ZMP
ARAP2
Ensembl ID:
Description:
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:16924]
Human Orthologue:
ARAP2
Human Description:
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:16924]
Mouse Orthologue:
Arap2
Mouse Description:
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 Gene [Source:MGI Symbol;Acc:MGI:2684416]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12743 | Nonsense | Available for shipment | Available now |
sa17957 | Essential Splice Site | Available for shipment | Available now |
sa9517 | Essential Splice Site | Available for shipment | Available now |
sa21116 | Splice Site, Nonsense | Available for shipment | Available now |
sa11046 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12743
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078816 | Nonsense | 306 | 1612 | 5 | 32 |
Genomic Location (Zv9):
Chromosome 7 (position 64318151)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 64114685 |
GRCz11 | 7 | 64531313 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTCACTCTACTATTTGTTTATTTATTTTTTTCAGACACAWGCAGACA[C/T]AAGCCAAAGAAAAAGTACATTATAACAACAAGCAAGACCTTTCCAAGCAA
Long Flanking Sequence:
GGTCTAATGAAAAATCTATTTTAGTTTCTCAAAATAGCAACGCGCCAGCAGTGCGCCTCAGAACGCCTTCCTCTTTAGACTAGAATGCCTATGGGCACACATATGAGCGCAAATGCATTTGCTGTTTAAAGAGCGTGGCGCAATGCCTCAAAATGACTCTTGCGCCAAGCTGAAACTAGCAAACAAGTATTGCGCCGCACCTTGCGCCACATTGCGCCGGTTGTATGATAGGGCCTCAAGTTCATCTTAGTAAATACATTAACTAACATTAACATATTAAACCTTATTGTAAAGTGTGACCAAAATGTGTACAGAAATGTTACCCAAACTTTTTTTTAAATTATAATTAGTGTCCAAACGAAGCTATTTGTTAATATTTAGCCTTGTTAAAATGTGTTTAACAATTTTTTGCTTAGTGCTCTTTCACTCTACTATTTGTTTCATTCTACATTTTTCACTCTACTATTTGTTTATTTATTTTTTTCAGACACAAGCAGACA[C/T]AAGCCAAAGAAAAAGTACATTATAACAACAAGCAAGACCTTTCCAAGCAACACATCGATGATGATAAGAATGTTGATGAAAATGATTATGATGATTACTCTACTGTCCAAGCATCCAGCTTTTGTCAGCAAATTACTAATGAACATCCCACACCTCCTACTCTTCTCTCTAGCACTGGACCCTCAGCTGTGTCAGCCCAGTCACAAGCAGATGTAAATGTTATATACAGTTTGGCACACGATGACCAACCAGGTCTCCTGAAACCCAGCGTTCCTCCTCGAACTGACCTGTCCATTTCTCCATACGCCTGCTTCTATGGGATCTGTAAGACTGCAACCAAAGCCGGCTGGCTGGACAAACTCTCCCCTCAAGGGTAAAGAATATGCAAAAAGCTCTGTTTCTTTATTTGCAATTTTTTTGCACTGATTTTAATATTATTCTTGACAATAGGCACAGGAATCTTTAGAAATTTCACAATTATTGTTACATACTGTATATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17957
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 |
---|---|---|---|---|---|
ENSDART00000078816 | Essential Splice Site | 430 | 1612 | 5 | 32 |
Genomic Location (Zv9):
Chromosome 7 (position 64318526)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 64114310 |
GRCz11 | 7 | 64530938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAAGACTGCAACYAAAGCCGGCTGGCTGGACAAACTCTCCCCTCAAGGG[T/C]AAAGAATATGYAAAAAGCNNNNNNTCTTTATTTGCAATTTTTTTGCACTG
Long Flanking Sequence:
ATTTAGCCTTGTTAAAATGTGTTTAACAATTTTTTGCTTAGTGCTCTTTCACTCTACTATTTGTTTCATTCTACATTTTTCACTCTACTATTTGTTTATTTATTTTTTTCAGACACAAGCAGACACAAGCCAAAGAAAAAGTACATTATAACAACAAGCAAGACCTTTCCAAGCAACACATCGATGATGATAAGAATGTTGATGAAAATGATTATGATGATTACTCTACTGTCCAAGCATCCAGCTTTTGTCAGCAAATTACTAATGAACATCCCACACCTCCTACTCTTCTCTCTAGCACTGGACCCTCAGCTGTGTCAGCCCAGTCACAAGCAGATGTAAATGTTATATACAGTTTGGCACACGATGACCAACCAGGTCTCCTGAAACCCAGCGTTCCTCCTCGAACTGACCTGTCCATTTCTCCATACGCCTGCTTCTATGGGATCTGTAAGACTGCAACCAAAGCCGGCTGGCTGGACAAACTCTCCCCTCAAGGG[T/C]AAAGAATATGCAAAAAGCTCTGTTTCTTTATTTGCAATTTTTTTGCACTGATTTTAATATTATTCTTGACAATAGGCACAGGAATCTTTAGAAATTTCACAATTATTGTTACATACTGTATATCTTAACTTTATTTTAATGGTCCATTTGAGTATTAGTAGACAGTCTGCTTAATATCGGTTGATACTGCTTTGCAAGTACATGTCAACTTACACTAACCCTAACCCAAACATTACAGTCTACTTGTAATCAAATGAGAATTAGTTAGCATGTAGATCATAATAAAGTGTGACCAAATATATAAACACATTTAGACATGTTTTTGTGCAAAAGCGTCAACTTTTTTAACTTTGGTGAGTTTTTTTTTTTACATCTTTCAAAATGGTTTCATCTTTTAGCCTAGACAACGGTGATCACAACAATATAAGAGTTTACGTTCATACTTTCACATTTTTTTTAAGAATAAAAAAAATATTCATTATGATAAAAATACTTTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9517
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078816 | Essential Splice Site | 928 | 1612 | 16 | 32 |
Genomic Location (Zv9):
Chromosome 7 (position 64415818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 64017018 |
GRCz11 | 7 | 64433646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGGAGACCTCGGACGCACACCAAGATTGGACAAACGCCATAGCCAAGG[T/G]CACACACATAGACACACACAYACATACATTTGTTTTTGTGAAYTGTGGGG
Long Flanking Sequence:
TTTAATGAATGTTTGCGCTTGAGCACCTTCTGTGGGTTAGAGGTTACAGAAAGAGTTTCAGATGTAAGTTTCTATTCACTAACAAACACAAAGAAATGAGAGCAAACTGACGTGTAGAGCAACCTCTAACCCGATTAGCGCGACTGTTGGGGAAATCTCTCGCTACCTTAACAAAAATATCCCATCCACAAAAAATGTGGGCCACAAATCAGAGCTGTTAAAGCCATTAAGAGAGTGACCTTTCCCCCTGGATTAATCTCCTGCGTTCAGCTGTTTATTGTAAGAGCAAAAGACTAACAGAGATTAATCACCATCCTTTCTGTTGCACAGCTGTGAGCATGTGTGTGTTTCAGTCATTGTGTGTGTGTTAATTGTACTGTTTCACACCTCCCTCAGGCCAGTGTTCACCTTTGAGTTGTACCTGCGCTCTCAAAGAGTGCTGGTGTTCGGAGTGGAGACCTCGGACGCACACCAAGATTGGACAAACGCCATAGCCAAGG[T/G]CACACACATAGACACACACATACATACATTTGTTTTTGTGAATTGTGGGGACATTTCATATGTTTCCATTAATTTTAAGACCATAAAAGCTGTATTTGCTAACGCTAAACCCCAAGTATGTTCCTTAACACCCCTCAACCCTCACAGGAAACTGTGTGCAGTTTTACTTTCTGGAAAAAAAACAAAACAAAAAAAAAAAACTGTTGTATTATTTATAAGCCTTTCGGCAATGAAGTCACCTTTTCCTTGTAATATTTTTGTCATACCCATGTCATACAAATTTGTGACCTGATATGTCAATAAAACACACACACACAAACACACAATTTACACAGATTGTTATTGGTGGTTTATTTATATTTTTAACCATTCTATTTGTAATTGATAATCTTTAGCTTGTCGATCTAATTCCAATTTTTGATCAAGTTTAAGTTTTTCATATTCGATTTTGTGCTGTTTTAGTAACTCCATAAATCTTGCTAATTCAACCTCCTTATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21116
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078816 | Splice Site, Nonsense | 1442 | 1612 | 30 | 32 |
Genomic Location (Zv9):
Chromosome 7 (position 64459377)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 63973463 |
