Mutagenetix > Incidental Mutation

Incidental Mutation 'FR4737:Mapk8ip3'

511745

Institutional Source

Beutler Lab

Gene Symbol

Mapk8ip3

Ensembl Gene

ENSMUSG00000024163

Gene Name

mitogen-activated protein kinase 8 interacting protein 3

Synonyms

JSAP1c, JSAP1b, JNK-interacting protein 3, Jip3, D17Wsu15e, JSAP1, JSAP1d, Syd2, sunday driver 2, JSAP1a, JUN/SAPK-associated protein 1, c-Jun NH2-terminal kinase (JNK)/stress-activated protein kinase-associated protein 1

Accession Numbers

Essential gene?

Probably essential (E-score: 0.843) question?

Stock #

FR4737 ()

Quality Score

155.033

Status

Not validated

Chromosome

Chromosomal Location

25116480-25155951 bp(-) (GRCm39)

Type of Mutation

splice site (159 bp from exon)

DNA Base Change (assembly)

G to A at 25121093 bp (GRCm39)

Zygosity

Homozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000136924 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024978] [ENSMUST00000088345] [ENSMUST00000115228] [ENSMUST00000115229] [ENSMUST00000117509] [ENSMUST00000119115] [ENSMUST00000120035] [ENSMUST00000121723] [ENSMUST00000121787] [ENSMUST00000146706] [ENSMUST00000146923] [ENSMUST00000178969] [ENSMUST00000154236]

AlphaFold

Q9ESN9

Predicted Effect

probably benign
Transcript: ENSMUST00000024978

SMART Domains

Protein: ENSMUSP00000024978
Gene: ENSMUSG00000073435

Domain	Start	End	E-Value	Type
NDK	21	158	1.06e-90	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000088345

SMART Domains

Protein: ENSMUSP00000085683
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	186	1.4e-72	PFAM
low complexity region	236	249	N/A	INTRINSIC
low complexity region	261	270	N/A	INTRINSIC
PDB:2W83\|D	417	472	6e-20	PDB
coiled coil region	525	555	N/A	INTRINSIC
low complexity region	582	596	N/A	INTRINSIC
low complexity region	754	769	N/A	INTRINSIC
low complexity region	893	901	N/A	INTRINSIC
low complexity region	928	940	N/A	INTRINSIC
SCOP:d1flga_	987	1167	4e-8	SMART
Blast:WD40	1075	1116	6e-18	BLAST
low complexity region	1260	1276	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000115228

SMART Domains

Protein: ENSMUSP00000110883
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	186	1.4e-72	PFAM
low complexity region	236	249	N/A	INTRINSIC
low complexity region	261	270	N/A	INTRINSIC
PDB:2W83\|D	411	466	7e-20	PDB
low complexity region	567	581	N/A	INTRINSIC
low complexity region	739	754	N/A	INTRINSIC
low complexity region	878	886	N/A	INTRINSIC
low complexity region	913	925	N/A	INTRINSIC
SCOP:d1flga_	972	1152	3e-8	SMART
Blast:WD40	1060	1101	6e-18	BLAST
low complexity region	1245	1261	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000115229

SMART Domains

Protein: ENSMUSP00000110884
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	184	2.9e-60	PFAM
low complexity region	244	257	N/A	INTRINSIC
low complexity region	269	278	N/A	INTRINSIC
Pfam:JIP_LZII	423	493	3.1e-32	PFAM
coiled coil region	533	563	N/A	INTRINSIC
low complexity region	590	604	N/A	INTRINSIC
low complexity region	762	777	N/A	INTRINSIC
low complexity region	901	909	N/A	INTRINSIC
low complexity region	936	948	N/A	INTRINSIC
SCOP:d1flga_	995	1175	4e-8	SMART
Blast:WD40	1083	1124	7e-18	BLAST
low complexity region	1268	1284	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000117509

SMART Domains

Protein: ENSMUSP00000112712
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	186	1.4e-72	PFAM
low complexity region	238	247	N/A	INTRINSIC
PDB:2W83\|D	394	449	7e-20	PDB
coiled coil region	502	532	N/A	INTRINSIC
low complexity region	559	573	N/A	INTRINSIC
low complexity region	731	746	N/A	INTRINSIC
low complexity region	870	878	N/A	INTRINSIC
low complexity region	905	917	N/A	INTRINSIC
SCOP:d1flga_	964	1144	3e-8	SMART
Blast:WD40	1052	1093	6e-18	BLAST
low complexity region	1237	1253	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000119115

SMART Domains

Protein: ENSMUSP00000112955
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	186	1.3e-72	PFAM
low complexity region	229	238	N/A	INTRINSIC
PDB:2W83\|D	385	440	7e-20	PDB
coiled coil region	493	523	N/A	INTRINSIC
low complexity region	550	564	N/A	INTRINSIC
low complexity region	722	737	N/A	INTRINSIC
low complexity region	861	869	N/A	INTRINSIC
low complexity region	896	908	N/A	INTRINSIC
SCOP:d1flga_	955	1135	3e-8	SMART
Blast:WD40	1043	1084	5e-18	BLAST
low complexity region	1228	1244	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000120035

