Mutagenetix > Incidental Mutation

Incidental Mutation 'R1766:Nrap'

194426

Institutional Source

Beutler Lab

Gene Symbol

Nrap

Ensembl Gene

ENSMUSG00000049134

Gene Name

nebulin-related anchoring protein

Synonyms

MMRRC Submission

039798-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1766 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

56308473-56378466 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 56323474 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 1366 (H1366L)

Ref Sequence

ENSEMBL: ENSMUSP00000128196 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040711] [ENSMUST00000073536] [ENSMUST00000095947] [ENSMUST00000166203] [ENSMUST00000167239]

AlphaFold

Q80XB4

Predicted Effect

possibly damaging
Transcript: ENSMUST00000040711
AA Change: H1366L

PolyPhen 2 Score 0.897 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000048364
Gene: ENSMUSG00000049134
AA Change: H1366L

Domain	Start	End	E-Value	Type
LIM	5	57	5.39e-11	SMART
NEBU	64	94	2.17e1	SMART
NEBU	168	197	1.94e-4	SMART
NEBU	202	232	1.39e-5	SMART
NEBU	239	268	2.23e-4	SMART
NEBU	308	337	2.83e-6	SMART
NEBU	346	376	3.82e-3	SMART
NEBU	382	412	1.18e-3	SMART
NEBU	450	480	8.97e-9	SMART
NEBU	485	515	1.73e-10	SMART
NEBU	521	551	8.12e-7	SMART
NEBU	555	585	1.73e-1	SMART
NEBU	590	620	2.33e-7	SMART
NEBU	621	651	1.49e-5	SMART
NEBU	655	686	5.12e-4	SMART
NEBU	689	719	8.12e-7	SMART
NEBU	724	754	2.64e-6	SMART
NEBU	760	790	3.48e-6	SMART
NEBU	798	828	2.35e-3	SMART
NEBU	833	863	6.11e-2	SMART
NEBU	864	894	1.69e-4	SMART
NEBU	899	929	3.88e-4	SMART
NEBU	932	962	4e-6	SMART
NEBU	967	997	4.22e-5	SMART
NEBU	1003	1033	2.64e-6	SMART
NEBU	1041	1071	3.68e-5	SMART
NEBU	1076	1106	4.16e-4	SMART
NEBU	1107	1137	1.1e-3	SMART
NEBU	1142	1172	1.68e1	SMART
NEBU	1175	1205	4.59e-6	SMART
NEBU	1210	1240	4.06e-7	SMART
NEBU	1246	1276	1.99e-1	SMART
NEBU	1284	1314	1.85e-1	SMART
NEBU	1319	1349	1.39e-5	SMART
NEBU	1350	1380	4.03e-2	SMART
NEBU	1385	1415	1.76e-2	SMART
NEBU	1418	1448	2.09e0	SMART
NEBU	1453	1483	6.4e-5	SMART
NEBU	1489	1519	8.63e-1	SMART
NEBU	1527	1557	1.33e-2	SMART
NEBU	1562	1592	1.84e-5	SMART
NEBU	1593	1623	7.24e-4	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000073536
AA Change: H1401L

PolyPhen 2 Score 0.834 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000073228
Gene: ENSMUSG00000049134
AA Change: H1401L