GRCz11 | 7 | 64390091 |
KASP Assay ID:
2259-9692.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTTCACTTGAGTGCTTCAGTGTTCACCTTTGCATCGTCTCTGAAACAG[G/A]TATTTCTGCTGTAAAGGGAATGATTCTCAGCAGGACTGGGTCACCTCCAT
Long Flanking Sequence:
TAGGTAAGCAGAAAATCTCAAAACAGACCATTTGTTTTTGTTATTCCAGTCAGCTGTCTGTGTAAATTAAGCTGAATTTAATGGTATCTTAGCACTTTAGAGGTTCAGCTTGTGGCACCATCAGGAAAAGCTGAATATAGCTGTAAATTGATGTGGAGAACCTGTATGAAATGCTGTGAAACTAATGGAATTCTTTTTTTGTTGTTGTTTTTCTGACAAATTTTCAACAGTTGGGGATTTACTGTTTATACTGAAAAGCAGCAGTGGTAAGTGCAATTAACTCTGTTCCTAATTACATAGTCAATCTCACGCTTCAGTACTGTTTTTAGGAAAAACATTTTGCTGGGACTGGGTAATATGTGCCTTTTTAATATTTCAGTCTGAAACTTATAAAGGCTTTTTGGTACAGCTTAATACATGAAGTACAGAACTGAAGGACTGCATTTCAAATAGTTCACTTGAGTGCTTCAGTGTTCACCTTTGCATCGTCTCTGAAACAG[G/A]TATTTCTGCTGTAAAGGGAATGATTCTCAGCAGGACTGGGTCACCTCCATTATCAGAATGAAGGTGAGCTTTTTCCTTTTCAGATGATGTGCAGTTAACATTCTTACAAATGGGCTGGTTTTTGTAATGCAATTTTAACATTTGATAATGTTTCACTTATTTTGAATTGAACAATCAAAAAAATAATAATTGCATTTCTCTTTCTTTGTATAAACAACGCATTCACTCACTGGCCACTTTATTAGATACACCTGTCCAACTGCTCGTTAATGCAAATTTCTAATCAGCCAATGACCTCATGAATAGCACAGGCCTCACCAAAATTATACAATAGAAGATTGAAAAAGCGATGCCTGTTCTGTCTCAAGTCTCGATTTCTGCTGCAACATTCGGATTGTAGGGTCAGAATTTGGCGTCAACAACATGAAAGCATGGATCCATCCTGCCTCGTATCAATGGTTCAGGCTGGTGATGGTGGTGGTGTTATGGTGTGGGGGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11046
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078816 | Nonsense | 1561 | 1612 | 32 | 32 |
Genomic Location (Zv9):
Chromosome 7 (position 64471242)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 63961598 |
GRCz11 | 7 | 64378226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGTGTCTCCAGGCTTGAAATGGTGATTGATGACACACTCCAGTCCCAA[C/T]GAAGGGCATCACTTCAACAAGACACTGCCACTCTAACCCAGATTTCACAA
Long Flanking Sequence:
CATCTCTACCTTATAACCTGAGCAGAAGGAGAACCTCCACTCAGAGCACCACACAGTCCAGCAATAAAAACCAAAGAGAGGTCAGCTCCAACGCTCACATAAACATCACAAACATTTAACAAACCACTTCATTTATTACTACTTAATGAATTTTTGCTTCAGTGAACACCTCTAAATGCCAGCACAGATCGCTGTTCTCCATCTTTGTTGACAGTTAAGCCAAATCCATGTCCTTTTAACCCACAAAACAGTTGTTAGAATTGGGCATCCAGTCTGTTCACTGCATACAAAACAACCGCTGACTATGATACACTTCCTTTTTTGTGCAGGTTAAAGGAAAGTCGGTGCTTACTACTAGTACAGAAGATTCAAATACACAAAACCAAATGGCCGCAGATGAGGGCATCCGACCGGACTCGCTGCATAAATTGGCAAGTGCTGAAGGAACTCCGGGTGTCTCCAGGCTTGAAATGGTGATTGATGACACACTCCAGTCCCAA[C/T]GAAGGGCATCACTTCAACAAGACACTGCCACTCTAACCCAGATTTCACAAAGGAAAGCCGCTATTCCCGGCAGAGGAGTGCAGTTGCCTCAAAACCTCATTAATGAGCTAAGTACTGTTCTCAACAAAACAGGACGCTCTCAGAAAGAAGCCGATTAGGAGAGACAGAAAGACAAGAGTCTTGTCCATTACACTTCCATGGTGCAAGAGGAAAATCAAACTCAGACCAAACCCAAAGTAAAGCTGCCTCTAAGTAAGCATAGTGCTATATGCATTGAAGATTTAAAGCATCTATGTTTAAGCTATGTAAGTATATGTAAGTATTAGCAGCTTTTTTTTAGTCAAAATGTATGAACAGAACTTTAAAACATAGATTTGCTTGAACGGGGTGTTCATTAGACTGGGTCACACTTTATTGTGATGGTCTGTTTGTTTAATTTAAGTTACTTTGCAACTTATTTTCATTAGAATATAAGTACACTGTTAGGTTGGGGTTAAGGT
Associated Phenotype:
Not determined