Incidental Mutation 'IGL01974:Mycbp2'
ID 181674
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mycbp2
Ensembl Gene ENSMUSG00000033004
Gene Name MYC binding protein 2
Synonyms C130061D10Rik, Phr1, Pam
Accession Numbers

Genbank: NM_207215; MGI: 2179432

Essential gene? Essential (E-score: 1.000) question?
Stock # IGL01974
Quality Score
Status
Chromosome 14
Chromosomal Location 103113411-103346814 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to C at 103143211 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Alanine at position 3670 (S3670A)
Ref Sequence ENSEMBL: ENSMUSP00000124601 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000159855] [ENSMUST00000160758]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000159855
AA Change: S3780A

PolyPhen 2 Score 0.477 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000124710
Gene: ENSMUSG00000033004
AA Change: S3780A

DomainStartEndE-ValueType
low complexity region 5 27 N/A INTRINSIC
low complexity region 47 55 N/A INTRINSIC
low complexity region 100 127 N/A INTRINSIC
low complexity region 178 191 N/A INTRINSIC
Pfam:RCC1_2 683 712 1.4e-10 PFAM
low complexity region 737 750 N/A INTRINSIC
low complexity region 793 815 N/A INTRINSIC
Pfam:RCC1_2 942 971 5.5e-10 PFAM
Pfam:RCC1 958 1006 4.8e-15 PFAM
Pfam:PHR 1235 1385 8.2e-44 PFAM
Pfam:PHR 1723 1880 1.4e-43 PFAM
low complexity region 1935 1948 N/A INTRINSIC
low complexity region 2182 2195 N/A INTRINSIC
Pfam:Filamin 2261 2431 7.5e-9 PFAM
Pfam:SH3_3 2472 2539 4.1e-9 PFAM
internal_repeat_3 2612 2679 1.69e-7 PROSPERO
low complexity region 2701 2710 N/A INTRINSIC
low complexity region 2884 2917 N/A INTRINSIC
low complexity region 2970 2984 N/A INTRINSIC
coiled coil region 3263 3290 N/A INTRINSIC
low complexity region 3352 3365 N/A INTRINSIC
low complexity region 3418 3433 N/A INTRINSIC
low complexity region 3678 3695 N/A INTRINSIC
APC10 3810 3968 1.11e-18 SMART
low complexity region 4103 4115 N/A INTRINSIC
low complexity region 4190 4212 N/A INTRINSIC
Blast:BBOX 4327 4370 7e-7 BLAST
RING 4496 4546 5.35e-5 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000160758
AA Change: S3670A

PolyPhen 2 Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000124601
Gene: ENSMUSG00000033004
AA Change: S3670A

DomainStartEndE-ValueType
low complexity region 14 22 N/A INTRINSIC
low complexity region 67 94 N/A INTRINSIC
low complexity region 145 158 N/A INTRINSIC
Pfam:RCC1_2 650 679 1e-10 PFAM
low complexity region 704 717 N/A INTRINSIC
low complexity region 760 782 N/A INTRINSIC
Pfam:RCC1_2 909 938 1.5e-9 PFAM
Pfam:RCC1 925 973 1.3e-15 PFAM
Pfam:PHR 1202 1353 1.6e-50 PFAM
Pfam:PHR 1690 1848 3.1e-58 PFAM
low complexity region 1902 1915 N/A INTRINSIC
low complexity region 2149 2162 N/A INTRINSIC
Pfam:Filamin 2228 2398 7.6e-9 PFAM
Pfam:SH3_3 2439 2507 2.3e-10 PFAM
internal_repeat_3 2554 2621 2e-7 PROSPERO
low complexity region 2643 2652 N/A INTRINSIC
low complexity region 2774 2807 N/A INTRINSIC
low complexity region 2860 2874 N/A INTRINSIC
coiled coil region 3153 3180 N/A INTRINSIC
low complexity region 3242 3255 N/A INTRINSIC
low complexity region 3308 3323 N/A INTRINSIC
low complexity region 3568 3585 N/A INTRINSIC
APC10 3700 3858 1.11e-18 SMART