SMART Domains

Protein: ENSMUSP00000114084
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	186	1.4e-72	PFAM
low complexity region	235	248	N/A	INTRINSIC
low complexity region	260	269	N/A	INTRINSIC
PDB:2W83\|D	416	471	6e-20	PDB
coiled coil region	524	554	N/A	INTRINSIC
low complexity region	581	595	N/A	INTRINSIC
low complexity region	753	768	N/A	INTRINSIC
low complexity region	892	900	N/A	INTRINSIC
low complexity region	927	939	N/A	INTRINSIC
SCOP:d1flga_	986	1166	3e-8	SMART
Blast:WD40	1074	1115	6e-18	BLAST
low complexity region	1259	1275	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000121723

SMART Domains

Protein: ENSMUSP00000113698
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	186	1e-72	PFAM
low complexity region	230	239	N/A	INTRINSIC
PDB:2W83\|D	386	441	7e-20	PDB
coiled coil region	494	524	N/A	INTRINSIC
low complexity region	551	565	N/A	INTRINSIC
low complexity region	723	738	N/A	INTRINSIC
low complexity region	862	870	N/A	INTRINSIC
low complexity region	897	909	N/A	INTRINSIC
SCOP:d1flga_	956	1136	3e-8	SMART
Blast:WD40	1044	1085	5e-18	BLAST
low complexity region	1229	1245	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000121787

SMART Domains

Protein: ENSMUSP00000113753
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	186	3.8e-73	PFAM
low complexity region	230	239	N/A	INTRINSIC
PDB:2W83\|D	380	435	8e-20	PDB
coiled coil region	488	518	N/A	INTRINSIC
low complexity region	545	559	N/A	INTRINSIC
low complexity region	717	732	N/A	INTRINSIC
low complexity region	856	864	N/A	INTRINSIC
low complexity region	891	903	N/A	INTRINSIC
SCOP:d1flga_	950	1130	3e-8	SMART
Blast:WD40	1038	1079	6e-18	BLAST
low complexity region	1223	1239	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133198

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144336

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145688

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145357

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132258

Predicted Effect

probably null
Transcript: ENSMUST00000146706

SMART Domains

Protein: ENSMUSP00000118422
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
low complexity region	55	64	N/A	INTRINSIC
Pfam:JIP_LZII	203	235	1.6e-17	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150500

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152486

Predicted Effect

probably benign
Transcript: ENSMUST00000146923

SMART Domains

Protein: ENSMUSP00000114802
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	186	1.4e-72	PFAM
low complexity region	236	249	N/A	INTRINSIC
low complexity region	261	270	N/A	INTRINSIC
PDB:2W83\|D	417	472	6e-20	PDB
coiled coil region	525	555	N/A	INTRINSIC
low complexity region	582	596	N/A	INTRINSIC
low complexity region	754	769	N/A	INTRINSIC
low complexity region	893	901	N/A	INTRINSIC
low complexity region	928	940	N/A	INTRINSIC
SCOP:d1flga_	987	1167	4e-8	SMART
Blast:WD40	1075	1116	6e-18	BLAST
low complexity region	1260	1276	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000125532

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000125648

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000147109

Predicted Effect

probably null
Transcript: ENSMUST00000178969

SMART Domains

Protein: ENSMUSP00000136924
Gene: ENSMUSG00000024163

Domain	Start	End	E-Value	Type
Pfam:Jnk-SapK_ap_N	29	186	1.1e-72	PFAM
low complexity region	236	249	N/A	INTRINSIC
low complexity region	261	270	N/A	INTRINSIC
PDB:2W83\|D	417	472	6e-20	PDB
coiled coil region	525	555	N/A	INTRINSIC
low complexity region	582	596	N/A	INTRINSIC
low complexity region	754	769	N/A	INTRINSIC
low complexity region	893	901	N/A	INTRINSIC
low complexity region	928	940	N/A	INTRINSIC
SCOP:d1flga_	987	1167	3e-8	SMART
Blast:WD40	1075	1116	6e-18	BLAST
low complexity region	1260	1276	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156663

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154321

Predicted Effect

probably benign
Transcript: ENSMUST00000154236

SMART Domains

Protein: ENSMUSP00000120985
Gene: ENSMUSG00000038880

Domain	Start	End	E-Value	Type
low complexity region	9	25	N/A	INTRINSIC
low complexity region	59	79	N/A	INTRINSIC
Blast:NDK	172	208	3e-12	BLAST

