ZMP
LOC799435
Ensembl ID:
Human Orthologue:
ARHGEF10L
Human Description:
Rho guanine nucleotide exchange factor (GEF) 10-like [Source:HGNC Symbol;Acc:25540]
Mouse Orthologue:
Arhgef10l
Mouse Description:
Rho guanine nucleotide exchange factor (GEF) 10-like Gene [Source:MGI Symbol;Acc:MGI:1920004]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30949 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44742 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35105 | Nonsense | Available for shipment | Available now |
sa21933 | Essential Splice Site | Available for shipment | Available now |
sa31839 | Nonsense | Available for shipment | Available now |
sa31838 | Nonsense | Available for shipment | Available now |
sa38849 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30949
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000131165 | Nonsense | 172 | 1342 | 4 | 27 |
Genomic Location (Zv9):
Chromosome 11 (position 30413708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29289694 |
GRCz11 | 11 | 29536868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGTTGTAATATGGCTGTATATTTGGGGAATGTTCCAGAGATCAAGCTT[C/A]AACAGACTCTACAGCACCAGAGGATTTAAATGAAGAGGAAGACCACACTT
Long Flanking Sequence:
TTTCCCATTTAGCACTCTAATGACTTTCATAACCGATTACATTTAAGCATATTAATATAATACAAATCCACATAAAGGGAGATATTTAATGCTAAATGAAATGCAATTCTGAAGGACTGTAACATTTTGAAGCATGATAACACCATGCAATAAAATATGTTTATCATCTTTTTTATTAAGTAGAAGGTATTAAGTGAAGATTAAATAACTTACATAAGACTGGACACATTACCATCTACATTCATACATACTGTACACCGTAAAAGCAAAATTTCCATCTCATTTCCATTTTCTCTACACAAAACACTGTGGCACACAAGTGAAAACACAAGTGCTTTTTGTGATGCTGACTATGTGGGGCTGATGGCATCTGAACTCTTCCCCTTCTCTCCTACACCCACCATCTAGTATTAGTTTTGAACTGATCTCAGTACGGTTATATCCTAGAAATTAGTTGTAATATGGCTGTATATTTGGGGAATGTTCCAGAGATCAAGCTT[C/A]AACAGACTCTACAGCACCAGAGGATTTAAATGAAGAGGAAGACCACACTTGCACTGTGGTGAAGATCCAGAGAGATACATGCACTATTAAAACAAACGCAGGGACAGAGGATTTCAGACACAGCCCATCACAAAATGCTGAAGGTAAGAGAAAAAACCTCAAATTTGTTTTAAAATGGACACCACTAGTAATCAAATGAACAGTAATCAAACTGCACATTTTAGTTTGAATGGATATTAGATAATATCAGAAAACTAGTTTGTAAAACAATCCTCTGTTTATTATTGTTTCAATATTCCAATTAGTATTGTTCAATTATGTTAGGCAATATTTTATATTTATTTTATATTCAACCACATTCAGGATAATGCAGTGACAGTATGGCTATTTATCTGTGGTTCTGTAATCACCTTTTATCATTATTTTAAACATTAAAAGAACATATACAACAAAAGTGAGCATATACAGACTTTCCTTAAAACTTCATGAGACGGAATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44742
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 |
---|---|---|---|---|---|
ENSDART00000131165 | Nonsense | 216 | 1342 | 4 | 27 |
