Busch Lab

ZMP

arhgap29b

Ensembl ID:
ENSDARG00000017748
ZFIN ID:
ZDB-GENE-031010-44
Description:
Rho GTPase-activating protein 29 [Source:UniProtKB/Swiss-Prot;Acc:Q6PCS4]
Human Orthologue:
ARHGAP29
Human Description:
Rho GTPase activating protein 29 [Source:HGNC Symbol;Acc:30207]
Mouse Orthologue:
Arhgap29
Mouse Description:
Rho GTPase activating protein 29 Gene [Source:MGI Symbol;Acc:MGI:2443818]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa18561 Essential Splice Site Available for shipment Available now
sa9978 Nonsense Available for shipment Available now
sa39792 Nonsense Mutation detected in F1 DNA Not yet available
sa6007 Nonsense Mutation detected in F1 DNA Not yet available
sa39793 Nonsense Mutation detected in F1 DNA Not yet available
sa9335 Nonsense Mutation detected in F1 DNA Not yet available
sa18723 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18561
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016071 Essential Splice Site 325 1337 10 24
ENSDART00000141921 Essential Splice Site 325 1337 10 23
Genomic Location (Zv9):
Chromosome 2 (position 14991766)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 15502593
GRCz11 2 15171183
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAACAARTCAATTCCTTAAATTCCACACATTTTCCCCTTATTCCAACA[G/A]CCACTGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAA
Long Flanking Sequence:
ATCTTTAATTAAATACCATAACCTACCCTCCTCCCTCGAATGCCTAAAGGAGTTACAGGAATTAATGACCTTAAATTACTATTTTAAAGTACAATAAAGGTCATTTCAGATTTTAATATGAGTTTGTAATCTTGTATATCACAAATTACAAGATTACATATTACATGTTTAGACATATAAAATCTTTTTTCACACTATTTATATTTTTATTGTGTTTTGAACCCTTTCTAAAATATTTTTAATAGTCAATTTCAGTGATAAAGTGACAGTATTTTAAAATTTTCTGTTTTTATCTTAAGGATTTCATGCCTTTCCGGGATATCTATGTCTCTGCCTTTAAAAATGAAATCGAGTACAATCATGTACTGCTCCAAACGGCTGCAGCTCTTCAGACCAACAAATTCACACAGGTAACCTCTATTGATTCCTCCGAACGCTTTTAGCCAACTATTCAACAAATCAATTCCTTAAATTCCACACATTTTCCCCTTATTCCAACA[G/A]CCACTGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAAAGAACAATGGCAAAGAGAGCTGAAGAAAATGGTACTAATGCCTATTTGAATTGGAATTTCATCACTAACTCAACATTTCTTCAAAATGATAGCACATAACCTACGTGTGTTTTCAGAACGAGTCAGAAAGTGCTTTAAAGAAGGCTCGGCTGTTGAAAATGCAGAAGAGGGAGGAATACGAGAAGGCCCGGAGCTCGACCAGCCGTACCGAGGAGGAGCAGCCAGCAGCTGGAGGCAGGACACTGGAGAAGAAACGCAGAGTTGAGGAAGAGGCCCTACAGAAGGTACTGTAGAAATTACACTATAAAAACTTTTAAAGCTTTTAATTCAACACACACACACAGACACACCCTTGAGTTTATTGTCCGCGTTTACTATGCATCAAAGCAGCAATAAGAAACACAGAGCTTGTGAGACTTTCCTTAACAACGATGTTATGTGTAAAAATAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9978