Coding Region Coverage

1x: 99.8%
3x: 99.6%
10x: 98.8%
20x: 97.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene shares similarity with the product of Drosophila syd gene, required for the functional interaction of kinesin I with axonal cargo. Studies of the similar gene in mouse suggested that this protein may interact with, and regulate the activity of numerous protein kinases of the JNK signaling pathway, and thus function as a scaffold protein in neuronal cells. The C. elegans counterpart of this gene is found to regulate synaptic vesicle transport possibly by integrating JNK signaling and kinesin-1 transport. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous inactivation of this gene results in impaired lung morphogenesis, causes absence of the telencephalic commissure with multiple defects in brain development and axon guidance, may affect synaptic transmission, and invariably leads to neonatal death due to respiratory failure. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 211 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700001K19Rik	TCT	TCTCCT	12: 110,634,882 (GRCm39)		probably benign	Het
A630001G21Rik	CTGTT	CT	1: 85,650,856 (GRCm39)		probably benign	Homo
Abcb11	C	A	2: 69,073,862 (GRCm39)	R1221L	probably damaging	Homo
Abcb4	GAAA	G	5: 8,946,597 (GRCm39)		probably benign	Homo
Ahdc1	CT	CTCGT	4: 132,790,070 (GRCm39)		probably benign	Homo
Alpk3	TCT	TCTACT	7: 80,727,510 (GRCm39)		probably benign	Het
Amfr	C	G	8: 94,731,787 (GRCm39)	G30R	probably damaging	Homo
Ankrd35	GC	GCTAC	3: 96,591,165 (GRCm39)		probably benign	Homo
Anxa7	C	T	14: 20,519,479 (GRCm39)	G113E	probably damaging	Homo
Apc	CAATAAAGC	CAATAAAGCTAATAAAGC	18: 34,415,052 (GRCm39)		probably benign	Homo
Apol6	GTTT	GTTTCTTT	15: 76,935,642 (GRCm39)		probably null	Homo
Arpc1b	GGTGGC	GGTGGCGTGGC	5: 145,063,597 (GRCm39)		probably null	Het
AY358078	C	T	14: 52,043,155 (GRCm39)	S281L	unknown	Homo
Blm	ACCTGC	ACCTGCCTGC	7: 80,113,519 (GRCm39)		probably null	Het
Blm	T	TACCA	7: 80,113,522 (GRCm39)		probably null	Het
Bltp1	TTATTAT	TTATTATTATTATTACTATTAT	3: 37,104,903 (GRCm39)		probably benign	Het
Blzf1	TTGT	TT	1: 164,131,486 (GRCm39)		probably null	Homo
Btnl10	A	AAGG	11: 58,814,757 (GRCm39)		probably benign	Homo
Cacna1a	ACC	ACCGCC	8: 85,365,349 (GRCm39)		probably benign	Het
Cacna1a	ACC	ACCCCC	8: 85,365,355 (GRCm39)		probably benign	Homo
Catsper2	TTC	TTCTTTTACTTTGTC	2: 121,228,021 (GRCm39)		probably benign	Homo
Ccdc170	ACC	ACCTCC	10: 4,511,023 (GRCm39)		probably benign	Het
Ccdc170	AC	ACCCC	10: 4,511,029 (GRCm39)		probably benign	Het
Ccdc73	TAAG	T	2: 104,822,185 (GRCm39)		probably benign	Homo
Ccnk	TTCCCAC	T	12: 108,168,766 (GRCm39)		probably benign	Het
Cdan1	A	C	2: 120,555,452 (GRCm39)	V763G	probably damaging	Het
Cdk6	A	G	5: 3,394,211 (GRCm39)		probably benign	Het
Cdx1	TGCTGC	TGCTGCCGCTGC	18: 61,152,946 (GRCm39)		probably benign	Het
Cdx1	GCTGCT	GCTGCTTCTGCT	18: 61,152,950 (GRCm39)		probably benign	Het
Cfap46	CCTTCT	CCTTCTTCT	7: 139,218,846 (GRCm39)		probably benign	Homo
