Incidental Mutation 'R1401:Srcap'
ID 160131
Institutional Source Beutler Lab
Gene Symbol Srcap
Ensembl Gene ENSMUSG00000053877
Gene Name Snf2-related CREBBP activator protein
Synonyms D030022P06Rik, B930091H02Rik, F630004O05Rik
MMRRC Submission 039463-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.960) question?
Stock # R1401 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 127111155-127160391 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 127159124 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000084563] [ENSMUST00000186954] [ENSMUST00000187040] [ENSMUST00000189629] [ENSMUST00000190278] [ENSMUST00000190390]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000084563
SMART Domains Protein: ENSMUSP00000081611
Gene: ENSMUSG00000106715

DomainStartEndE-ValueType
low complexity region 2 29 N/A INTRINSIC
AT_hook 62 74 4.04e0 SMART
low complexity region 114 134 N/A INTRINSIC
AT_hook 142 154 4.46e-1 SMART
low complexity region 155 166 N/A INTRINSIC
low complexity region 175 202 N/A INTRINSIC
AT_hook 206 218 3.94e-1 SMART
low complexity region 251 262 N/A INTRINSIC
low complexity region 263 273 N/A INTRINSIC
low complexity region 360 396 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000186954
AA Change: I2843T
SMART Domains Protein: ENSMUSP00000139536
Gene: ENSMUSG00000053877
AA Change: I2843T

DomainStartEndE-ValueType
low complexity region 26 48 N/A INTRINSIC
HSA 125 196 5.4e-25 SMART
low complexity region 257 280 N/A INTRINSIC
low complexity region 283 310 N/A INTRINSIC
low complexity region 322 347 N/A INTRINSIC
low complexity region 396 420 N/A INTRINSIC
low complexity region 480 558 N/A INTRINSIC
low complexity region 577 592 N/A INTRINSIC
DEXDc 626 818 5e-37 SMART
low complexity region 993 1001 N/A INTRINSIC
low complexity region 1027 1042 N/A INTRINSIC
low complexity region 1046 1063 N/A INTRINSIC
low complexity region 1175 1194 N/A INTRINSIC
internal_repeat_1 1202 1245 2.24e-5 PROSPERO
low complexity region 1274 1302 N/A INTRINSIC
low complexity region 1304 1318 N/A INTRINSIC
low complexity region 1335 1353 N/A INTRINSIC
low complexity region 1355 1370 N/A INTRINSIC
low complexity region 1414 1441 N/A INTRINSIC
low complexity region 1452 1466 N/A INTRINSIC
low complexity region 1504 1533 N/A INTRINSIC
internal_repeat_1 1536 1579 2.24e-5 PROSPERO
internal_repeat_2 1537 1559 5.66e-5 PROSPERO
internal_repeat_2 1569 1589 5.66e-5 PROSPERO
low complexity region 1590 1607 N/A INTRINSIC
low complexity region 1609 1627 N/A INTRINSIC
low complexity region 1644 1678 N/A INTRINSIC
low complexity region 1713 1726 N/A INTRINSIC
low complexity region 1828 1840 N/A INTRINSIC
HELICc 1916 1999 1.2e-28 SMART
low complexity region 2058 2078 N/A INTRINSIC
coiled coil region 2166 2201 N/A INTRINSIC
low complexity region 2282 2348 N/A INTRINSIC
low complexity region 2374 2409 N/A INTRINSIC
low complexity region 2588 2600 N/A INTRINSIC
low complexity region 2642 2657 N/A INTRINSIC
low complexity region 2685 2712 N/A INTRINSIC
AT_hook 2745 2757 2.4e-2 SMART
low complexity region 2797 2817 N/A INTRINSIC
