ZMP
asap2b
Ensembl ID:
ZFIN ID:
Description:
ArfGAP with SH3 domain, ankyrin repeat and PH domain 2b [Source:RefSeq peptide;Acc:NP_001038398]
Human Orthologue:
ASAP2
Human Description:
ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:2721]
Mouse Orthologue:
6530401G17Rik
Mouse Description:
RIKEN cDNA 6530401G17 gene Gene [Source:MGI Symbol;Acc:MGI:1923478]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37060 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3052 | Essential Splice Site | F2 line generated | Not yet available |
sa37061 | Essential Splice Site | Available for shipment | Available now |
sa14060 | Nonsense | Available for shipment | Available now |
sa45704 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14030 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37060
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101556 | Nonsense | 352 | 1024 | 12 | 28 |
Genomic Location (Zv9):
Chromosome 20 (position 29685938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29757151 |
GRCz11 | 20 | 29660030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTCTGTTTCCCTTGCAGCCCAATGCACCGCCAGCAAACCTGAACCTCT[T/G]AACCTGCCAAGTGAAGCGTAACCCAGATGAGAAAAAATGCTTTGATCTCA
Long Flanking Sequence:
ACAGTTACTAAGTCCATTAGGTTTATGTGATGAAGGCTTTTCTCCACATTACAGACTGAGGAAAGTTTGGCAGAAAAGGAAGTGCTCTGTGAAAAATGGATTGTTGACTATTTCACATGGAACGGTAGGAGAACAAAGCAACACTCTAACTTTGTAATTCATGTTTGTTAATTTATACAAGCTAATACCTGCACCATTTTCACAACATACTGAATGTTAAGGACAATGATGTATTTGTGTCAACATAATCTCAAAATATCATGTCATGATTTGGGAAAATAAGAATGTTAAATTGTTAAATATTAAAACATGTTTTGTTTTCAGCTAATGTTTATATTATTTTATGTAACAAAAACATTGAGTTACTATTATTTATGTATATTAACCCTGATTTATGGATAATAATTCTATAAATGCCATCAGTTTTCCTTGTTCTCTCCTAATGTATCCGTCTCTGTTTCCCTTGCAGCCCAATGCACCGCCAGCAAACCTGAACCTCT[T/G]AACCTGCCAAGTGAAGCGTAACCCAGATGAGAAAAAATGCTTTGATCTCATATCACGTAATGTAGTTTTACAATCACAGCACAAAACTGACATAAATTCACAGCCAGTATCATCAGAGTCTGTCAAGGCTCATATGGCTGATTGATCCCCTCACGTTTCTCCTCCATCTTCTAGATGACAGAACGTATCACTTCCAGACTGAGGATGAGGCAGAGTGTCAGGTGTAAGTATGTGCACATAGCGAGTGTGCAATTTCACATGAAATTTACTTGAACATATTAAGAGACTGCTTAAATTCTCAGTTTTTCTGGCTTTAGTGAATTTATTAGATATGGCTTTGGAAATTATTTTAATTTTTATTTTCTACTTTACAGTTCAGATTGAATTTAAAACTGAATTTAAATTAAAATAGTCATTTATAGCCTTTTTTTTCAAAAACTGACAGTCAGAATAACAAGGCTGCATCCAAATATTGCTACTAGATTTGAATTTACTTCACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3052
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000101556 | Essential Splice Site | 370 | 1024 | 12 | 28 |
Genomic Location (Zv9):