Chd4	GC	GCTCCCCC	6: 125,099,094 (GRCm39)		probably benign	Homo
Cluh	GAGCCT	GAGCCTAAGCCT	11: 74,560,350 (GRCm39)		probably benign	Het
Cluh	CC	CCTGAGGC	11: 74,560,359 (GRCm39)		probably benign	Het
Cluh	CCCCGAGCC	CCCCGAGCCCGAGCC	11: 74,560,340 (GRCm39)		probably benign	Het
Cluh	AGCCTG	AGCCTGCGCCTG	11: 74,560,345 (GRCm39)		probably benign	Het
Cntnap1	GCCCCA	GCCCCACCCCCA	11: 101,080,408 (GRCm39)		probably benign	Het
Cntnap1	CCCAGC	CCCAGCGCCAGC	11: 101,080,416 (GRCm39)		probably benign	Het
Cntnap1	AGCCCC	AGCCCCCGCCCC	11: 101,080,395 (GRCm39)		probably benign	Het
Cntnap1	GCCCCA	GCCCCAACCCCA	11: 101,080,402 (GRCm39)		probably benign	Het
Cracdl	T	A	1: 37,664,116 (GRCm39)	E594V	probably benign	Homo
Cracdl	C	A	1: 37,664,117 (GRCm39)	E594*	probably null	Homo
Cul9	CTC	CTCTTC	17: 46,811,784 (GRCm39)		probably benign	Het
Cul9	CTCTTC	CTCTTCTTC	17: 46,811,772 (GRCm39)		probably benign	Het
Cyth2	C	A	7: 45,462,466 (GRCm39)	S102I	possibly damaging	Het
Dbr1	AGGAGG	AGGAGGCGGAGG	9: 99,465,739 (GRCm39)		probably benign	Het
Dbr1	GGAGG	GGAGGACGAGG	9: 99,465,752 (GRCm39)		probably benign	Het
Dennd2b	CACCACACTGGGGCAGCCCACACTGGGGCAG	CCCCACACTGGGGCAG	7: 109,156,128 (GRCm39)		probably benign	Het
Dhx8	GACCGA	GACCGATACCGA	11: 101,629,005 (GRCm39)		probably benign	Homo
Dhx8	GAGACC	GAGACCCAGACC	11: 101,629,015 (GRCm39)		probably benign	Homo
Dhx8	CGAGAC	CGAGACGGAGAC	11: 101,629,008 (GRCm39)		probably benign	Homo
Dnaaf9	CC	CCTGC	2: 130,612,672 (GRCm39)		probably benign	Het
Dnah8	ACTGCCCCT	ACT	17: 30,854,439 (GRCm39)		probably benign	Het
Dnah8	CCTCCCG	C	17: 30,854,451 (GRCm39)		probably benign	Homo
Dnajb5	AGGTG	A	4: 42,957,126 (GRCm39)		probably null	Het
Dusp10	G	T	1: 183,769,253 (GRCm39)	C73F	probably damaging	Homo
E4f1	CCG	CCGACG	17: 24,674,166 (GRCm39)		probably benign	Homo
Eif3a	TTA	TTATTATA	19: 60,763,727 (GRCm39)		probably benign	Het
Fam81b	TTC	TTCGTC	13: 76,419,438 (GRCm39)		probably benign	Het
Fbxo22	G	A	9: 55,116,666 (GRCm39)	R56H	probably damaging	Het
Fcgr1	CTTCT	C	3: 96,191,820 (GRCm39)		probably null	Het
Fcgr1	T	C	3: 96,194,410 (GRCm39)	D159G	probably benign	Homo
Fmn1	CC	CCTCCTTC	2: 113,356,129 (GRCm39)		probably benign	Het
Fmn1	CCTCCT	CCTCCTACTCCT	2: 113,356,123 (GRCm39)		probably benign	Het
Fmn1	CC	CCCCCTGC	2: 113,356,126 (GRCm39)		probably benign	Het
G530012D18Rik	GA	GACAGAGATA	1: 85,504,899 (GRCm39)		probably null	Het
Gli3	G	A	13: 15,818,942 (GRCm39)	R248H	probably damaging	Het
Gm16503	G	A	4: 147,625,710 (GRCm39)	G68E	unknown	Het
Gm19345	GGATGGCAGGTG	GG	7: 19,591,527 (GRCm39)		probably null	Het
Gm4340	AGC	AGCTGC	10: 104,031,958 (GRCm39)		probably benign	Het
Gm4340	AG	AGCGG	10: 104,031,961 (GRCm39)		probably benign	Het
Gm4340	GCA	GCAACA	10: 104,031,938 (GRCm39)		probably benign	Het
Gm6309	C	T	5: 146,104,993 (GRCm39)	V307I	probably benign	Het
Gpatch11	AAGAGG	AAGAGGCAGAGG	17: 79,149,600 (GRCm39)		probably benign	Het
Gpatch11	AGGAA	AGGAAGCGGAA	17: 79,149,609 (GRCm39)		probably benign	Het
Hoxa10	T	A	6: 52,211,166 (GRCm39)	Q250L	possibly damaging	Homo
Hrh1	T	C	6: 114,458,084 (GRCm39)	I455T	possibly damaging	Het
