Mutagenetix > Incidental Mutation

Incidental Mutation 'R4998:Dip2a'

389655

Institutional Source

Beutler Lab

Gene Symbol

Dip2a

Ensembl Gene

ENSMUSG00000020231

Gene Name

disco interacting protein 2 homolog A

Synonyms

Dip2, Kiaa0184-hp, 4931420H10Rik

MMRRC Submission

042592-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4998 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

76098581-76181194 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 76155390 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Stop codon at position 65 (L65*)

Ref Sequence

ENSEMBL: ENSMUSP00000125184 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000036033] [ENSMUST00000105417] [ENSMUST00000160048]

AlphaFold

Q8BWT5

Predicted Effect

probably null
Transcript: ENSMUST00000036033
AA Change: L104*

SMART Domains

Protein: ENSMUSP00000043710
Gene: ENSMUSG00000020231
AA Change: L104*

Domain	Start	End	E-Value	Type
DMAP_binding	9	122	2.55e-35	SMART
low complexity region	173	208	N/A	INTRINSIC
low complexity region	281	293	N/A	INTRINSIC
Pfam:AMP-binding	330	806	4.3e-26	PFAM
Pfam:AMP-binding	982	1456	1.4e-52	PFAM
low complexity region	1487	1498	N/A	INTRINSIC
low complexity region	1511	1532	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000105417
AA Change: L104*

SMART Domains

Protein: ENSMUSP00000101057
Gene: ENSMUSG00000020231
AA Change: L104*

Domain	Start	End	E-Value	Type
DMAP_binding	9	122	2.55e-35	SMART
low complexity region	173	208	N/A	INTRINSIC
low complexity region	281	293	N/A	INTRINSIC
Pfam:AMP-binding	330	806	6.6e-28	PFAM
Pfam:AMP-binding	992	1466	7.3e-65	PFAM
low complexity region	1497	1508	N/A	INTRINSIC
low complexity region	1521	1542	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000160048
AA Change: L65*

SMART Domains

Protein: ENSMUSP00000125184
Gene: ENSMUSG00000020231
AA Change: L65*

Domain	Start	End	E-Value	Type
DMAP_binding	9	83	7.94e-23	SMART
low complexity region	134	169	N/A	INTRINSIC
low complexity region	242	254	N/A	INTRINSIC
Pfam:AMP-binding	291	767	5.3e-26	PFAM
Pfam:AMP-binding	943	1417	1.7e-52	PFAM
low complexity region	1448	1459	N/A	INTRINSIC
low complexity region	1472	1493	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000162766

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.6%
20x: 93.3%

Validation Efficiency

97% (91/94)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene may be involved in axon patterning in the central nervous system. This gene is not highly expressed. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

