Incidental Mutation 'IGL02739:Nomo1'
ID 305824
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Nomo1
Ensembl Gene ENSMUSG00000030835
Gene Name nodal modulator 1
Synonyms D7Ertd156e, Nomo, PM5
Accession Numbers
Essential gene? Possibly essential (E-score: 0.672) question?
Stock # IGL02739
Quality Score
Status
Chromosome 7
Chromosomal Location 45683122-45733636 bp(+) (GRCm39)
Type of Mutation splice site (4 bp from exon)
DNA Base Change (assembly) A to G at 45693731 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000033121 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000033121]
AlphaFold Q6GQT9
Predicted Effect probably null
Transcript: ENSMUST00000033121
SMART Domains Protein: ENSMUSP00000033121
Gene: ENSMUSG00000030835

DomainStartEndE-ValueType
low complexity region 2 21 N/A INTRINSIC
internal_repeat_1 22 215 2.35e-7 PROSPERO
Pfam:CarboxypepD_reg 322 395 3.5e-12 PFAM
Pfam:DUF2012 331 401 5.7e-10 PFAM
low complexity region 709 732 N/A INTRINSIC
low complexity region 881 893 N/A INTRINSIC
Blast:FN3 913 1017 6e-22 BLAST
low complexity region 1156 1164 N/A INTRINSIC
low complexity region 1203 1214 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI

All alleles(8) : Gene trapped(8)

Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aasdh A T 5: 77,026,364 (GRCm39) C887S possibly damaging Het
Adamdec1 C A 14: 68,807,605 (GRCm39) E352* probably null Het
Bglap2 A T 3: 88,285,319 (GRCm39) probably null Het
Bsn A T 9: 107,989,745 (GRCm39) H2002Q probably benign Het
Chtop T A 3: 90,409,557 (GRCm39) Q165L possibly damaging Het
Clcn1 A T 6: 42,263,714 (GRCm39) probably null Het
Ctsr T C 13: 61,309,658 (GRCm39) T184A probably benign Het
Defb36 T C 2: 152,446,439 (GRCm39) L11P unknown Het
Dock8 A G 19: 25,165,852 (GRCm39) E1912G probably damaging Het
Dpp3 A G 19: 4,973,756 (GRCm39) Y106H probably damaging Het
Epas1 A G 17: 87,112,710 (GRCm39) T103A probably damaging Het
Epcam A T 17: 87,947,922 (GRCm39) T131S probably benign Het
Fam169a A G 13: 97,230,563 (GRCm39) probably benign Het
Gh T A 11: 106,192,559 (GRCm39) probably benign Het
Kif20a A T 18: 34,761,996 (GRCm39) K399* probably null Het
Lrp1b A G 2: 41,388,227 (GRCm39) I466T probably damaging Het
Nlk A G 11: 78,465,677 (GRCm39) V409A probably benign Het
Nr2c1 T A 10: 93,992,834 (GRCm39) M16K probably damaging Het
Nxph2 A T 2: 23,289,912 (GRCm39) Q88L probably benign Het
Or51a39 A G 7: 102,363,521 (GRCm39) I33T possibly damaging Het
Pkdrej T A 15: 85,703,895 (GRCm39) R680S probably benign Het
Pkhd1l1 A T 15: 44,404,346 (GRCm39) N2325I probably benign Het
Pnliprp2 T C 19: 58,748,941 (GRCm39) probably null Het
Ppp1r42 T A 1: 10,039,078 (GRCm39) K347N probably benign Het
Prtg T C 9: 72,758,867 (GRCm39) V407A possibly damaging Het
Psmb8 C A 17: 34,419,728 (GRCm39) S194* probably null Het
