ZMP
LOC100332271
Ensembl ID:
Human Orthologue:
IQGAP1
Human Description:
IQ motif containing GTPase activating protein 1 [Source:HGNC Symbol;Acc:6110]
Mouse Orthologue:
Iqgap1
Mouse Description:
IQ motif containing GTPase activating protein 1 Gene [Source:MGI Symbol;Acc:MGI:1352757]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41010 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7084 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11898 | Essential Splice Site | Available for shipment | Available now |
sa15628 | Essential Splice Site | Available for shipment | Available now |
sa41009 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34178 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9487 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41010
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110283 | Essential Splice Site | 154 | 1655 | 5 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 52165618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50435458 |
GRCz11 | 7 | 50708240 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACAGGAAGAACATGCCACGCTGTATCTATTGCATACATGCTCTCAGG[T/A]AATCTAATATGTCACTGTGGGCTCATTCAGAAAACTCGTGTTAGGGAGCA
Long Flanking Sequence:
CGGCGTTTATCTGGCCAAGCTGGGAAACTTCTTTGCCCCCAATGTGGTCTCTCTCAAAAGAATCTATGACCGTGAACAAACACGCTACAAGGTGAGACTGACTTTATTTCTTTCAGGAGCTCTGACGGAAATAGCAGACGGTTTGAATTAAAATGTTACTCCTTTCTTTTCCCCCCTCTGCTTTGTCTTGTTTGTAGGCCACTGGGCTCCATTTCAGACACACAGACAATATCATCCAGTGGCTGAATGCAATGACAGATAAGGGCCTCCCTAAGGTGAGTCTGCATGGATCTGTCATTAGCGGCATTTCTTCAGCTTTACCGAGACATGACAGAGCTTGCCTCTCAGCTTCTTCTCCATGTTTGGCAACAGTGCTGCCTTCGGTCTCATCAAAGTACATGTTTTTTGTCTCTCCACGTTAGATTTTCTATCCTGAGACAACAGACATCTATGACAGGAAGAACATGCCACGCTGTATCTATTGCATACATGCTCTCAGG[T/A]AATCTAATATGTCACTGTGGGCTCATTCAGAAAACTCGTGTTAGGGAGCAGCCAACTATAATGCTGGGTTCACACACCAGACGGGAAGCATCTCAACATTGCTCTAGATTACTTGCTGGGGAGTTTTTTTTTCGCCTCACACTAATTTTCTGCTCAAGTTTATTTTAAATCATTTATTTATTTATTTTTTACTTATGGTGAATTGGACGTGTTCAGTTTCACGTCATTCACACCACCCGATGGAAATTCGCCCCCATTCTTGCATTTGCATTGTCTACTCATGTGAATACTTCAATATGTATTGGTAACACTTAATGTCAGTTAATGCAGTTACTAACATCAACAAAGAATGAAAGATAAGTTTGTTATAGTAACCTTTATTAGGCTTTGTTAACATTTTAATGAAGATTAAGTTGTTAGTTGTTGTTAACTCACAGTGCTTTAACTAATGTTAACAATCATAAGTTTGGGATTTTAATAATGCATTATTTAATCAGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7084
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110283 | Nonsense | 186 | 1655 | 7 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 52159909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50429749 |
GRCz11 | 7 | 50702531 |
KASP Assay ID:
554-4428.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGTCTGTCYTTTATCTTTTCAGAGGAGGAGATCAACAAMATGAAGATC[G/T]AATTAGAGAAATACAACATTCAAATGCCAGCCTTCAGCAAAATCGGTGGR
Long Flanking Sequence:
GACTTTCTGTTTTCTCTATAGCCTCTACCTGTTTAAACTTGGTCTTGCGCCCCAGATTACAGACCTGTATGGCAAGGTCGCCTTCACAGGTGAGTCAACTCATCACGGTATTAAACTAAGCCTGGATTTTATATGGTATGATCTGGAAAGGCTGCTGTTCCTGGGAGCTGTGTTCAATGTGAAAAGCATTATCAATTGTTTGAGGGTTTCCTGCCATTTTGGCTGGCTCAAACCGCCTGCCAAGTCCCTGGATGGAGAACATTATTTACCAGACTTGCTGAGAACAATGTCCAGCCGACTCCATCAAAGAGGGGAAAAACGCTCAGCTGAGATTACCTTCTAAAAGGTTACCCAGCAGAATTTATCCAGAGTCATACAGTATAAAATAATAAAAACCTAATTCATAACATAAAGCCAAATAATCACCATTTTCACTAATATTTGCAATGCTGAGTCTGTCCTTTATCTTTTCAGAGGAGGAGATCAACAACATGAAGATC[G/T]AATTAGAGAAATACAACATTCAAATGCCAGCCTTCAGCAAAATCGGTGGGATTTTAGCCAACGAGTTATCAGTGGACGAAGCAGCCTGTGAGTTTCACGCTTTCAAAAGTCAAATTCCTCTTGGCTCTTTGGCACAGATCCTTCCCGCGCAAACAATAAACTACTAGACTTAACTTGTACAGCCAAGAGTTTAACAGCACAGTAATTACGATCTGTTTTACATCCCTCTGAGCTCAAAATATCTGCATTATCTTTTGTTGTAACGATTCAGTGCATGCTGCTGTGATCGCCATCAATGATGCCATTGACCATGGAGTTCCTGAGGGCACTTTAGCTGCCATGAGAAACCCGAACGCCATGTTGCTGCAGCTGGATGAAAGCGCTGCCCAGCAGTACCAGGACACCCTGTTCCAGGCCAAGAGTGAGAAAGTGGCCAACTCCCGAAAGAGAGTACGAACTGCACTCTACTATTAAGAGATTTGTTGTACTTGAGTTACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11898
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110283 | Essential Splice Site | 274 | 1655 | 8 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 52159457)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50429297 |
GRCz11 | 7 | 50702079 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACCCTGTTCCAGGCCAAGAGTGAGAAAGTGGCCAACTCCCGAAAGAGAG[T/C]ACGAACTGCACTSTACWATTAAGAGATTTGTTGTACTTGAGTTACTAAGG
Long Flanking Sequence:
AGTCTGTCCTTTATCTTTTCAGAGGAGGAGATCAACAACATGAAGATCGAATTAGAGAAATACAACATTCAAATGCCAGCCTTCAGCAAAATCGGTGGGATTTTAGCCAACGAGTTATCAGTGGACGAAGCAGCCTGTGAGTTTCACGCTTTCAAAAGTCAAATTCCTCTTGGCTCTTTGGCACAGATCCTTCCCGCGCAAACAATAAACTACTAGACTTAACTTGTACAGCCAAGAGTTTAACAGCACAGTAATTACGATCTGTTTTACATCCCTCTGAGCTCAAAATATCTGCATTATCTTTTGTTGTAACGATTCAGTGCATGCTGCTGTGATCGCCATCAATGATGCCATTGACCATGGAGTTCCTGAGGGCACTTTAGCTGCCATGAGAAACCCGAACGCCATGTTGCTGCAGCTGGATGAAAGCGCTGCCCAGCAGTACCAGGACACCCTGTTCCAGGCCAAGAGTGAGAAAGTGGCCAACTCCCGAAAGAGAG[T/C]ACGAACTGCACTCTACTATTAAGAGATTTGTTGTACTTGAGTTACTAAGGGTGTTTTTTGCAATATGTACATATCATATCTCTTCAAAAACTTAGTGACTAGCATAACTAGACTGTAAAATGGGTAAAGTCTAAATTGAACATGCAGCCGGCCAAAAGTGTGATATGCACATCAATATAGCAGCATTTTTTTAAGAACACTGAATAACAATAATTAATACTTTACAGTACTGTGATTATTGTGTTTAGGGTTGGGGTGTGTGTAGGTGTTAAAAATACAATTTTATTGGGTGATTTAATAGATAGCATAAACAATACGCTGTACAACTACTGTTTTTACGTTTCTGTGATGGTTAGGTTTAGGGTTGGTGTGGTGGTAGACATTAATAAAATACAATAAATGGGAAATGTATTAAATAATATAACTATTTCTCGTTAGCTTCCATCCGCAACCATATCCAATCTAGCCACAACCTAGAAAGTTGGGTAACACTTTTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15628
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110283 | Essential Splice Site | 677 | 1655 | 17 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 52134199)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50404039 |
GRCz11 | 7 | 50676821 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCTACCAGGATGACCTGCTGCGRATTAAAGACGACAAGAGAAAGGAAG[G/A]TGAGATGGGCTCTTCTGTTGATTYTTTAATATYTGGTACWAAACAAGTAT