AT_hook 2825 2837 2.6e-3 SMART
low complexity region 2838 2849 N/A INTRINSIC
low complexity region 2858 2885 N/A INTRINSIC
AT_hook 2889 2901 2.4e-3 SMART
low complexity region 2934 2945 N/A INTRINSIC
low complexity region 2946 2956 N/A INTRINSIC
low complexity region 3043 3079 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000187040
AA Change: I3000T
SMART Domains Protein: ENSMUSP00000140036
Gene: ENSMUSG00000053877
AA Change: I3000T

DomainStartEndE-ValueType
low complexity region 26 48 N/A INTRINSIC
HSA 125 196 5.4e-25 SMART
low complexity region 257 280 N/A INTRINSIC
low complexity region 283 310 N/A INTRINSIC
low complexity region 322 347 N/A INTRINSIC
low complexity region 396 420 N/A INTRINSIC
low complexity region 480 558 N/A INTRINSIC
low complexity region 577 592 N/A INTRINSIC
DEXDc 626 818 5e-37 SMART
low complexity region 993 1001 N/A INTRINSIC
low complexity region 1027 1042 N/A INTRINSIC
low complexity region 1046 1063 N/A INTRINSIC
low complexity region 1120 1143 N/A INTRINSIC
low complexity region 1150 1178 N/A INTRINSIC
low complexity region 1277 1305 N/A INTRINSIC
low complexity region 1332 1351 N/A INTRINSIC
internal_repeat_1 1359 1402 1.78e-5 PROSPERO
low complexity region 1431 1459 N/A INTRINSIC
low complexity region 1461 1475 N/A INTRINSIC
low complexity region 1492 1510 N/A INTRINSIC
low complexity region 1512 1527 N/A INTRINSIC
low complexity region 1571 1598 N/A INTRINSIC
low complexity region 1609 1623 N/A INTRINSIC
low complexity region 1661 1690 N/A INTRINSIC
internal_repeat_1 1693 1736 1.78e-5 PROSPERO
internal_repeat_2 1694 1716 4.56e-5 PROSPERO
internal_repeat_2 1726 1746 4.56e-5 PROSPERO
low complexity region 1747 1764 N/A INTRINSIC
low complexity region 1766 1784 N/A INTRINSIC
low complexity region 1801 1835 N/A INTRINSIC
low complexity region 1870 1883 N/A INTRINSIC
low complexity region 1985 1997 N/A INTRINSIC
HELICc 2073 2156 1.2e-28 SMART
low complexity region 2215 2235 N/A INTRINSIC
coiled coil region 2323 2358 N/A INTRINSIC
low complexity region 2439 2505 N/A INTRINSIC
low complexity region 2531 2566 N/A INTRINSIC
low complexity region 2745 2757 N/A INTRINSIC
low complexity region 2799 2814 N/A INTRINSIC
low complexity region 2842 2869 N/A INTRINSIC
AT_hook 2902 2914 2.4e-2 SMART
low complexity region 2954 2974 N/A INTRINSIC
AT_hook 2982 2994 2.6e-3 SMART
low complexity region 2995 3006 N/A INTRINSIC
low complexity region 3015 3042 N/A INTRINSIC
AT_hook 3046 3058 2.4e-3 SMART
low complexity region 3091 3102 N/A INTRINSIC
low complexity region 3103 3113 N/A INTRINSIC
low complexity region 3200 3236 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000189629
AA Change: I2824T
SMART Domains Protein: ENSMUSP00000139644
Gene: ENSMUSG00000107023
AA Change: I2824T

DomainStartEndE-ValueType
low complexity region 7 29 N/A INTRINSIC
HSA 106 177 5.4e-25 SMART
low complexity region 238 261 N/A INTRINSIC
low complexity region 264 291 N/A INTRINSIC
low complexity region 303 328 N/A INTRINSIC
low complexity region 377 401 N/A INTRINSIC