Hspa1b	GCGCC	GC	17: 35,176,105 (GRCm39)		probably benign	Homo
Iba57	GAAA	GAAAAA	11: 59,052,331 (GRCm39)		probably null	Homo
Igf1r	TGGAGC	TGGAGCTGGAGAGGGAGC	7: 67,875,929 (GRCm39)		probably benign	Het
Il17rd	CGG	CGGAGG	14: 26,804,637 (GRCm39)		probably benign	Het
Il2	TGG	TGGGGCTTGAAGCGG	3: 37,179,977 (GRCm39)		probably benign	Het
Il2	AGGTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG	AGCTGCTGCTGCTGCTGCTGCTGCTG	3: 37,179,913 (GRCm39)		probably benign	Het
Kcng4	G	T	8: 120,360,258 (GRCm39)	Y39*	probably null	Homo
Klra2	G	GAAATCCACAT	6: 131,198,815 (GRCm39)		probably null	Het
Kmt2b	CCTCCT	CCTCCTTCTCCT	7: 30,285,792 (GRCm39)		probably benign	Het
Kmt2b	CCTCCT	CCTCCTGCTCCT	7: 30,285,795 (GRCm39)		probably benign	Het
Kmt2b	TCCTCC	TCCTCCCCCTCC	7: 30,285,803 (GRCm39)		probably benign	Het
Kmt2b	TCCTCC	TCCTCCCCCTCC	7: 30,285,791 (GRCm39)		probably benign	Het
Krt10	TCCTCC	TCCTCCGCCTCC	11: 99,280,099 (GRCm39)		probably benign	Het
Krt10	TCCGCC	TCCGCCGCC	11: 99,277,023 (GRCm39)		probably benign	Homo
Krt10	TCC	TCCTCCACC	11: 99,280,105 (GRCm39)		probably benign	Homo
Krtap28-10	TCCCACA	TCCCACACCCACA	1: 83,019,844 (GRCm39)		probably benign	Homo
Krtap4-2	A	ACAC	11: 99,525,839 (GRCm39)		probably benign	Het
Krtap9-3	AC	ACAGGTGTCGC	11: 99,488,830 (GRCm39)		probably benign	Het
Las1l	AGG	AGGGGG	X: 94,984,427 (GRCm39)		probably benign	Het
Las1l	GAG	GAGCAG	X: 94,984,435 (GRCm39)		probably benign	Het
Las1l	AGG	AGGCGG	X: 94,984,433 (GRCm39)		probably benign	Het
Lrit3	TGC	TGCAGC	3: 129,582,455 (GRCm39)		probably benign	Het
Lrit3	AC	ACATTC	3: 129,597,562 (GRCm39)		probably null	Homo
Lrit3	GCT	GCTTCT	3: 129,582,459 (GRCm39)		probably benign	Het
Luzp1	A	AGGTGGCCTCTTCAGT	4: 136,270,507 (GRCm39)		probably benign	Het
Mamld1	AGC	AGCCGC	X: 70,162,441 (GRCm39)		probably benign	Het
Mamld1	GCA	GCAACA	X: 70,162,445 (GRCm39)		probably benign	Het
Mbd1	TGTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC	TATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC	18: 74,406,644 (GRCm39)		probably benign	Het
Nat8f2	T	A	6: 85,844,668 (GRCm39)	L231F	possibly damaging	Homo
Nfxl1	CC	CCGGGGAC	5: 72,716,464 (GRCm39)		probably benign	Het
Noc2l	CTG	CTGTTG	4: 156,324,552 (GRCm39)		probably benign	Het
Noc2l	GGTAG	GG	4: 156,325,958 (GRCm39)		probably benign	Homo
Noc2l	GCT	GCTTCT	4: 156,324,551 (GRCm39)		probably benign	Het
Nxpe5	C	T	5: 138,228,196 (GRCm39)		probably benign	Het
Or10j2	GGGCTGCTTGTGGCAAT	G	1: 173,098,197 (GRCm39)		probably null	Het
Or51a43	G	C	7: 103,720,499 (GRCm39)		probably benign	Homo
Or51f2	CT	CTAATTGCCTT	7: 102,526,440 (GRCm39)		probably benign	Homo
Or8b41	A	G	9: 38,054,484 (GRCm39)	I13V	probably benign	Homo
Or8u3-ps	CAG	CAGAG	2: 85,953,104 (GRCm39)		probably null	Homo
Osmr	C	CTCA	15: 6,867,187 (GRCm39)		probably null	Homo
Patl2	GC	GCTAC	2: 121,956,625 (GRCm39)		probably null	Het
Patl2	C	CTGA	2: 121,956,626 (GRCm39)		probably benign	Het
Patl2	CTG	CTGTTG	2: 121,956,617 (GRCm39)		probably benign	Het
Pdik1l	GTTTTTGTTTT	GTTTTTGTTTTTTTTTTGTTTT	4: 134,006,678 (GRCm39)		probably null	Homo