Long Flanking Sequence:
AAACATAATTGTTGTTTTTTTCCTTTTTATAATAGTTTTTTTTTCTTTCTTTTCTTTTTTCCAGGAATCTGGAGATCCATCTGCGGTGCTTTGGCTAGATGAGATTCAGGATGCAATCCTGAGAGCCAACAAGGACTCAGAGGAAGCTCTGCAGTGTAATGCTTATTAAAATCTTTATTCATTTAGCCTCTCTGTTTATCTCTTTATCTCTTTGTCTTAATAAATATCTATAACATATATTAAGATATAACATATTTTAATATATAACAGGTGATTCTTTTCTTTAAATTATGTCAGCTTTTTTCTAAAGAATGATCTTTGTCTGCCTTCAGTCTCTCAGGCGATCCAGGCCATTAATGAGGCTGTAGATAATAAGGACTCTTCTCAGACACTGGCGGCCTTGCGATCCCCTGCTGCTGGCATGTATGGAGTCACATCTGAATGTGCTCAAACCTACCAGGATGACCTGCTGCGAATTAAAGACGACAAGAGAAAGGAAG[G/A]TGAGATGGGCTCTTCTGTTGATTCTTTAATATTTGGTACTAAACAAGTATTGCCATATTTATGTTAAAATAACTGACATTTGTGCTAATTTTCTCAAAAGATGAAGATAAATATCCTTATCACAAGCTCTTGGTGACTATATATTGTTATCATGTAATAGTAATACTATACTATGAGTTTGTCTAAAACTATTTTCTGTTTACATACAGTTGAAGTCAGAGTTATTAGCCTCCCTGAATTATTAGCCCCCGTTTAATTTTTTCCCCAATTTCTGTTTAACGGAGAGCAGATTTTTTCAACACATTTCCAAACATAATAGTTTTAATAACTCATTTTTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAAAATTTGACTAGATATTTTTCAAGACACTTCTATACAGCTGAAAGTGATATTTAAAGGCTTAACTAGGTTTACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTATAATGATGGTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41009
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110283 | Nonsense | 1253 | 1655 | 28 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 52111383)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50381223 |
GRCz11 | 7 | 50654005 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAAGATGTTCCTTGGAGACAACGCACATTTGAACCCCATCAACGAATA[C/A]CTCGCCAACTCCTACCAGAAATTTAGGTAAAAGTGATATCAGTGCTTCTG
Long Flanking Sequence:
GCAGTGGAAGCCATTACAATGAATGGGTTTCATAGCGCAGAACTTTCCTTGTCTGGTGTGAAAGCTACTTTACACTGCAGTGACTATAGCTAGTGGTACTGTGAAACAAGTGCACTGAACATTACAGCATTTAAGTATAGTCTTTATTCTGTTCATTTTTTTTGCCAAAGCATTAAATCCATTTTCTGCCAATAATTTTTAGTGCGTCCATCATAGAAACAGCATTTTTTTAAACTGCATAGCTTTTGTATTTACTTGAAAATGAAAACATGGCCATGTTTCTCATTCTTTAAGATTGTGGGCAACCTGCTTTACTACCGTTACATGAATCCTGCCATTGTGGCTCCTGATGCGTTTGACATCATCGATATATCAGCTGGGGGTCAGCTGACCACAGAACAGAGGCGAAATCTGGGGTCAATCGCCAAAATGCTGCAACACGCAGCCTCAAACAAGATGTTCCTTGGAGACAACGCACATTTGAACCCCATCAACGAATA[C/A]CTCGCCAACTCCTACCAGAAATTTAGGTAAAAGTGATATCAGTGCTTCTGTTTGTTGTTTTCCAGTTGTTTGGTTTATAATCACTCCATACTGATGCAAGAACCCTTCTGTCTTCCAGACGTTTCTTTTTGTCCGCTTGTGACGTCCCTACTTTGGAGGACAAGTTCAATGTGGATCAGTACTCAGACGTGGTCACCTTGACCAAGCCTGTGATCTACATTACCATCGGGGAGATCATCAACACTCACACGGTAACAATCCAAGACTCATGGTATGCTTACATACCCCTTTTCTACCAAGGCTAGTTCCAAATCGTTTTTTTGACACCCAAATCACCAGCTGTGAAACAGGAAAAGTGCTTCTTAAGTAGCACCAAAACATTGCTGAGCTAGAACTAGTCATGTCAAGGGCTGAGTTGTATTCTCCATCTATACAAAGTGTTACTATGGCACACTGCATGAATGCAATGGATTTGCTGTGCGAAATAGGTTTGCTAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34178
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110283 | Essential Splice Site | 1416 | 1655 | 33 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 52108799)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50378639 |