Domain	Start	End	E-Value	Type
LIM	5	57	5.39e-11	SMART
NEBU	64	94	2.17e1	SMART
NEBU	168	197	1.94e-4	SMART
NEBU	202	232	1.39e-5	SMART
NEBU	239	268	2.23e-4	SMART
NEBU	308	337	2.83e-6	SMART
NEBU	346	376	7.24e-4	SMART
NEBU	381	411	3.46e-1	SMART
NEBU	417	447	1.18e-3	SMART
NEBU	485	515	8.97e-9	SMART
NEBU	520	550	1.73e-10	SMART
NEBU	556	586	8.12e-7	SMART
NEBU	590	620	1.73e-1	SMART
NEBU	625	655	2.33e-7	SMART
NEBU	656	686	1.49e-5	SMART
NEBU	690	721	5.12e-4	SMART
NEBU	724	754	8.12e-7	SMART
NEBU	759	789	2.64e-6	SMART
NEBU	795	825	3.48e-6	SMART
NEBU	833	863	2.35e-3	SMART
NEBU	868	898	6.11e-2	SMART
NEBU	899	929	1.69e-4	SMART
NEBU	934	964	3.88e-4	SMART
NEBU	967	997	4e-6	SMART
NEBU	1002	1032	4.22e-5	SMART
NEBU	1038	1068	2.64e-6	SMART
NEBU	1076	1106	3.68e-5	SMART
NEBU	1111	1141	4.16e-4	SMART
NEBU	1142	1172	1.1e-3	SMART
NEBU	1177	1207	1.68e1	SMART
NEBU	1210	1240	4.59e-6	SMART
NEBU	1245	1275	4.06e-7	SMART
NEBU	1281	1311	1.99e-1	SMART
NEBU	1319	1349	1.85e-1	SMART
NEBU	1354	1384	1.39e-5	SMART
NEBU	1385	1415	4.03e-2	SMART
NEBU	1420	1450	1.76e-2	SMART
NEBU	1453	1483	2.09e0	SMART
NEBU	1488	1518	6.4e-5	SMART
NEBU	1524	1554	8.63e-1	SMART
NEBU	1562	1592	1.33e-2	SMART
NEBU	1597	1627	1.84e-5	SMART
NEBU	1628	1658	7.24e-4	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000095947
AA Change: H1284L

PolyPhen 2 Score 0.897 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000093640
Gene: ENSMUSG00000049134
AA Change: H1284L

Domain	Start	End	E-Value	Type
NEBU	86	115	1.2e-6	SMART
NEBU	120	150	9.1e-8	SMART
NEBU	157	186	1.4e-6	SMART
NEBU	226	255	1.8e-8	SMART
NEBU	264	294	2.5e-5	SMART
NEBU	300	330	7.8e-6	SMART
NEBU	368	398	6e-11	SMART
NEBU	403	433	1.1e-12	SMART
NEBU	439	469	5.2e-9	SMART
NEBU	473	503	1.1e-3	SMART
NEBU	508	538	1.5e-9	SMART
NEBU	539	569	1e-7	SMART
NEBU	573	604	3.3e-6	SMART
NEBU	607	637	5.4e-9	SMART
NEBU	642	672	1.7e-8	SMART
NEBU	678	708	2.3e-8	SMART
NEBU	716	746	1.5e-5	SMART
NEBU	751	781	4.1e-4	SMART
NEBU	782	812	1.1e-6	SMART
NEBU	817	847	2.6e-6	SMART
NEBU	850	880	2.6e-8	SMART
NEBU	885	915	2.7e-7	SMART
NEBU	921	951	1.7e-8	SMART
NEBU	959	989	2.4e-7	SMART
NEBU	994	1024	2.7e-6	SMART
NEBU	1025	1055	7.2e-6	SMART
NEBU	1060	1090	1.1e-1	SMART
NEBU	1093	1123	3e-8	SMART
NEBU	1128	1158	2.6e-9	SMART
NEBU	1164	1194	1.3e-3	SMART
NEBU	1202	1232	1.2e-3	SMART
NEBU	1237	1267	8.8e-8	SMART
NEBU	1268	1298	2.7e-4	SMART
NEBU	1303	1333	1.2e-4	SMART
NEBU	1336	1366	1.4e-2	SMART
NEBU	1371	1401	4.3e-7	SMART
NEBU	1407	1437	5.6e-3	SMART
NEBU	1445	1475	8.8e-5	SMART
NEBU	1480	1510	1.2e-7	SMART
NEBU	1511	1541	4.8e-6	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000166203
AA Change: H1365L

PolyPhen 2 Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000132582
Gene: ENSMUSG00000049134
AA Change: H1365L