Pdik1l	ACCACC	ACCACCCCCACC	4: 134,006,817 (GRCm39)		probably benign	Het
Phc1	GCTG	GCTGCTTCTG	6: 122,300,557 (GRCm39)		probably benign	Het
Piezo1	G	A	8: 123,222,308 (GRCm39)	R503W	probably damaging	Homo
Pitrm1	TTTTA	T	13: 6,610,632 (GRCm39)		probably benign	Homo
Pkdrej	TG	TGGGAGCG	15: 85,703,881 (GRCm39)		probably benign	Homo
Pla2g4e	AGGG	A	2: 120,075,205 (GRCm39)		probably benign	Homo
Plekhs1	AC	ACCTCCCCCGAGCC	19: 56,468,295 (GRCm39)		probably benign	Het
Pnma8a	CCTCATGATGCACCTGCTTCAACATC	CCTCATGATGCACCTGCTTCAACATCTCATGATGCACCTGCTTCAACATC	7: 16,695,350 (GRCm39)		probably benign	Homo
Pnma8b	TGGA	T	7: 16,679,931 (GRCm39)		probably benign	Het
Ppp1r3f	C	A	X: 7,426,575 (GRCm39)	G562V	probably damaging	Homo
Prr13	CTC	CTCATC	15: 102,370,608 (GRCm39)		probably benign	Het
Prss41	CACA	C	17: 24,063,071 (GRCm39)		probably benign	Het
Prtg	GTAAC	G	9: 72,764,363 (GRCm39)		probably benign	Het
Ptk2b	C	T	14: 66,411,298 (GRCm39)	R411Q	possibly damaging	Homo
Ptms	TCT	TCTGCT	6: 124,891,420 (GRCm39)		probably benign	Homo
Ptms	C	CTTG	6: 124,891,424 (GRCm39)		probably benign	Homo
Ptms	TTC	TTCGTC	6: 124,891,422 (GRCm39)		probably benign	Homo
Ptpn23	G	T	9: 110,216,701 (GRCm39)	P1052T	probably benign	Homo
Rab3il1	C	A	19: 10,011,115 (GRCm39)	A264E	probably damaging	Homo
Rbm6	GCTGT	G	9: 107,659,954 (GRCm39)		probably null	Homo
Rtbdn	TAG	TAGGGGCAG	8: 85,682,790 (GRCm39)		probably benign	Het
Rtbdn	GGC	GGCAGCTGC	8: 85,682,806 (GRCm39)		probably benign	Het
Rtbdn	CGGC	CGGCAGGGGC	8: 85,682,805 (GRCm39)		probably benign	Het
Rtbdn	AGCG	AGCGTCCGCG	8: 85,682,797 (GRCm39)		probably benign	Het
Sbp	CAAAG	CAAAGCTGCTGACAAAAAAG	17: 24,164,356 (GRCm39)		probably benign	Het
Sbp	G	GCTGACAACAAAGATC	17: 24,164,363 (GRCm39)		probably benign	Het
Setd1a	GTGGTAGTG	GTGGTAGTGTTGGTAGTG	7: 127,384,484 (GRCm39)		probably benign	Het
Sfswap	GCCCACTC	GCCCACTCATCCCACTC	5: 129,646,820 (GRCm39)		probably benign	Het
Six3	GGC	GGCAGC	17: 85,928,785 (GRCm39)		probably benign	Het
Six3	GCG	GCGCCG	17: 85,928,786 (GRCm39)		probably benign	Het
Six3	CGG	CGGGGG	17: 85,928,790 (GRCm39)		probably benign	Het
Six3	GGC	GGCAGC	17: 85,928,791 (GRCm39)		probably benign	Het
Six3	CGG	CGGGGG	17: 85,928,793 (GRCm39)		probably benign	Het
Six3	CGG	CGGGGG	17: 85,928,796 (GRCm39)		probably benign	Het
Slc12a1	ACC	ACCTTTGGCCACAACTCC	2: 124,996,134 (GRCm39)		probably benign	Homo
Smarca2	CAGCAGCAGCAGCAGCAGCA	CAGCAGCAGCAGCAGCAGCAGCAGCA	19: 26,608,399 (GRCm39)		probably benign	Homo
Spaca1	TCGCTC	TCGCTCGCGCTC	4: 34,049,836 (GRCm39)		probably benign	Het
Spag1	TTC	TTCGTC	15: 36,197,879 (GRCm39)		probably benign	Het
Spag17	AGG	AGGCGG	3: 99,963,573 (GRCm39)		probably benign	Het
Spata31h1	TTCA	T	10: 82,121,303 (GRCm39)		probably benign	Homo
Srebf2	G	T	15: 82,069,536 (GRCm39)	A693S	probably damaging	Homo
Srpk2	T	C	5: 23,750,194 (GRCm39)		probably null	Homo
Sry	AACTGCT	A	Y: 2,663,195 (GRCm39)		probably benign	Het
Sry	GTG	GTGTTG	Y: 2,662,837 (GRCm39)		probably benign	Homo
Sry	TGG	TGGGGG	Y: 2,662,838 (GRCm39)		probably benign	Homo