low complexity region 461 539 N/A INTRINSIC
low complexity region 558 573 N/A INTRINSIC
DEXDc 607 799 5e-37 SMART
low complexity region 974 982 N/A INTRINSIC
low complexity region 1008 1023 N/A INTRINSIC
low complexity region 1027 1044 N/A INTRINSIC
low complexity region 1156 1175 N/A INTRINSIC
internal_repeat_1 1183 1226 2e-5 PROSPERO
low complexity region 1255 1283 N/A INTRINSIC
low complexity region 1285 1299 N/A INTRINSIC
low complexity region 1316 1334 N/A INTRINSIC
low complexity region 1336 1351 N/A INTRINSIC
low complexity region 1395 1422 N/A INTRINSIC
low complexity region 1433 1447 N/A INTRINSIC
low complexity region 1485 1514 N/A INTRINSIC
internal_repeat_1 1517 1560 2e-5 PROSPERO
internal_repeat_2 1518 1540 5.08e-5 PROSPERO
internal_repeat_2 1550 1570 5.08e-5 PROSPERO
low complexity region 1571 1588 N/A INTRINSIC
low complexity region 1590 1608 N/A INTRINSIC
low complexity region 1625 1659 N/A INTRINSIC
low complexity region 1694 1707 N/A INTRINSIC
low complexity region 1809 1821 N/A INTRINSIC
HELICc 1897 1980 1.2e-28 SMART
low complexity region 2039 2059 N/A INTRINSIC
coiled coil region 2147 2182 N/A INTRINSIC
low complexity region 2263 2329 N/A INTRINSIC
low complexity region 2355 2390 N/A INTRINSIC
low complexity region 2569 2581 N/A INTRINSIC
low complexity region 2623 2638 N/A INTRINSIC
low complexity region 2666 2693 N/A INTRINSIC
AT_hook 2726 2738 2.4e-2 SMART
low complexity region 2778 2798 N/A INTRINSIC
AT_hook 2806 2818 2.6e-3 SMART
low complexity region 2819 2830 N/A INTRINSIC
low complexity region 2839 2866 N/A INTRINSIC
AT_hook 2870 2882 2.4e-3 SMART
low complexity region 2915 2926 N/A INTRINSIC
low complexity region 2927 2937 N/A INTRINSIC
low complexity region 3024 3060 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000190278
SMART Domains Protein: ENSMUSP00000144111
Gene: ENSMUSG00000106715

DomainStartEndE-ValueType
transmembrane domain 33 55 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000190390
AA Change: I2939T
SMART Domains Protein: ENSMUSP00000139399
Gene: ENSMUSG00000053877
AA Change: I2939T

DomainStartEndE-ValueType
low complexity region 26 48 N/A INTRINSIC
HSA 125 196 5.4e-25 SMART
low complexity region 257 280 N/A INTRINSIC
low complexity region 283 310 N/A INTRINSIC
low complexity region 322 347 N/A INTRINSIC
low complexity region 396 420 N/A INTRINSIC
low complexity region 480 558 N/A INTRINSIC
low complexity region 577 592 N/A INTRINSIC
DEXDc 626 818 5e-37 SMART
low complexity region 993 1001 N/A INTRINSIC
low complexity region 1027 1042 N/A INTRINSIC
low complexity region 1046 1063 N/A INTRINSIC
low complexity region 1120 1143 N/A INTRINSIC
low complexity region 1150 1178 N/A INTRINSIC
low complexity region 1271 1290 N/A INTRINSIC
internal_repeat_1 1298 1341 2.01e-5 PROSPERO
low complexity region 1370 1398 N/A INTRINSIC
low complexity region 1400 1414 N/A INTRINSIC
low complexity region 1431 1449 N/A INTRINSIC
low complexity region 1451 1466 N/A INTRINSIC
low complexity region 1510 1537 N/A INTRINSIC
low complexity region 1548 1562 N/A INTRINSIC
