Incidental Mutation 'R0468:Map9'
ID41731
Institutional Source Beutler Lab
Gene Symbol Map9
Ensembl Gene ENSMUSG00000033900
Gene Namemicrotubule-associated protein 9
SynonymsASAP, 5330427D05Rik, Mtap9, 5033421J10Rik
MMRRC Submission 038668-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.208) question?
Stock #R0468 (G1)
Quality Score225
Status Validated
Chromosome3
Chromosomal Location82358044-82395268 bp(+) (GRCm38)
Type of Mutationcritical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to C at 82374203 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000142206 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091014] [ENSMUST00000091014] [ENSMUST00000192595] [ENSMUST00000192595] [ENSMUST00000193559] [ENSMUST00000193559] [ENSMUST00000195471] [ENSMUST00000195471] [ENSMUST00000195640] [ENSMUST00000195640]
Predicted Effect probably null
Transcript: ENSMUST00000091014
SMART Domains Protein: ENSMUSP00000088535
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
Pfam:DUF4207 340 566 3.6e-10 PFAM
low complexity region 607 622 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000091014
SMART Domains Protein: ENSMUSP00000088535
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
Pfam:DUF4207 340 566 3.6e-10 PFAM
low complexity region 607 622 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000192595
SMART Domains Protein: ENSMUSP00000141828
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000192595
SMART Domains Protein: ENSMUSP00000141828
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000193559
SMART Domains Protein: ENSMUSP00000142014
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
low complexity region 356 365 N/A INTRINSIC
coiled coil region 476 513 N/A INTRINSIC
low complexity region 516 537 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000193559
SMART Domains Protein: ENSMUSP00000142014
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
low complexity region 356 365 N/A INTRINSIC
coiled coil region 476 513 N/A INTRINSIC
low complexity region 516 537 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000195471
SMART Domains Protein: ENSMUSP00000141282
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
low complexity region 356 365 N/A INTRINSIC
coiled coil region 476 513 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000195471
SMART Domains Protein: ENSMUSP00000141282
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
low complexity region 356 365 N/A INTRINSIC
coiled coil region 476 513 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000195640
SMART Domains Protein: ENSMUSP00000142206
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
Pfam:DUF4207 332 562 4.4e-11 PFAM
low complexity region 564 596 N/A INTRINSIC
low complexity region 607 622 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000195640
SMART Domains Protein: ENSMUSP00000142206
Gene: ENSMUSG00000033900

DomainStartEndE-ValueType
low complexity region 41 52 N/A INTRINSIC
Pfam:DUF4207 332 562 4.4e-11 PFAM
low complexity region 564 596 N/A INTRINSIC
low complexity region 607 622 N/A INTRINSIC
Meta Mutation Damage Score 0.9487 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.2%
Validation Efficiency 100% (61/61)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] ASAP is a microtubule-associated protein required for spindle function, mitotic progression, and cytokinesis (Saffin et al., 2005 [PubMed 16049101]).[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik A G 12: 71,193,310 H1298R possibly damaging Het
5530400C23Rik T C 6: 133,294,458 L155P probably benign Het
6820408C15Rik A T 2: 152,441,266 R283S probably benign Het
Aldh1l2 T A 10: 83,518,678 E104D probably benign Het
Anxa3 T C 5: 96,811,099 V22A probably benign Het
Bcl7b T C 5: 135,180,883 F188L probably benign Het
Brinp1 T A 4: 68,762,776 I506F probably damaging Het
Bsdc1 T C 4: 129,461,718 probably benign Het
Ccdc180 T C 4: 45,923,271 I1075T possibly damaging Het
Cep162 A G 9: 87,193,697 L1294P probably damaging Het