Stard9	C	CTAAGGGACTAGTAGG	2: 120,526,566 (GRCm39)		probably benign	Het
Supt20	CAGCAG	CAGCAGGAGCAG	3: 54,635,079 (GRCm39)		probably benign	Het
Supt20	CAGCAG	CAGCAGAAGCAG	3: 54,635,082 (GRCm39)		probably benign	Het
Supt20	GCAGCA	GCAGCAACAGCA	3: 54,635,078 (GRCm39)		probably benign	Het
Tcof1	GGGTA	G	18: 60,961,722 (GRCm39)		probably benign	Homo
Tdpoz3	A	C	3: 93,733,981 (GRCm39)	N219H	probably benign	Het
Tesk1	C	CCCCG	4: 43,447,004 (GRCm39)		probably null	Homo
Tob1	GCA	GCAACA	11: 94,105,290 (GRCm39)		probably benign	Het
Tob1	CACA	CACAACA	11: 94,105,277 (GRCm39)		probably benign	Het
Tob1	A	AGCC	11: 94,105,304 (GRCm39)		probably benign	Het
Trav15-2-dv6-2	AG	AGAGG	14: 53,887,213 (GRCm39)		probably benign	Homo
Trav15-2-dv6-2	G	GAAA	14: 53,887,214 (GRCm39)		probably benign	Homo
Trim63	GAGT	G	4: 134,055,036 (GRCm39)		probably benign	Het
Tsbp1	CAG	CAGAAG	17: 34,679,025 (GRCm39)		probably benign	Het
Tsbp1	GCA	GCATCA	17: 34,679,042 (GRCm39)		probably benign	Het
Tsen2	G	GAGA	6: 115,537,038 (GRCm39)		probably benign	Het
Ttf2	TC	TCCCC	3: 100,870,476 (GRCm39)		probably benign	Homo
Tusc1	ACCGCC	ACCGCCCCCGCC	4: 93,223,550 (GRCm39)		probably benign	Homo
Ubqlnl	TGAG	T	7: 103,799,042 (GRCm39)		probably benign	Homo
Ubtf	CCT	CCTACT	11: 102,197,774 (GRCm39)		probably null	Het
Ubtf	TCC	TCCACC	11: 102,197,776 (GRCm39)		probably benign	Het
Vps13b	G	T	15: 35,847,103 (GRCm39)	A2629S	probably damaging	Homo
Wasf3	G	T	5: 146,407,060 (GRCm39)	R460L	probably damaging	Het
Zc3h13	TGCGAGATG	TGCGAGATGAGCGAGATG	14: 75,561,039 (GRCm39)		probably benign	Homo
Zc3h13	ATGTGCGAG	ATGTGCGAGGTGTGCGAG	14: 75,561,036 (GRCm39)		probably benign	Homo
Zfhx3	GCAACA	GCAACAACAACAACA	8: 109,682,720 (GRCm39)		probably benign	Het
Zfhx3	GCA	GCAACAGCACCA	8: 109,682,735 (GRCm39)		probably benign	Het
Zfhx3	AGCA	AGCAACAGACGCA	8: 109,682,734 (GRCm39)		probably benign	Het
Zfp111	TCA	TCAACA	7: 23,899,230 (GRCm39)		probably benign	Homo
Zfp112	CATGA	CATGATGA	7: 23,824,832 (GRCm39)		probably benign	Homo
Zfp26	C	A	9: 20,349,842 (GRCm39)	A241S	probably benign	Homo
Zfp282	CGG	CGGGGG	6: 47,881,724 (GRCm39)		probably benign	Het
Zfp282	CGG	CGGGGG	6: 47,881,733 (GRCm39)		probably benign	Het
Zfp335	TC	TCCCC	2: 164,749,404 (GRCm39)		probably benign	Het
Zfp335	TCC	TCCGCC	2: 164,749,395 (GRCm39)		probably benign	Het
Zfp335	CTC	CTCGTC	2: 164,749,394 (GRCm39)		probably benign	Het
Zfp462	CCACC	CCACCTCAGCCACAGTCACC	4: 55,009,758 (GRCm39)		probably benign	Het
Zfp462	ACC	ACCTCAGCCACAGTCGCC	4: 55,009,760 (GRCm39)		probably benign	Het
Zfp598	ACCACC	ACCACCCCCACC	17: 24,899,750 (GRCm39)		probably benign	Het
Zfp598	AC	ACCACCGC	17: 24,899,765 (GRCm39)		probably benign	Het
Zfp598	ACCACC	ACCACCGCCACC	17: 24,899,756 (GRCm39)		probably benign	Het
Zfp831	TCC	TCCCCC	2: 174,487,264 (GRCm39)		probably benign	Het
Zfp831	TC	TCCGC	2: 174,487,276 (GRCm39)		probably benign	Het
Zfp831	CTC	CTCATC	2: 174,487,269 (GRCm39)		probably benign	Het
Zfp93	CAGGCATAG	CAG	7: 23,974,814 (GRCm39)		probably benign	Homo
Zscan10	TGACG	TG	17: 23,828,419 (GRCm39)		probably benign	Homo