low complexity region 1600 1629 N/A INTRINSIC
internal_repeat_1 1632 1675 2.01e-5 PROSPERO
internal_repeat_2 1633 1655 5.11e-5 PROSPERO
internal_repeat_2 1665 1685 5.11e-5 PROSPERO
low complexity region 1686 1703 N/A INTRINSIC
low complexity region 1705 1723 N/A INTRINSIC
low complexity region 1740 1774 N/A INTRINSIC
low complexity region 1809 1822 N/A INTRINSIC
low complexity region 1924 1936 N/A INTRINSIC
HELICc 2012 2095 1.2e-28 SMART
low complexity region 2154 2174 N/A INTRINSIC
coiled coil region 2262 2297 N/A INTRINSIC
low complexity region 2378 2444 N/A INTRINSIC
low complexity region 2470 2505 N/A INTRINSIC
low complexity region 2684 2696 N/A INTRINSIC
low complexity region 2738 2753 N/A INTRINSIC
low complexity region 2781 2808 N/A INTRINSIC
AT_hook 2841 2853 2.4e-2 SMART
low complexity region 2893 2913 N/A INTRINSIC
AT_hook 2921 2933 2.6e-3 SMART
low complexity region 2934 2945 N/A INTRINSIC
low complexity region 2954 2981 N/A INTRINSIC
AT_hook 2985 2997 2.4e-3 SMART
low complexity region 3030 3041 N/A INTRINSIC
low complexity region 3042 3052 N/A INTRINSIC
low complexity region 3139 3175 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000206825
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190938
Meta Mutation Damage Score 0.0611 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.8%
  • 20x: 91.4%
Validation Efficiency 98% (87/89)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the core catalytic component of the multiprotein chromatin-remodeling SRCAP complex. The encoded protein is an ATPase that is necessary for the incorporation of the histone variant H2A.Z into nucleosomes. It can function as a transcriptional activator in Notch-mediated, CREB-mediated and steroid receptor-mediated transcription. Mutations in this gene cause Floating-Harbor syndrome, a rare disorder characterized by short stature, language deficits and dysmorphic facial features. [provided by RefSeq, Feb 2012]
Allele List at MGI
Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930433I11Rik A T 7: 40,642,480 (GRCm39) T141S probably benign Het
Abcg1 T A 17: 31,333,132 (GRCm39) I625N possibly damaging Het
Adam33 C A 2: 130,893,391 (GRCm39) probably benign Het
Adgrl2 A T 3: 148,528,617 (GRCm39) I1185N probably damaging Het
Afp A T 5: 90,649,486 (GRCm39) probably benign Het
Aggf1 A G 13: 95,501,356 (GRCm39) V342A probably benign Het
Ankrd11 A T 8: 123,619,789 (GRCm39) S1333R probably benign Het
Arhgef11 C A 3: 87,640,776 (GRCm39) S1311* probably null Het
Atp6v1g1 T C 4: 63,466,878 (GRCm39) Y47H probably benign Het
Atp8b4 T C 2: 126,165,013 (GRCm39) probably null Het
Barx2 A G 9: 31,770,327 (GRCm39) L67P probably damaging Het
Bbs7 G A 3: 36,627,706 (GRCm39) P694S probably benign Het
Btbd10 A T 7: 112,946,266 (GRCm39) V33E probably benign Het
C2 T C 17: 35,091,457 (GRCm39) T69A possibly damaging Het
C8b T G 4: 104,641,679 (GRCm39) L205R possibly damaging Het
Cct4 T G 11: 22,944,333 (GRCm39) N72K probably damaging Het
Cd300lg C A 11: 101,944,981 (GRCm39) P353H possibly damaging Het