GRCz11 | 7 | 50651421 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAAGCTTTATCAAACTTTGTAATAAAGTCAGCACTTTTATTTGAAACA[G/A]GAAGCAGAGTACCAGCGAGCTATGCAGCGGCGAGCCATTCGCGATGCAAA
Long Flanking Sequence:
ATTAATGTTACTTGTCACCCACTTATGTCACTTCAGAGATACAAGTGATAATACAACCAGAAAATTTGTCCAAAAGAATATTACTAATTGGGGAACCAGGTTTGGAGGCTATTCTCCCATGATCACCTTCCTGTAAATATCAGATGCACAACCCCCTATACAAATCACCTTTTGAATCTCATATACAGAGAAGAATGCAATTGCTTTCTAATTGAGTTTGCAAGTAATTGCTGGCTGTCTTAATTACTAGTTTCTGAAACTAGTAGAACTTGGGCATTTACTTGTTTTACTTATTCACAAATCTGCCCCTTTTGTCTTGCTCATTTAGCACCAAGAGGCTCATAGTAGATGTGATCAGATTTCAGCCAGGAGACACACTTACTGAGATTCTGGAGACTGTAGCTTCACCTGAGCAGGTACTTTAATTGCTATTTATTTTTCAAGAATGGAAGTAAGCTTTATCAAACTTTGTAATAAAGTCAGCACTTTTATTTGAAACA[G/A]GAAGCAGAGTACCAGCGAGCTATGCAGCGGCGAGCCATTCGCGATGCAAAGACCCCAGAGAAGATGAAGCAAGCCAAACCAGTTGTAGATGACAGTCTTACTTTGCAAGGCAAGAAGGACAAGATCAAGAGCAACCTGCAAAGACTGGGAGAGTTGGGCAAAGTACACCCTGAGAAGAAATACCAGGACCTAATCAATGACATCGCCAAGGTACTGTTCTTGGATGTGTCCTAGCATTTACATTCTGCATGTCAAGGGTGTCCAAACTTGGTCCTTGAGAGCTGGTGTCCTGCAAATTTTAGCTTCAACTTGTCTCAAGACACCTGCAAGGATGTTTCTAGAAAGCCTAGTAAGAACTTGATTAGTTAGCCCAGGTGTGTCTGATTGGAGTTGGAACTAAACTTTGCAGGACACCGGCCCTCCAGGACCGAGTTTAGTCACCACTGCTTTATGAGAACACAAAACTTCTAGCATTTCATTTTCACACTAAAGCAGGGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9487
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110283 | Essential Splice Site | 1485 | 1655 | 33 | 37 |
Genomic Location (Zv9):
Chromosome 7 (position 52108587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50378427 |
GRCz11 | 7 | 50651209 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTACACCCTGAGAAGAAATACCAGGACCTAATCAATGACATCGCCAAGG[T/C]ACTGTWCTTGGATGTGTCCTAGCATTTACATTCTGCATGTCAAGGGTGTC
Long Flanking Sequence:
TGAGTTTGCAAGTAATTGCTGGCTGTCTTAATTACTAGTTTCTGAAACTAGTAGAACTTGGGCATTTACTTGTTTTACTTATTCACAAATCTGCCCCTTTTGTCTTGCTCATTTAGCACCAAGAGGCTCATAGTAGATGTGATCAGATTTCAGCCAGGAGACACACTTACTGAGATTCTGGAGACTGTAGCTTCACCTGAGCAGGTACTTTAATTGCTATTTATTTTTCAAGAATGGAAGTAAGCTTTATCAAACTTTGTAATAAAGTCAGCACTTTTATTTGAAACAGGAAGCAGAGTACCAGCGAGCTATGCAGCGGCGAGCCATTCGCGATGCAAAGACCCCAGAGAAGATGAAGCAAGCCAAACCAGTTGTAGATGACAGTCTTACTTTGCAAGGCAAGAAGGACAAGATCAAGAGCAACCTGCAAAGACTGGGAGAGTTGGGCAAAGTACACCCTGAGAAGAAATACCAGGACCTAATCAATGACATCGCCAAGG[T/C]ACTGTTCTTGGATGTGTCCTAGCATTTACATTCTGCATGTCAAGGGTGTCCAAACTTGGTCCTTGAGAGCTGGTGTCCTGCAAATTTTAGCTTCAACTTGTCTCAAGACACCTGCAAGGATGTTTCTAGAAAGCCTAGTAAGAACTTGATTAGTTAGCCCAGGTGTGTCTGATTGGAGTTGGAACTAAACTTTGCAGGACACCGGCCCTCCAGGACCGAGTTTAGTCACCACTGCTTTATGAGAACACAAAACTTCTAGCATTTCATTTTCACACTAAAGCAGGGGTATCAAACTCGGTCCTAGAGAGTTTAGTTTTGGCCCCAATTAGACACACCTAAACCAGCTGATCAAGCTCTTTTTAGGTATGCTAGAAACCTCCAGGCACAAGTTTTGAAGGGAGTTGGAGCTAAACTATGCAGGACAACGACCCTTCAGGGCCGAGTTAGGGCACCCCTGCACTAAAGCATCTTCATTTACTTGTTAATGGTTTTTGTAGGAC
Associated Phenotype:
Not determined