Other mutations in Mapk8ip3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00578:Mapk8ip3	APN	17	25,119,793 (GRCm39)	missense	probably damaging	1.00
IGL01018:Mapk8ip3	APN	17	25,118,693 (GRCm39)	splice site	probably benign
IGL01066:Mapk8ip3	APN	17	25,120,692 (GRCm39)	missense	probably benign	0.00
IGL01656:Mapk8ip3	APN	17	25,137,003 (GRCm39)	missense	probably damaging	0.99
IGL01991:Mapk8ip3	APN	17	25,146,835 (GRCm39)	missense	possibly damaging	0.78
IGL02014:Mapk8ip3	APN	17	25,122,254 (GRCm39)	splice site	probably benign
IGL02219:Mapk8ip3	APN	17	25,118,532 (GRCm39)	missense	probably damaging	1.00
IGL03006:Mapk8ip3	APN	17	25,120,489 (GRCm39)	missense	probably benign
ANU74:Mapk8ip3	UTSW	17	25,119,551 (GRCm39)	missense	possibly damaging	0.94
R0028:Mapk8ip3	UTSW	17	25,123,871 (GRCm39)	splice site	probably benign
R0401:Mapk8ip3	UTSW	17	25,128,145 (GRCm39)	intron	probably benign
R0496:Mapk8ip3	UTSW	17	25,133,424 (GRCm39)	splice site	probably benign
R1456:Mapk8ip3	UTSW	17	25,125,923 (GRCm39)	missense	probably damaging	1.00
R1503:Mapk8ip3	UTSW	17	25,123,897 (GRCm39)	missense	probably damaging	1.00
R1554:Mapk8ip3	UTSW	17	25,122,033 (GRCm39)	missense	probably benign	0.14
R1680:Mapk8ip3	UTSW	17	25,119,985 (GRCm39)	missense	probably damaging	1.00
R1733:Mapk8ip3	UTSW	17	25,155,824 (GRCm39)	missense	possibly damaging	0.70
R1741:Mapk8ip3	UTSW	17	25,118,828 (GRCm39)	missense	probably damaging	1.00
R1750:Mapk8ip3	UTSW	17	25,133,433 (GRCm39)	missense	probably null	1.00
R1774:Mapk8ip3	UTSW	17	25,143,119 (GRCm39)	critical splice donor site	probably null
R1845:Mapk8ip3	UTSW	17	25,133,557 (GRCm39)	missense	probably benign	0.29
R1911:Mapk8ip3	UTSW	17	25,123,025 (GRCm39)	missense	probably benign	0.00
R1993:Mapk8ip3	UTSW	17	25,133,562 (GRCm39)	missense	probably damaging	1.00
R2512:Mapk8ip3	UTSW	17	25,133,677 (GRCm39)	nonsense	probably null
R2656:Mapk8ip3	UTSW	17	25,131,781 (GRCm39)	missense	probably damaging	1.00
R2990:Mapk8ip3	UTSW	17	25,124,266 (GRCm39)	missense	probably benign	0.00
R4587:Mapk8ip3	UTSW	17	25,123,761 (GRCm39)	missense	probably damaging	1.00
R4617:Mapk8ip3	UTSW	17	25,123,761 (GRCm39)	missense	probably damaging	1.00
R4627:Mapk8ip3	UTSW	17	25,122,267 (GRCm39)	missense	probably benign
R4649:Mapk8ip3	UTSW	17	25,123,726 (GRCm39)	missense	probably damaging	1.00
R4868:Mapk8ip3	UTSW	17	25,120,389 (GRCm39)	missense	probably benign	0.04
R4903:Mapk8ip3	UTSW	17	25,120,183 (GRCm39)	missense	probably benign
R4915:Mapk8ip3	UTSW	17	25,128,127 (GRCm39)	missense	possibly damaging	0.75
R5447:Mapk8ip3	UTSW	17	25,118,163 (GRCm39)	missense	probably benign
R5642:Mapk8ip3	UTSW	17	25,122,285 (GRCm39)	missense	possibly damaging	0.63
R6320:Mapk8ip3	UTSW	17	25,125,879 (GRCm39)	missense	probably damaging	0.99
R6900:Mapk8ip3	UTSW	17	25,128,097 (GRCm39)	splice site	probably null
R7178:Mapk8ip3	UTSW	17	25,120,728 (GRCm39)	missense	probably benign	0.02
R7273:Mapk8ip3	UTSW	17	25,125,148 (GRCm39)	missense	probably benign	0.00
R7317:Mapk8ip3	UTSW	17	25,120,692 (GRCm39)	missense	probably benign	0.00
R7323:Mapk8ip3	UTSW	17	25,120,135 (GRCm39)	missense	probably benign
R7701:Mapk8ip3	UTSW	17	25,120,378 (GRCm39)	missense	possibly damaging	0.93
R7873:Mapk8ip3	UTSW	17	25,125,146 (GRCm39)	missense	probably benign	0.01
R8070:Mapk8ip3	UTSW	17	25,120,078 (GRCm39)	critical splice donor site	probably null
R8314:Mapk8ip3	UTSW	17	25,120,748 (GRCm39)	missense	probably benign	0.09
R8356:Mapk8ip3	UTSW	17	25,123,925 (GRCm39)	missense	probably damaging	1.00
R8441:Mapk8ip3	UTSW	17	25,139,474 (GRCm39)	intron	probably benign
R8537:Mapk8ip3	UTSW	17	25,120,652 (GRCm39)	nonsense	probably null
R8802:Mapk8ip3	UTSW	17	25,124,206 (GRCm39)	missense	probably damaging	1.00
R8864:Mapk8ip3	UTSW	17	25,118,492 (GRCm39)	missense	probably damaging	1.00
R8918:Mapk8ip3	UTSW	17	25,131,727 (GRCm39)	missense	probably damaging	1.00
R9312:Mapk8ip3	UTSW	17	25,146,925 (GRCm39)	critical splice acceptor site	probably null
R9599:Mapk8ip3	UTSW	17	25,118,124 (GRCm39)	missense	probably damaging	1.00
R9638:Mapk8ip3	UTSW	17	25,118,023 (GRCm39)	missense	probably benign
R9640:Mapk8ip3	UTSW	17	25,155,647 (GRCm39)	missense	possibly damaging	0.46
R9723:Mapk8ip3	UTSW	17	25,132,585 (GRCm39)	missense	possibly damaging	0.83
X0024:Mapk8ip3	UTSW	17	25,122,947 (GRCm39)	missense	possibly damaging	0.69

Predicted Primers

Posted On

2018-04-05