Domain	Start	End	E-Value	Type
LIM	5	57	5.39e-11	SMART
NEBU	64	94	2.17e1	SMART
NEBU	168	197	1.94e-4	SMART
NEBU	202	232	1.39e-5	SMART
NEBU	239	268	2.23e-4	SMART
NEBU	308	337	2.83e-6	SMART
NEBU	346	376	7.24e-4	SMART
NEBU	381	411	3.46e-1	SMART
NEBU	417	447	1.18e-3	SMART
NEBU	485	515	8.97e-9	SMART
NEBU	520	550	1.06e-10	SMART
NEBU	554	584	1.73e-1	SMART
NEBU	589	619	2.33e-7	SMART
NEBU	620	650	1.49e-5	SMART
NEBU	654	685	5.12e-4	SMART
NEBU	688	718	8.12e-7	SMART
NEBU	723	753	2.64e-6	SMART
NEBU	759	789	3.48e-6	SMART
NEBU	797	827	2.35e-3	SMART
NEBU	832	862	6.11e-2	SMART
NEBU	863	893	1.69e-4	SMART
NEBU	898	928	3.88e-4	SMART
NEBU	931	961	4e-6	SMART
NEBU	966	996	4.22e-5	SMART
NEBU	1002	1032	2.64e-6	SMART
NEBU	1040	1070	3.68e-5	SMART
NEBU	1075	1105	4.16e-4	SMART
NEBU	1106	1136	1.1e-3	SMART
NEBU	1141	1171	1.68e1	SMART
NEBU	1174	1204	4.59e-6	SMART
NEBU	1209	1239	4.06e-7	SMART
NEBU	1245	1275	1.99e-1	SMART
NEBU	1283	1313	1.85e-1	SMART
NEBU	1318	1348	1.39e-5	SMART
NEBU	1349	1379	4.03e-2	SMART
NEBU	1384	1414	1.76e-2	SMART
NEBU	1417	1447	2.09e0	SMART
NEBU	1452	1482	6.4e-5	SMART
NEBU	1488	1518	8.63e-1	SMART
NEBU	1526	1556	1.33e-2	SMART
NEBU	1561	1591	1.84e-5	SMART
NEBU	1592	1622	7.24e-4	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000167239
AA Change: H1366L

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000128196
Gene: ENSMUSG00000049134
AA Change: H1366L

Domain	Start	End	E-Value	Type
LIM	5	57	5.39e-11	SMART
NEBU	64	94	2.17e1	SMART
NEBU	168	197	1.94e-4	SMART
NEBU	202	232	1.39e-5	SMART
NEBU	239	268	2.23e-4	SMART
NEBU	308	337	2.83e-6	SMART
NEBU	346	376	3.82e-3	SMART
NEBU	382	412	1.18e-3	SMART
NEBU	450	480	8.97e-9	SMART
NEBU	485	515	1.73e-10	SMART
NEBU	521	551	8.12e-7	SMART
NEBU	555	585	1.73e-1	SMART
NEBU	590	620	2.33e-7	SMART
NEBU	621	651	1.49e-5	SMART
NEBU	655	686	5.12e-4	SMART
NEBU	689	719	8.12e-7	SMART
NEBU	724	754	2.64e-6	SMART
NEBU	760	790	3.48e-6	SMART
NEBU	798	828	2.35e-3	SMART
NEBU	833	863	6.11e-2	SMART
NEBU	864	894	1.69e-4	SMART
NEBU	899	929	3.88e-4	SMART
NEBU	932	962	4e-6	SMART
NEBU	967	997	4.22e-5	SMART
NEBU	1003	1033	2.64e-6	SMART
NEBU	1041	1071	3.68e-5	SMART
NEBU	1076	1106	4.16e-4	SMART
NEBU	1107	1137	1.1e-3	SMART
NEBU	1142	1172	1.68e1	SMART
NEBU	1175	1205	4.59e-6	SMART
NEBU	1210	1240	4.06e-7	SMART
NEBU	1246	1276	1.99e-1	SMART
NEBU	1284	1314	1.85e-1	SMART
NEBU	1319	1349	1.39e-5	SMART
NEBU	1350	1380	4.03e-2	SMART
NEBU	1385	1415	3.06e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000169099

SMART Domains

Protein: ENSMUSP00000125889
Gene: ENSMUSG00000049134

Domain	Start	End	E-Value	Type
NEBU	32	61	2.83e-6	SMART
NEBU	70	100	7.24e-4	SMART
NEBU	105	135	3.46e-1	SMART
NEBU	141	171	1.18e-3	SMART
NEBU	209	239	8.97e-9	SMART
NEBU	244	274	1.73e-10	SMART
NEBU	280	310	8.12e-7	SMART
NEBU	314	344	1.73e-1	SMART