Allele List at MGI

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310022A10Rik	T	C	7: 27,271,088 (GRCm39)	V135A	probably damaging	Het
Ankrd42	T	C	7: 92,273,282 (GRCm39)	N115S	possibly damaging	Het
Baz1a	T	C	12: 55,021,922 (GRCm39)	E120G	probably damaging	Het
Calcrl	A	T	2: 84,169,658 (GRCm39)	V341E	probably damaging	Het
Card6	T	C	15: 5,129,564 (GRCm39)	R611G	probably benign	Het
Cd70	A	T	17: 57,453,311 (GRCm39)	S118T	probably damaging	Het
Chil5	T	A	3: 105,927,248 (GRCm39)	I188F	probably damaging	Het
Clca4b	C	T	3: 144,621,269 (GRCm39)	V602I	probably benign	Het
Cldn10	G	A	14: 119,025,725 (GRCm39)	G53S	possibly damaging	Het
Col6a4	A	G	9: 105,867,977 (GRCm39)		probably benign	Het
Cox8b	T	C	7: 140,479,001 (GRCm39)	E38G	probably damaging	Het
Cx3cl1	C	G	8: 95,507,053 (GRCm39)	L353V	probably damaging	Het
Cyp2a4	G	T	7: 26,006,786 (GRCm39)	Q48H	probably damaging	Het
Defb8	T	C	8: 19,497,603 (GRCm39)	I3V	probably benign	Het
Dnaaf4	A	G	9: 72,867,960 (GRCm39)	T74A	possibly damaging	Het
Dsg2	A	T	18: 20,734,578 (GRCm39)	D852V	probably benign	Het
Edar	T	C	10: 58,441,915 (GRCm39)	R326G	probably damaging	Het
Egfr	A	G	11: 16,831,493 (GRCm39)	E554G	possibly damaging	Het
Eif2b3	A	C	4: 116,923,589 (GRCm39)	K268T	probably benign	Het
Enox1	A	T	14: 77,738,875 (GRCm39)		probably benign	Het
Enpp3	C	A	10: 24,683,436 (GRCm39)	M260I	probably benign	Het
Espn	A	T	4: 152,220,040 (GRCm39)	M361K	possibly damaging	Het
Fam107a	T	C	14: 8,299,514 (GRCm38)	N108S	possibly damaging	Het
Fbn2	A	T	18: 58,205,703 (GRCm39)	V1125D	probably damaging	Het
Fbxo30	T	A	10: 11,166,507 (GRCm39)	S410T	probably damaging	Het
Fchsd1	C	T	18: 38,092,926 (GRCm39)		probably benign	Het
Fcsk	G	A	8: 111,614,435 (GRCm39)	A618V	probably damaging	Het
Gm10715	T	G	9: 3,038,073 (GRCm39)		probably benign	Het
Gm10722	A	C	9: 3,001,041 (GRCm39)	Y39S	probably benign	Het
Gm17416	C	A	2: 152,411,427 (GRCm39)	P57Q	probably damaging	Het
Gm27013	A	T	6: 130,653,501 (GRCm39)	C654S	probably damaging	Het
Gon4l	G	T	3: 88,807,305 (GRCm39)	E1666D	probably damaging	Het
Gypa	T	A	8: 81,222,964 (GRCm39)	S23T	unknown	Het
Gys1	C	A	7: 45,100,968 (GRCm39)		probably benign	Het
Hdac10	T	A	15: 89,008,143 (GRCm39)	Q569L	possibly damaging	Het
Icos	A	G	1: 61,032,941 (GRCm39)	T47A	possibly damaging	Het
Igfn1	T	A	1: 135,882,404 (GRCm39)	I2814F	probably damaging	Het
Kif27	A	G	13: 58,440,957 (GRCm39)	S1153P	probably damaging	Het
Lin28a	A	C	4: 133,746,028 (GRCm39)	F9V	possibly damaging	Het
Lrriq3	T	A	3: 154,893,695 (GRCm39)	N465K	probably benign	Het
Lsm14a	T	C	7: 34,074,799 (GRCm39)	E47G	probably damaging	Het
Mmel1	A	G	4: 154,969,967 (GRCm39)	K177R	probably benign	Het
