ZMP
srgap2a
Ensembl ID:
ZFIN ID:
Description:
SLIT-ROBO Rho GTPase activating protein 2a [Source:RefSeq peptide;Acc:NP_001041700]
Human Orthologue:
SRGAP2
Human Description:
SLIT-ROBO Rho GTPase activating protein 2 [Source:HGNC Symbol;Acc:19751]
Mouse Orthologue:
Srgap2
Mouse Description:
SLIT-ROBO Rho GTPase activating protein 2 Gene [Source:MGI Symbol;Acc:MGI:109605]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11022 | Nonsense | Available for shipment | Available now |
sa17814 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11022
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045391 | Nonsense | 18 | 1100 | 1 | 22 |
ENSDART00000103865 | Nonsense | 18 | 1100 | 2 | 23 |
ENSDART00000045391 | Nonsense | 18 | 1100 | 1 | 22 |
ENSDART00000103865 | Nonsense | 18 | 1100 | 2 | 23 |
The following transcripts of ENSDARG00000032161 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 22416053)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 21422284 |
GRCz11 | 11 | 21582852 |
KASP Assay ID:
2260-4216.1 (used for ordering genotyping assays)
KASP Sequence:
TGACGTCTCCTGCTAAATTCCGAAAGGACAAGGAAATTATAGCCGAATAT[G/T]AAACGCAAGTTAAAGGTAAGTGAAATGTGTCGCTTTATGTTGCRTTTTYA
Long Flanking Sequence:
GAAGTTTACTGGAAGGAAGTAGTCTTTAGAAATCTGATCCGCTGAACTTTTCTTTGCCCTGTGTGTGCCCAGTGTGATGCTGGGAAATCCTATCCATGCCTTCATCCAGCTCTGAGGAGACTCACTCACACGTCTGACCGCCAGAGGAAAGACTGAAACTTTTGAAGACGCTGCGTCTGGTCGTGGGGATCCAGTGTGAGTGGACGGTGGGATGAAACTCTTCTCTTGCTTCATTCCTCTGCTGTTACGGACATATTACTCTACCTTGGAAGCCATCGGCAGCTCTTAACTAATAATGCGGCGTGATTGATCATCGACAGGAGACAATACCCATCCACTGCTTTCCATTCCCACATATTCGCTGGATATCTGTAGACGAAGTGCGGGCGAAGAGGCTTTTGTTCTGCGGTGTTTCTCGCTGTGACGGGACTTATTGTGTTTAGATCAATATGACGTCTCCTGCTAAATTCCGAAAGGACAAGGAAATTATAGCCGAATAT[G/T]AAACGCAAGTTAAAGGTAAGTGAAATGTGTCGCTTTATGTTGCATTTTCACTCGGTTCACCTTTGTGTTACGTGGTGGCTAGGTTACAGTGTATTTCTATATGAGCACAGCTGGTGCAAACCCTGTCGTATTACTGCAGAAAACGCTATTTATTTGAGTTTGTGAGAAACAATGCTAGCGCTTCTCCACATGTGGCAACGGAATGATAGATGTGCGATCGGTCAGTCAGTCAGTCAGTCAGTCGCCTAAAGCTATATTGTCTGTAGATACACAACTTAAACCGTTTATAACAACGCTTTTACTTTAAAAATGCATTGATGTGTGATTAATGTTACGTTTGTGCTGTGTTGTACTGTTTTCCCTCATTCAGCTTGTGTAGGTTGTACGTATAGACAAGGCAGGGCGTTTTCTTTTGCCCTGCGTGTCTCTATGAGCTGGTGCGGTGCTGTTCAACCTATTGATTTTTTAAAAGTCAGGTTAGCTGACATTGATGTTTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17814
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 |
---|---|---|---|---|---|
ENSDART00000045391 | Nonsense | 926 | 1100 | 21 | 22 |
ENSDART00000103865 | Nonsense | 926 | 1100 | 22 | 23 |
The following transcripts of ENSDARG00000032161 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 22247096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 21253327 |
GRCz11 | 11 | 21413895 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAGACTAAAGTAGARGGTCCTCAAGTTCGCAAATCCACAYCTACTGGA[C/T]GATCCAAGAGCTTCAGCAAYCACAGACCCCTCGACCCAGARGTRATCGCG
Long Flanking Sequence:
CCCTTAACAAGTGGGAGGAACATATGCAAACTGTTGTAATTCCTACAGCGTTCACCTGATTTGGATGTAAGTACCTTCAAATTAAAGCTGATAGTCTGCAGTTAAAGTACATGTTGTTTGTTTTATTTTAAATCTATTGTGTTGGTGTATAGAGCCAAAAATGTTAGAATTGTGTCGATGTCCAATTGTTTATGAACCGAACCGTTCAAAGACAAATAAAAGAGTGTATGTGAGAGTTTGTACTTACACATATTTATCTCAGGTTGAGGAAGCGTCCAGAAGCGACGAGCATCCGGAGAACCATCCGGCCTGTGGAGGAGGGCTCATCAGGAGCAGCAGGGGGCTTAAAGACCTCCTCTATGCCTGCTGGAGGACTGGCCAAGGACAGCTCAGACAAGCGTCCTGTCAGCGCTCACAGCGTCCTGAACTCCATCACCAGACACTCGTCTCTCAAGACTAAAGTAGAGGGTCCTCAAGTTCGCAAATCCACACCTACTGGA[C/T]GATCCAAGAGCTTCAGCAACCACAGACCCCTCGACCCAGAGGTGATCGCGCAGGTGGAGCACAGCTCACAGGTACGGGACACTTCAGAAATATTATTAGAAACAAGCAGCATTCAAACCCTGTCAGCTTTCATCTAAACTTTCTGGCTCAAGCAGACATCACTGTTGTCCAATCACAACCCATTAGGCAAATGATGACATCAAACTTACATCTCAGTTGATAAAGTATGTAAATCAAACTGATGTCAGAATCTTGACATGGTTTTGTTTTGATGTAAATTGAATGGCAAACATATTGGCATTCATGTCATTAAACCAATTTAAGTGTTATTAACCCCCCCCCTACCCCCACCCCCTAAATAATCACCGATATCACTGTCCAAACTGAATTTATAATTATGTTACAGCATCGTGATCAAGTCTTAAGTAACAACTTATCAGAATGATATCAAGACCTGCCAGAAAACAATTTGTGTGGTAGTTAATATATGCAAATATATG
Associated Phenotype:
Not determined