low complexity region 3993 4005 N/A INTRINSIC
low complexity region 4080 4102 N/A INTRINSIC
Blast:BBOX 4217 4260 7e-7 BLAST
RING 4386 4436 5.35e-5 SMART
Predicted Effect unknown
Transcript: ENSMUST00000161008
AA Change: S493A
SMART Domains Protein: ENSMUSP00000124443
Gene: ENSMUSG00000033004
AA Change: S493A

DomainStartEndE-ValueType
low complexity region 66 79 N/A INTRINSIC
low complexity region 132 147 N/A INTRINSIC
low complexity region 392 409 N/A INTRINSIC
APC10 524 682 1.11e-18 SMART
low complexity region 820 832 N/A INTRINSIC
low complexity region 907 929 N/A INTRINSIC
Blast:BBOX 1042 1085 2e-6 BLAST
RING 1213 1263 5.35e-5 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000162762
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a targeted allele exhibit neonatal lethality, defective diaphragm innervation, abnormal brain morphology and defective axonal guidance. [provided by MGI curators]
Allele List at MGI

All alleles(10) : Targeted, knock-out(1) Targeted, other(1) Gene trapped(5) Chemically induced(3)

Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik T C 14: 32,659,805 (GRCm38) D1401G possibly damaging Het
Adamts2 G A 11: 50,776,174 (GRCm38) G433S probably damaging Het
Cacna2d2 A C 9: 107,517,422 (GRCm38) S598R probably benign Het
Cdkl3 A G 11: 52,011,237 (GRCm38) Q91R probably damaging Het
Celf2 T C 2: 6,604,031 (GRCm38) Y313C probably damaging Het
Clint1 C A 11: 45,909,035 (GRCm38) N558K probably benign Het
Dcbld1 A G 10: 52,304,681 (GRCm38) H147R probably benign Het
Dusp27 A T 1: 166,100,536 (GRCm38) C502* probably null Het
Ednrb A C 14: 103,820,818 (GRCm38) Y350D probably damaging Het
Elp2 C T 18: 24,626,203 (GRCm38) P539L probably damaging Het
Fam217b G A 2: 178,421,227 (GRCm38) R328Q probably damaging Het
Gm9991 G T 1: 90,675,475 (GRCm38) noncoding transcript Het
Herc4 T G 10: 63,299,241 (GRCm38) probably null Het
Hus1 T C 11: 9,000,088 (GRCm38) N211S possibly damaging Het
Immt A G 6: 71,872,858 (GRCm38) D454G probably damaging Het
Itga4 G A 2: 79,273,127 (GRCm38) probably benign Het
Kank1 A T 19: 25,410,232 (GRCm38) N423I possibly damaging Het
Kynu T A 2: 43,681,340 (GRCm38) probably benign Het
Ndufv3 T C 17: 31,521,609 (GRCm38) V30A probably benign Het
Olfr1048 G T 2: 86,235,960 (GRCm38) L292I probably benign Het
Per2 C T 1: 91,423,718 (GRCm38) R1022Q probably benign Het
Rad23a T C 8: 84,838,939 (GRCm38) E30G probably damaging Het
Ropn1l T A 15: 31,449,109 (GRCm38) Y91F probably benign Het
Sertad4 C A 1: 192,846,966 (GRCm38) E181* probably null Het
Tnfrsf1b G A 4: 145,215,851 (GRCm38) P454L probably damaging Het
Ttbk2 G A 2: 120,786,083 (GRCm38) R110W probably damaging Het
Usp17le G T 7: 104,768,435 (GRCm38) S500Y probably benign Het
Other mutations in Mycbp2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00094:Mycbp2 APN 14 103,223,050 (GRCm38) missense probably damaging 1.00
IGL00518:Mycbp2 APN 14 103,155,808 (GRCm38) missense probably damaging 1.00
IGL00650:Mycbp2 APN 14 103,143,228 (GRCm38) missense probably damaging 0.97
IGL00653:Mycbp2 APN 14 103,143,228 (GRCm38) missense probably damaging 0.97
IGL00742:Mycbp2 APN 14 103,201,352 (GRCm38) missense probably damaging 1.00
IGL00755:Mycbp2 APN 14 103,194,621 (GRCm38) missense possibly damaging 0.72