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.3%
20x: 92.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Afg1l	T	C	10: 42,330,491 (GRCm39)	T59A	probably benign	Het
Ankrd17	T	A	5: 90,412,656 (GRCm39)	M1223L	possibly damaging	Het
Ankrd24	G	A	10: 81,474,472 (GRCm39)	S68N	probably benign	Het
Arhgap31	A	G	16: 38,445,952 (GRCm39)	I131T	probably damaging	Het
Arhgef10	A	T	8: 15,029,836 (GRCm39)	I874F	probably damaging	Het
Arl5b	T	C	2: 15,074,648 (GRCm39)	V43A	probably benign	Het
BC051665	G	A	13: 60,932,854 (GRCm39)	H36Y	probably benign	Het
Cdh9	A	G	15: 16,778,392 (GRCm39)	D69G	probably damaging	Het
Chd6	G	A	2: 160,808,559 (GRCm39)	L1552F	probably damaging	Het
Chrd	A	G	16: 20,556,191 (GRCm39)	H584R	probably damaging	Het
Dnhd1	G	A	7: 105,343,179 (GRCm39)	V1508I	possibly damaging	Het
Dpy19l4	C	T	4: 11,303,360 (GRCm39)	G187D	probably damaging	Het
Dync2h1	T	C	9: 7,015,526 (GRCm39)		probably null	Het
Ehbp1l1	A	G	19: 5,766,434 (GRCm39)	V1303A	probably damaging	Het
Eif4e1b	G	A	13: 54,934,704 (GRCm39)	E182K	probably damaging	Het
Fam170b	A	T	14: 32,557,843 (GRCm39)	Q226L	possibly damaging	Het
Fam193a	C	T	5: 34,619,475 (GRCm39)	P760L	probably damaging	Het
Gabra5	A	T	7: 57,157,796 (GRCm39)	L6H	probably benign	Het
Gabrq	G	A	X: 71,876,989 (GRCm39)	R161H	probably damaging	Het
Gm10608	CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	9: 118,989,784 (GRCm39)		probably null	Het
Gm7334	T	A	17: 51,006,006 (GRCm39)	D97E	probably damaging	Het
Gpsm1	G	A	2: 26,215,395 (GRCm39)	A286T	probably damaging	Het
Gsta4	C	A	9: 78,111,611 (GRCm39)	Y79*	probably null	Het
Hcn1	T	A	13: 117,793,270 (GRCm39)	V174D	probably benign	Het
Hic1	G	T	11: 75,056,620 (GRCm39)	C756*	probably null	Het
Hivep3	C	T	4: 119,953,868 (GRCm39)	T728I	probably benign	Het
Ice1	T	C	13: 70,752,561 (GRCm39)	E1175G	possibly damaging	Het
Igsf3	T	A	3: 101,338,598 (GRCm39)	L304Q	probably damaging	Het
Kpna6	T	C	4: 129,551,235 (GRCm39)	D90G	probably benign	Het
Krt73	C	T	15: 101,702,363 (GRCm39)	G500D	probably damaging	Het
Lama3	A	G	18: 12,535,119 (GRCm39)	K156E	probably damaging	Het
Mdm2	T	C	10: 117,531,927 (GRCm39)	K94E	probably damaging	Het
Mitf	T	C	6: 97,918,060 (GRCm39)	S26P	probably damaging	Het
Myh4	C	A	11: 67,147,121 (GRCm39)	Q1589K	possibly damaging	Het
Nlrp4c	T	A	7: 6,076,113 (GRCm39)	V671E	probably benign	Het
Nop9	C	T	14: 55,989,591 (GRCm39)	A407V	possibly damaging	Het
Ntrk1	A	T	3: 87,685,825 (GRCm39)	C766S	probably damaging	Het
Oog3	C	T	4: 143,885,692 (GRCm39)	G302D	possibly damaging	Het
