Mutagenetix > Incidental Mutation

Incidental Mutation 'R5541:Cercam'

435941

Institutional Source

Beutler Lab

Gene Symbol

Cercam

Ensembl Gene

ENSMUSG00000039787

Gene Name

cerebral endothelial cell adhesion molecule

Synonyms

CerCAM, Ceecam1

MMRRC Submission

043099-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5541 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

29759176-29772852 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 29765641 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 261 (D261G)

Ref Sequence

ENSEMBL: ENSMUSP00000041622 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000047521] [ENSMUST00000134152] [ENSMUST00000154464]

AlphaFold

A3KGW5

Predicted Effect

probably benign
Transcript: ENSMUST00000047521
AA Change: D261G

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

SMART Domains

Protein: ENSMUSP00000041622
Gene: ENSMUSG00000039787
AA Change: D261G

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
Pfam:Glyco_tranf_2_4	37	157	2.6e-15	PFAM
Pfam:Glyco_transf_25	316	500	3.2e-33	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000134152

SMART Domains

Protein: ENSMUSP00000115902
Gene: ENSMUSG00000039787

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153863

Predicted Effect

probably benign
Transcript: ENSMUST00000154464

SMART Domains

Protein: ENSMUSP00000119476
Gene: ENSMUSG00000039787

Domain	Start	End	E-Value	Type
low complexity region	11	28	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000155355

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.4%
20x: 95.2%

Validation Efficiency

100% (63/63)

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700113H08Rik	A	G	10: 87,061,808 (GRCm39)	K86R	probably benign	Het
Abca13	T	C	11: 9,241,545 (GRCm39)	V1136A	probably benign	Het
Arfgap2	G	A	2: 91,106,114 (GRCm39)	R530H	probably benign	Het
Arhgap30	T	C	1: 171,231,707 (GRCm39)		probably null	Het
Asb7	T	C	7: 66,329,017 (GRCm39)	R8G	probably benign	Het
Bod1l	T	C	5: 41,949,276 (GRCm39)	N2949D	probably benign	Het
Ccdc86	T	C	19: 10,925,918 (GRCm39)	E227G	probably damaging	Het
Chd9	A	T	8: 91,778,132 (GRCm39)	E2714D	probably benign	Het
Dcp1a	T	A	14: 30,224,796 (GRCm39)	S126R	probably damaging	Het
Defa17	T	A	8: 22,146,565 (GRCm39)	C64S	probably damaging	Het
Depdc5	A	T	5: 33,021,973 (GRCm39)		probably benign	Het
Dhx29	A	G	13: 113,076,908 (GRCm39)	N259S	possibly damaging	Het
Dnah6	A	T	6: 73,169,971 (GRCm39)	L323Q	possibly damaging	Het
Dnah9	T	C	11: 66,036,162 (GRCm39)	Y416C	probably damaging	Het
Faap100	T	A	11: 120,268,458 (GRCm39)	E105V	possibly damaging	Het
Fbxw15	T	G	9: 109,394,498 (GRCm39)	I106L	probably benign	Het
Flacc1	A	G	1: 58,697,588 (GRCm39)	M384T	probably benign	Het
Gm10610	A	G	7: 83,198,614 (GRCm39)		noncoding transcript	Het
Gpr22	A	G	12: 31,759,348 (GRCm39)	F258S	probably damaging	Het
Grip1	A	T	10: 119,908,623 (GRCm39)	I618F	probably damaging	Het
Hspg2	C	T	4: 137,247,862 (GRCm39)	T1233I	probably damaging	Het
Hspg2	C	A	4: 137,270,136 (GRCm39)	Q2365K	probably benign	Het
Intu	A	G	3: 40,647,017 (GRCm39)		probably null	Het
Kdm1b	T	C	13: 47,232,672 (GRCm39)	M714T	probably damaging	Het
Kif21a	A	G	15: 90,852,316 (GRCm39)	M924T	probably damaging	Het
Klb	A	T	5: 65,536,577 (GRCm39)	M636L	probably benign	Het
Klrb1a	G	A	6: 128,586,699 (GRCm39)	H219Y	probably benign	Het
Macroh2a2	T	C	10: 61,583,496 (GRCm39)	I215V	probably benign	Het
Marchf10	C	T	11: 105,280,957 (GRCm39)	D443N	probably damaging	Het
Nos1	A	G	5: 118,043,459 (GRCm39)	E578G	probably damaging	Het
Or8b39	T	C	9: 37,996,419 (GRCm39)	C96R	probably damaging	Het
Or9i1	T	C	19: 13,839,328 (GRCm39)	I57T	probably benign	Het
Pard3b	A	G	1: 61,678,502 (GRCm39)	Y34C	probably damaging	Het
Pcdh17	T	A	14: 84,684,856 (GRCm39)	V441E	probably damaging	Het
Pde6g	A	T	11: 120,338,998 (GRCm39)	I64N	probably damaging	Het
Pdia4	C	T	6: 47,773,571 (GRCm39)	V593M	probably damaging	Het
Pnn	T	G	12: 59,118,716 (GRCm39)	V433G	possibly damaging	Het
Rbak	G	A	5: 143,159,745 (GRCm39)	S436F	probably damaging	Het
Rpl11	A	G	4: 135,780,043 (GRCm39)		probably benign	Het
Ryr1	G	T	7: 28,785,610 (GRCm39)	Q1701K	probably damaging	Het
Scn1a	T	A	2: 66,154,977 (GRCm39)	T661S	probably benign	Het
Smg1	T	A	7: 117,756,386 (GRCm39)		probably benign	Het
St8sia2	T	C	7: 73,616,648 (GRCm39)	D109G	probably benign	Het
Stk-ps1	T	A	17: 36,709,105 (GRCm39)		noncoding transcript	Het
Stxbp3-ps	C	T	19: 9,535,334 (GRCm39)		noncoding transcript	Het
Taf1d	T	A	9: 15,220,146 (GRCm39)	F132I	probably damaging	Het
Tfap2b	A	G	1: 19,284,250 (GRCm39)	S35G	possibly damaging	Het
Tnk2	C	T	16: 32,488,341 (GRCm39)	T198I	probably benign	Het
Trappc2b	T	C	11: 51,576,796 (GRCm39)	H34R	probably benign	Het
Ube2q2	T	A	9: 55,099,163 (GRCm39)	V168E	possibly damaging	Het
Ucma	A	G	2: 4,986,141 (GRCm39)	R105G	probably benign	Het
Vmn2r97	C	T	17: 19,148,617 (GRCm39)	Q171*	probably null	Het
Wapl	T	C	14: 34,452,619 (GRCm39)		probably null	Het
Zfand4	T	A	6: 116,291,256 (GRCm39)	C397S	possibly damaging	Het
Zfhx3	A	G	8: 109,675,583 (GRCm39)	N2211S	probably damaging	Het
Zfp143	G	T	7: 109,669,687 (GRCm39)	G39C	probably benign	Het
Zfp568	T	A	7: 29,722,301 (GRCm39)	D414E	possibly damaging	Het
Zfp574	C	T	7: 24,781,375 (GRCm39)	A799V	probably damaging	Het