IGL00793:Mycbp2 APN 14 103,126,753 (GRCm38) missense possibly damaging 0.77
IGL00916:Mycbp2 APN 14 103,291,283 (GRCm38) splice site probably benign
IGL00960:Mycbp2 APN 14 103,229,384 (GRCm38) missense possibly damaging 0.95
IGL00977:Mycbp2 APN 14 103,172,642 (GRCm38) missense probably damaging 0.98
IGL01349:Mycbp2 APN 14 103,122,547 (GRCm38) missense probably damaging 0.98
IGL01369:Mycbp2 APN 14 103,155,510 (GRCm38) missense possibly damaging 0.61
IGL01410:Mycbp2 APN 14 103,229,492 (GRCm38) splice site probably null
IGL01586:Mycbp2 APN 14 103,140,869 (GRCm38) critical splice donor site probably null
IGL01593:Mycbp2 APN 14 103,291,287 (GRCm38) critical splice donor site probably null
IGL01693:Mycbp2 APN 14 103,127,979 (GRCm38) missense probably damaging 0.99
IGL01730:Mycbp2 APN 14 103,135,204 (GRCm38) nonsense probably null
IGL01820:Mycbp2 APN 14 103,188,501 (GRCm38) missense probably damaging 1.00
IGL02071:Mycbp2 APN 14 103,154,907 (GRCm38) nonsense probably null
IGL02178:Mycbp2 APN 14 103,224,366 (GRCm38) missense probably benign 0.01
IGL02324:Mycbp2 APN 14 103,242,207 (GRCm38) missense probably damaging 1.00
IGL02442:Mycbp2 APN 14 103,314,375 (GRCm38) missense probably benign
IGL02607:Mycbp2 APN 14 103,285,273 (GRCm38) missense probably damaging 1.00
IGL02679:Mycbp2 APN 14 103,205,185 (GRCm38) missense probably benign
IGL02702:Mycbp2 APN 14 103,220,124 (GRCm38) missense probably benign 0.01
IGL02709:Mycbp2 APN 14 103,155,261 (GRCm38) missense probably damaging 0.97
IGL02736:Mycbp2 APN 14 103,114,242 (GRCm38) splice site probably benign
IGL02866:Mycbp2 APN 14 103,129,992 (GRCm38) missense probably damaging 0.98
IGL02939:Mycbp2 APN 14 103,177,279 (GRCm38) missense probably benign
IGL03082:Mycbp2 APN 14 103,204,369 (GRCm38) missense probably benign 0.23
IGL03142:Mycbp2 APN 14 103,298,776 (GRCm38) missense probably damaging 0.99
IGL03155:Mycbp2 APN 14 103,155,453 (GRCm38) missense probably benign 0.06
IGL03236:Mycbp2 APN 14 103,298,698 (GRCm38) missense probably damaging 0.99
IGL03256:Mycbp2 APN 14 103,188,589 (GRCm38) missense possibly damaging 0.92
IGL03303:Mycbp2 APN 14 103,247,758 (GRCm38) missense probably damaging 1.00
compost UTSW 14 103,156,453 (GRCm38) missense probably damaging 1.00
decompose UTSW 14 103,219,979 (GRCm38) missense probably benign 0.12
moulder UTSW 14 103,188,592 (GRCm38) missense probably damaging 1.00
N/A - 293:Mycbp2 UTSW 14 103,224,462 (GRCm38) splice site probably benign
R0040:Mycbp2 UTSW 14 103,224,272 (GRCm38) missense probably benign 0.11
R0040:Mycbp2 UTSW 14 103,224,272 (GRCm38) missense probably benign 0.11
R0057:Mycbp2 UTSW 14 103,152,142 (GRCm38) missense probably damaging 0.97
R0063:Mycbp2 UTSW 14 103,156,634 (GRCm38) unclassified probably benign
R0097:Mycbp2 UTSW 14 103,155,762 (GRCm38) missense probably damaging 1.00
R0097:Mycbp2 UTSW 14 103,155,762 (GRCm38) missense probably damaging 1.00
R0268:Mycbp2 UTSW 14 103,314,325 (GRCm38) nonsense probably null
R0388:Mycbp2 UTSW 14 103,156,667 (GRCm38) missense probably benign 0.01
R0410:Mycbp2 UTSW 14 103,135,133 (GRCm38) missense probably damaging 1.00
R0530:Mycbp2 UTSW 14 103,182,459 (GRCm38) missense probably damaging 1.00
R0591:Mycbp2 UTSW 14 103,196,391 (GRCm38) unclassified probably benign