Or4q3	T	C	14: 50,583,677 (GRCm39)	Y43C	probably damaging	Het
Or52z15	A	G	7: 103,332,068 (GRCm39)	N38D	possibly damaging	Het
Or6c38	T	C	10: 128,929,616 (GRCm39)	I76V	probably benign	Het
Or7g27	A	G	9: 19,250,154 (GRCm39)	T133A	probably benign	Het
Pdzph1	C	T	17: 59,280,747 (GRCm39)	V512I	probably benign	Het
Phf2	A	C	13: 48,973,033 (GRCm39)	S408A	unknown	Het
Pigk	T	G	3: 152,445,793 (GRCm39)	L135V	probably damaging	Het
Ppp2ca	C	A	11: 52,012,773 (GRCm39)	T301N	probably benign	Het
Ppp4r3a	A	G	12: 101,024,741 (GRCm39)	S253P	probably damaging	Het
Ptgfrn	A	T	3: 100,957,438 (GRCm39)	I712N	probably benign	Het
Rapgef2	A	T	3: 79,000,010 (GRCm39)	D579E	probably damaging	Het
Rims2	T	A	15: 39,325,976 (GRCm39)	D769E	probably damaging	Het
Rptor	T	A	11: 119,615,887 (GRCm39)	C134S	probably damaging	Het
S100a1	A	G	3: 90,418,599 (GRCm39)	F72L	probably damaging	Het
Scube1	T	A	15: 83,606,146 (GRCm39)	D42V	probably damaging	Het
Sh3glb1	T	C	3: 144,418,446 (GRCm39)	D39G	probably damaging	Het
Sh3pxd2a	T	C	19: 47,261,689 (GRCm39)	T397A	probably benign	Het
Siglece	G	A	7: 43,300,956 (GRCm39)	T453M	probably damaging	Het
Slc26a1	G	A	5: 108,819,658 (GRCm39)	R514W	probably damaging	Het
Slc4a8	T	C	15: 100,685,093 (GRCm39)	V156A	probably benign	Het
Smchd1	A	T	17: 71,698,374 (GRCm39)	V1134E	probably damaging	Het
Sorbs2	A	G	8: 46,223,613 (GRCm39)	Y222C	probably damaging	Het
Sorcs3	G	T	19: 48,592,314 (GRCm39)	W326C	possibly damaging	Het
Taf2	A	G	15: 54,934,793 (GRCm39)	V45A	probably benign	Het
Tex16	T	C	X: 111,150,782 (GRCm39)	Y22H	probably benign	Het
Tiparp	A	T	3: 65,439,470 (GRCm39)	H80L	probably damaging	Het
Tmem71	T	A	15: 66,413,548 (GRCm39)	T175S	probably benign	Het
Tmem87b	T	A	2: 128,681,090 (GRCm39)	V338D	probably damaging	Het
Trdn	A	G	10: 33,240,004 (GRCm39)	K445R	probably damaging	Het
Trim14	A	G	4: 46,522,039 (GRCm39)	F213L	probably benign	Het
Tubgcp5	T	A	7: 55,464,768 (GRCm39)	S550T	probably benign	Het
Tufm	A	G	7: 126,089,644 (GRCm39)	D446G	probably benign	Het
Vipr1	A	T	9: 121,490,485 (GRCm39)	Y177F	possibly damaging	Het
Vmn2r116	A	C	17: 23,620,740 (GRCm39)	I825L	probably damaging	Het
Vmn2r12	G	T	5: 109,239,910 (GRCm39)	Q218K	probably damaging	Het
Vwa7	G	T	17: 35,242,919 (GRCm39)		probably null	Het
Ywhae	T	C	11: 75,646,491 (GRCm39)	V119A	probably damaging	Het
Zfand5	A	G	19: 21,257,888 (GRCm39)	R199G	probably damaging	Het
Zfp810	T	C	9: 22,189,828 (GRCm39)	Y360C	possibly damaging	Het
Zrsr2-ps1	A	G	11: 22,923,637 (GRCm39)	D137G	probably benign	Het