Other mutations in Cercam

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01885:Cercam	APN	2	29,771,015 (GRCm39)	missense	probably damaging	1.00
IGL02619:Cercam	APN	2	29,770,686 (GRCm39)	missense	probably benign	0.05
IGL03088:Cercam	APN	2	29,771,699 (GRCm39)	splice site	probably benign
I1329:Cercam	UTSW	2	29,761,097 (GRCm39)	missense	probably damaging	1.00
P0042:Cercam	UTSW	2	29,771,095 (GRCm39)	missense	probably damaging	1.00
R0086:Cercam	UTSW	2	29,761,076 (GRCm39)	missense	probably damaging	1.00
R0829:Cercam	UTSW	2	29,761,079 (GRCm39)	missense	probably damaging	0.98
R1442:Cercam	UTSW	2	29,770,652 (GRCm39)	missense	probably benign
R1558:Cercam	UTSW	2	29,766,251 (GRCm39)	missense	probably benign	0.35
R1997:Cercam	UTSW	2	29,762,935 (GRCm39)	missense	probably benign	0.11
R4678:Cercam	UTSW	2	29,759,689 (GRCm39)	missense	probably damaging	1.00
R4889:Cercam	UTSW	2	29,771,845 (GRCm39)	missense	probably damaging	0.96
R4891:Cercam	UTSW	2	29,759,283 (GRCm39)	unclassified	probably benign
R4967:Cercam	UTSW	2	29,761,033 (GRCm39)	critical splice acceptor site	probably null
R5052:Cercam	UTSW	2	29,765,639 (GRCm39)	missense	probably damaging	1.00
R5650:Cercam	UTSW	2	29,771,827 (GRCm39)	missense	probably damaging	1.00
R7072:Cercam	UTSW	2	29,771,936 (GRCm39)	missense	probably benign	0.00
R7422:Cercam	UTSW	2	29,762,892 (GRCm39)	missense	possibly damaging	0.81
R7585:Cercam	UTSW	2	29,771,743 (GRCm39)	missense	probably damaging	1.00
R7725:Cercam	UTSW	2	29,762,574 (GRCm39)	critical splice acceptor site	probably null
R7730:Cercam	UTSW	2	29,762,574 (GRCm39)	critical splice acceptor site	probably null
R7747:Cercam	UTSW	2	29,761,298 (GRCm39)	missense	probably benign	0.02
R8504:Cercam	UTSW	2	29,771,829 (GRCm39)	missense	possibly damaging	0.86
R9010:Cercam	UTSW	2	29,766,071 (GRCm39)	missense	possibly damaging	0.95
R9185:Cercam	UTSW	2	29,766,033 (GRCm39)	missense	possibly damaging	0.53
RF016:Cercam	UTSW	2	29,759,317 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- ACCATGATGAGGTGCTGGTG -3'
(R):5'- AAGGCTGGCATGCAAATATG -3'

Sequencing Primer
(F):5'- AAGTTCAGCCCAGTGCCCTAG -3'
(R):5'- GTGCTTCCAAAATGAGGTG -3'

Posted On

2016-10-24