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016071 Nonsense 343 1337 10 24
ENSDART00000141921 Nonsense 343 1337 10 23
Genomic Location (Zv9):
Chromosome 2 (position 14991821)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 15502648
GRCz11 2 15171238
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAAAGAA[C/T]AATGGCAAAGAGAGCTGAAGAAAATGGTACTAATGCCTATTTGAATTGGA
Long Flanking Sequence:
CAGGAATTAATGACCTTAAATTACTATTTTAAAGTACAATAAAGGTCATTTCAGATTTTAATATGAGTTTGTAATCTTGTATATCACAAATTACAAGATTACATATTACATGTTTAGACATATAAAATCTTTTTTCACACTATTTATATTTTTATTGTGTTTTGAACCCTTTCTAAAATATTTTTAATAGTCAATTTCAGTGATAAAGTGACAGTATTTTAAAATTTTCTGTTTTTATCTTAAGGATTTCATGCCTTTCCGGGATATCTATGTCTCTGCCTTTAAAAATGAAATCGAGTACAATCATGTACTGCTCCAAACGGCTGCAGCTCTTCAGACCAACAAATTCACACAGGTAACCTCTATTGATTCCTCCGAACGCTTTTAGCCAACTATTCAACAAATCAATTCCTTAAATTCCACACATTTTCCCCTTATTCCAACAGCCACTGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAAAGAA[C/T]AATGGCAAAGAGAGCTGAAGAAAATGGTACTAATGCCTATTTGAATTGGAATTTCATCACTAACTCAACATTTCTTCAAAATGATAGCACATAACCTACGTGTGTTTTCAGAACGAGTCAGAAAGTGCTTTAAAGAAGGCTCGGCTGTTGAAAATGCAGAAGAGGGAGGAATACGAGAAGGCCCGGAGCTCGACCAGCCGTACCGAGGAGGAGCAGCCAGCAGCTGGAGGCAGGACACTGGAGAAGAAACGCAGAGTTGAGGAAGAGGCCCTACAGAAGGTACTGTAGAAATTACACTATAAAAACTTTTAAAGCTTTTAATTCAACACACACACACAGACACACCCTTGAGTTTATTGTCCGCGTTTACTATGCATCAAAGCAGCAATAAGAAACACAGAGCTTGTGAGACTTTCCTTAACAACGATGTTATGTGTAAAAATACGAGTGCTAGAAAACCTAGCAAATGCTTGAATGTTGTTCTAGTGTTTTGCTCACAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39792
Status:
Mutation detected in F1 DNA
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
ENSDART00000016071 Nonsense 406 1337 11 24
ENSDART00000141921 Nonsense 406 1337 11 23
Genomic Location (Zv9):
Chromosome 2 (position 14992095)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 15502922
GRCz11 2 15171512
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGGCAGGACACTGGAGAAGAAACGCAGAGTTGAGGAAGAGGCCCTA[C/T]AGAAGGTACTGTAGAAATTACACTATAAAAACTTTTAAAGCTTTTAATTC
Long Flanking Sequence:
