ZMP
iqgap2
Ensembl ID:
ZFIN ID:
Description:
IQ motif containing GTPase activating protein 2 [Source:RefSeq peptide;Acc:NP_001121812]
Human Orthologue:
IQGAP2
Human Description:
IQ motif containing GTPase activating protein 2 [Source:HGNC Symbol;Acc:6111]
Mouse Orthologue:
Iqgap2
Mouse Description:
IQ motif containing GTPase activating protein 2 Gene [Source:MGI Symbol;Acc:MGI:2449975]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38499 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1554 | Nonsense | Available for shipment | Available now |
sa33696 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40546 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38499
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084069 | Essential Splice Site | 112 | 1526 | 3 | 34 |
ENSDART00000138055 | Essential Splice Site | 139 | 1680 | 4 | 38 |
Genomic Location (Zv9):
Chromosome 5 (position 47725806)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 45514546 |
GRCz11 | 5 | 46114699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACACCGTGCAGTGGCTCAGAGCCATGGAGTCCATTGGTTTGCCCAAGG[T/C]GAGGCCCACACATACACACACAGACACACACACCTCTTTGAAGATAATAC
Long Flanking Sequence:
TGTTCTATAGTTATTCGTTCATTCGTTTTCTTGTCGGCTTAATCCCTTTATTAATCCAGGGTTGCCACAGCTGAATGAAGCACCAACATATCCAGCACGTTTTTACGCCTCGAATGCCCTTCCAGCCGCAACCCATCTCCGGGAAAGTGTTCTATAGTGTTTGCTAATAATAAAAATAAAAAAAATTTTAAATACTGAAATACCTCAAAATAAATAGTAAAAATAATACTTTAAATAGTATTGTGCTTTTCTAATTCCTTCCAATTGCTTATTTACCTCGCATATTTCTGTTGCATACATAACAGACTAAACACAGAGCATTTTCAAAGCAGCTTTATATATAATTCTGTTTTAATTAAAATTGTGCCGTCATGTTTTATTTATTCGTATTTATTCGTGTTTTGTTTTGCACTTTCTCCAGCTCTCAGGACTTCATTTCAGACACACTGATAACACCGTGCAGTGGCTCAGAGCCATGGAGTCCATTGGTTTGCCCAAGG[T/C]GAGGCCCACACATACACACACAGACACACACACCTCTTTGAAGATAATACTATGTTTATTGCACTTACACTCAAAGAAATCAAGCCGTGGTTCAGAATTATGTCCTGTTTGCTTTATGTGCCCATTTGTTGGTTTGGAAAGGAGTGTGAATAATTAATTTACAACTGTCATAAGAAGAATGCATAAGCCTATTACTGAACATTTACTCTTGGTATAAGTTATCAATCATTTGGTTTATGTTTCTTACCCTTTCGCTCAAGAGCAGAAAAAACGAAGAAAGGCATCCTCCAGGTATACAGCGGAAACCTGGTGCAGTGCACAGCGCATTACACAAAGCCACAGAATCAAAATGTCGCTATGTTTACATATATGGTAAAATTTGGCAAAACCTAATATGACACCAAATTATACACTGCCTGACAAAAGTCTTGTTGTCAATCTCAGTTTTAAGAGTAGAAAATAATAACTTCTAGTTAATCATTTGGAAAAGTGTCAGAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1554
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084069 | Nonsense | 719 | 1526 | 18 | 34 |
