Mutagenetix > Incidental Mutations

Incidental Mutation 'R3849:Ccl27a'

474214

Institutional Source

Beutler Lab

Gene Symbol

Ccl27a

Ensembl Gene

ENSMUSG00000073888

Gene Name

chemokine (C-C motif) ligand 27A

Synonyms

ALP, Ccl27, CTACK, CTAK, ESkine, ESkine, ILC, mILC, PESKY, Scya27, Scya27a, skinskine

MMRRC Submission

040897-MU

Accession Numbers

Is this an essential gene?

Not available question?

Stock #

R3849 (G1)

Quality Score

125

Status

Not validated

Chromosome

Chromosomal Location

41769467-41774247 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 41773232 bp

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 76 (T76S)

Ref Sequence

ENSEMBL: ENSMUSP00000133827 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000074387] [ENSMUST00000098132] [ENSMUST00000108032] [ENSMUST00000108033] [ENSMUST00000108035] [ENSMUST00000108036] [ENSMUST00000108037] [ENSMUST00000108040] [ENSMUST00000108041] [ENSMUST00000108042] [ENSMUST00000131349] [ENSMUST00000155240] [ENSMUST00000173865] [ENSMUST00000151142] [ENSMUST00000155322]

Predicted Effect

probably benign
Transcript: ENSMUST00000074387

SMART Domains

Protein: ENSMUSP00000073990
Gene: ENSMUSG00000073888

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
SCY	31	97	5.12e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000098132

SMART Domains

Protein: ENSMUSP00000095736
Gene: ENSMUSG00000073889

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
IG	33	108	5.75e-4	SMART
FN3	112	204	2.18e-2	SMART
FN3	218	304	4.93e-1	SMART
low complexity region	354	365	N/A	INTRINSIC
transmembrane domain	369	391	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000108032
AA Change: T76S

PolyPhen 2 Score 0.080 (Sensitivity: 0.93; Specificity: 0.85)

Predicted Effect

probably benign
Transcript: ENSMUST00000108033

SMART Domains

Protein: ENSMUSP00000103668
Gene: ENSMUSG00000073888

Domain	Start	End	E-Value	Type
signal peptide	1	24	N/A	INTRINSIC
SCY	30	96	5.12e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000108035

SMART Domains

Protein: ENSMUSP00000103670
Gene: ENSMUSG00000073888

Domain	Start	End	E-Value	Type
SCY	38	104	5.12e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000108036

SMART Domains

Protein: ENSMUSP00000103671
Gene: ENSMUSG00000073888

Domain	Start	End	E-Value	Type
SCY	75	141	5.12e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000108037

SMART Domains

Protein: ENSMUSP00000103672
Gene: ENSMUSG00000073888

Domain	Start	End	E-Value	Type
SCY	75	141	5.12e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000108040

SMART Domains

Protein: ENSMUSP00000103675
Gene: ENSMUSG00000073889

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
IG	33	108	5.75e-4	SMART
FN3	112	204	2.18e-2	SMART
FN3	218	304	4.93e-1	SMART
low complexity region	354	365	N/A	INTRINSIC
transmembrane domain	369	391	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000108041

SMART Domains

Protein: ENSMUSP00000103676
Gene: ENSMUSG00000073889

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
IG	33	108	5.75e-4	SMART
FN3	112	204	2.18e-2	SMART
FN3	218	304	4.93e-1	SMART
low complexity region	354	365	N/A	INTRINSIC
transmembrane domain	369	391	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000108042

SMART Domains

Protein: ENSMUSP00000103677
Gene: ENSMUSG00000073889

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
IG	33	108	5.75e-4	SMART
FN3	112	204	2.18e-2	SMART
FN3	218	304	4.93e-1	SMART
low complexity region	354	365	N/A	INTRINSIC
transmembrane domain	369	391	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126759

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000130197

Predicted Effect

probably benign
Transcript: ENSMUST00000131349

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133556

Predicted Effect

probably benign
Transcript: ENSMUST00000155240
AA Change: T76S

PolyPhen 2 Score 0.080 (Sensitivity: 0.93; Specificity: 0.85)

Predicted Effect

probably benign
Transcript: ENSMUST00000173865
AA Change: T76S

PolyPhen 2 Score 0.080 (Sensitivity: 0.93; Specificity: 0.85)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144090