R0671:Mycbp2 UTSW 14 103,194,588 (GRCm38) missense possibly damaging 0.95
R0755:Mycbp2 UTSW 14 103,174,794 (GRCm38) missense probably damaging 1.00
R0817:Mycbp2 UTSW 14 103,229,418 (GRCm38) missense probably damaging 0.99
R0818:Mycbp2 UTSW 14 103,229,418 (GRCm38) missense probably damaging 0.99
R0819:Mycbp2 UTSW 14 103,229,418 (GRCm38) missense probably damaging 0.99
R0881:Mycbp2 UTSW 14 103,220,013 (GRCm38) missense probably benign
R0903:Mycbp2 UTSW 14 103,275,857 (GRCm38) missense probably damaging 0.99
R0940:Mycbp2 UTSW 14 103,262,693 (GRCm38) unclassified probably benign
R0961:Mycbp2 UTSW 14 103,184,835 (GRCm38) missense probably damaging 1.00
R1004:Mycbp2 UTSW 14 103,140,917 (GRCm38) missense probably benign 0.00
R1138:Mycbp2 UTSW 14 103,174,826 (GRCm38) missense possibly damaging 0.84
R1170:Mycbp2 UTSW 14 103,200,152 (GRCm38) nonsense probably null
R1211:Mycbp2 UTSW 14 103,120,563 (GRCm38) missense probably benign 0.31
R1268:Mycbp2 UTSW 14 103,208,782 (GRCm38) missense probably damaging 1.00
R1298:Mycbp2 UTSW 14 103,155,898 (GRCm38) missense probably damaging 1.00
R1341:Mycbp2 UTSW 14 103,298,867 (GRCm38) splice site probably benign
R1469:Mycbp2 UTSW 14 103,188,520 (GRCm38) missense probably damaging 0.99
R1469:Mycbp2 UTSW 14 103,188,520 (GRCm38) missense probably damaging 0.99
R1513:Mycbp2 UTSW 14 103,204,389 (GRCm38) missense probably damaging 1.00
R1528:Mycbp2 UTSW 14 103,232,597 (GRCm38) missense possibly damaging 0.91
R1564:Mycbp2 UTSW 14 103,169,851 (GRCm38) splice site probably null
R1565:Mycbp2 UTSW 14 103,252,509 (GRCm38) missense possibly damaging 0.82
R1656:Mycbp2 UTSW 14 103,247,758 (GRCm38) missense probably damaging 1.00
R1694:Mycbp2 UTSW 14 103,227,511 (GRCm38) missense probably damaging 1.00
R1709:Mycbp2 UTSW 14 103,224,416 (GRCm38) missense probably damaging 1.00
R1728:Mycbp2 UTSW 14 103,155,178 (GRCm38) missense probably damaging 0.98
R1751:Mycbp2 UTSW 14 103,248,405 (GRCm38) missense probably damaging 0.98
R1767:Mycbp2 UTSW 14 103,248,405 (GRCm38) missense probably damaging 0.98
R1772:Mycbp2 UTSW 14 103,182,419 (GRCm38) missense probably damaging 1.00
R1784:Mycbp2 UTSW 14 103,155,178 (GRCm38) missense probably damaging 0.98
R1823:Mycbp2 UTSW 14 103,252,509 (GRCm38) missense possibly damaging 0.82
R1824:Mycbp2 UTSW 14 103,252,509 (GRCm38) missense possibly damaging 0.82
R1844:Mycbp2 UTSW 14 103,155,714 (GRCm38) missense possibly damaging 0.94
R1916:Mycbp2 UTSW 14 103,184,883 (GRCm38) missense probably damaging 1.00
R1944:Mycbp2 UTSW 14 103,229,404 (GRCm38) missense probably damaging 1.00
R1983:Mycbp2 UTSW 14 103,145,971 (GRCm38) missense probably damaging 0.97
R2002:Mycbp2 UTSW 14 103,248,403 (GRCm38) missense probably damaging 0.98
R2031:Mycbp2 UTSW 14 103,188,592 (GRCm38) missense probably damaging 1.00
R2035:Mycbp2 UTSW 14 103,260,239 (GRCm38) missense probably damaging 1.00
R2048:Mycbp2 UTSW 14 103,232,524 (GRCm38) critical splice donor site probably null
R2061:Mycbp2 UTSW 14 103,287,260 (GRCm38) missense probably damaging 0.99
R2113:Mycbp2 UTSW 14 103,220,076 (GRCm38) missense probably damaging 0.99
R2128:Mycbp2 UTSW 14 103,201,230 (GRCm38) missense probably benign 0.01
R2134:Mycbp2 UTSW 14 103,208,893 (GRCm38) missense probably damaging 1.00
