Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02391:Clec3a'

293856

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Clec3a

Ensembl Gene

ENSMUSG00000008874

Gene Name

C-type lectin domain family 3, member a

Synonyms

LOC330844, 1110019O10Rik, Clecsf1

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.065) question?

Stock #

IGL02391

Quality Score

Status

Chromosome

Chromosomal Location

114418086-114425846 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 114425500 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Leucine at position 82 (S82L)

Ref Sequence

ENSEMBL: ENSMUSP00000009018 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000009018]

AlphaFold

Q9EPW4

Predicted Effect

probably benign
Transcript: ENSMUST00000009018
AA Change: S82L

PolyPhen 2 Score 0.300 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000009018
Gene: ENSMUSG00000008874
AA Change: S82L

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
CLECT	68	192	6.72e-26	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 44 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc4	T	A	14: 118,553,352	N748Y	probably damaging	Het
Actbl2	A	G	13: 111,255,167	D12G	possibly damaging	Het
Adamts10	T	C	17: 33,528,811	S74P	probably benign	Het
Adprhl2	C	T	4: 126,317,908		probably benign	Het
Amn1	A	G	6: 149,169,446		probably null	Het
Antxr1	A	T	6: 87,287,056	I144N	probably damaging	Het
Atp2a3	C	A	11: 72,975,339	H262N	probably benign	Het
Cabp5	A	T	7: 13,398,344	R13*	probably null	Het
Cacna1e	A	G	1: 154,421,113	Y1669H	probably damaging	Het
Ccdc174	A	G	6: 91,898,282	E364G	possibly damaging	Het
Ccdc18	C	T	5: 108,136,052	P74S	probably damaging	Het
Cnih3	A	G	1: 181,406,513	D43G	probably damaging	Het
Dpp10	G	A	1: 123,650,358	T128M	probably damaging	Het
Edar	A	T	10: 58,628,581	F79I	probably damaging	Het
Eif2ak4	T	A	2: 118,420,791	H199Q	probably benign	Het
Fermt1	A	G	2: 132,941,951	L46P	probably damaging	Het
Glipr1	A	G	10: 111,988,894		probably benign	Het
Gsdmc	T	C	15: 63,803,579	N129S	probably damaging	Het
Ift88	T	C	14: 57,481,414	S619P	possibly damaging	Het
Itga9	T	A	9: 118,850,805	V262E	probably benign	Het
Med17	G	A	9: 15,277,667	R101*	probably null	Het
Mta1	T	A	12: 113,136,583	I688N	possibly damaging	Het
Muc4	A	T	16: 32,752,076	R651S	probably benign	Het
Olfr109	C	T	17: 37,466,586	P127S	probably damaging	Het
Olfr1342	A	G	4: 118,690,341	L37P	probably damaging	Het
Olfr824	A	G	10: 130,126,904	V51A	possibly damaging	Het
Opcml	A	G	9: 28,675,264	I93V	probably damaging	Het
Parg	T	G	14: 32,262,681		probably null	Het
Rps3a3	A	G	13: 108,670,883		probably benign	Het
Safb	T	A	17: 56,600,813		probably benign	Het
Sat2	G	T	11: 69,622,749	C54F	probably damaging	Het
Scin	T	A	12: 40,077,531	Y420F	probably benign	Het
Slc22a29	A	T	19: 8,169,353	S362T	probably benign	Het
Smchd1	T	C	17: 71,431,259	D537G	probably null	Het
Spred3	A	G	7: 29,166,405	S126P	probably benign	Het
Ssh1	C	T	5: 113,942,517	E951K	probably damaging	Het
Ssmem1	A	G	6: 30,512,442	E28G	possibly damaging	Het
Stox1	A	T	10: 62,659,676		probably benign	Het
Syn3	T	C	10: 86,064,906	I373V	probably benign	Het
Tecrl	A	T	5: 83,354,827	F58L	probably benign	Het
Trp53bp1	T	C	2: 121,202,710	N1655S	possibly damaging	Het
Usp2	G	T	9: 44,091,227	Q147H	probably damaging	Het
Usp24	T	A	4: 106,407,129	N1751K	possibly damaging	Het
Wipf1	T	A	2: 73,434,143	D438V	probably damaging	Het

Other mutations in Clec3a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01564:Clec3a	APN	8	114425542	missense	probably damaging	1.00
R0569:Clec3a	UTSW	8	114425736	missense	probably damaging	1.00
R4988:Clec3a	UTSW	8	114418087	start codon destroyed	probably null	0.98
R5344:Clec3a	UTSW	8	114422972	missense	probably damaging	1.00
R5443:Clec3a	UTSW	8	114418153	missense	probably benign	0.10
R6023:Clec3a	UTSW	8	114418143	missense	possibly damaging	0.52
R6523:Clec3a	UTSW	8	114425605	missense	probably damaging	1.00
R8263:Clec3a	UTSW	8	114425629	missense	probably benign	0.00
R8320:Clec3a	UTSW	8	114425629	missense	probably benign	0.00
R9068:Clec3a	UTSW	8	114425635	missense	probably damaging	1.00
R9623:Clec3a	UTSW	8	114418147	missense	probably benign
Z1187:Clec3a	UTSW	8	114418119	missense	possibly damaging	0.91
Z1188:Clec3a	UTSW	8	114418119	missense	possibly damaging	0.91
Z1190:Clec3a	UTSW	8	114418119	missense	possibly damaging	0.91

Posted On

2015-04-16