Other mutations in Nrap

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00500:Nrap	APN	19	56,361,341 (GRCm39)	missense	probably damaging	1.00
IGL00570:Nrap	APN	19	56,326,545 (GRCm39)	missense	probably benign	0.10
IGL00946:Nrap	APN	19	56,329,058 (GRCm39)	splice site	probably null
IGL01070:Nrap	APN	19	56,317,516 (GRCm39)	missense	probably damaging	1.00
IGL01111:Nrap	APN	19	56,333,990 (GRCm39)	missense	probably damaging	1.00
IGL01138:Nrap	APN	19	56,343,970 (GRCm39)	missense	probably damaging	1.00
IGL01290:Nrap	APN	19	56,350,180 (GRCm39)	missense	probably damaging	1.00
IGL01352:Nrap	APN	19	56,368,268 (GRCm39)	missense	probably benign	0.00
IGL01372:Nrap	APN	19	56,317,534 (GRCm39)	critical splice acceptor site	probably null
IGL01395:Nrap	APN	19	56,350,225 (GRCm39)	missense	probably damaging	1.00
IGL01413:Nrap	APN	19	56,377,823 (GRCm39)	missense	probably damaging	0.99
IGL01734:Nrap	APN	19	56,338,741 (GRCm39)	missense	probably damaging	1.00
IGL01933:Nrap	APN	19	56,377,250 (GRCm39)	missense	probably damaging	1.00
IGL02156:Nrap	APN	19	56,309,432 (GRCm39)	missense	probably damaging	1.00
IGL02415:Nrap	APN	19	56,370,741 (GRCm39)	missense	probably damaging	1.00
IGL02447:Nrap	APN	19	56,333,951 (GRCm39)	nonsense	probably null
IGL02864:Nrap	APN	19	56,338,806 (GRCm39)	missense	probably damaging	1.00
IGL02993:Nrap	APN	19	56,333,965 (GRCm39)	missense	probably damaging	1.00
IGL03003:Nrap	APN	19	56,310,384 (GRCm39)	missense	probably damaging	1.00
IGL03006:Nrap	APN	19	56,335,596 (GRCm39)	missense	probably benign	0.02
IGL03084:Nrap	APN	19	56,353,886 (GRCm39)	missense	probably damaging	1.00
IGL03136:Nrap	APN	19	56,330,687 (GRCm39)	missense	possibly damaging	0.69
IGL03272:Nrap	APN	19	56,334,000 (GRCm39)	intron	probably benign
IGL03389:Nrap	APN	19	56,340,148 (GRCm39)	missense	probably benign	0.10
R0116:Nrap	UTSW	19	56,343,978 (GRCm39)	missense	probably damaging	1.00
R0374:Nrap	UTSW	19	56,340,054 (GRCm39)	missense	probably damaging	1.00
R0715:Nrap	UTSW	19	56,345,757 (GRCm39)	missense	probably damaging	0.98
R0828:Nrap	UTSW	19	56,333,990 (GRCm39)	missense	probably damaging	1.00
R0883:Nrap	UTSW	19	56,333,906 (GRCm39)	missense	probably damaging	1.00
R1416:Nrap	UTSW	19	56,315,725 (GRCm39)	missense	possibly damaging	0.60
R1459:Nrap	UTSW	19	56,372,562 (GRCm39)	missense	probably benign	0.00
R1616:Nrap	UTSW	19	56,378,255 (GRCm39)	missense	probably damaging	1.00
R1676:Nrap	UTSW	19	56,323,687 (GRCm39)	missense	probably damaging	1.00
R1687:Nrap	UTSW	19	56,343,961 (GRCm39)	missense	probably damaging	0.99
R1792:Nrap	UTSW	19	56,367,590 (GRCm39)	missense	probably benign	0.00
R1817:Nrap	UTSW	19	56,372,487 (GRCm39)	unclassified	probably benign
R1972:Nrap	UTSW	19	56,345,785 (GRCm39)	missense	probably damaging	1.00
R1982:Nrap	UTSW	19	56,372,537 (GRCm39)	missense	probably damaging	0.99
R2258:Nrap	UTSW	19	56,310,394 (GRCm39)	missense	possibly damaging	0.80