R2135:Mycbp2 UTSW 14 103,208,893 (GRCm38) missense probably damaging 1.00
R2135:Mycbp2 UTSW 14 103,145,942 (GRCm38) missense probably benign
R2146:Mycbp2 UTSW 14 103,155,922 (GRCm38) missense probably damaging 0.97
R2147:Mycbp2 UTSW 14 103,155,922 (GRCm38) missense probably damaging 0.97
R2148:Mycbp2 UTSW 14 103,155,922 (GRCm38) missense probably damaging 0.97
R2150:Mycbp2 UTSW 14 103,155,922 (GRCm38) missense probably damaging 0.97
R2163:Mycbp2 UTSW 14 103,169,855 (GRCm38) critical splice donor site probably null
R2248:Mycbp2 UTSW 14 103,169,859 (GRCm38) missense possibly damaging 0.50
R2265:Mycbp2 UTSW 14 103,262,749 (GRCm38) missense probably benign 0.39
R2272:Mycbp2 UTSW 14 103,144,338 (GRCm38) missense probably null 0.66
R2379:Mycbp2 UTSW 14 103,174,950 (GRCm38) missense probably benign
R2495:Mycbp2 UTSW 14 103,200,118 (GRCm38) missense probably damaging 0.99
R2508:Mycbp2 UTSW 14 103,131,245 (GRCm38) missense probably damaging 0.99
R2510:Mycbp2 UTSW 14 103,155,255 (GRCm38) missense probably damaging 0.96
R2851:Mycbp2 UTSW 14 103,144,333 (GRCm38) missense probably damaging 0.99
R2852:Mycbp2 UTSW 14 103,144,333 (GRCm38) missense probably damaging 0.99
R2965:Mycbp2 UTSW 14 103,297,358 (GRCm38) missense probably benign 0.00
R3156:Mycbp2 UTSW 14 103,208,743 (GRCm38) splice site probably benign
R3404:Mycbp2 UTSW 14 103,200,114 (GRCm38) missense probably damaging 0.99
R3410:Mycbp2 UTSW 14 103,135,117 (GRCm38) missense probably damaging 1.00
R3429:Mycbp2 UTSW 14 103,229,430 (GRCm38) missense probably damaging 1.00
R3706:Mycbp2 UTSW 14 103,156,414 (GRCm38) missense probably benign 0.31
R3772:Mycbp2 UTSW 14 103,133,788 (GRCm38) missense possibly damaging 0.82
R3778:Mycbp2 UTSW 14 103,197,285 (GRCm38) missense probably damaging 0.99
R3883:Mycbp2 UTSW 14 103,295,250 (GRCm38) missense probably damaging 0.97
R3884:Mycbp2 UTSW 14 103,295,250 (GRCm38) missense probably damaging 0.97
R3887:Mycbp2 UTSW 14 103,174,797 (GRCm38) missense probably damaging 0.98
R3923:Mycbp2 UTSW 14 103,126,713 (GRCm38) missense probably damaging 1.00
R3926:Mycbp2 UTSW 14 103,204,500 (GRCm38) missense probably damaging 1.00
R3959:Mycbp2 UTSW 14 103,295,252 (GRCm38) missense probably benign 0.00
R3966:Mycbp2 UTSW 14 103,138,725 (GRCm38) splice site probably benign
R4021:Mycbp2 UTSW 14 103,152,157 (GRCm38) missense probably damaging 0.97
R4363:Mycbp2 UTSW 14 103,248,457 (GRCm38) missense probably damaging 1.00
R4405:Mycbp2 UTSW 14 103,123,445 (GRCm38) missense probably damaging 1.00
R4407:Mycbp2 UTSW 14 103,287,228 (GRCm38) missense probably damaging 1.00
R4410:Mycbp2 UTSW 14 103,135,266 (GRCm38) missense probably damaging 1.00
R4434:Mycbp2 UTSW 14 103,133,789 (GRCm38) missense probably damaging 0.99
R4448:Mycbp2 UTSW 14 103,188,502 (GRCm38) missense possibly damaging 0.89
R4452:Mycbp2 UTSW 14 103,155,658 (GRCm38) missense probably damaging 0.99
R4573:Mycbp2 UTSW 14 103,346,297 (GRCm38) missense probably benign 0.05
R4589:Mycbp2 UTSW 14 103,177,313 (GRCm38) missense probably benign 0.04
R4621:Mycbp2 UTSW 14 103,219,979 (GRCm38) missense probably benign 0.12
R4622:Mycbp2 UTSW 14 103,219,979 (GRCm38) missense probably benign 0.12
R4729:Mycbp2 UTSW 14 103,188,591 (GRCm38) missense probably damaging 1.00