Cdh20 A T 1: 104,875,222 (GRCm39) I335L possibly damaging Het
Cfhr2 T A 1: 139,738,757 (GRCm39) H268L probably benign Het
Chia1 T A 3: 106,036,255 (GRCm39) D278E probably benign Het
Cntn6 A G 6: 104,781,359 (GRCm39) T482A possibly damaging Het
Cst13 T A 2: 148,665,016 (GRCm39) F4I probably benign Het
Ctsc T A 7: 87,930,706 (GRCm39) V95E probably damaging Het
Ddhd1 A T 14: 45,842,508 (GRCm39) probably null Het
Dmxl2 A T 9: 54,322,712 (GRCm39) probably null Het
Dnah5 A C 15: 28,402,059 (GRCm39) T3407P probably damaging Het
Dock1 T A 7: 134,735,665 (GRCm39) Y1344* probably null Het
Eif4g3 T C 4: 137,933,395 (GRCm39) V1740A probably damaging Het
Epb41l5 A G 1: 119,506,634 (GRCm39) probably benign Het
Flt4 C T 11: 49,527,166 (GRCm39) probably benign Het
Fnbp1l C T 3: 122,339,955 (GRCm39) R499Q probably damaging Het
Gm10033 T C 8: 69,826,022 (GRCm39) noncoding transcript Het
Gm12790 A G 4: 101,825,396 (GRCm39) L6P probably benign Het
Gramd4 A G 15: 86,009,397 (GRCm39) D210G probably damaging Het
Hectd3 T C 4: 116,859,466 (GRCm39) S697P possibly damaging Het
Hsf4 T C 8: 106,002,235 (GRCm39) V399A probably benign Het
Hyal6 T A 6: 24,743,434 (GRCm39) C377S probably damaging Het
Myb C T 10: 21,028,844 (GRCm39) V85M probably damaging Het
Mypn A G 10: 62,988,636 (GRCm39) V463A probably damaging Het
Nav1 T A 1: 135,388,163 (GRCm39) I1144L probably benign Het
Nckap5 A G 1: 125,942,398 (GRCm39) probably benign Het
Nipbl A T 15: 8,401,657 (GRCm39) S30T probably damaging Het
Nmt1 T C 11: 102,948,307 (GRCm39) F277S probably damaging Het
Nploc4 A C 11: 120,274,115 (GRCm39) probably benign Het
Nup54 C A 5: 92,576,080 (GRCm39) R137I probably damaging Het
Or52n2b T C 7: 104,565,963 (GRCm39) Y180C probably damaging Het
Oxtr C T 6: 112,454,138 (GRCm39) R42Q probably benign Het
Pkd1l1 G T 11: 8,804,487 (GRCm39) Y1701* probably null Het
Plekhg6 T C 6: 125,340,072 (GRCm39) T763A probably damaging Het
Pmepa1 C T 2: 173,070,368 (GRCm39) probably null Het
Ppfia2 A G 10: 106,666,518 (GRCm39) E408G possibly damaging Het
Pramel13 G A 4: 144,121,658 (GRCm39) T122M probably benign Het
Prl8a2 G A 13: 27,537,979 (GRCm39) V218I possibly damaging Het
Ptpro T A 6: 137,420,592 (GRCm39) V1007D probably damaging Het
Rims4 C T 2: 163,705,849 (GRCm39) V262M possibly damaging Het
Shisal2b A T 13: 105,000,113 (GRCm39) C37S probably damaging Het
Slc13a1 A T 6: 24,118,082 (GRCm39) probably null Het
Slc17a8 T A 10: 89,427,076 (GRCm39) T342S probably damaging Het
Slc30a9 A G 5: 67,510,005 (GRCm39) E519G probably benign Het
Slc35e1 T C 8: 73,246,415 (GRCm39) probably benign Het
Slc39a5 G A 10: 128,233,610 (GRCm39) L296F probably damaging Het
Slco6b1 A C 1: 96,857,610 (GRCm39) noncoding transcript Het
Slco6d1 G A 1: 98,418,341 (GRCm39) G509D probably damaging Het
Spen A G 4: 141,199,132 (GRCm39) V3142A probably damaging Het
Spta1 T A 1: 174,050,250 (GRCm39) H1763Q probably damaging Het
Stard9 T C 2: 120,543,328 (GRCm39) probably benign Het
Stat4 A G 1: 52,111,106 (GRCm39) probably benign Het
Svbp T A 4: 119,053,225 (GRCm39) probably benign Het