TCTGCCTTTAAAAATGAAATCGAGTACAATCATGTACTGCTCCAAACGGCTGCAGCTCTTCAGACCAACAAATTCACACAGGTAACCTCTATTGATTCCTCCGAACGCTTTTAGCCAACTATTCAACAAATCAATTCCTTAAATTCCACACATTTTCCCCTTATTCCAACAGCCACTGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAAAGAACAATGGCAAAGAGAGCTGAAGAAAATGGTACTAATGCCTATTTGAATTGGAATTTCATCACTAACTCAACATTTCTTCAAAATGATAGCACATAACCTACGTGTGTTTTCAGAACGAGTCAGAAAGTGCTTTAAAGAAGGCTCGGCTGTTGAAAATGCAGAAGAGGGAGGAATACGAGAAGGCCCGGAGCTCGACCAGCCGTACCGAGGAGGAGCAGCCAGCAGCTGGAGGCAGGACACTGGAGAAGAAACGCAGAGTTGAGGAAGAGGCCCTA[C/T]AGAAGGTACTGTAGAAATTACACTATAAAAACTTTTAAAGCTTTTAATTCAACACACACACACAGACACACCCTTGAGTTTATTGTCCGCGTTTACTATGCATCAAAGCAGCAATAAGAAACACAGAGCTTGTGAGACTTTCCTTAACAACGATGTTATGTGTAAAAATACGAGTGCTAGAAAACCTAGCAAATGCTTGAATGTTGTTCTAGTGTTTTGCTCACACTTGAACAGTTGAACATCTACTAATACATGATTAAAATTCATGGTTTTAATATTAGTTAATGCTTTGATGGTTAACTTAAATTAACAGCGAAGAGGTTTAATGGTAACACTTTAAAATAATGGTCCATTATGTGTTTACTAACATGAACACACTATTAGTAATACATTTATTACTCTATTCATTCATCGTTGTTCAAGCTAGTTATATTACTTAAGTTAAATAACATTAGTTCATGTTAACTGACTGTGCATTAACTAATGTTAACAAGCACAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6007
Status:
Mutation detected in F1 DNA
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
ENSDART00000016071 Nonsense 414 1337 12 24
ENSDART00000141921 Nonsense 414 1337 12 23
Genomic Location (Zv9):
Chromosome 2 (position 14994766)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 15505593
GRCz11 2 15174183
KASP Assay ID:
554-3734.1 (used for ordering genotyping assays)
KASP Sequence:
TGGCTGATGGTCTGTTTTTGTGGTAACTCCAGGCAGAGGAAGCGCAGGAG[C/T]AGTATAAAGCCTGTGTGGCYGATCTGGAGGCCAAGAAGGTCAGCCTGTCA
Long Flanking Sequence:
GCGTTATATAAATACACATTACATTACATGACAACAGCCATTCTTCTCCTTGGGCAGTTTTGAAAAAAAATATTTGATTCACTTCGAATGTTCATTGCTGTTAATAAAATTATTAGAAATAGCATCTGATATAGTGTGTTGAAGTAGGTATATAAAATTTGCAATTTGCCCAACTTGTATAGTGCTGGAAAAGTTTGACCTTAAAAGTGTTTGAAAAGCGCTTAAATTTGATGTTGGGAAAGGTGTATAAACCCTGATGGACATTAAACTATACATTATTGTTGCTGTATCATTCTGTAAACCTCTAACAACTAAAAGAAATTACCTCACATACCATTTGAAAAAAAACAAATGAGCAGGATTTTTCTTTCTAAAATGTATTTTGAATGGCTTGATGGCACAGAAATGACATAAAACAGGCTAGTAAAATGACTGTACTCGTGTTTTGCTTGGCTGATGGTCTGTTTTTGTGGTAACTCCAGGCAGAGGAAGCGCAGGAG[C/T]AGTATAAAGCCTGTGTGGCCGATCTGGAGGCCAAGAAGGTCAGCCTGTCAAACGCTAAGAGTGAGATCCTCGCACAGATTCGGAAGCTGGTCTTCCAATGTGACCTGACCCTCAAAGCGGTCTGTATCCCTGTCACAACACTATTACACACTACTGTTGAAAAATGCGCAGCGGTTTTCTTCTTCTTCTTCTTTGTTTAATTCTTCTTCATTTAATTCTTATATAAGAAGCTTCGGTTTTTAATAATAATTTTATATGTACAGTTGAAGTCAGAATTATTAGCCTTTTTTTTTTTTTTTTCAAACGACGTTAAACAGCAAGGAGTTTTTCCACAGTATTTCCTATAAAAAAAAATTCTTCTGGAGAAAGTCTTATTTGATTTATTTTGGCTAGAATAAACACAATTTAAATGTTTTGAAACCCTTTTTTAATCAATATTATTAAATCCCTAAAGCAATATTTTTTTTAATTGTCTACAGAACAAATTTAACAATTTAACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39793
Status:
Mutation detected in F1 DNA
