ZMP
zgc:153345
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC566129 [Source:RefSeq peptide;Acc:NP_001071081]
Human Orthologues:
ARHGAP11A, ARHGAP11B
Human Descriptions:
Rho GTPase activating protein 11A [Source:HGNC Symbol;Acc:15783]
Rho GTPase activating protein 11B [Source:HGNC Symbol;Acc:15782]
Rho GTPase activating protein 11B [Source:HGNC Symbol;Acc:15782]
Mouse Orthologue:
Arhgap11a
Mouse Description:
Rho GTPase activating protein 11A Gene [Source:MGI Symbol;Acc:MGI:2444300]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21766 | Essential Splice Site | Available for shipment | Available now |
sa21767 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21766
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 |
---|---|---|---|---|---|
ENSDART00000078012 | Essential Splice Site | 74 | 922 | 2 | 14 |
ENSDART00000115379 | Essential Splice Site | 74 | 270 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 34422480)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33450445 |
GRCz11 | 10 | 33394305 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTGCTCCCTCAGCATGACCTGCCTGACAATGGCGGTACAGTACCTCGG[T/C]ATGTTTAATAACATCACTTGTTTATTAGATAACGAAATCTGAAGCTGGCT
Long Flanking Sequence:
GGTGACGAGCGGAAACTACCTGCCACCAATCACTACAAGCAGTCCATACGAAAACATCTCCGAGGCTGCGCGGTGCTAGTTAACAAAAATTGACCGCTTCCATGATTTATCCGTTTAAGTACATTTATATTATTTTAATCAATACACTTTGGATTTAAACAGTAAGGTTTGTAGCGGTACAGGACGTTAAATTATGGGTGGTTTAACGGAAGAGCGTGTGCGCGTGGTGGCGATCATTCAGGCGCTCAAAGCTGTCGGAATTCGCGTGAAAAACTGGAAAAATTTTCTAAATGGAAATTCAAACTGCGAACAAACCTTGTGTCAGGTATAAACCCCATTTGCAAGGATGGGCATTTATTCGATGTCTAATAAGTGTAGTGGAATTTACAGATGCTGAATTTGTCTCTCAGGAGAACGCGTCCCAACGCTTTGCTTTTGGACGTGACCTGCACTTGCTCCCTCAGCATGACCTGCCTGACAATGGCGGTACAGTACCTCGG[T/C]ATGTTTAATAACATCACTTGTTTATTAGATAACGAAATCTGAAGCTGGCTTTTACATATGTGACAGTAGTTGACAGATTCTTGTGCTGGTTTTCAGGTTCTTGGTTGAGGCCTGTGTGTTTCTGTCACAGCATCTCAATACAGAGGGTCTTTTCAGGAAGACTGGATCTCTTACTCGGATCAGAGCTCTGAGGGTAAGTTAAAATCAGTCAAAATGTCACTGACAAGTGTTAAATTTATGCAGTAATTTATGTTACACCAGTTTTTCTGATAATGATTAACGTTAATTTATTTAAACAAAAAAACAACAGTATAATAAAAATATTAGTATCAGATAAAGTAAAGTTAACTGTTGTCTAATTTTATATATTTAACGTGTATGTTTTTCCTGTGATGATAAAGCTGATTATTTACCATCATTATACCAGTCTGTAGTGTCACACAACCCTTTAGAAACTGTCTAATGTTTTGCTTTCATCTTGAAGAAACTTCTTTTTATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21767
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 |
---|---|---|---|---|---|
ENSDART00000078012 | Nonsense | 298 | 922 | 6 | 14 |
ENSDART00000115379 | None | None | 270 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 34427259)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33455224 |
GRCz11 | 10 | 33399084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATGTTTAGTAAGAGGACTGGACTCAGTGTTTACAGAAGTCTGAGAAGA[C/T]AACGAAGGCGAAGTGTTGGTGGTGAGACTTTGATGTGATTGTAATGAAGG
Long Flanking Sequence:
TGTCCCTTTATGTTGGCTGAATTGTTAAATGTGATACTTAATCTTAGACAAACGCATAGTAAAGAAGCTCATTTCCTCATTTGTCTTTGTTCAGATGCAGTGAGAACAGAATGGATGCAAGCAGCCTGGCTGTTGTTATTGCTCCTAACCTGCTGCAGTGTCCAACACAACCCAACAAACTCACTCTGGACACTGAGAAACATTTAGACCAGCAGACCTCAGTGATCAAATCACTCATTCTTAATGCAGATCGCATTGGTAATTATGTATAAGATTAGCATTAACAATTAGTTACTCATCCTTTGCTGGTTGCAGCAATAGGTTGATAAGTTTATTTGGGCAAACTAAATATCTAAGTGAACTTTGTCTTTTCAGGTGTTGTTCCATCATGTCTGCTGGAGCCATCAAAATCAACAGGGGGAATTGGGACACCGTCTCCTGTGGGTGGCACTATGTTTAGTAAGAGGACTGGACTCAGTGTTTACAGAAGTCTGAGAAGA[C/T]AACGAAGGCGAAGTGTTGGTGGTGAGACTTTGATGTGATTGTAATGAAGGCTTTTAGGGCTGCTCATCAGTCTTTTTTCTTTTTTTATAAATCATAACTCTGGGGGTATCATGGTTATTTTTATGAAATCATGTTTATTTTATAACATTTAATGTAAGGTGGATATAAAAAATATTTTTGTTCATCAAATGTTCTTAAAGAAAATGTATATTGAAAATAAACAGCACAGCATTTGATGATAAATGTTTTTAGAACACCAAATCAGCATATTAGATTAATCTTCTTAATGAACTACTAGATTTAATAGTTTGTTAGATTAAAAGATTACTCAGTTTTATCATTTCGCCTGTTTTTTTTATAAATAAAGTTGCAGTTTTAATCAAAAGTTATTCTCTCAGAAATATTTGTAGATGCTTTTTCCAAATTGAAGCCGTGTCGTACTCCCACTGAACCAGCAATTGTCTTGGGTGTCGCATCAGGTGAGCCACAGTATTTTGCAT
Associated Phenotype:
Not determined