Genomic Location (Zv9):
Chromosome 11 (position 30413577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29289563 |
GRCz11 | 11 | 29536737 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACTATTAAAACAAACGCAGGGACAGAGGATTTCAGACACAGCCCATCA[C/T]AAAATGCTGAAGGTAAGAGAAAAAACCTCAAATTTGTTTTAAAATGGACA
Long Flanking Sequence:
GCATGATAACACCATGCAATAAAATATGTTTATCATCTTTTTTATTAAGTAGAAGGTATTAAGTGAAGATTAAATAACTTACATAAGACTGGACACATTACCATCTACATTCATACATACTGTACACCGTAAAAGCAAAATTTCCATCTCATTTCCATTTTCTCTACACAAAACACTGTGGCACACAAGTGAAAACACAAGTGCTTTTTGTGATGCTGACTATGTGGGGCTGATGGCATCTGAACTCTTCCCCTTCTCTCCTACACCCACCATCTAGTATTAGTTTTGAACTGATCTCAGTACGGTTATATCCTAGAAATTAGTTGTAATATGGCTGTATATTTGGGGAATGTTCCAGAGATCAAGCTTCAACAGACTCTACAGCACCAGAGGATTTAAATGAAGAGGAAGACCACACTTGCACTGTGGTGAAGATCCAGAGAGATACATGCACTATTAAAACAAACGCAGGGACAGAGGATTTCAGACACAGCCCATCA[C/T]AAAATGCTGAAGGTAAGAGAAAAAACCTCAAATTTGTTTTAAAATGGACACCACTAGTAATCAAATGAACAGTAATCAAACTGCACATTTTAGTTTGAATGGATATTAGATAATATCAGAAAACTAGTTTGTAAAACAATCCTCTGTTTATTATTGTTTCAATATTCCAATTAGTATTGTTCAATTATGTTAGGCAATATTTTATATTTATTTTATATTCAACCACATTCAGGATAATGCAGTGACAGTATGGCTATTTATCTGTGGTTCTGTAATCACCTTTTATCATTATTTTAAACATTAAAAGAACATATACAACAAAAGTGAGCATATACAGACTTTCCTTAAAACTTCATGAGACGGAATTTTTGAGGACTAATTGCAGTAAATGAATTTACATGGTGAAAAGTGTGATCAGGAAAACATTAAGTCCACATCAATTTTACAAGTGTCTAGAAACTGAAAGGTCTTCTCGTGGCCAGCTGCATAAATGCTATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35105
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 |
---|---|---|---|---|---|
ENSDART00000131165 | Nonsense | 563 | 1342 | 14 | 27 |
Genomic Location (Zv9):
Chromosome 11 (position 30378249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29254235 |
GRCz11 | 11 | 29501409 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGGACATGCTGAAGAACACTCCCACTGGCCATGTGGACAGACTGCCCT[T/A]GCAACTGGCTCTGACTGAATTGGAGACCCTCGCTGAGAAACTCAATGAGC
Long Flanking Sequence:
ACTCGAGCCCGGTCGTCGTCCCAGCGGCCGGCTCCTCCTCCTCTGGGGCCTCCGCTCAGCCGACGCAACGCTGTGAGCTAAGCGGACAAACTGGTTGCATTGGGAAAGCCCTCCACTCGGGGGACGGAGCGGCGCCACACCCCCCCGCAGCGTTCGCTCGGAAAAAACTAAACGCGGCCTTACGTACCTCCGGCCACGTAAATCGCGGTCTCCAGAAATGTCCGCGGGGCTACGTTTCCAGAATGAGCTTGGGTTGAACTTATTATTTACAAACTGCTACTCTGATGATTTGAATTGCTGTTTTATCCTCACTTGCAAGTTGCTTTGGATAAAAAGTGTCTGCTAAATGACTACATGTAAATGTAAAGAAAACAATTGGCCTTTGATTGCAAAAGCGAAACAAAAAAGCATTCGGTGTGATCAGGGCCTGACTTACTATGTTCTCTGCCTTTAGGACATGCTGAAGAACACTCCCACTGGCCATGTGGACAGACTGCCCT[T/A]GCAACTGGCTCTGACTGAATTGGAGACCCTCGCTGAGAAACTCAATGAGCAGAAAAGGGTGGCTGATCAGATCACTGAGACACAGCAGCTGGCCCGCTGTGTCAGTGACCGTTCTCTCAGCAAGGTGAGGAAAACACACACATGCGCCCTTTTTTCTTCCTCAGCTGTGATGGCAGAATGATGCTGCTGCCGCCTTGATGTAATCAGAGGAGTGTAAATCCTAATCACAAAACCATTTCATGGTTTCTTTCTGACTTCCTATTTTCTTAGACCTTTTTGCAATTACTTTACACCAGCTGGTCCCAAGGTCATTGTGTTCACACTGCTCTCATTGTAGCGAACCACAGATGTGGTTCATCACATTAACTGTTACACTTGCGTTTGACAAGCAGAAAATGTCACAGTGCTTTAGTCTTAATTATGAAATGGCTGTCTATTATTCCATTTTATCTTTTGAAAAAAAATGCAATCACAAGAATGAGGAAATTAGCCACTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21933
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000131165 | Essential Splice Site | 605 | 1342 | 15 | 27 |
Genomic Location (Zv9):
Chromosome 11 (position 30368180)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29244166 |
GRCz11 | 11 | 29491340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTTGTAAGACTTGCGTGTAATCAGTGTGTCCCCTGTCTTTTTCTTCA[G/A]TTGCTCAACTCGGAGCAGAGCTCTTTGATCCTTTGTGAGACGCTGATTGA
Long Flanking Sequence:
GTGCATAAAACTCAAATGGGTTTCTAAATTGAATTCAAATTGATGGAGCAGACCCTGCAAGTGAATGAACAATCAAAAGTGCTGCAACAAATGACATTTATTTGAAAGCAGTTTTAAGGTAAGTAAGGTCATAATGACATTATAAATGCCTCTTCAGTTTAGACATCATTCTAAAACTATTTATGTAATAAAAGAACCTTTAGTGGTCCTCTATTTTTATTGTACACATGCAGTCAAATTTAGATAGTTTGTGGATGCAACTTTGTGCTTGTCAATTCAGTTTGAAAGGAGTATTTTCTTCAAGATTGGCTTTTATTCCCACAACCTTTTCCACTACAAATCTACCACTGTGTTTCCAATCTTCTGTGGTGCCTGCCTGTGAACCTTCAAGTGTCTTATATGCCACGCTGTGGCCTCTAAGTAAGTGTGTAGCCATGTAATTGTAGCCTCTATTTTGTAAGACTTGCGTGTAATCAGTGTGTCCCCTGTCTTTTTCTTCA[G/A]TTGCTCAACTCGGAGCAGAGCTCTTTGATCCTTTGTGAGACGCTGATTGAGACGGTGTACGGTGAACGAGGACAGGTCCTCAAGTCTAAGGAGCGGAAAGTCTTTCTCTTCGGTGACGTGCTCATCTGTGCCAACATCAATGTCAAGTATGTGTCCTGTGCAAGGTCGATTGACTTTTTCTTTCTTCCTCCATCCCTCTTTTGACAGATTGTCGCTCATCAGCCGATCTAAATATGAGTCTCCTGAAGCATTACAGTGACGTTCCCCCCAAATACCCCCCAGTCAATGTTAGAGGGTTAGCTAATGGCTAAGGCACAGGACAGAATTGAGCAGAGTCAAATGGGCCATCATTATCTGGGGACAAATAGCGGGGTGTTTAGCTACAGAGACAGGAATTATCCCCATAGATCACTGGCATAAAGCGCTCTTCTGTTCCACTCAAATAGATTATCTATGACAGCTCCATTGATCACATCTCAGCAGTGCAAAAGGTAAACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31839
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 |
---|---|---|---|---|---|
ENSDART00000131165 | Nonsense | 783 | 1342 | 18 | 27 |
Genomic Location (Zv9):
Chromosome 11 (position 30348025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29224011 |
GRCz11 | 11 | 29471185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCCGCATCAAAGAAGACCAAATTCAGAACGCCAACAAGTGCCGTTTA[C/T]GACTGCAAGTTCCTGGCAGACCAGACAAGTAAGTGAAGAGGAAACTTGAA