Rnf214 T C 9: 45,780,772 (GRCm39) I406V probably benign Het
Rreb1 C T 13: 38,077,797 (GRCm39) S3L probably damaging Het
Sdad1 C T 5: 92,437,931 (GRCm39) A539T probably benign Het
Sema3a A G 5: 13,501,128 (GRCm39) Y57C probably damaging Het
Susd5 A G 9: 113,925,101 (GRCm39) E328G possibly damaging Het
Syngr3 T C 17: 24,905,372 (GRCm39) T175A probably damaging Het
Tcf20 T A 15: 82,740,281 (GRCm39) Q390L probably damaging Het
Tex15 A G 8: 34,071,721 (GRCm39) T2423A possibly damaging Het
Tlr1 T C 5: 65,084,469 (GRCm39) N36S probably benign Het
Uchl4 C T 9: 64,142,819 (GRCm39) T100M probably damaging Het
Uhrf1 A G 17: 56,612,129 (GRCm39) K11R probably benign Het
Vps13b T A 15: 35,880,046 (GRCm39) D3040E probably damaging Het
Wdr62 A T 7: 29,941,885 (GRCm39) Y640* probably null Het
Zkscan17 T G 11: 59,394,352 (GRCm39) E83A probably damaging Het
Other mutations in Nomo1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00331:Nomo1 APN 7 45,694,760 (GRCm39) missense possibly damaging 0.66
IGL00811:Nomo1 APN 7 45,732,732 (GRCm39) missense possibly damaging 0.95
IGL01710:Nomo1 APN 7 45,687,980 (GRCm39) missense probably damaging 1.00
IGL01797:Nomo1 APN 7 45,706,086 (GRCm39) missense probably damaging 0.96
IGL01973:Nomo1 APN 7 45,732,651 (GRCm39) splice site probably benign
IGL02506:Nomo1 APN 7 45,727,480 (GRCm39) missense possibly damaging 0.50
IGL02863:Nomo1 APN 7 45,696,340 (GRCm39) missense probably damaging 0.98
P0005:Nomo1 UTSW 7 45,686,981 (GRCm39) critical splice acceptor site probably null
PIT4243001:Nomo1 UTSW 7 45,693,705 (GRCm39) missense probably damaging 1.00
R0106:Nomo1 UTSW 7 45,687,056 (GRCm39) missense probably damaging 1.00
R0106:Nomo1 UTSW 7 45,687,056 (GRCm39) missense probably damaging 1.00
R0124:Nomo1 UTSW 7 45,732,652 (GRCm39) splice site probably benign
R0239:Nomo1 UTSW 7 45,729,018 (GRCm39) critical splice donor site probably null
R0239:Nomo1 UTSW 7 45,729,018 (GRCm39) critical splice donor site probably null
R0417:Nomo1 UTSW 7 45,718,122 (GRCm39) missense possibly damaging 0.51
R0467:Nomo1 UTSW 7 45,721,911 (GRCm39) splice site probably null
R0535:Nomo1 UTSW 7 45,721,941 (GRCm39) missense probably damaging 0.99
R0829:Nomo1 UTSW 7 45,725,596 (GRCm39) splice site probably benign
R0940:Nomo1 UTSW 7 45,683,329 (GRCm39) missense possibly damaging 0.56
R1480:Nomo1 UTSW 7 45,710,337 (GRCm39) missense probably damaging 0.98
R1601:Nomo1 UTSW 7 45,696,379 (GRCm39) missense probably damaging 0.96
R1743:Nomo1 UTSW 7 45,719,461 (GRCm39) critical splice donor site probably null
R1765:Nomo1 UTSW 7 45,715,717 (GRCm39) missense possibly damaging 0.59
R1861:Nomo1 UTSW 7 45,727,525 (GRCm39) missense probably benign 0.06
R1998:Nomo1 UTSW 7 45,683,368 (GRCm39) missense possibly damaging 0.69
R1999:Nomo1 UTSW 7 45,706,151 (GRCm39) missense possibly damaging 0.95
R2145:Nomo1 UTSW 7 45,715,928 (GRCm39) missense probably damaging 1.00