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133572

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143676

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152748

Predicted Effect

probably benign
Transcript: ENSMUST00000151142

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000142059

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151909

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000155538

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000136768

Predicted Effect

probably benign
Transcript: ENSMUST00000155322

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000138337

Coding Region Coverage

1x: 99.3%
3x: 98.8%
10x: 97.7%
20x: 96.1%

Validation Efficiency

100% (52/52)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9430038I01Rik	A	T	7: 137,376,340	N102K	possibly damaging	Het
Abca1	C	T	4: 53,061,481		probably benign	Het
Adamts17	T	A	7: 66,840,467	L99Q	possibly damaging	Het
Adamtsl1	A	T	4: 86,418,546	Q1564L	probably damaging	Het
Aspm	T	A	1: 139,458,286	V556E	probably benign	Het
Axin1	T	A	17: 26,187,797	Y455N	probably benign	Het
BC017158	C	T	7: 128,285,208	V201I	probably damaging	Het
Cacna2d3	A	G	14: 29,347,120		probably null	Het
Car8	T	A	4: 8,189,353	I154F	probably benign	Het
Cep170	G	A	1: 176,755,843	A990V	probably benign	Het
Chd1	A	T	17: 15,731,871	T291S	probably damaging	Het
Col3a1	C	A	1: 45,321,990	P112T	unknown	Het
Cpa4	T	C	6: 30,590,873	F390S	probably damaging	Het
Cul5	T	G	9: 53,617,986	M800L	probably benign	Het
Dst	C	T	1: 34,212,319	S4165F	probably damaging	Het
Dusp8	T	C	7: 142,090,065	E37G	probably damaging	Het
Efr3b	T	C	12: 3,983,414	N131S	probably benign	Het
Fan1	T	C	7: 64,372,371	Y378C	probably damaging	Het
Fcgr2b	T	C	1: 170,968,135	N75S	possibly damaging	Het
Foxp4	A	G	17: 47,875,528	I442T	unknown	Het
Gp9	A	G	6: 87,779,151	I49M	probably benign	Het
Grip1	G	A	10: 119,929,958	G65D	probably damaging	Het
Hoxc10	T	C	15: 102,967,444	V196A	probably benign	Het
Hpx	A	G	7: 105,596,291	C92R	probably damaging	Het
Ighv1-22	A	G	12: 114,746,681	F9S	possibly damaging	Het
Kif24	C	T	4: 41,404,734	R422H	probably damaging	Het
Klk1b1	T	C	7: 43,969,327	Y43H	probably damaging	Het
Lmo7	A	G	14: 101,922,095		probably null	Het
Lrguk	A	G	6: 34,073,768	D387G	probably damaging	Het
Lysmd1	G	A	3: 95,138,461	G203D	probably damaging	Het
Mpnd	T	C	17: 56,011,692	S150P	probably damaging	Het
Mrc2	T	C	11: 105,292,903		probably null	Het
Mtr	A	G	13: 12,247,365	S152P	probably benign	Het
Naip2	A	T	13: 100,179,432	L280Q	probably damaging	Het
Naip2	G	C	13: 100,179,433	L280V	probably damaging	Het
Ndufa13	T	C	8: 69,901,610	D9G	probably damaging	Het
Nek1	T	A	8: 61,072,315	F596I	probably damaging	Het
Nsd1	A	G	13: 55,246,691	T702A	probably benign	Het
Olfr77	A	T	9: 19,920,809	Y200F	probably damaging	Het
Pam	T	A	1: 97,854,756		probably benign	Het
Plxna1	C	A	6: 89,356,519	R376L	probably damaging	Het
Plxnc1	A	G	10: 94,794,432	V1535A	probably benign	Het
Prdx5	A	G	19: 6,906,850	L166P	probably damaging	Het
Prol1	A	T	5: 88,328,617	I289F	unknown	Het
Prss23	T	C	7: 89,509,751	Y370C	probably damaging	Het
Rimbp3	A	T	16: 17,210,299	H529L	probably benign	Het
Rnase2b	T	A	14: 51,162,748	H95Q	probably damaging	Het
Rnf103	C	G	6: 71,508,875	C163W	probably damaging	Het
Rnf17	T	C	14: 56,512,296	V1433A	probably damaging	Het
Syne2	C	T	12: 76,046,065	Q5150*	probably null	Het
Tas2r110	T	A	6: 132,868,675	I223N	probably damaging	Het
Tead2	T	A	7: 45,232,328		probably null	Het
Vwa3a	A	T	7: 120,762,464	K133*	probably null	Het
Vwce	T	C	19: 10,646,905	S387P	probably damaging	Het
Zbtb41	T	A	1: 139,423,996	H282Q	probably benign	Het

Other mutations in Ccl27a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R2869:Ccl27a	UTSW	4	41769640	missense	probably benign	0.20
R2869:Ccl27a	UTSW	4	41769640	missense	probably benign	0.20
R6730:Ccl27a	UTSW	4	41773342	missense	probably damaging	0.97
R7619:Ccl27a	UTSW	4	41774166	start gained	probably benign

Predicted Primers

Posted On

2017-04-14