ENSDART00000138055 | Nonsense | 746 | 1680 | 19 | 38 |
Genomic Location (Zv9):
Chromosome 5 (position 47773076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 45561816 |
GRCz11 | 5 | 46161969 |
KASP Assay ID:
554-1497.1 (used for ordering genotyping assays)
KASP Sequence:
ATGCNTTTTTTTTATAAATAGAATGTTTTGAGCAGTGTAACAGCGGAGTA[T/G]AATAGAGAGCAGCTGTGGTTGGCCAATGAGCCGTTTATCATCCAGCTGCA
Long Flanking Sequence:
AACGCGCCCGACAACACCGCTCTTCAGTACGTGCGCGACAACAACAACACCCCCACCCCACTCCTCAAAAAATGTATCCTGCACATGCCCTTTGGACGGTCTCTGCATGGGCCTGCATTATCATATTAGTTGAAAATATTCCTTTCAAACTTCATCTAAAACCTTTACTGATCATTTTATTTTAGACTGAACCAAATGTTTATATTTTCATACTTATATTATGCTTCTGTTTTCCGTAGGCACCAGTGGCAGTTCATGGGTGCAACACAAGATCAAGGATAAATATGATTACTTCTACAACATTGAATGCAAAGAAGGCACGTGGGTTGAGCCTGAACATTTTGTCCATGACAGTTCACAGCTCAGCAGAGAGGATATCCAGGTATGACTTTAGCACAGAAATTGTGTTGAGTTGTGTTGACTTGAATGAAATGAGCTGTATTTCAGTTGATGCTTTTTTTTTATAAATAGAATGTTTTGAGCAGTGTAACAGCGGAGTA[T/G]AATAGAGAGCAGCTGTGGTTGGCCAATGAGCCGTTTATCATCCAGCTGCAGGCTCTGATTCGTGGATATCTGGTGAGGCGGGCACATCAGGACAGACTGGAGTACCTGCGAAAACAAGAGCCAAGTGTCATCAAACTACAGGTGCTTAAGTGTATTATATTAGAGTTGACTCATAGCCTTTTGATTTACCTTGTGATTTGTTTACATTTTACTGTTCACATTTTTATGTTATTACCAATTACACAAAAAAAGTACAATAATTTGTCACTGTAAATTATTCAGAACGTTTTCATAGAACGCAAAATTACCCTTTATGCTTTGCGTGTATGCATTAGAAAGATGCTTCCAGCTTCCGCTTGATGCATATAAAGATTTACATTTGGACAGATTTGAAAAAAAAAATGTTTTAATGTATTTTACCAGAGGGGTCTGGATGCAGACCTAGTGCAGCAGATGCAATCTGAGCTGCATGCAATGCTTTTGAATGGGCTCACCTAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33696
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 |
---|---|---|---|---|---|
ENSDART00000084069 | Nonsense | 1178 | 1526 | 28 | 34 |
ENSDART00000138055 | Nonsense | 1204 | 1680 | 29 | 38 |
Genomic Location (Zv9):
Chromosome 5 (position 47785679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 45574419 |
GRCz11 | 5 | 46174572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGCTGTCTTCTTCCCTCAGATTGTAGGGACTCTTCTGTATTACCGCTA[C/A]ATGAATCCTGCCATTGTGGCTCCAGACGGCTTTGACATCATTGACATGAC
Long Flanking Sequence:
GGTGCCCTTTAAAGCTTGACTCTATAGTTTCAATGTTTACTAAGACTGGTGGAAAATGAAAAGTTATTATGCCAGAATGTCATATTAGCCTAGAAAATATCAATTTGTTTTATTTTCTGTCAGACATAATGCAATAGATACTAAATCAAAACTCTTTTTTTAAAATTCTTTTTAAGTGAGATGCTAATGTTAAAATTTGATTCAATGATTTATACTAAGCTAAAAGTGCTCCTGCTAGAAAAAGAGATCAGCTGAATGGACTAAAAACGGTTAAAACTCATCTGTTTAGTTTTAGTTAAGTTGTAAAATAGGCACATTTTTCAAAAAAGTGTTAGTAAAGTTTAAATGTAGATGTCATTTCTTGACACATCAAACCAAGACAGAATAAGGACCAAATCACCTTTTGACTCAACATTTCAAAAACCAAGATATAATAAGCATAATATAATTATTGCTGTCTTCTTCCCTCAGATTGTAGGGACTCTTCTGTATTACCGCTA[C/A]ATGAATCCTGCCATTGTGGCTCCAGACGGCTTTGACATCATTGACATGACAGCGGGAGGGCAGGTTCATTCGGAGCAGAGGAGGAATTTGGCGTCCGTGGCTAAGATGCTTCAGCATGCAGCTGCAAACAAACTATTTGAGGACGAGAGCGACCACCTCACTCCCATGAACAGCTACATCTCCCAGACCTACCAGAAATTCAGGTGAGGAGAACAGAGCTTCTCATCAGTATCCGTCTTTACATCAAATGTAGAGAATTTTCTTTATGTGCAAATAAAGCATCGTTTCTATTCCAAGTGTTTAACAGAATAAAAGGGTCAGGCGGGTAATCCATGTTAGCCCTTTTTTCTTCCACAGGAATTTTTTATAGGTATACAGTTTATTCCTATTTCGAGGCTTTGTTTTTATGCAATAAAACATGGTATAGGAATAGGTTAATGGAAGGTAGGAGGGCATATTCCTGGATCAAGATCTATGTTTATCCTGGAACAACATTACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40546
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084069 | Essential Splice Site | 1246 | 1526 | 28 | 34 |
ENSDART00000138055 | Essential Splice Site | 1272 | 1680 | 29 | 38 |
Genomic Location (Zv9):
Chromosome 5 (position 47785884)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 45574624 |
GRCz11 | 5 | 46174777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTCACTCCCATGAACAGCTACATCTCCCAGACCTACCAGAAATTCAGG[T/C]GAGGAGAACAGAGCTTCTCATCAGTATCCGTCTTTACATCAAATGTAGAG
Long Flanking Sequence:
TGATTTATACTAAGCTAAAAGTGCTCCTGCTAGAAAAAGAGATCAGCTGAATGGACTAAAAACGGTTAAAACTCATCTGTTTAGTTTTAGTTAAGTTGTAAAATAGGCACATTTTTCAAAAAAGTGTTAGTAAAGTTTAAATGTAGATGTCATTTCTTGACACATCAAACCAAGACAGAATAAGGACCAAATCACCTTTTGACTCAACATTTCAAAAACCAAGATATAATAAGCATAATATAATTATTGCTGTCTTCTTCCCTCAGATTGTAGGGACTCTTCTGTATTACCGCTACATGAATCCTGCCATTGTGGCTCCAGACGGCTTTGACATCATTGACATGACAGCGGGAGGGCAGGTTCATTCGGAGCAGAGGAGGAATTTGGCGTCCGTGGCTAAGATGCTTCAGCATGCAGCTGCAAACAAACTATTTGAGGACGAGAGCGACCACCTCACTCCCATGAACAGCTACATCTCCCAGACCTACCAGAAATTCAGG[T/C]GAGGAGAACAGAGCTTCTCATCAGTATCCGTCTTTACATCAAATGTAGAGAATTTTCTTTATGTGCAAATAAAGCATCGTTTCTATTCCAAGTGTTTAACAGAATAAAAGGGTCAGGCGGGTAATCCATGTTAGCCCTTTTTTCTTCCACAGGAATTTTTTATAGGTATACAGTTTATTCCTATTTCGAGGCTTTGTTTTTATGCAATAAAACATGGTATAGGAATAGGTTAATGGAAGGTAGGAGGGCATATTCCTGGATCAAGATCTATGTTTATCCTGGAACAACATTACACTCAGCCAATCAGGTTTAATTGAACAGTTTATGCTAATTTTAGGTTTACAATTAGGGTTATGTACTACCATCATTGTTATCTAACTATTATTCCCCTCTGATTTTGAGAATTTTTTTTTTTTTTTTTTTTAATTCAGTAATAAGTTGGACTTGGAAAATGCCAGTGGAAAGAATTTGTATAATTTGTGTGTCAGATGTTTTCATAA
Associated Phenotype:
Not determined