ZMP
si:ch211-142p3.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate Rho guanine nucleotide exchange factor (GEF) 12 (ARHGEF12) [Sour
Human Orthologue:
ARHGEF12
Human Description:
Rho guanine nucleotide exchange factor (GEF) 12 [Source:HGNC Symbol;Acc:14193]
Mouse Orthologue:
Arhgef12
Mouse Description:
Rho guanine nucleotide exchange factor (GEF) 12 Gene [Source:MGI Symbol;Acc:MGI:1916882]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25313 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40576 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44622 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17710 | Nonsense | Available for shipment | Available now |
sa20550 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25313
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087610 | Nonsense | 657 | 1336 | 19 | 35 |
ENSDART00000144670 | None | None | 248 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 60191163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 58052781 |
GRCz11 | 5 | 58722490 |
KASP Assay ID:
554-7853.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGTGAAGATGATCAGTGTGTTGAAGCCGAACTCGAGCCTCCAAACT[G/A]GCAGACACTAGTGAGCAGAGACGTCCTGTCCACACTCACGCCTCAGGAAA
Long Flanking Sequence:
AAATATATATTTTTGCGCCATTTTGAATTTTACTTGAATACAAATACAAATACAAATACTTTTCCCCCCTCAACAAATACAAATACCGGCTGCTCCGCACATCCCTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATTTTTAAAGATTAAATAAAGTGTGATTAAAGTTTTATTAATTAATTTGAACAGTTTTTTTTTTAATCATAAAACACAAGAAAATTAGAACAAAATACAGAATATTGTGAAAAAACTGCATGAAATTTGGTTTGGACATTTGGCTTTTCTTTGTTCACATGCTAATAAGTTATGTTGAAGTTTTCTACATTGCGTTAGGCCTGTTTTAATCAATTTGTGGTGTGTTTGAGCAGCAGGATGGATCCGCTGGGCTCTGGAGAGGTGCAGAGTGAAGATGATCAGTGTGTTGAAGCCGAACTCGAGCCTCCAAACT[G/A]GCAGACACTAGTGAGCAGAGACGTCCTGTCCACACTCACGCCTCAGGAAATTAAGAGACAAGAAGTCATCAATGGTGAGCAACTTTCTGAAATAATTAGTTTAGATTTGATTTATGTATAATTTTATATAATGTTACATAACATTTTATATAGACAACCATATATGGTGTACCCGCTTCATAATATGAACTATATTTTAGTTTATCTTTGTTCTTTATAAATGTCTACATGAAATCAAAATTCACCGTGTTCATTTTACTATCTGTGCAAGTAAGTTCACTGAATTTATTTATTTATTTTTTCAGCGCTTAAATCAAAATCTTATCAGTAGCAGTAATCTTCTGATGATGTCAGTTTGACGGCTAGGGCGAAATATTCTTAGACACACCCCTCCAGCCATTAGTTTGCTGCGAATTAAAAATAAGAGGAGGTGCTCCGAAATAGCCCCGCCCTTACTCAATATTCCATCTCAGCTGGAAATGCGTCATCATACTTAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40576
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087610 | Nonsense | 855 | 1336 | 24 | 35 |
ENSDART00000144670 | None | None | 248 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 60186250)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 58047868 |
GRCz11 | 5 | 58717577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGGACTCTGAGGAGAGAAGTAAAGTGAAACGGGCTGGCGAATGCTG[T/A]AGAAAGATCCTCACTCACGTCAACCAGGAGGTGAAGGAAGCGGAAAACAA
Long Flanking Sequence:
TATATAAAATGTTAGATGCAATAATGCAAATTCCATCACAAACTTTAGTTTGTCACAATTTGTGCTAATAACTACTAGCTTATTACCTGCCCATTATTAAGATATAAACTGTTTATTAATATTTATAAAGTATGATCTTAATCTACATCCCCAATCCTACCGATTACCTAAACCCAACTACCACCTTACTAACTATAAATAAGCAGCAAATTAGTAGTTTATTGAGCTAATAGTCTTAGTTAATGGTTTGTTAATAGTGTGAATTGTGACTTAAGATAAAGTGTTACCTAACATTGCATACTGTTGAATGAAAGTATTCGATTGTGGATTTGAAACTTTTTAAACAGATTGATGTAATAAACTGATTGTGTAATAATGGTGGCAGGCTAAATGACAGAAATATTTAGCTGTGTAAGTCTGTAATCCTTCAATGATTCTTGTTGTTGGATGGCAGAGGACTCTGAGGAGAGAAGTAAAGTGAAACGGGCTGGCGAATGCTG[T/A]AGAAAGATCCTCACTCACGTCAACCAGGAGGTGAAGGAAGCGGAAAACAAGCAGGTTAGCAGATAATACAGTGGAAAACCTGACTTTAGCTCAGTCCACACAATCTGACACAATCAAACCATGATTCTTACTTTCTGCTGCCCCCAGAGGCTGGAGGACTACCAGAGAAGACTGGACCTGTCCTCACTGAAGCAGAGCGAAAACCCCATGATCGCAGAGTTCAAGGTCAGAGCACGCTTATTAACCTAGAACCTATAAAAAAAATAAAAAAAATGTACAATAAGGTGCACAAGTGTTCTCCTATCAACACAATAATAAATAATAAATAATTATCTTTAAATATTAAGATATTTGTAAATTTTACCAAATTGTTGACTATACGACATATTTTTCTACCATGTTACTTTATTTTTGTGTTTTCATTAGCAAAAATACAAATATTATATCAGTAGTAATATTTTACATATTAATATCTACTGATCTGGCAAATATTATTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44622
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 |
---|---|---|---|---|---|
ENSDART00000087610 | Nonsense | 941 | 1336 | 27 | 35 |
ENSDART00000144670 | None | None | 248 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 60181930)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 58043548 |
GRCz11 | 5 | 58713257 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGCTGTACACGTTGCTGCTGGAGGATATATTGGTGCTACTTCAAAGG[C/T]AGGATGAGAAGCTGATCTTAAAATGCCACAGTAAGAATCTGGCGGGCACC
Long Flanking Sequence:
AGTAAAATAGCATAAAAACTATGTAAAAACTAACTAACAATAGTTATTATACCCTTTTATGTGTTGCAGGCATATTTAAATGTTAAGACATCTGCTAATTTAACAAATATCATTTACCATTTTATATCTATTTCATGATTTTTTTTTCTCTCCATGTCCAGAGCTTGGACTTGACCAAGAGGAAGATGGTGCACGAGGGGCCGCTGTCCTGGAAGGTCAACAAAGACAAAACCATTGGTGGGTGTGGCTTTTTTACAGAATTAATATATATAGACCAAACTCACAGTAGGTCAATATCCTAAAGATCTCTTACAGGTGCAGTAATTCTGAAGAAGAAAATCACTTTTGACTGTGTTTTCCACAAAGCGACATCAAGGCAAAACCGAATGCTGTGAACGAGTGATGTCTTGTAATGTCATTGTGAAATGATTTCATGTGCGTGTGTGTTTTCAGAGCTGTACACGTTGCTGCTGGAGGATATATTGGTGCTACTTCAAAGG[C/T]AGGATGAGAAGCTGATCTTAAAATGCCACAGTAAGAATCTGGCGGGCACCGCTGAGACCAAACACATCTTCAGCCCCATCATCAAGCTCAGCACTGTGATGGTGCGCTCCGTTGCCACCGGTACGATAACAGAGATGTTAAAATCTGACAATGTGAATGCTTAAAGCTGTAGTTCACGGAACAATTTTTCAAATGATCTTATAATTATCAAAAAACAGAGAAATATTCTGTAGCATTTTCTTTAAAGGTGCAGTAGGTGATCTGCCAGAATGCTAGCGTTAGCATAATAGCTTACGTCCCTTCACTGCCATCAAATACCATGGAACCCGCACCGAATAGATGATGAACTGATGATGATAGACAACCTTATATAGCTCTAGACCATGTCATTCACCAGTTAGAAAAATCTTTGAAGACACACACTTTGTCCAGCATAGTTGTTGACAGCCCGGGGGGTGCAGGAAATGTATTTCCCCAAAACTGGCATTGGGGTAAAGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17710
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087610 | Nonsense | 947 | 1336 | 27 | 35 |
ENSDART00000144670 | None | None | 248 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 60181911)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 58043529 |