Chromosome 20 (position 29685995)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29757208 |
GRCz11 | 20 | 29660087 |
KASP Assay ID:
554-2583.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAGTGAAGCGTAACCCAGATGAGAAAAAATGCTTTGATCTCATATCAC[G/A]TAATGTAGTTTTACAATCACAGCACAAAACTGWCATAAATTCACAGCCAG
Long Flanking Sequence:
GAGGAAAGTTTGGCAGAAAAGGAAGTGCTCTGTGAAAAATGGATTGTTGACTATTTCACATGGAACGGTAGGAGAACAAAGCAACACTCTAACTTTGTAATTCATGTTTGTTAATTTATACAAGCTAATACCTGCACCATTTTCACAACATACTGAATGTTAAGGACAATGATGTATTTGTGTCAACATAATCTCAAAATATCATGTCATGATTTGGGAAAATAAGAATGTTAAATTGTTAAATATTAAAACATGTTTTGTTTTCAGCTAATGTTTATATTATTTTATGTAACAAAAACATTGAGTTACTATTATTTATGTATATTAACCCTGATTTATGGATAATAATTCTATAAATGCCATCAGTTTTCCTTGTTCTCTCCTAATGTATCCGTCTCTGTTTCCCTTGCAGCCCAATGCACCGCCAGCAAACCTGAACCTCTTAACCTGCCAAGTGAAGCGTAACCCAGATGAGAAAAAATGCTTTGATCTCATATCAC[G/A]TAATGTAGTTTTACAATCACAGCACAAAACTGACATAAATTCACAGCCAGTATCATCAGAGTCTGTCAAGGCTCATATGGCTGATTGATCCCCTCACGTTTCTCCTCCATCTTCTAGATGACAGAACGTATCACTTCCAGACTGAGGATGAGGCAGAGTGTCAGGTGTAAGTATGTGCACATAGCGAGTGTGCAATTTCACATGAAATTTACTTGAACATATTAAGAGACTGCTTAAATTCTCAGTTTTTCTGGCTTTAGTGAATTTATTAGATATGGCTTTGGAAATTATTTTAATTTTTATTTTCTACTTTACAGTTCAGATTGAATTTAAAACTGAATTTAAATTAAAATAGTCATTTATAGCCTTTTTTTTCAAAAACTGACAGTCAGAATAACAAGGCTGCATCCAAATATTGCTACTAGATTTGAATTTACTTCACGGCTGTTAGAAAAGCAGGTTCTATATAGTTTAAATGTGAGTTATGTGAATGGAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37061
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 |
---|---|---|---|---|---|
ENSDART00000101556 | Essential Splice Site | 371 | 1024 | 12 | 28 |
Genomic Location (Zv9):
Chromosome 20 (position 29685996)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29757209 |
GRCz11 | 20 | 29660088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGTGAAGCGTAACCCAGATGAGAAAAAATGCTTTGATCTCATATCACG[T/C]AATGTAGTTTTACAATCACAGCACAAAACTGACATAAATTCACAGCCAGT
Long Flanking Sequence:
AGGAAAGTTTGGCAGAAAAGGAAGTGCTCTGTGAAAAATGGATTGTTGACTATTTCACATGGAACGGTAGGAGAACAAAGCAACACTCTAACTTTGTAATTCATGTTTGTTAATTTATACAAGCTAATACCTGCACCATTTTCACAACATACTGAATGTTAAGGACAATGATGTATTTGTGTCAACATAATCTCAAAATATCATGTCATGATTTGGGAAAATAAGAATGTTAAATTGTTAAATATTAAAACATGTTTTGTTTTCAGCTAATGTTTATATTATTTTATGTAACAAAAACATTGAGTTACTATTATTTATGTATATTAACCCTGATTTATGGATAATAATTCTATAAATGCCATCAGTTTTCCTTGTTCTCTCCTAATGTATCCGTCTCTGTTTCCCTTGCAGCCCAATGCACCGCCAGCAAACCTGAACCTCTTAACCTGCCAAGTGAAGCGTAACCCAGATGAGAAAAAATGCTTTGATCTCATATCACG[T/C]AATGTAGTTTTACAATCACAGCACAAAACTGACATAAATTCACAGCCAGTATCATCAGAGTCTGTCAAGGCTCATATGGCTGATTGATCCCCTCACGTTTCTCCTCCATCTTCTAGATGACAGAACGTATCACTTCCAGACTGAGGATGAGGCAGAGTGTCAGGTGTAAGTATGTGCACATAGCGAGTGTGCAATTTCACATGAAATTTACTTGAACATATTAAGAGACTGCTTAAATTCTCAGTTTTTCTGGCTTTAGTGAATTTATTAGATATGGCTTTGGAAATTATTTTAATTTTTATTTTCTACTTTACAGTTCAGATTGAATTTAAAACTGAATTTAAATTAAAATAGTCATTTATAGCCTTTTTTTTCAAAAACTGACAGTCAGAATAACAAGGCTGCATCCAAATATTGCTACTAGATTTGAATTTACTTCACGGCTGTTAGAAAAGCAGGTTCTATATAGTTTAAATGTGAGTTATGTGAATGGAATTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14060
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101556 | Nonsense | 385 | 1024 | 13 | 28 |
Genomic Location (Zv9):
Chromosome 20 (position 29686156)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29757369 |
GRCz11 | 20 | 29660248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCTAGATGACAGAACGTATCACTTCCAGACTGAGGATGAGGCAGAGTG[T/A]CAGGTGTAAGTAWGTGCACATAKCRAGTGTGCMATTTCACATGAAATTTA
Long Flanking Sequence:
AAGGACAATGATGTATTTGTGTCAACATAATCTCAAAATATCATGTCATGATTTGGGAAAATAAGAATGTTAAATTGTTAAATATTAAAACATGTTTTGTTTTCAGCTAATGTTTATATTATTTTATGTAACAAAAACATTGAGTTACTATTATTTATGTATATTAACCCTGATTTATGGATAATAATTCTATAAATGCCATCAGTTTTCCTTGTTCTCTCCTAATGTATCCGTCTCTGTTTCCCTTGCAGCCCAATGCACCGCCAGCAAACCTGAACCTCTTAACCTGCCAAGTGAAGCGTAACCCAGATGAGAAAAAATGCTTTGATCTCATATCACGTAATGTAGTTTTACAATCACAGCACAAAACTGACATAAATTCACAGCCAGTATCATCAGAGTCTGTCAAGGCTCATATGGCTGATTGATCCCCTCACGTTTCTCCTCCATCTTCTAGATGACAGAACGTATCACTTCCAGACTGAGGATGAGGCAGAGTG[T/A]CAGGTGTAAGTATGTGCACATAGCGAGTGTGCAATTTCACATGAAATTTACTTGAACATATTAAGAGACTGCTTAAATTCTCAGTTTTTCTGGCTTTAGTGAATTTATTAGATATGGCTTTGGAAATTATTTTAATTTTTATTTTCTACTTTACAGTTCAGATTGAATTTAAAACTGAATTTAAATTAAAATAGTCATTTATAGCCTTTTTTTTCAAAAACTGACAGTCAGAATAACAAGGCTGCATCCAAATATTGCTACTAGATTTGAATTTACTTCACGGCTGTTAGAAAAGCAGGTTCTATATAGTTTAAATGTGAGTTATGTGAATGGAATTCAGACGTACTACAACTGCCATTTGTCATTATCACATGATCTACCCTCGTCAGTTGCGTTGCTTCTGTCCCATTTATGAATTCTCTCACATGGCATCATGGGATAGCGGAGTGCCCATTGGATGCACACTTCAGAATCTCACCGGAAGTAGTAAGCCATCCGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45704
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101556 | Nonsense | 472 | 1024 | 15 | 28 |
Genomic Location (Zv9):
Chromosome 20 (position 29688992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29760205 |
GRCz11 | 20 | 29663084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGCATTGAATGCTCTGGGATCCATCGGGAAATGGGCGTCCACTACTCC[C/T]GAATACAGTCTCTGACACTGGACCTCTTAGGCACATCTGAACTATTGGTA
Long Flanking Sequence:
AAAAGAAAAATAACTATAAATTAGGCAAATAAAATAAAAATAAAAAGATTAAATTAAATTATAAATTTATTTGTTACCAAAGTGCATCTTTAAACATTTCTACAACAAAATATTATTGTTAAATGAAATCACCGAATTTTTGTTGTTGTTTTTTTTTTTCCTGCTTGATGTGCACAAACTAAAATAAATATTTTAGGAGAGTGATTATTGCCCCAACTCGCACTGCTTTTTTCATATCAAATCAACACCCTGTGCTTCCTGTTTTGCATCTGGTCTTTTGGCTGGTCTTTGTGCATTGTAGTAAACTTAGTCATCCCAGTAGAACTTGTTTGTATAGTTATTCAGATAGAAAAAGATAACCCTGGATGAAATTCAAATAAAACATCAGTGGCTTTTCTCTGTTGTTGTCTACAGATCCAACATGGCTCTCCACAAACCTGGGTGTGTTGATTTGCATTGAATGCTCTGGGATCCATCGGGAAATGGGCGTCCACTACTCC[C/T]GAATACAGTCTCTGACACTGGACCTCTTAGGCACATCTGAACTATTGGTAATATGGTAACATTCTTTCTTTCCTTTTTAGGCAGGAATTTTATATATTTTATATATAACATTACTGAATGCTTTGCAGCTTGCTAACAGTGTGGGAAATGCAGCATTCAATGAAATCATGGAAGCAAAACTGTCTTCAGAGATCCCAAAACCCAACCCTTCTAGTGACATGTAAGCAACACATCTGTTGTTATCTTTAGTAATCTTTAGTCCTATATTTGTATTTTATGTTTTAAACTGCCGTGCAAAATATATTTAGAGTATCTACATAACCAGCCAGTGTTTAAAAATATCTCTTTACATTAGTCTGATGTACAGTGGTAAGTTTGTAATGATGTTTTACAACTTTAGTGGAGCCGGTAGGTTTTTACGTATACAAGTGTAATAAAATTAGCTGCCATTCATCTTCGCATTTTCAGTAGGACTCCCAGTTAAGGATCGGTTATAGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14030
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 |
---|---|---|---|---|---|
ENSDART00000101556 | Nonsense | 815 | 1024 | 23 | 28 |
Genomic Location (Zv9):
Chromosome 20 (position 29695155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29766368 |
GRCz11 | 20 | 29669247 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGGTAGACARAGGTCATGTTCAGAWCCTGCAAACCCTCAAACTCCTGAA[C/T]AAAATAACTCTGTGTATGGTGAGTCTGACCTCCTGACAGCGACTTGATTT
Long Flanking Sequence:
GCGCTCTGGCTCGGGACGTGGCCAATGTGGTCAATAATAAGCAGAGGGCTTTTATTCCGAGCATGATGATGAACGAGACTTACGGCACCATGCTCGATCCCAACTCTCCACCACTGGGTTTACCAGGAGTACCTGGCATTCCTCTTTTACCCCCTCGGCCCTTGGGAAGGGGTGAGTAGCAGTCAGTCCGAGGAGCTTTAAATAGATAGTTCAACAAAAAATCAAGCTTTGCTGTTAATTTACTCACCCTAGGGTCATCCGATATATAGATAACAATTTTCTGCAGTAGAACTTTAAGAAGATTTTTAGCTAAATCTGTTGTCCTTGGTGTGATTTATACAAAGCAACTGCTTGGGCTTTAAGATGTAGGATGTACAGCAAATGTCTGTTAATGCACCTGGACTTACCCTGTGTGTGTGATGTCAGGATGGAGTCCACCAATGGAGAACATCGGTAGACAGAGGTCATGTTCAGATCCTGCAAACCCTCAAACTCCTGAA[C/T]AAAATAACTCTGTGTATGGTGAGTCTGACCTCCTGACAGCGACTTGATTTCATTATAAATAATCATATAAAGTGCTGGGTAGTTACTGATTTTACTGTATAATATGCAACTGAACAACTATTAGCCCTTTTGTGAATTTTCTTTTTTAAACATTTCCCAAACAATGATTAACAGAGCAAAGGATTTTTCACAGTATTTCCTAAAAATTTTTTCTTCTGGAAAAAGTCTTATTTATTTTATTTGGGCTACAATAAAAGCAGTTTTTAGAAACATTTTAAGGTCAAAATTGTTAGCCCCTTTAAGCTATATATTTTTTTTAGATTGTCTACAGAACAAACTGTTATACAATCACTTGCCTAATTTAGCTAATTAACCTGATTAAGCCTTTAAATGTCACGTTAAATACTAGTATATGGTAAAAAATTATTTTAATAATTCTGACTTCAATTTTATATAGAAAGTTACAAATTAGCAAAATTATTTGAATTAGAAAATGCTTA
Associated Phenotype:
Not determined