R4770:Mycbp2 UTSW 14 103,219,944 (GRCm38) missense probably benign 0.41
R4790:Mycbp2 UTSW 14 103,229,437 (GRCm38) missense probably damaging 1.00
R4884:Mycbp2 UTSW 14 103,211,295 (GRCm38) missense probably damaging 1.00
R4885:Mycbp2 UTSW 14 103,145,946 (GRCm38) missense possibly damaging 0.86
R4956:Mycbp2 UTSW 14 103,287,239 (GRCm38) missense probably damaging 0.99
R4980:Mycbp2 UTSW 14 103,260,385 (GRCm38) splice site probably null
R4994:Mycbp2 UTSW 14 103,169,994 (GRCm38) missense probably benign
R5029:Mycbp2 UTSW 14 103,156,510 (GRCm38) missense probably benign 0.21
R5038:Mycbp2 UTSW 14 103,296,939 (GRCm38) missense probably damaging 1.00
R5044:Mycbp2 UTSW 14 103,139,235 (GRCm38) critical splice donor site probably null
R5231:Mycbp2 UTSW 14 103,346,214 (GRCm38) critical splice donor site probably null
R5305:Mycbp2 UTSW 14 103,346,321 (GRCm38) missense probably benign 0.00
R5322:Mycbp2 UTSW 14 103,185,683 (GRCm38) critical splice acceptor site probably null
R5376:Mycbp2 UTSW 14 103,242,432 (GRCm38) nonsense probably null
R5414:Mycbp2 UTSW 14 103,306,261 (GRCm38) missense probably damaging 1.00
R5453:Mycbp2 UTSW 14 103,201,401 (GRCm38) missense probably damaging 0.99
R5462:Mycbp2 UTSW 14 103,200,126 (GRCm38) missense probably damaging 1.00
R5499:Mycbp2 UTSW 14 103,242,179 (GRCm38) missense probably damaging 1.00
R5502:Mycbp2 UTSW 14 103,173,814 (GRCm38) missense probably damaging 1.00
R5524:Mycbp2 UTSW 14 103,295,237 (GRCm38) missense probably damaging 1.00
R5533:Mycbp2 UTSW 14 103,282,645 (GRCm38) nonsense probably null
R5569:Mycbp2 UTSW 14 103,135,243 (GRCm38) missense probably damaging 1.00
R5574:Mycbp2 UTSW 14 103,142,767 (GRCm38) missense possibly damaging 0.94
R5579:Mycbp2 UTSW 14 103,291,333 (GRCm38) missense probably damaging 0.98
R5590:Mycbp2 UTSW 14 103,123,355 (GRCm38) missense probably damaging 1.00
R5592:Mycbp2 UTSW 14 103,194,677 (GRCm38) missense probably benign 0.02
R5643:Mycbp2 UTSW 14 103,287,334 (GRCm38) missense probably damaging 1.00
R5644:Mycbp2 UTSW 14 103,287,334 (GRCm38) missense probably damaging 1.00
R5645:Mycbp2 UTSW 14 103,188,615 (GRCm38) critical splice acceptor site probably null
R5645:Mycbp2 UTSW 14 103,188,608 (GRCm38) missense probably damaging 1.00
R5646:Mycbp2 UTSW 14 103,169,910 (GRCm38) missense probably benign 0.09
R5648:Mycbp2 UTSW 14 103,291,342 (GRCm38) missense probably damaging 1.00
R5651:Mycbp2 UTSW 14 103,282,665 (GRCm38) missense probably null 0.99
R5668:Mycbp2 UTSW 14 103,120,519 (GRCm38) missense possibly damaging 0.62
R5745:Mycbp2 UTSW 14 103,156,453 (GRCm38) missense possibly damaging 0.94
R5751:Mycbp2 UTSW 14 103,148,550 (GRCm38) missense probably damaging 0.99
R5756:Mycbp2 UTSW 14 103,133,974 (GRCm38) missense probably damaging 0.99
R5837:Mycbp2 UTSW 14 103,124,403 (GRCm38) missense probably damaging 1.00
R5984:Mycbp2 UTSW 14 103,126,684 (GRCm38) missense probably damaging 0.98
R6005:Mycbp2 UTSW 14 103,156,723 (GRCm38) missense probably benign
R6063:Mycbp2 UTSW 14 103,135,146 (GRCm38) missense probably damaging 1.00
R6091:Mycbp2 UTSW 14 103,223,046 (GRCm38) missense probably damaging 1.00
R6120:Mycbp2 UTSW 14 103,275,887 (GRCm38) missense probably benign 0.01