Ncstn	T	A	1: 171,899,087 (GRCm39)	N348I	possibly damaging	Het
Ninl	A	G	2: 150,795,284 (GRCm39)	I619T	probably damaging	Het
Npb	T	C	11: 120,499,401 (GRCm39)	Y23H	probably damaging	Het
Npepps	A	G	11: 97,096,933 (GRCm39)		probably benign	Het
Or8k30	T	C	2: 86,339,699 (GRCm39)	Y299H	probably benign	Het
Otop1	G	A	5: 38,451,892 (GRCm39)		probably null	Het
Pcdha1	T	C	18: 37,065,469 (GRCm39)	L711P	probably damaging	Het
Pcyt1a	A	G	16: 32,270,660 (GRCm39)		probably benign	Het
Pdpr	G	T	8: 111,841,400 (GRCm39)	V211F	probably damaging	Het
Pip4k2b	T	C	11: 97,613,261 (GRCm39)	N245S	possibly damaging	Het
Platr26	G	A	2: 71,561,214 (GRCm39)		noncoding transcript	Het
Plek	A	G	11: 16,933,194 (GRCm39)		probably null	Het
Potefam3c	G	C	8: 69,906,010 (GRCm39)	N13K	probably benign	Het
Prdm15	A	T	16: 97,595,689 (GRCm39)	D1046E	probably damaging	Het
Prr29	T	G	11: 106,267,779 (GRCm39)	C175G	probably benign	Het
Ptpru	A	G	4: 131,504,196 (GRCm39)	V1097A	probably damaging	Het
Ramp2	T	A	11: 101,138,247 (GRCm39)		probably benign	Het
Rap1gap	A	G	4: 137,455,595 (GRCm39)	D381G	possibly damaging	Het
Rbbp6	T	A	7: 122,589,549 (GRCm39)	D412E	probably benign	Het
Rgs4	C	T	1: 169,572,802 (GRCm39)	V45I	probably benign	Het
Ryr2	C	T	13: 11,658,781 (GRCm39)	R3614Q	probably damaging	Het
Shc3	G	A	13: 51,596,856 (GRCm39)		probably null	Het
Shmt2	A	T	10: 127,354,139 (GRCm39)	C412S	probably damaging	Het
Slc25a45	A	T	19: 5,934,945 (GRCm39)	N265Y	probably damaging	Het
Slc4a10	G	C	2: 62,074,783 (GRCm39)	E316Q	probably benign	Het
Slc5a8	T	C	10: 88,743,919 (GRCm39)		probably null	Het
Snx31	A	G	15: 36,539,513 (GRCm39)	V121A	probably damaging	Het
Socs3	T	C	11: 117,858,542 (GRCm39)	E172G	probably damaging	Het
Tg	A	G	15: 66,545,899 (GRCm39)	D207G	probably damaging	Het
Them4	G	T	3: 94,237,088 (GRCm39)	V183F	probably damaging	Het
Tkt	G	A	14: 30,287,499 (GRCm39)	W136*	probably null	Het
Tlcd3b	C	T	7: 126,426,795 (GRCm39)	R73C	probably damaging	Het
Tmc3	C	A	7: 83,271,529 (GRCm39)	R894S	probably benign	Het
Tmem132a	G	T	19: 10,836,305 (GRCm39)	P742T	probably benign	Het
Tmem202	A	G	9: 59,432,129 (GRCm39)	L66P	probably damaging	Het
Trbc1	G	A	6: 41,516,270 (GRCm39)		probably benign	Het
Trhr2	A	G	8: 123,085,511 (GRCm39)	F158L	probably benign	Het
Ttc13	A	T	8: 125,406,795 (GRCm39)	N595K	probably damaging	Het
Ucp1	A	G	8: 84,024,484 (GRCm39)		probably null	Het
Zbtb4	C	T	11: 69,669,497 (GRCm39)	T740I	probably benign	Het
Zfp69	A	T	4: 120,804,522 (GRCm39)	D116E	possibly damaging	Het
Zfp879	A	G	11: 50,728,796 (GRCm39)	L66S	probably damaging	Het
Zfp955b	T	A	17: 33,524,125 (GRCm39)		probably benign	Het
Zfyve1	T	C	12: 83,594,839 (GRCm39)	I718V	possibly damaging	Het

