25	G	A	8: 123,400,698		probably null	Het
Tsc22d1	A	T	14: 76,506,483	K24*	probably null	Het
Vmn2r30	A	G	7: 7,312,548	F762S	probably damaging	Het
Xrcc6	A	G	15: 82,029,122	T319A	probably benign	Het
Zbtb1	C	T	12: 76,386,211	R324*	probably null	Het
Zc3h7a	A	G	16: 11,145,671	Y729H	probably damaging	Het
Zfp329	C	A	7: 12,806,530		probably benign	Het
Zfp456	A	T	13: 67,366,265	S441T	probably benign	Het

Other mutations in Cdcp1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01757:Cdcp1	APN	9	123180001	nonsense	probably null
IGL01883:Cdcp1	APN	9	123183598	missense	probably benign	0.18
IGL02029:Cdcp1	APN	9	123183834	splice site	probably benign
IGL02115:Cdcp1	APN	9	123185397	missense	probably damaging	1.00
IGL02516:Cdcp1	APN	9	123173637	missense	possibly damaging	0.86
IGL02709:Cdcp1	APN	9	123173814	missense	probably damaging	1.00
IGL03263:Cdcp1	APN	9	123180087	missense	probably benign	0.12
IGL03406:Cdcp1	APN	9	123185313	missense	probably benign	0.00
R0242:Cdcp1	UTSW	9	123180172	missense	probably benign	0.00
R0242:Cdcp1	UTSW	9	123180172	missense	probably benign	0.00
R0939:Cdcp1	UTSW	9	123183690	missense	probably damaging	1.00
R1411:Cdcp1	UTSW	9	123190112	missense	probably damaging	0.99
R1460:Cdcp1	UTSW	9	123180027	missense	possibly damaging	0.69
R1538:Cdcp1	UTSW	9	123173588	missense	probably damaging	1.00
R1660:Cdcp1	UTSW	9	123185362	missense	probably benign	0.09
R1673:Cdcp1	UTSW	9	123178021	nonsense	probably null
R1794:Cdcp1	UTSW	9	123190094	missense	probably benign	0.37
R1794:Cdcp1	UTSW	9	123215831	missense	probably benign
R2472:Cdcp1	UTSW	9	123185107	missense	probably benign	0.07
R3961:Cdcp1	UTSW	9	123182381	missense	possibly damaging	0.73
R3962:Cdcp1	UTSW	9	123182381	missense	possibly damaging	0.73
R4288:Cdcp1	UTSW	9	123183628	missense	probably damaging	0.99
R4888:Cdcp1	UTSW	9	123182129	intron	probably benign
R4953:Cdcp1	UTSW	9	123180023	missense	probably benign	0.00
R5236:Cdcp1	UTSW	9	123185193	missense	probably damaging	1.00
R5546:Cdcp1	UTSW	9	123178029	missense	probably damaging	1.00
R5848:Cdcp1	UTSW	9	123183705	missense	possibly damaging	0.87
R5903:Cdcp1	UTSW	9	123173772	nonsense	probably null
R6052:Cdcp1	UTSW	9	123185331	missense	probably benign	0.04
R6344:Cdcp1	UTSW	9	123182382	missense	possibly damaging	0.69
R7038:Cdcp1	UTSW	9	123173597	missense	probably damaging	1.00
R7092:Cdcp1	UTSW	9	123183613	missense	probably benign	0.20
R7262:Cdcp1	UTSW	9	123173615	missense	probably damaging	1.00
R7275:Cdcp1	UTSW	9	123185054	missense	possibly damaging	0.79
R7294:Cdcp1	UTSW	9	123177921	missense	probably benign	0.01
R7373:Cdcp1	UTSW	9	123177900	missense	probably damaging	1.00
R7394:Cdcp1	UTSW	9	123173813	missense	probably damaging	1.00
R7527:Cdcp1	UTSW	9	123185107	missense	probably benign	0.26
R7674:Cdcp1	UTSW	9	123216006	start gained	probably benign
R7680:Cdcp1	UTSW	9	123183519	missense	probably damaging	1.00
R8079:Cdcp1	UTSW	9	123173790	missense	probably damaging	1.00
R8355:Cdcp1	UTSW	9	123173823	missense	probably benign	0.16
X0028:Cdcp1	UTSW	9	123185184	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGTCCACCTCTGGTTGGATG -3'
(R):5'- TTGGTTTCCCTGAAGTCTATCAG -3'

Sequencing Primer
(F):5'- CACCTCTGGTTGGATGAAGGATCC -3'
(R):5'- AAGATCCGTCAGTTTCCACCTTGG -3'

Posted On

2018-11-06