Tm2d1 A T 4: 98,258,833 (GRCm39) probably benign Het
Trpv1 C A 11: 73,130,952 (GRCm39) probably null Het
Trrap A G 5: 144,794,232 (GRCm39) D3713G possibly damaging Het
Ubr1 T A 2: 120,786,125 (GRCm39) D165V probably benign Het
Utrn C A 10: 12,524,897 (GRCm39) M2195I probably benign Het
Vmn1r229 G A 17: 21,034,904 (GRCm39) V50I possibly damaging Het
Vmn1r44 A T 6: 89,870,632 (GRCm39) H126L probably benign Het
Vmn2r116 T C 17: 23,605,570 (GRCm39) probably benign Het
Vmn2r27 A C 6: 124,168,591 (GRCm39) Y846* probably null Het
Vmn2r84 T A 10: 130,227,859 (GRCm39) S126C possibly damaging Het
Xylb T A 9: 119,197,133 (GRCm39) probably benign Het
Zfp282 A T 6: 47,867,108 (GRCm39) K232* probably null Het
Zfp39 C A 11: 58,781,149 (GRCm39) V538L probably benign Het
Zfp560 T C 9: 20,263,149 (GRCm39) N76D possibly damaging Het
Zmym4 C T 4: 126,804,962 (GRCm39) V433I probably benign Het
Zscan5b A G 7: 6,233,425 (GRCm39) E83G probably damaging Het
Other mutations in Srcap
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00323:Srcap APN 7 127,141,885 (GRCm39) splice site probably benign
IGL00475:Srcap APN 7 127,152,093 (GRCm39) missense possibly damaging 0.92
IGL01064:Srcap APN 7 127,159,064 (GRCm39) unclassified probably benign
IGL01129:Srcap APN 7 127,120,823 (GRCm39) missense probably damaging 1.00
IGL01670:Srcap APN 7 127,127,604 (GRCm39) missense probably damaging 1.00
IGL01861:Srcap APN 7 127,124,457 (GRCm39) splice site probably benign
IGL02237:Srcap APN 7 127,133,864 (GRCm39) splice site probably benign
IGL02665:Srcap APN 7 127,140,075 (GRCm39) missense probably damaging 1.00
IGL02688:Srcap APN 7 127,141,625 (GRCm39) missense probably benign 0.04
IGL02744:Srcap APN 7 127,133,838 (GRCm39) missense probably damaging 1.00
IGL02810:Srcap APN 7 127,120,835 (GRCm39) critical splice donor site probably null
IGL03184:Srcap APN 7 127,129,674 (GRCm39) unclassified probably benign
IGL03309:Srcap APN 7 127,129,965 (GRCm39) missense probably damaging 0.99
PIT4453001:Srcap UTSW 7 127,148,492 (GRCm39) missense possibly damaging 0.52
R1340:Srcap UTSW 7 127,159,910 (GRCm39) intron probably benign
R1455:Srcap UTSW 7 127,129,822 (GRCm39) missense probably damaging 0.99
R1470:Srcap UTSW 7 127,158,899 (GRCm39) unclassified probably benign
R1470:Srcap UTSW 7 127,158,899 (GRCm39) unclassified probably benign
R1761:Srcap UTSW 7 127,134,017 (GRCm39) missense probably damaging 1.00
R1911:Srcap UTSW 7 127,133,994 (GRCm39) missense probably damaging 0.99
R2483:Srcap UTSW 7 127,141,319 (GRCm39) missense probably damaging 0.99
R2892:Srcap UTSW 7 127,138,237 (GRCm39) missense probably damaging 0.99
R2893:Srcap UTSW 7 127,138,237 (GRCm39) missense probably damaging 0.99
R3623:Srcap UTSW 7 127,141,319 (GRCm39) missense probably damaging 0.99
R3976:Srcap UTSW 7 127,148,411 (GRCm39) missense probably benign 0.18
R4001:Srcap UTSW 7 127,131,339 (GRCm39) missense probably damaging 1.00
R4015:Srcap UTSW 7 127,124,595 (GRCm39) missense probably benign 0.27
R4581:Srcap UTSW 7 127,157,482 (GRCm39) unclassified probably benign