R6129:Mycbp2 UTSW 14 103,285,400 (GRCm38) missense probably benign 0.21
R6147:Mycbp2 UTSW 14 103,155,509 (GRCm38) nonsense probably null
R6161:Mycbp2 UTSW 14 103,298,747 (GRCm38) missense probably damaging 1.00
R6187:Mycbp2 UTSW 14 103,147,017 (GRCm38) missense probably damaging 1.00
R6208:Mycbp2 UTSW 14 103,295,228 (GRCm38) missense probably benign 0.11
R6228:Mycbp2 UTSW 14 103,260,229 (GRCm38) missense probably benign 0.24
R6301:Mycbp2 UTSW 14 103,155,426 (GRCm38) missense probably damaging 1.00
R6311:Mycbp2 UTSW 14 103,262,740 (GRCm38) missense possibly damaging 0.93
R6329:Mycbp2 UTSW 14 103,155,852 (GRCm38) missense probably benign 0.00
R6439:Mycbp2 UTSW 14 103,155,475 (GRCm38) missense probably benign 0.00
R6462:Mycbp2 UTSW 14 103,136,557 (GRCm38) critical splice donor site probably null
R6528:Mycbp2 UTSW 14 103,142,881 (GRCm38) missense probably damaging 0.99
R6736:Mycbp2 UTSW 14 103,191,567 (GRCm38) missense probably null 1.00
R6821:Mycbp2 UTSW 14 103,139,409 (GRCm38) missense probably damaging 1.00
R6851:Mycbp2 UTSW 14 103,260,194 (GRCm38) critical splice donor site probably null
R6948:Mycbp2 UTSW 14 103,285,267 (GRCm38) missense possibly damaging 0.94
R6977:Mycbp2 UTSW 14 103,154,906 (GRCm38) missense probably damaging 0.99
R6985:Mycbp2 UTSW 14 103,206,681 (GRCm38) missense possibly damaging 0.79
R7035:Mycbp2 UTSW 14 103,174,981 (GRCm38) missense probably benign
R7054:Mycbp2 UTSW 14 103,156,098 (GRCm38) missense possibly damaging 0.90
R7108:Mycbp2 UTSW 14 103,122,603 (GRCm38) missense probably damaging 1.00
R7117:Mycbp2 UTSW 14 103,154,077 (GRCm38) missense probably benign 0.21
R7137:Mycbp2 UTSW 14 103,282,679 (GRCm38) missense possibly damaging 0.94
R7169:Mycbp2 UTSW 14 103,260,200 (GRCm38) missense possibly damaging 0.78
R7218:Mycbp2 UTSW 14 103,133,846 (GRCm38) missense probably benign
R7234:Mycbp2 UTSW 14 103,215,337 (GRCm38) missense probably damaging 0.98
R7238:Mycbp2 UTSW 14 103,156,297 (GRCm38) missense probably damaging 1.00
R7244:Mycbp2 UTSW 14 103,208,909 (GRCm38) missense probably damaging 0.98
R7265:Mycbp2 UTSW 14 103,197,243 (GRCm38) critical splice donor site probably null
R7286:Mycbp2 UTSW 14 103,120,591 (GRCm38) missense probably damaging 1.00
R7332:Mycbp2 UTSW 14 103,197,357 (GRCm38) missense probably damaging 0.97
R7332:Mycbp2 UTSW 14 103,156,453 (GRCm38) missense probably damaging 1.00
R7384:Mycbp2 UTSW 14 103,276,393 (GRCm38) missense probably damaging 0.99
R7392:Mycbp2 UTSW 14 103,243,128 (GRCm38) missense probably damaging 0.99
R7392:Mycbp2 UTSW 14 103,152,191 (GRCm38) missense probably damaging 1.00
R7409:Mycbp2 UTSW 14 103,288,744 (GRCm38) missense probably damaging 1.00
R7486:Mycbp2 UTSW 14 103,197,254 (GRCm38) missense probably damaging 0.97
R7643:Mycbp2 UTSW 14 103,346,265 (GRCm38) missense probably benign
R7661:Mycbp2 UTSW 14 103,212,623 (GRCm38) missense probably damaging 1.00
R7663:Mycbp2 UTSW 14 103,191,609 (GRCm38) missense probably damaging 0.99
R7730:Mycbp2 UTSW 14 103,123,355 (GRCm38) missense probably damaging 0.99
R7757:Mycbp2 UTSW 14 103,191,619 (GRCm38) missense probably damaging 1.00
R7773:Mycbp2 UTSW 14 103,248,404 (GRCm38) missense probably damaging 0.97
R7787:Mycbp2 UTSW 14 103,127,097 (GRCm38) missense probably damaging 1.00