Other mutations in Dip2a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00422:Dip2a	APN	10	76,149,070 (GRCm39)	missense	probably benign
IGL00849:Dip2a	APN	10	76,128,152 (GRCm39)	missense	probably damaging	0.99
IGL01685:Dip2a	APN	10	76,163,583 (GRCm39)	missense	probably damaging	1.00
IGL01825:Dip2a	APN	10	76,108,514 (GRCm39)	nonsense	probably null
IGL02343:Dip2a	APN	10	76,155,312 (GRCm39)	missense	probably benign	0.00
IGL02437:Dip2a	APN	10	76,134,101 (GRCm39)	missense	probably benign	0.09
IGL02981:Dip2a	APN	10	76,112,255 (GRCm39)	missense	possibly damaging	0.84
IGL03122:Dip2a	APN	10	76,110,880 (GRCm39)	missense	probably benign	0.00
IGL03261:Dip2a	APN	10	76,140,982 (GRCm39)	missense	possibly damaging	0.80
R0369:Dip2a	UTSW	10	76,134,621 (GRCm39)	missense	probably damaging	1.00
R0522:Dip2a	UTSW	10	76,157,365 (GRCm39)	missense	probably benign	0.03
R0962:Dip2a	UTSW	10	76,128,266 (GRCm39)	unclassified	probably benign
R1164:Dip2a	UTSW	10	76,112,231 (GRCm39)	missense	possibly damaging	0.72
R1309:Dip2a	UTSW	10	76,115,610 (GRCm39)	missense	probably damaging	1.00
R1426:Dip2a	UTSW	10	76,115,654 (GRCm39)	unclassified	probably benign
R1636:Dip2a	UTSW	10	76,157,412 (GRCm39)	missense	probably benign	0.01
R1823:Dip2a	UTSW	10	76,114,336 (GRCm39)	nonsense	probably null
R1830:Dip2a	UTSW	10	76,153,797 (GRCm39)	missense	probably damaging	1.00
R1876:Dip2a	UTSW	10	76,153,925 (GRCm39)	missense	probably damaging	1.00
R2284:Dip2a	UTSW	10	76,149,027 (GRCm39)	missense	probably benign	0.01
R2369:Dip2a	UTSW	10	76,149,030 (GRCm39)	missense	probably benign
R4050:Dip2a	UTSW	10	76,114,441 (GRCm39)	missense	probably damaging	1.00
R4089:Dip2a	UTSW	10	76,114,323 (GRCm39)	splice site	probably null
R4231:Dip2a	UTSW	10	76,155,304 (GRCm39)	missense	probably damaging	1.00
R4715:Dip2a	UTSW	10	76,132,240 (GRCm39)	missense	probably benign	0.34
R4752:Dip2a	UTSW	10	76,112,491 (GRCm39)	missense	probably damaging	1.00
R4846:Dip2a	UTSW	10	76,157,327 (GRCm39)	missense	probably damaging	1.00
R4849:Dip2a	UTSW	10	76,130,367 (GRCm39)	missense	probably damaging	1.00
R4892:Dip2a	UTSW	10	76,116,593 (GRCm39)	missense	probably benign	0.02
R5068:Dip2a	UTSW	10	76,153,877 (GRCm39)	missense	possibly damaging	0.82
R5141:Dip2a	UTSW	10	76,106,287 (GRCm39)	missense	probably damaging	1.00
R5253:Dip2a	UTSW	10	76,135,831 (GRCm39)	missense	probably damaging	1.00
R5304:Dip2a	UTSW	10	76,130,357 (GRCm39)	missense	possibly damaging	0.67
R5324:Dip2a	UTSW	10	76,132,227 (GRCm39)	missense	probably damaging	1.00
R5369:Dip2a	UTSW	10	76,128,194 (GRCm39)	missense	probably damaging	1.00
R6272:Dip2a	UTSW	10	76,122,241 (GRCm39)	makesense	probably null
R6884:Dip2a	UTSW	10	76,108,366 (GRCm39)	critical splice donor site	probably null
R7143:Dip2a	UTSW	10	76,133,625 (GRCm39)	missense	probably damaging	1.00
R7247:Dip2a	UTSW	10	76,108,366 (GRCm39)	critical splice donor site	probably null
R7252:Dip2a	UTSW	10	76,109,036 (GRCm39)	missense	not run
R7327:Dip2a	UTSW	10	76,108,396 (GRCm39)	missense	probably benign	0.41
R7334:Dip2a	UTSW	10	76,110,080 (GRCm39)	missense	possibly damaging	0.91
R7349:Dip2a	UTSW	10	76,121,426 (GRCm39)	missense	probably damaging	1.00
R7360:Dip2a	UTSW	10	76,114,394 (GRCm39)	missense	probably damaging	1.00
R7513:Dip2a	UTSW	10	76,149,069 (GRCm39)	missense	probably benign
R7793:Dip2a	UTSW	10	76,114,417 (GRCm39)	missense	probably benign	0.06
R7794:Dip2a	UTSW	10	76,112,459 (GRCm39)	missense	probably damaging	1.00
R7819:Dip2a	UTSW	10	76,126,862 (GRCm39)	missense	probably benign	0.06
R8079:Dip2a	UTSW	10	76,123,155 (GRCm39)	missense	probably benign
R8280:Dip2a	UTSW	10	76,100,610 (GRCm39)	missense	possibly damaging	0.75
R8281:Dip2a	UTSW	10	76,112,438 (GRCm39)	missense	probably damaging	1.00
R8286:Dip2a	UTSW	10	76,122,297 (GRCm39)	missense	probably benign
R8350:Dip2a	UTSW	10	76,100,690 (GRCm39)	missense	probably damaging	1.00
R8450:Dip2a	UTSW	10	76,100,690 (GRCm39)	missense	probably damaging	1.00
R8525:Dip2a	UTSW	10	76,110,115 (GRCm39)	critical splice acceptor site	probably null
R8824:Dip2a	UTSW	10	76,114,320 (GRCm39)	critical splice donor site	probably null
R8897:Dip2a	UTSW	10	76,110,098 (GRCm39)	missense	probably benign	0.22
R9039:Dip2a	UTSW	10	76,163,553 (GRCm39)	missense	probably benign	0.00
R9286:Dip2a	UTSW	10	76,138,096 (GRCm39)	missense	probably benign	0.05
R9504:Dip2a	UTSW	10	76,132,189 (GRCm39)	missense	probably damaging	1.00
R9523:Dip2a	UTSW	10	76,112,438 (GRCm39)	missense	probably damaging	1.00
R9628:Dip2a	UTSW	10	76,142,993 (GRCm39)	missense	probably damaging	0.99
R9732:Dip2a	UTSW	10	76,110,077 (GRCm39)	missense	probably benign	0.11
Z1088:Dip2a	UTSW	10	76,121,462 (GRCm39)	missense	probably benign	0.06
Z1176:Dip2a	UTSW	10	76,116,654 (GRCm39)	missense	probably damaging	0.97
Z1176:Dip2a	UTSW	10	76,102,157 (GRCm39)	missense	possibly damaging	0.94
Z1177:Dip2a	UTSW	10	76,132,234 (GRCm39)	missense	probably damaging	1.00
Z1177:Dip2a	UTSW	10	76,102,156 (GRCm39)	missense	possibly damaging	0.51

Predicted Primers

PCR Primer
(F):5'- AAACCTGTACCATGGACTATAAAGG -3'
(R):5'- GTTCAAAAGTTGAGTCCTCAGG -3'

Sequencing Primer
(F):5'- AATACCTGGAGGCGTGTA -3'
(R):5'- TTCAAAAGTTGAGTCCTCAGGCAAAG -3'

Posted On

2016-06-06