R2869:Nomo1 UTSW 7 45,696,361 (GRCm39) missense probably damaging 0.96
R2869:Nomo1 UTSW 7 45,696,361 (GRCm39) missense probably damaging 0.96
R2870:Nomo1 UTSW 7 45,696,361 (GRCm39) missense probably damaging 0.96
R2870:Nomo1 UTSW 7 45,696,361 (GRCm39) missense probably damaging 0.96
R2871:Nomo1 UTSW 7 45,696,361 (GRCm39) missense probably damaging 0.96
R2871:Nomo1 UTSW 7 45,696,361 (GRCm39) missense probably damaging 0.96
R2873:Nomo1 UTSW 7 45,696,361 (GRCm39) missense probably damaging 0.96
R4116:Nomo1 UTSW 7 45,683,320 (GRCm39) missense probably benign 0.06
R4404:Nomo1 UTSW 7 45,706,092 (GRCm39) missense probably benign 0.00
R4406:Nomo1 UTSW 7 45,706,092 (GRCm39) missense probably benign 0.00
R4560:Nomo1 UTSW 7 45,690,904 (GRCm39) missense probably damaging 0.99
R4633:Nomo1 UTSW 7 45,699,684 (GRCm39) splice site probably benign
R4651:Nomo1 UTSW 7 45,717,866 (GRCm39) missense probably damaging 0.99
R4653:Nomo1 UTSW 7 45,711,237 (GRCm39) missense probably benign 0.01
R4752:Nomo1 UTSW 7 45,706,626 (GRCm39) missense probably damaging 1.00
R4792:Nomo1 UTSW 7 45,693,643 (GRCm39) splice site probably null
R4838:Nomo1 UTSW 7 45,733,139 (GRCm39) missense unknown
R4876:Nomo1 UTSW 7 45,715,915 (GRCm39) missense probably damaging 1.00
R4915:Nomo1 UTSW 7 45,693,656 (GRCm39) missense probably benign 0.30
R4953:Nomo1 UTSW 7 45,700,155 (GRCm39) intron probably benign
R5463:Nomo1 UTSW 7 45,712,426 (GRCm39) missense possibly damaging 0.47
R5664:Nomo1 UTSW 7 45,725,581 (GRCm39) missense probably benign
R5956:Nomo1 UTSW 7 45,692,037 (GRCm39) missense possibly damaging 0.51
R6037:Nomo1 UTSW 7 45,712,423 (GRCm39) missense possibly damaging 0.64
R6037:Nomo1 UTSW 7 45,712,423 (GRCm39) missense possibly damaging 0.64
R6307:Nomo1 UTSW 7 45,683,260 (GRCm39) unclassified probably benign
R6695:Nomo1 UTSW 7 45,715,885 (GRCm39) missense probably benign 0.16
R6970:Nomo1 UTSW 7 45,695,391 (GRCm39) missense probably damaging 0.97
R7334:Nomo1 UTSW 7 45,732,692 (GRCm39) missense probably damaging 1.00
R7394:Nomo1 UTSW 7 45,715,903 (GRCm39) missense probably benign 0.26
R7556:Nomo1 UTSW 7 45,715,642 (GRCm39) missense probably damaging 1.00
R7834:Nomo1 UTSW 7 45,706,162 (GRCm39) critical splice donor site probably null
R7979:Nomo1 UTSW 7 45,690,986 (GRCm39) missense probably null
R8193:Nomo1 UTSW 7 45,692,037 (GRCm39) missense possibly damaging 0.51
R8841:Nomo1 UTSW 7 45,707,911 (GRCm39) missense probably benign 0.00
R8906:Nomo1 UTSW 7 45,722,004 (GRCm39) missense probably benign 0.06
R9049:Nomo1 UTSW 7 45,715,597 (GRCm39) missense probably benign 0.01
R9087:Nomo1 UTSW 7 45,732,748 (GRCm39) missense probably benign 0.00
R9176:Nomo1 UTSW 7 45,730,828 (GRCm39) missense possibly damaging 0.88
Z1177:Nomo1 UTSW 7 45,715,697 (GRCm39) missense probably benign 0.17
Posted On 2015-04-16