Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02826:Ceacam19'

361196

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Ceacam19

Ensembl Gene

ENSMUSG00000049848

Gene Name

carcinoembryonic antigen-related cell adhesion molecule 19

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.051) question?

Stock #

IGL02826

Quality Score

Status

Chromosome

Chromosomal Location

19875742-19887965 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 19882610 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 193 (T193I)

Ref Sequence

ENSEMBL: ENSMUSP00000057433 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052605]

AlphaFold

Q3TQ88

Predicted Effect

probably benign
Transcript: ENSMUST00000052605
AA Change: T193I

PolyPhen 2 Score 0.205 (Sensitivity: 0.92; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000057433
Gene: ENSMUSG00000049848
AA Change: T193I

Domain	Start	End	E-Value	Type
low complexity region	14	25	N/A	INTRINSIC
IG	37	140	3.83e0	SMART
transmembrane domain	157	179	N/A	INTRINSIC
low complexity region	227	249	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 45 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110004E09Rik	A	C	16: 90,926,062 (GRCm38)	D261E	probably benign	Het
1810041L15Rik	A	G	15: 84,420,129 (GRCm38)		probably benign	Het
4930404N11Rik	A	G	10: 81,364,736 (GRCm38)		probably benign	Het
A3galt2	T	C	4: 128,761,509 (GRCm38)		probably benign	Het
Alk	C	T	17: 71,869,536 (GRCm38)	G1591D	probably damaging	Het
Angptl2	T	C	2: 33,228,315 (GRCm38)	S34P	probably benign	Het
Atp2a2	A	G	5: 122,489,291 (GRCm38)	V137A	probably benign	Het
Atp8b5	A	G	4: 43,366,770 (GRCm38)	M845V	probably damaging	Het
Camk1d	A	G	2: 5,565,760 (GRCm38)	V30A	possibly damaging	Het
Chst15	T	A	7: 132,266,746 (GRCm38)	D315V	probably damaging	Het
Cux1	G	T	5: 136,308,003 (GRCm38)	P885Q	probably damaging	Het
Cyth1	C	T	11: 118,185,481 (GRCm38)	E88K	possibly damaging	Het
Dido1	A	G	2: 180,683,958 (GRCm38)	V479A	probably benign	Het
Dlc1	G	T	8: 36,570,275 (GRCm38)		probably benign	Het
H2-Ab1	G	A	17: 34,264,911 (GRCm38)	R82Q	probably damaging	Het
Hps6	T	A	19: 46,006,041 (GRCm38)	*806K	probably null	Het
Ilf3	T	C	9: 21,398,044 (GRCm38)	S486P	probably benign	Het
Kdm1b	C	A	13: 47,080,467 (GRCm38)	T759K	probably damaging	Het
Kirrel	C	A	3: 87,088,485 (GRCm38)	V381F	probably damaging	Het
Kmt2b	A	T	7: 30,577,144 (GRCm38)	V1701E	probably damaging	Het
Lrmda	T	C	14: 22,828,737 (GRCm38)	Y100H	probably damaging	Het
Mastl	T	C	2: 23,145,409 (GRCm38)	I169V	probably damaging	Het
Mroh2b	A	G	15: 4,962,148 (GRCm38)	E1576G	probably damaging	Het
Nek3	A	T	8: 22,160,368 (GRCm38)		probably null	Het
Nipal3	G	T	4: 135,468,550 (GRCm38)	Y247*	probably null	Het
Nt5e	A	C	9: 88,355,705 (GRCm38)	K229N	probably damaging	Het
Olfr237-ps1	A	G	6: 43,153,577 (GRCm38)	I91V	possibly damaging	Het
Olfr974	G	T	9: 39,942,958 (GRCm38)	G233C	probably damaging	Het
Opa1	A	G	16: 29,610,887 (GRCm38)	M290V	probably null	Het
Parp2	T	A	14: 50,815,415 (GRCm38)	I155K	probably benign	Het
Pde4dip	G	T	3: 97,767,087 (GRCm38)	A171E	probably damaging	Het
Prom2	C	T	2: 127,531,116 (GRCm38)	E678K	probably benign	Het
Rab12	A	G	17: 66,498,116 (GRCm38)		probably benign	Het
Rgs8	A	T	1: 153,670,799 (GRCm38)	T13S	probably damaging	Het
Setd3	A	G	12: 108,112,124 (GRCm38)		probably benign	Het
Slx4ip	G	A	2: 137,004,973 (GRCm38)	V53I	probably damaging	Het
Stil	A	G	4: 115,024,098 (GRCm38)	D613G	probably benign	Het
Tjp3	T	A	10: 81,273,689 (GRCm38)	S858C	probably damaging	Het
Tmem215	A	G	4: 40,474,632 (GRCm38)	*236W	probably null	Het
Ttbk1	A	G	17: 46,470,660 (GRCm38)	V389A	probably benign	Het
Wdfy4	A	G	14: 32,971,750 (GRCm38)	F2706S	possibly damaging	Het
Xpo4	C	A	14: 57,629,420 (GRCm38)	V222L	possibly damaging	Het
Zfc3h1	A	G	10: 115,400,904 (GRCm38)	S428G	probably benign	Het
Zfp286	T	C	11: 62,787,960 (GRCm38)	Q47R	probably damaging	Het
Zfp318	A	G	17: 46,398,754 (GRCm38)	K468E	probably damaging	Het

Other mutations in Ceacam19

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0791:Ceacam19	UTSW	7	19,882,632 (GRCm38)	splice site	probably null
R6084:Ceacam19	UTSW	7	19,882,887 (GRCm38)	missense	probably benign	0.00
R6492:Ceacam19	UTSW	7	19,882,592 (GRCm38)	missense	probably benign	0.00
R7596:Ceacam19	UTSW	7	19,881,887 (GRCm38)	missense	possibly damaging	0.90
R7734:Ceacam19	UTSW	7	19,886,595 (GRCm38)	missense	probably benign	0.00
R7874:Ceacam19	UTSW	7	19,886,438 (GRCm38)	missense	probably damaging	1.00
Z1177:Ceacam19	UTSW	7	19,886,449 (GRCm38)	missense	probably damaging	1.00
Z1177:Ceacam19	UTSW	7	19,882,844 (GRCm38)	missense	probably damaging	0.99

Posted On

2015-12-18