R4643:Srcap UTSW 7 127,140,948 (GRCm39) missense probably damaging 1.00
R4644:Srcap UTSW 7 127,151,770 (GRCm39) missense probably damaging 1.00
R4690:Srcap UTSW 7 127,137,186 (GRCm39) missense probably damaging 1.00
R4693:Srcap UTSW 7 127,137,716 (GRCm39) missense probably damaging 1.00
R4719:Srcap UTSW 7 127,140,731 (GRCm39) missense probably benign 0.13
R4728:Srcap UTSW 7 127,140,096 (GRCm39) critical splice donor site probably null
R4740:Srcap UTSW 7 127,148,471 (GRCm39) missense probably damaging 1.00
R4752:Srcap UTSW 7 127,158,172 (GRCm39) unclassified probably benign
R4834:Srcap UTSW 7 127,156,782 (GRCm39) critical splice donor site probably null
R4837:Srcap UTSW 7 127,158,134 (GRCm39) unclassified probably benign
R4884:Srcap UTSW 7 127,121,189 (GRCm39) missense probably damaging 1.00
R4889:Srcap UTSW 7 127,137,719 (GRCm39) missense possibly damaging 0.94
R5088:Srcap UTSW 7 127,140,833 (GRCm39) missense probably benign 0.02
R5102:Srcap UTSW 7 127,129,795 (GRCm39) missense probably damaging 1.00
R5358:Srcap UTSW 7 127,139,492 (GRCm39) missense probably damaging 1.00
R5372:Srcap UTSW 7 127,156,785 (GRCm39) splice site probably null
R5397:Srcap UTSW 7 127,152,468 (GRCm39) critical splice donor site probably null
R5481:Srcap UTSW 7 127,131,369 (GRCm39) missense probably damaging 1.00
R5566:Srcap UTSW 7 127,124,475 (GRCm39) missense probably damaging 0.99
R5584:Srcap UTSW 7 127,127,651 (GRCm39) missense probably damaging 1.00
R5693:Srcap UTSW 7 127,118,988 (GRCm39) missense probably damaging 1.00
R5769:Srcap UTSW 7 127,158,994 (GRCm39) unclassified probably benign
R5805:Srcap UTSW 7 127,141,211 (GRCm39) missense possibly damaging 0.87
R5806:Srcap UTSW 7 127,158,335 (GRCm39) unclassified probably benign
R5921:Srcap UTSW 7 127,158,005 (GRCm39) unclassified probably benign
R5942:Srcap UTSW 7 127,137,180 (GRCm39) missense probably damaging 1.00
R6014:Srcap UTSW 7 127,137,922 (GRCm39) missense probably benign 0.01
R6057:Srcap UTSW 7 127,140,528 (GRCm39) missense probably damaging 0.99
R6113:Srcap UTSW 7 127,159,453 (GRCm39) unclassified probably benign
R6150:Srcap UTSW 7 127,134,000 (GRCm39) missense probably damaging 1.00
R6212:Srcap UTSW 7 127,148,861 (GRCm39) missense probably damaging 1.00
R6299:Srcap UTSW 7 127,129,626 (GRCm39) unclassified probably benign
R6437:Srcap UTSW 7 127,127,722 (GRCm39) splice site probably null
R6492:Srcap UTSW 7 127,121,317 (GRCm39) nonsense probably null
R6537:Srcap UTSW 7 127,141,392 (GRCm39) missense probably damaging 0.97
R6659:Srcap UTSW 7 127,141,563 (GRCm39) missense probably damaging 1.00
R6713:Srcap UTSW 7 127,134,089 (GRCm39) missense probably benign 0.28
R6717:Srcap UTSW 7 127,157,482 (GRCm39) unclassified probably benign
R6941:Srcap UTSW 7 127,141,769 (GRCm39) missense probably damaging 1.00
R7068:Srcap UTSW 7 127,141,115 (GRCm39) missense probably benign 0.00
R7097:Srcap UTSW 7 127,138,213 (GRCm39) missense probably damaging 1.00
R7394:Srcap UTSW 7 127,134,000 (GRCm39) missense probably damaging 1.00
R7426:Srcap UTSW 7 127,137,689 (GRCm39) missense possibly damaging 0.90