R2448:Nrap	UTSW	19	56,310,462 (GRCm39)	missense	possibly damaging	0.90
R3034:Nrap	UTSW	19	56,352,437 (GRCm39)	missense	probably damaging	1.00
R3801:Nrap	UTSW	19	56,310,211 (GRCm39)	missense	probably damaging	1.00
R3804:Nrap	UTSW	19	56,310,211 (GRCm39)	missense	probably damaging	1.00
R3923:Nrap	UTSW	19	56,368,688 (GRCm39)	missense	probably damaging	0.99
R3964:Nrap	UTSW	19	56,330,576 (GRCm39)	missense	probably damaging	1.00
R3965:Nrap	UTSW	19	56,330,576 (GRCm39)	missense	probably damaging	1.00
R3966:Nrap	UTSW	19	56,330,576 (GRCm39)	missense	probably damaging	1.00
R3980:Nrap	UTSW	19	56,369,984 (GRCm39)	missense	probably benign	0.01
R4182:Nrap	UTSW	19	56,338,759 (GRCm39)	missense	probably damaging	1.00
R4499:Nrap	UTSW	19	56,339,913 (GRCm39)	missense	probably damaging	0.97
R4573:Nrap	UTSW	19	56,330,770 (GRCm39)	critical splice acceptor site	probably null
R4603:Nrap	UTSW	19	56,323,456 (GRCm39)	critical splice donor site	probably null
R4689:Nrap	UTSW	19	56,374,458 (GRCm39)	missense	probably damaging	0.97
R4749:Nrap	UTSW	19	56,368,669 (GRCm39)	missense	probably damaging	0.96
R4845:Nrap	UTSW	19	56,339,902 (GRCm39)	missense	probably benign	0.16
R4937:Nrap	UTSW	19	56,335,652 (GRCm39)	missense	probably damaging	1.00
R4962:Nrap	UTSW	19	56,366,575 (GRCm39)	missense	probably damaging	1.00
R5156:Nrap	UTSW	19	56,360,277 (GRCm39)	missense	possibly damaging	0.94
R5181:Nrap	UTSW	19	56,333,960 (GRCm39)	missense	possibly damaging	0.85
R5202:Nrap	UTSW	19	56,323,583 (GRCm39)	missense	probably damaging	1.00
R5262:Nrap	UTSW	19	56,308,655 (GRCm39)	missense	possibly damaging	0.95
R5301:Nrap	UTSW	19	56,367,541 (GRCm39)	missense	probably damaging	1.00
R5380:Nrap	UTSW	19	56,370,035 (GRCm39)	missense	probably damaging	1.00
R5576:Nrap	UTSW	19	56,310,414 (GRCm39)	missense	probably damaging	0.99
R5631:Nrap	UTSW	19	56,342,553 (GRCm39)	missense	probably benign	0.19
R5754:Nrap	UTSW	19	56,377,916 (GRCm39)	missense	possibly damaging	0.55
R5799:Nrap	UTSW	19	56,330,601 (GRCm39)	nonsense	probably null
R5899:Nrap	UTSW	19	56,329,006 (GRCm39)	missense	possibly damaging	0.80
R5910:Nrap	UTSW	19	56,330,743 (GRCm39)	missense	probably benign	0.00
R5994:Nrap	UTSW	19	56,340,031 (GRCm39)	nonsense	probably null
R6124:Nrap	UTSW	19	56,374,458 (GRCm39)	missense	probably damaging	0.97
R6149:Nrap	UTSW	19	56,377,885 (GRCm39)	missense	possibly damaging	0.79
R6182:Nrap	UTSW	19	56,350,130 (GRCm39)	missense	probably benign
R6245:Nrap	UTSW	19	56,368,307 (GRCm39)	missense	possibly damaging	0.80
R6245:Nrap	UTSW	19	56,342,653 (GRCm39)	missense	probably damaging	1.00
R6270:Nrap	UTSW	19	56,308,630 (GRCm39)	missense	probably benign	0.00
R6274:Nrap	UTSW	19	56,350,153 (GRCm39)	missense	probably benign	0.21
R6340:Nrap	UTSW	19	56,335,616 (GRCm39)	missense	probably damaging	1.00
R6547:Nrap	UTSW	19	56,339,998 (GRCm39)	missense	probably benign	0.00
R6734:Nrap	UTSW	19	56,333,941 (GRCm39)	missense	probably damaging	0.99
R6770:Nrap	UTSW	19	56,370,969 (GRCm39)	splice site	probably null