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
ENSDART00000016071 Nonsense 1012 1337 22 24
ENSDART00000141921 Nonsense 1012 1337 22 23
Genomic Location (Zv9):
Chromosome 2 (position 15013431)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 15524258
GRCz11 2 15192848
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTCTACAAGAGACACTCGTCTGTGATCATCCCAGCTCAGCTCATGGAG[G/T]AAGGGAAGGAAATGAAGACTGGAGACCACAGAGTACAAACATCTGGTTAG
Long Flanking Sequence:
GTGAAATATAACCCAGCACTTAATCACATTTTTGTTAATTGTTCTGCAGAGTTTCAGAGCAAGCTGAGGAGAACAAGATGACCGCTAGTAACCTGGGCATCATCTTTGGCCCCACGCTCATTAAGCCCAGACATTTGGAGGCAGAAGTGTCGCTTTCCTCCCTGGTTGACTATCCTCACCAGGCCCGCATGGTGGAGCTGCTCATCAAACACCATCAGATGATCTTTGACGTGCCCCTCAGCCCCATGTCTCCAACCAGTCCAACTGTATCACAGGCTTCCTTTGGGTCCAGCATCCAGGACAAAGAGTCCAAACTCAGCCGTCACTCTAGATCCCTGATGGACATCAAAGAGGTAGGATGGCCTAGAGAATAGAAACCAGACTCGGTAGGATTAATTTAAGGAGATATTAAAGTTTTTGATTTGTTTTTTCTCCTCATTCAGAGTGCAAAACTCTACAAGAGACACTCGTCTGTGATCATCCCAGCTCAGCTCATGGAG[G/T]AAGGGAAGGAAATGAAGACTGGAGACCACAGAGTACAAACATCTGGTTAGTATGAGACTACATTTACACTAATCCAGATAAATCTGAAAATGACTCTTTGGTCTAATAGCAGTCTGCATGTACACAATCATTCTTTTCCACTAAAATTGGTCACCCACACACTGAAATGACAGAAAATGCTTTTGTCCTTGCTTTCGTTTTTGAAGTGACCAAAAGTAGCCAAGCTCAAAGAGTTTTAGATACTGATTGTACCACGATTATAATAGTTTTTTTTTAATTAGTTTTAGTTGTTATTTTGTTTTGAGTTTTTGTTTTCAAATCCAGTTAGTTCTAATTAGTTTTTAGGGGCAGATTTACAAATTTTTATTAGTTTCTATATTTTGAAATCGCTTGGTTTTAGTTTAGTTTTGATTAGTTTCAGTATTAGTTTTATAAATTAGAGTATTTGTTAGGTGCAAGATACAAAATCATCAGAATATACTATAATAACTCAACCAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9335
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016071 Nonsense 1037 1337 23 24
ENSDART00000141921 Nonsense 1037 1337 23 23
ENSDART00000016071 Nonsense 1037 1337 23 24
ENSDART00000141921 Nonsense 1037 1337 23 23
Genomic Location (Zv9):
Chromosome 2 (position 15015301)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 15526128
GRCz11 2 15194718
KASP Assay ID:
2259-1746.1 (used for ordering genotyping assays)
KASP Sequence:
GTATTTTTTYTCTCAARCAGGTGAGGGCTCAGATGTCAACGGGGTTGGTT[T/A]GACTTCTGTTGACTCCACATCTGTGTTCAAYCGGCCTGGTGCCAGCAGCC
Long Flanking Sequence:
TAAAACTGGCATTGTGGAGTTAATAGATTTCCTTCTAAAAGGCTTATATATTAAATACATTTACAAAGGCAAAAAAGAAGGACGTTTTTGCTATAATTTTAGTTAGTTTCAGTTAGTTTTGTATGTACACAATACATTTTCAGTTATTTCTAGTTTTTTTTTATTTTTAAAAACTCTTTTTTTTATTTTTATTTCAGTTAACGAAAAGGATTTTTCAATTCTAGTTTTGTTTTTTCGTTAATTTTCGTTAACAATAATAACCTTGAACAGAACCTGTATTTGTCAATTTAAAGGGATAGTTCACTTTATAATGAAAACTGCTGCCCCTTAAGTAGGCTAAAATTTTAAAGATCGACAATCTTGAGCACCTAAGGTTTAAAAAAAAGTGTAATATAACATTTTAACTCTATTCAGATGTTTGTTTTGATGTGTATGTAATTGTATAAAAAAGTATTTTTTTTCTCAAGCAGGTGAGGGCTCAGATGTCAACGGGGTTGGTT[T/A]GACTTCTGTTGACTCCACATCTGTGTTCAACCGGCCTGGTGCCAGCAGCCGAATGGTGCAGCTGAGACCTCAGCGTGCCAAGCCGGTGTCTCGACCAATCAGCATGCCCATAGACCGCCTACTCAACGAACGCAACAGCCGCAACACAGTGGAGCATGATCACTCACCCGCCGCCATTGAGGAGACCACTGAACCAGAGAAACCGACAACACCACGGCACACCAACTTTTACAGGAACCCCTTCATTGACACTCAGACGCTGAGGAGGACCTGGGACAGGCAGTACAGACATTATGACGTCACGCCCAGGACTGCAATGATAGTGGCCAACCTGCCACCTTCCGGTGTGCAGAAACAGCCTGAAATTAGTATGGGATCCCAAAGCAGCACCTCTAGAAAAGATGGTACAAGCCAGTCTGGTGTGGCTCCAATATCGTTCAGAGCAGCACGGACACTAAAACCCTCTTCTCCTGGAACGTTCTATAGACCTCCCTCTGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18723
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016071 Nonsense 1037 1337 23 24
ENSDART00000141921 Nonsense 1037 1337 23 23
ENSDART00000016071 Nonsense 1037 1337 23 24
ENSDART00000141921 Nonsense 1037 1337 23 23
Genomic Location (Zv9):
Chromosome 2 (position 15015301)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 15526128
GRCz11 2 15194718
KASP Assay ID:
2259-1746.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTTTTTTTCTCAAGCAGGTGAGGGCTCAGATGTCAACGGGGTTGGTT[T/A]GACTTCTGTTGACTCCACATCTGTGTTCAACCGGCCTGGTGCCAGCAGCC
Long Flanking Sequence:
TAAAACTGGCATTGTGGAGTTAATAGATTTCCTTCTAAAAGGCTTATATATTAAATACATTTACAAAGGCAAAAAAGAAGGACGTTTTTGCTATAATTTTAGTTAGTTTCAGTTAGTTTTGTATGTACACAATACATTTTCAGTTATTTCTAGTTTTTTTTTATTTTTAAAAACTCTTTTTTTTATTTTTATTTCAGTTAACGAAAAGGATTTTTCAATTCTAGTTTTGTTTTTTCGTTAATTTTCGTTAACAATAATAACCTTGAACAGAACCTGTATTTGTCAATTTAAAGGGATAGTTCACTTTATAATGAAAACTGCTGCCCCTTAAGTAGGCTAAAATTTTAAAGATCGACAATCTTGAGCACCTAAGGTTTAAAAAAAAGTGTAATATAACATTTTAACTCTATTCAGATGTTTGTTTTGATGTGTATGTAATTGTATAAAAAAGTATTTTTTTTCTCAAGCAGGTGAGGGCTCAGATGTCAACGGGGTTGGTT[T/A]GACTTCTGTTGACTCCACATCTGTGTTCAACCGGCCTGGTGCCAGCAGCCGAATGGTGCAGCTGAGACCTCAGCGTGCCAAGCCGGTGTCTCGACCAATCAGCATGCCCATAGACCGCCTACTCAACGAACGCAACAGCCGCAACACAGTGGAGCATGATCACTCACCCGCCGCCATTGAGGAGACCACTGAACCAGAGAAACCGACAACACCACGGCACACCAACTTTTACAGGAACCCCTTCATTGACACTCAGACGCTGAGGAGGACCTGGGACAGGCAGTACAGACATTATGACGTCACGCCCAGGACTGCAATGATAGTGGCCAACCTGCCACCTTCCGGTGTGCAGAAACAGCCTGAAATTAGTATGGGATCCCAAAGCAGCACCTCTAGAAAAGATGGTACAAGCCAGTCTGGTGTGGCTCCAATATCGTTCAGAGCAGCACGGACACTAAAACCCTCTTCTCCTGGAACGTTCTATAGACCTCCCTCTGGAG
Associated Phenotype:
Not determined