GRCz11 | 5 | 58713238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGGAGGATATATTGGTGCTACTTCAAAGGCAGGATGAGAAGCTGATCT[T/G]AAAATGCCACAGTAAGAATCTGGCRGGCACCGCTGAGACCAAACACAWCT
Long Flanking Sequence:
TATGTAAAAACTAACTAACAATAGTTATTATACCCTTTTATGTGTTGCAGGCATATTTAAATGTTAAGACATCTGCTAATTTAACAAATATCATTTACCATTTTATATCTATTTCATGATTTTTTTTTCTCTCCATGTCCAGAGCTTGGACTTGACCAAGAGGAAGATGGTGCACGAGGGGCCGCTGTCCTGGAAGGTCAACAAAGACAAAACCATTGGTGGGTGTGGCTTTTTTACAGAATTAATATATATAGACCAAACTCACAGTAGGTCAATATCCTAAAGATCTCTTACAGGTGCAGTAATTCTGAAGAAGAAAATCACTTTTGACTGTGTTTTCCACAAAGCGACATCAAGGCAAAACCGAATGCTGTGAACGAGTGATGTCTTGTAATGTCATTGTGAAATGATTTCATGTGCGTGTGTGTTTTCAGAGCTGTACACGTTGCTGCTGGAGGATATATTGGTGCTACTTCAAAGGCAGGATGAGAAGCTGATCT[T/G]AAAATGCCACAGTAAGAATCTGGCGGGCACCGCTGAGACCAAACACATCTTCAGCCCCATCATCAAGCTCAGCACTGTGATGGTGCGCTCCGTTGCCACCGGTACGATAACAGAGATGTTAAAATCTGACAATGTGAATGCTTAAAGCTGTAGTTCACGGAACAATTTTTCAAATGATCTTATAATTATCAAAAAACAGAGAAATATTCTGTAGCATTTTCTTTAAAGGTGCAGTAGGTGATCTGCCAGAATGCTAGCGTTAGCATAATAGCTTACGTCCCTTCACTGCCATCAAATACCATGGAACCCGCACCGAATAGATGATGAACTGATGATGATAGACAACCTTATATAGCTCTAGACCATGTCATTCACCAGTTAGAAAAATCTTTGAAGACACACACTTTGTCCAGCATAGTTGTTGACAGCCCGGGGGGTGCAGGAAATGTATTTCCCCAAAACTGGCATTGGGGTAAAGTTGGTTTTATATTGGCACAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20550
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 |
---|---|---|---|---|---|
ENSDART00000087610 | Essential Splice Site | 981 | 1336 | 27 | 35 |
ENSDART00000144670 | None | None | 248 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 60181808)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 58043426 |
GRCz11 | 5 | 58713135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCCCATCATCAAGCTCAGCACTGTGATGGTGCGCTCCGTTGCCACCGG[T/C]ACGATAACAGAGATGTTAAAATCTGACAATGTGAATGCTTAAAGCTGTAG
Long Flanking Sequence:
TATATCTATTTCATGATTTTTTTTTCTCTCCATGTCCAGAGCTTGGACTTGACCAAGAGGAAGATGGTGCACGAGGGGCCGCTGTCCTGGAAGGTCAACAAAGACAAAACCATTGGTGGGTGTGGCTTTTTTACAGAATTAATATATATAGACCAAACTCACAGTAGGTCAATATCCTAAAGATCTCTTACAGGTGCAGTAATTCTGAAGAAGAAAATCACTTTTGACTGTGTTTTCCACAAAGCGACATCAAGGCAAAACCGAATGCTGTGAACGAGTGATGTCTTGTAATGTCATTGTGAAATGATTTCATGTGCGTGTGTGTTTTCAGAGCTGTACACGTTGCTGCTGGAGGATATATTGGTGCTACTTCAAAGGCAGGATGAGAAGCTGATCTTAAAATGCCACAGTAAGAATCTGGCGGGCACCGCTGAGACCAAACACATCTTCAGCCCCATCATCAAGCTCAGCACTGTGATGGTGCGCTCCGTTGCCACCGG[T/C]ACGATAACAGAGATGTTAAAATCTGACAATGTGAATGCTTAAAGCTGTAGTTCACGGAACAATTTTTCAAATGATCTTATAATTATCAAAAAACAGAGAAATATTCTGTAGCATTTTCTTTAAAGGTGCAGTAGGTGATCTGCCAGAATGCTAGCGTTAGCATAATAGCTTACGTCCCTTCACTGCCATCAAATACCATGGAACCCGCACCGAATAGATGATGAACTGATGATGATAGACAACCTTATATAGCTCTAGACCATGTCATTCACCAGTTAGAAAAATCTTTGAAGACACACACTTTGTCCAGCATAGTTGTTGACAGCCCGGGGGGTGCAGGAAATGTATTTCCCCAAAACTGGCATTGGGGTAAAGTTGGTTTTATATTGGCACAATTACAATAATATAAATTCGGAAAAGTACTGTTTGCAAACTCTACATAGTGAAATCATATAATCAGCCAATGACTATAAAATACAACATCGTTTACTGTCAATAGT
Associated Phenotype:
Not determined