Cltc G A 11: 86,704,626 probably benign Het
Col11a1 T C 3: 114,217,058 probably benign Het
Col14a1 A T 15: 55,388,646 Y566F unknown Het
Dhx29 A G 13: 112,963,277 Q1148R probably benign Het
Ehbp1 A G 11: 22,169,184 probably benign Het
Ehd3 A G 17: 73,805,379 H46R probably damaging Het
Fam171a1 T C 2: 3,225,396 V522A probably benign Het
Gm4553 C A 7: 142,165,625 C22F unknown Het
Hibadh C T 6: 52,557,770 probably benign Het
Hspg2 G A 4: 137,533,529 C1613Y probably damaging Het
Hydin G T 8: 110,413,223 C708F possibly damaging Het
Ifi208 A T 1: 173,683,481 M401L probably benign Het
Igsf8 G A 1: 172,318,796 V454M probably damaging Het
Irx4 G T 13: 73,266,720 probably benign Het
Kcnh4 C T 11: 100,746,932 G633E probably benign Het
Kcnn2 C T 18: 45,559,471 T38M possibly damaging Het
L3mbtl3 C T 10: 26,327,732 R400H unknown Het
Lrp6 T C 6: 134,485,661 T679A possibly damaging Het
Men1 T A 19: 6,336,923 V5E probably null Het
Mettl14 T C 3: 123,371,412 D93G probably damaging Het
Neb G T 2: 52,211,556 R4601S probably damaging Het
Nell1 A G 7: 50,228,846 T272A probably damaging Het
Olfr1115 A T 2: 87,252,255 N106I probably benign Het
Olfr319 A T 11: 58,701,793 I31F probably damaging Het
Pclo C A 5: 14,677,288 probably benign Het
Pdia5 A G 16: 35,397,507 L502P probably damaging Het
Pkd1l3 C G 8: 109,623,649 D375E possibly damaging Het
Plxna4 C A 6: 32,215,246 C803F probably damaging Het
Pmfbp1 A G 8: 109,513,968 probably null Het
Ptgs1 A G 2: 36,249,193 Y468C probably damaging Het
Pxdn G T 12: 29,994,486 G488W probably damaging Het
Safb C T 17: 56,606,025 R914C probably damaging Het
Sec31b T A 19: 44,518,508 probably benign Het
Shank3 G A 15: 89,549,275 V1333I probably benign Het
Slamf1 A G 1: 171,792,371 probably benign Het
Slc23a3 T A 1: 75,133,230 Q131L possibly damaging Het
Slc7a11 A G 3: 50,384,051 V303A probably damaging Het
Slc7a13 T A 4: 19,841,500 V449D probably benign Het
Srp68 A T 11: 116,248,764 I453K probably damaging Het
Steap3 A T 1: 120,234,300 V414D probably damaging Het
Tagln2 A G 1: 172,506,221 N131D probably benign Het
Tmem132d T C 5: 128,269,203 Y85C probably damaging Het
Vcam1 A T 3: 116,115,946 Y577* probably null Het
Vmn1r214 A G 13: 23,035,253 T306A probably benign Het
Zfyve1 A T 12: 83,555,274 probably benign Het
Zgrf1 T A 3: 127,562,041 N305K possibly damaging Het
Other mutations in Map9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00742:Map9 APN 3 82363420 missense probably benign 0.37
IGL01520:Map9 APN 3 82378965 missense probably damaging 0.99
IGL02281:Map9 APN 3 82391146 missense possibly damaging 0.53
IGL02931:Map9 APN 3 82377121 missense possibly damaging 0.86
IGL02937:Map9 APN 3 82363512 missense possibly damaging 0.95
IGL02985:Map9 APN 3 82359902 nonsense probably null
IGL03113:Map9 APN 3 82359978 splice site probably benign
R0134:Map9 UTSW 3 82359983 splice site probably benign
R0225:Map9 UTSW 3 82359983 splice site probably benign
R1027:Map9 UTSW 3 82377094 missense probably damaging 1.00
R1794:Map9 UTSW 3 82380221 missense probably damaging 1.00
R4008:Map9 UTSW 3 82359083 missense probably damaging 1.00
R5728:Map9 UTSW 3 82363335 missense probably benign 0.00
R5905:Map9 UTSW 3 82380248 critical splice donor site probably null
R6028:Map9 UTSW 3 82380248 critical splice donor site probably null
R6334:Map9 UTSW 3 82383305 missense probably damaging 1.00
R6798:Map9 UTSW 3 82380164 missense probably damaging 1.00
R7135:Map9 UTSW 3 82363458 missense probably benign 0.03
R7443:Map9 UTSW 3 82371356 missense possibly damaging 0.72
R7694:Map9 UTSW 3 82358983 start gained probably benign
R8224:Map9 UTSW 3 82359063 missense probably benign 0.33
R8237:Map9 UTSW 3 82377160 missense probably damaging 0.97
R8395:Map9 UTSW 3 82381969 missense probably benign 0.06
R8504:Map9 UTSW 3 82377169 critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- GTGTTTCCTTCCTGAGACTTTGGCA -3'
(R):5'- ATCTCCCCAGTTCTCCTTGAGAGTATG -3'

Sequencing Primer
(F):5'- tggaagagcaggaagcac -3'
(R):5'- agagccttttgagacaggac -3'
Posted On2013-05-23