R7822:Mycbp2 UTSW 14 103,139,415 (GRCm38) missense probably benign 0.00
R7838:Mycbp2 UTSW 14 103,177,293 (GRCm38) missense probably benign 0.10
R7841:Mycbp2 UTSW 14 103,146,831 (GRCm38) critical splice donor site probably null
R7858:Mycbp2 UTSW 14 103,156,305 (GRCm38) missense probably damaging 1.00
R7873:Mycbp2 UTSW 14 103,156,146 (GRCm38) missense probably damaging 1.00
R7911:Mycbp2 UTSW 14 103,200,185 (GRCm38) missense probably damaging 0.99
R7942:Mycbp2 UTSW 14 103,155,238 (GRCm38) missense probably damaging 0.99
R7951:Mycbp2 UTSW 14 103,215,462 (GRCm38) missense probably damaging 0.99
R7958:Mycbp2 UTSW 14 103,129,964 (GRCm38) missense probably benign 0.00
R8235:Mycbp2 UTSW 14 103,198,674 (GRCm38) missense probably damaging 0.99
R8246:Mycbp2 UTSW 14 103,155,204 (GRCm38) missense probably damaging 0.99
R8338:Mycbp2 UTSW 14 103,135,265 (GRCm38) missense probably damaging 1.00
R8343:Mycbp2 UTSW 14 103,160,675 (GRCm38) splice site probably null
R8361:Mycbp2 UTSW 14 103,138,814 (GRCm38) missense probably damaging 1.00
R8490:Mycbp2 UTSW 14 103,208,831 (GRCm38) missense probably benign 0.00
R8524:Mycbp2 UTSW 14 103,155,459 (GRCm38) missense probably benign 0.23
R8525:Mycbp2 UTSW 14 103,212,719 (GRCm38) missense probably damaging 1.00
R8711:Mycbp2 UTSW 14 103,169,994 (GRCm38) missense probably benign 0.08
R8735:Mycbp2 UTSW 14 103,223,150 (GRCm38) missense probably damaging 0.99
R8825:Mycbp2 UTSW 14 103,229,435 (GRCm38) missense probably damaging 1.00
R8928:Mycbp2 UTSW 14 103,156,345 (GRCm38) missense probably benign
R8974:Mycbp2 UTSW 14 103,124,421 (GRCm38) missense probably damaging 1.00
R8987:Mycbp2 UTSW 14 103,208,796 (GRCm38) missense probably damaging 1.00
R9021:Mycbp2 UTSW 14 103,314,316 (GRCm38) missense probably benign 0.08
R9062:Mycbp2 UTSW 14 103,242,360 (GRCm38) missense probably benign 0.00
R9077:Mycbp2 UTSW 14 103,232,538 (GRCm38) missense probably damaging 1.00
R9208:Mycbp2 UTSW 14 103,295,228 (GRCm38) missense probably benign 0.01
R9285:Mycbp2 UTSW 14 103,197,317 (GRCm38) missense probably damaging 0.97
R9290:Mycbp2 UTSW 14 103,188,524 (GRCm38) missense probably damaging 0.99
R9362:Mycbp2 UTSW 14 103,260,206 (GRCm38) missense probably damaging 0.97
R9520:Mycbp2 UTSW 14 103,260,269 (GRCm38) missense probably benign 0.02
R9557:Mycbp2 UTSW 14 103,135,261 (GRCm38) missense probably benign 0.03
R9639:Mycbp2 UTSW 14 103,196,381 (GRCm38) missense probably damaging 1.00
R9666:Mycbp2 UTSW 14 103,134,038 (GRCm38) missense probably damaging 0.98
R9732:Mycbp2 UTSW 14 103,211,313 (GRCm38) missense probably damaging 1.00
R9736:Mycbp2 UTSW 14 103,197,416 (GRCm38) missense probably damaging 0.96
R9739:Mycbp2 UTSW 14 103,282,793 (GRCm38) missense probably benign 0.11
R9755:Mycbp2 UTSW 14 103,314,370 (GRCm38) missense probably benign
X0024:Mycbp2 UTSW 14 103,146,942 (GRCm38) missense probably damaging 1.00
Z1176:Mycbp2 UTSW 14 103,346,249 (GRCm38) missense probably benign
Z1176:Mycbp2 UTSW 14 103,156,637 (GRCm38) missense probably benign 0.06
Z1177:Mycbp2 UTSW 14 103,169,873 (GRCm38) missense possibly damaging 0.83
Z1177:Mycbp2 UTSW 14 103,135,123 (GRCm38) missense probably damaging 1.00
Z1177:Mycbp2 UTSW 14 103,127,063 (GRCm38) critical splice donor site probably null
Posted On 2014-05-07