R7434:Srcap UTSW 7 127,159,414 (GRCm39) missense unknown
R7559:Srcap UTSW 7 127,129,722 (GRCm39) missense unknown
R7638:Srcap UTSW 7 127,137,920 (GRCm39) missense probably benign 0.39
R7677:Srcap UTSW 7 127,158,980 (GRCm39) missense unknown
R7715:Srcap UTSW 7 127,148,460 (GRCm39) missense probably damaging 0.99
R7757:Srcap UTSW 7 127,129,966 (GRCm39) missense probably damaging 0.99
R7811:Srcap UTSW 7 127,141,221 (GRCm39) missense probably damaging 0.97
R7821:Srcap UTSW 7 127,129,499 (GRCm39) unclassified probably benign
R7869:Srcap UTSW 7 127,138,366 (GRCm39) missense possibly damaging 0.92
R7870:Srcap UTSW 7 127,159,730 (GRCm39) missense unknown
R7941:Srcap UTSW 7 127,157,462 (GRCm39) unclassified probably benign
R7994:Srcap UTSW 7 127,140,930 (GRCm39) missense probably benign 0.00
R8035:Srcap UTSW 7 127,141,784 (GRCm39) missense probably benign 0.05
R8066:Srcap UTSW 7 127,120,804 (GRCm39) missense probably damaging 1.00
R8066:Srcap UTSW 7 127,139,484 (GRCm39) missense possibly damaging 0.74
R8168:Srcap UTSW 7 127,141,695 (GRCm39) missense probably damaging 1.00
R8194:Srcap UTSW 7 127,138,369 (GRCm39) missense probably damaging 1.00
R8288:Srcap UTSW 7 127,130,528 (GRCm39) missense probably damaging 1.00
R8307:Srcap UTSW 7 127,124,541 (GRCm39) missense probably damaging 1.00
R8308:Srcap UTSW 7 127,152,353 (GRCm39) missense possibly damaging 0.82
R8309:Srcap UTSW 7 127,148,529 (GRCm39) missense probably damaging 0.98
R8311:Srcap UTSW 7 127,156,969 (GRCm39) missense probably damaging 0.99
R8321:Srcap UTSW 7 127,140,068 (GRCm39) missense probably damaging 1.00
R8365:Srcap UTSW 7 127,148,869 (GRCm39) missense probably damaging 1.00
R8424:Srcap UTSW 7 127,141,560 (GRCm39) missense probably benign 0.00
R8815:Srcap UTSW 7 127,158,037 (GRCm39) missense unknown
R8817:Srcap UTSW 7 127,152,395 (GRCm39) missense probably benign 0.23
R8924:Srcap UTSW 7 127,158,204 (GRCm39) missense unknown
R8933:Srcap UTSW 7 127,151,566 (GRCm39) missense probably damaging 1.00
R8961:Srcap UTSW 7 127,141,101 (GRCm39) missense probably damaging 1.00
R9000:Srcap UTSW 7 127,130,943 (GRCm39) missense possibly damaging 0.91
R9098:Srcap UTSW 7 127,151,816 (GRCm39) missense probably damaging 0.99
R9124:Srcap UTSW 7 127,159,874 (GRCm39) missense unknown
R9163:Srcap UTSW 7 127,121,162 (GRCm39) missense unknown
R9332:Srcap UTSW 7 127,158,812 (GRCm39) missense unknown
R9389:Srcap UTSW 7 127,141,455 (GRCm39) missense probably damaging 1.00
R9464:Srcap UTSW 7 127,137,273 (GRCm39) missense possibly damaging 0.95
R9467:Srcap UTSW 7 127,139,531 (GRCm39) missense probably damaging 0.98
R9554:Srcap UTSW 7 127,151,577 (GRCm39) missense probably damaging 1.00
R9596:Srcap UTSW 7 127,131,036 (GRCm39) missense probably damaging 1.00
R9597:Srcap UTSW 7 127,121,219 (GRCm39) missense possibly damaging 0.91
X0025:Srcap UTSW 7 127,159,277 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- ACAGTAACTGTTGCAGAACCTGACC -3'
(R):5'- TCCCTTCAGCTTCAAGCCGAAGAC -3'

Sequencing Primer
(F):5'- GACCTCAGGCCCCAATTTG -3'
(R):5'- AGAGGAACTGCCTTCACTTTCTG -3'
Posted On 2014-03-14