R6812:Nrap	UTSW	19	56,340,108 (GRCm39)	missense	probably damaging	1.00
R6843:Nrap	UTSW	19	56,368,651 (GRCm39)	missense	probably damaging	1.00
R7207:Nrap	UTSW	19	56,333,953 (GRCm39)	missense	probably damaging	1.00
R7214:Nrap	UTSW	19	56,366,567 (GRCm39)	missense	probably benign	0.09
R7313:Nrap	UTSW	19	56,330,700 (GRCm39)	missense	probably damaging	0.97
R7515:Nrap	UTSW	19	56,354,859 (GRCm39)	missense	possibly damaging	0.94
R7662:Nrap	UTSW	19	56,308,715 (GRCm39)	missense	probably benign	0.00
R7819:Nrap	UTSW	19	56,323,720 (GRCm39)	missense	probably benign
R7836:Nrap	UTSW	19	56,338,729 (GRCm39)	missense	probably benign	0.00
R7895:Nrap	UTSW	19	56,342,584 (GRCm39)	missense	probably benign	0.00
R8041:Nrap	UTSW	19	56,352,768 (GRCm39)	nonsense	probably null
R8046:Nrap	UTSW	19	56,308,683 (GRCm39)	missense	possibly damaging	0.46
R8066:Nrap	UTSW	19	56,342,562 (GRCm39)	missense	possibly damaging	0.94
R8129:Nrap	UTSW	19	56,355,068 (GRCm39)	splice site	probably null
R8188:Nrap	UTSW	19	56,325,010 (GRCm39)	nonsense	probably null
R8323:Nrap	UTSW	19	56,378,255 (GRCm39)	missense	probably benign	0.00
R8353:Nrap	UTSW	19	56,312,352 (GRCm39)	missense	probably damaging	1.00
R8453:Nrap	UTSW	19	56,312,352 (GRCm39)	missense	probably damaging	1.00
R8693:Nrap	UTSW	19	56,310,384 (GRCm39)	missense	probably damaging	1.00
R8703:Nrap	UTSW	19	56,323,703 (GRCm39)	missense	probably damaging	1.00
R8810:Nrap	UTSW	19	56,352,843 (GRCm39)	critical splice acceptor site	probably benign
R8872:Nrap	UTSW	19	56,308,627 (GRCm39)	makesense	probably null
R8980:Nrap	UTSW	19	56,343,970 (GRCm39)	missense	probably damaging	1.00
R9201:Nrap	UTSW	19	56,340,093 (GRCm39)	missense	probably damaging	1.00
R9229:Nrap	UTSW	19	56,310,339 (GRCm39)	missense	probably benign	0.01
R9235:Nrap	UTSW	19	56,330,760 (GRCm39)	nonsense	probably null
R9323:Nrap	UTSW	19	56,378,255 (GRCm39)	missense	probably benign	0.00
R9327:Nrap	UTSW	19	56,340,100 (GRCm39)	missense	probably benign	0.25
R9329:Nrap	UTSW	19	56,350,277 (GRCm39)	missense	probably damaging	1.00
R9468:Nrap	UTSW	19	56,330,632 (GRCm39)	missense	possibly damaging	0.52
R9517:Nrap	UTSW	19	56,360,277 (GRCm39)	missense	probably benign	0.00
R9639:Nrap	UTSW	19	56,333,948 (GRCm39)	missense	possibly damaging	0.63
R9657:Nrap	UTSW	19	56,352,377 (GRCm39)	missense	probably benign	0.27
R9709:Nrap	UTSW	19	56,317,453 (GRCm39)	missense	probably benign	0.08
R9709:Nrap	UTSW	19	56,317,452 (GRCm39)	missense	probably damaging	0.98
X0028:Nrap	UTSW	19	56,323,652 (GRCm39)	nonsense	probably null
Z1176:Nrap	UTSW	19	56,333,949 (GRCm39)	frame shift	probably null
Z1177:Nrap	UTSW	19	56,333,196 (GRCm39)	missense	probably benign	0.01
Z1177:Nrap	UTSW	19	56,326,524 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTGCACAAGCATGGGGCATGAC -3'
(R):5'- AAGGAGCGTGGACAGCTCATTG -3'

Sequencing Primer
(F):5'- gaaacgacctgacatctgaac -3'
(R):5'- TACTGCACTGCCTACGGATG -3'

Posted On

2014-05-23