Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL02043:0610037L13Rik'

List |< first << previous [record 61 of 527231] next >> last >|

184862

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

0610037L13Rik

Ensembl Gene

ENSMUSG00000028608

Gene Name

RIKEN cDNA 0610037L13 gene

Synonyms

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.125) question?

Stock #

IGL02043

Quality Score

Status

Chromosome

Chromosomal Location

107889813-107899384 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

T to G at 107894868 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000114234 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000106726] [ENSMUST00000106727] [ENSMUST00000119394] [ENSMUST00000120473] [ENSMUST00000125107] [ENSMUST00000128474] [ENSMUST00000132417] [ENSMUST00000134254] [ENSMUST00000135454]

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000030346

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000030347

Predicted Effect

probably benign
Transcript: ENSMUST00000106726

SMART Domains

Protein: ENSMUSP00000102337
Gene: ENSMUSG00000028608

Domain	Start	End	E-Value	Type
Pfam:DUF866	1	114	1.9e-53	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000106727

SMART Domains

Protein: ENSMUSP00000102338
Gene: ENSMUSG00000028608

Domain	Start	End	E-Value	Type
Pfam:DUF866	1	154	1.2e-62	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000119394

SMART Domains

Protein: ENSMUSP00000113991
Gene: ENSMUSG00000028608

Domain	Start	End	E-Value	Type
Pfam:DUF866	1	146	8.1e-63	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000120473

SMART Domains

Protein: ENSMUSP00000113866
Gene: ENSMUSG00000028608

Domain	Start	End	E-Value	Type
Pfam:DUF866	1	138	2.7e-62	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000125107

SMART Domains

Protein: ENSMUSP00000119565
Gene: ENSMUSG00000028608

Domain	Start	End	E-Value	Type
Pfam:DUF866	40	194	2.2e-61	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127715

Predicted Effect

probably benign
Transcript: ENSMUST00000128474

SMART Domains

Protein: ENSMUSP00000115797
Gene: ENSMUSG00000028608

Domain	Start	End	E-Value	Type
Pfam:DUF866	2	66	4.2e-27	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000132417

SMART Domains

Protein: ENSMUSP00000117717
Gene: ENSMUSG00000028608

Domain	Start	End	E-Value	Type
Pfam:DUF866	37	98	1.4e-20	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000134254

SMART Domains

Protein: ENSMUSP00000119309
Gene: ENSMUSG00000028608

Domain	Start	End	E-Value	Type
Pfam:DUF866	1	46	3e-16	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000135454

SMART Domains

Protein: ENSMUSP00000114234
Gene: ENSMUSG00000028608

Domain	Start	End	E-Value	Type
Pfam:DUF866	1	160	1.7e-74	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153593

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156888

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Atp1b2	T	C	11: 69,605,276	T33A	probably benign	Het
Brd2	A	T	17: 34,112,616		probably benign	Het
Carmil1	T	C	13: 24,024,316		probably benign	Het
Cdh9	A	T	15: 16,856,232	D786V	probably damaging	Het
Cep128	A	C	12: 91,266,730		probably benign	Het
Cep85	T	C	4: 134,155,727	T284A	probably benign	Het
Chrna1	C	T	2: 73,568,106	E330K	probably benign	Het
Clec2l	T	C	6: 38,676,850	Y104H	probably damaging	Het
Clybl	G	T	14: 122,379,252	K226N	probably damaging	Het
Cmip	T	A	8: 117,445,328	D467E	probably benign	Het
Cpne3	A	T	4: 19,543,340		probably null	Het
Crisp4	A	G	1: 18,134,100	V46A	probably damaging	Het
Csnk2a1	T	C	2: 152,274,150	Y261H	probably damaging	Het
Cul5	C	A	9: 53,658,673	G86V	probably benign	Het
Depdc7	T	C	2: 104,730,281	T123A	probably benign	Het
Edem2	T	C	2: 155,705,741	T384A	probably damaging	Het
F8	C	T	X: 75,332,641	M377I	probably benign	Het
Fan1	T	A	7: 64,371,619		probably null	Het
Fez2	T	C	17: 78,381,622	D366G	probably damaging	Het
Gm4841	A	C	18: 60,270,965	S19A	probably benign	Het
Gm4862	T	A	3: 139,128,635		noncoding transcript	Het
Hk3	T	A	13: 55,015,095	Q44L	probably damaging	Het
Irgm1	C	A	11: 48,866,815	L56F	probably damaging	Het
Ldlr	A	G	9: 21,733,499	T108A	probably benign	Het
Lgr4	T	A	2: 110,011,290	M516K	probably damaging	Het
Lrp1b	T	C	2: 40,697,525	N3906S	probably null	Het
Lrrtm4	A	G	6: 80,021,862	N86D	possibly damaging	Het
Map3k2	A	G	18: 32,207,534	D198G	probably damaging	Het
Mapkapk3	C	T	9: 107,262,422		probably null	Het
Mvp	A	T	7: 126,993,618	Y374N	probably damaging	Het
Myo3a	T	C	2: 22,399,965	S711P	probably benign	Het
Myom3	A	G	4: 135,770,675	K189E	probably damaging	Het
Naip1	T	A	13: 100,426,796	K620N	probably benign	Het
Nlrp10	T	C	7: 108,925,502	E257G	probably damaging	Het
Nptn	T	G	9: 58,640,729	M139R	possibly damaging	Het
Nrk	T	G	X: 138,988,795	M1105R	possibly damaging	Het
Olfr357	T	A	2: 36,997,465	Y218*	probably null	Het
Olfr519	A	T	7: 108,893,839	C189*	probably null	Het
Olfr963	T	G	9: 39,669,078	V7G	probably damaging	Het
Pcdhb16	A	G	18: 37,479,195	T403A	probably benign	Het
Pcyt1b	A	G	X: 93,702,116	E50G	possibly damaging	Het
Pigg	C	T	5: 108,344,324	T892I	probably damaging	Het
Ppig	T	G	2: 69,735,983		probably null	Het
Prr12	A	G	7: 45,050,005		probably benign	Het
Slc5a5	G	T	8: 70,892,429	A78E	possibly damaging	Het
Slc7a2	T	G	8: 40,911,058	M436R	probably benign	Het
Sp7	T	A	15: 102,359,255	M39L	probably benign	Het
Spag8	T	A	4: 43,653,134		probably benign	Het
Svep1	A	G	4: 58,068,556	S3077P	probably benign	Het
Tmem30a	A	T	9: 79,774,089		probably benign	Het
Tmem63a	C	T	1: 180,972,788	T714I	probably benign	Het
Trank1	T	C	9: 111,363,960	L535P	probably damaging	Het
Tuba8	A	C	6: 121,220,511	N44T	probably benign	Het
Wnk1	A	G	6: 119,949,078		probably benign	Het
Zfp654	A	T	16: 64,785,028	I396K	probably benign	Het

Other mutations in 0610037L13Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
horribilis	UTSW	4	107891998	missense	probably damaging	1.00
R0787:0610037L13Rik	UTSW	4	107890129	missense	probably damaging	1.00
R3500:0610037L13Rik	UTSW	4	107891513	missense	probably damaging	1.00
R4778:0610037L13Rik	UTSW	4	107891998	missense	probably damaging	1.00
R5940:0610037L13Rik	UTSW	4	107893288	intron	probably benign
R6644:0610037L13Rik	UTSW	4	107894922	missense	probably damaging	0.99
R7164:0610037L13Rik	UTSW	4	107894890	missense	not run
R7535:0610037L13Rik	UTSW	4	107894900	missense	probably benign	0.36

Posted On

2014-05-07