Long Flanking Sequence:
CTGAGGCCAAAAACCACAATTAACATAAAAAAGTGTTTTTTATGTTTTTAATCTGGTATCAAGGTCTATTTATATATGGTTGGCTAAACAATGCCACATTTCACATGTGTATATTTGGGAAATAAATCAGTTTGTGATGTTTTATTCAGCAAGGATGCAGTGATTTCATCAAAAAATGACATAAAGACATTTATAATGTAACAAAAAAATATATATATAATAAGGCTCTTTGGTTAAACCTCCTAAACCTATTTTTTCATCTTTAGTTTTACTAAAATGCTCTGTATTTTTGTTCAGTCAGTAATGGTTTTTATAATTATTGCAGTAGTCTATAATTGTTAAACACTTAGAAAATCACTGAGATTGTGAATGCTTGTTGTCACTATTTGCTGCATTTCCAGAATCTGAACACCACAGTGGCGCAGGACTGGTGTTTGGCACTGCAAAGGCTGATCCGCATCAAAGAAGACCAAATTCAGAACGCCAACAAGTGCCGTTTA[C/T]GACTGCAAGTTCCTGGCAGACCAGACAAGTAAGTGAAGAGGAAACTTGAAACTTCGCTCAGTTTGACATGCCATGAATTTTATAAAAGCATCGTTAATGTTTTCTTGACTTCAACTACAGTGGTACAAATACATTTTTTAAAATAAAAATTTCATTAAATATAATTGGCGCTTTCAGTTTGTTCCACTGAAAAAGAGGTCATAAATATATCAATGACCCAATGGGCTGAATGCACAGCTTGGGTTTTTTCAGCCAATGTTAAACTTCCGGTGAAAGCTTAATGTGACTATTTTTAATTTCATACGTTTTCTTTTACAGCATTGCTGTTGTGATGGAATTCAAATATAATCAGTGAAATAGACTTTAGCGTTCATTTAGTTGTTCAAGCGTTAAAAAAAAAATTAAAGACCATATAAACGCAGGCGCCATCATTAGCAGCAGGCTAGCACAGAAACTCCATTGAAAATACTGGGGTAAAATGAATTTCCATATTTTAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31838
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 |
---|---|---|---|---|---|
ENSDART00000131165 | Nonsense | 924 | 1342 | 22 | 27 |
Genomic Location (Zv9):
Chromosome 11 (position 30266076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29142062 |
GRCz11 | 11 | 29389236 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACATCTTCTCCTTGAACAGACCCACACCTCGGCCTGTAAAATCCCTC[C/T]AGATGGGAGCTCAAGTGAGGTGTCTGGAGTATGTGCCTGAGCCCAGCCCA
Long Flanking Sequence:
AAGATGTTTGAAGTTCTCGGGCTGACGCTGGGAATGCATTAGGGGTGATAGCGCATGCATTTTAGAGGCTTTATCAAGTGGAAGACTATGAGTTAGATTTTTACGAGATATGTGATTTTAACTTTCCTGTTTTTGTGAAATTGAAATTGACAAGAATAAAATAACAGGGTTGAAAAGCATTAAAGTACACAGGAAGTGAAAGAGAGTTTTCTGCTGTTTGGAAATTTCCTCCGTCTTGTTCTTGGAACTGGAAGTGAAAGCACAAAGCTGGGGGAGTGTTTAAAAGTGGCAGAACAACACAAAGATCCTTCCATTCCTCTGCCATTTTCTTTCTCTACCTGTACAGTCATAGATATGAGAGCAGTTTTGGTTGGATGACTGCCCGTAATAGTGGTGCCCTTGCTCTGTTTTTGCAGGTAGCTAGTGGAGCTGATTCCACTCAAGGCCAGGTGGACATCTTCTCCTTGAACAGACCCACACCTCGGCCTGTAAAATCCCTC[C/T]AGATGGGAGCTCAAGTGAGGTGTCTGGAGTATGTGCCTGAGCCCAGCCCATCAGAGGATGCGGAAACCAGCCTGCACAGCTCCACTGAAGTTGGAAATACTATCTGTGTAGGACTTGATGATGGCAGGTAATATATAGACTGCTTAAAATGTGCAATATGTTCCTCAGTACAATTATAAAATACTTATTAATTCTGATAAAAATGTACTATAATAACACCAGTGTTGGGCAGTAGCGTTGCTACAAGTAGTGATGCTAGTAGCTTAGCTACATTTCTCAGTAGTGTGGTAATGTTGCTACTTTCTACATCAATTAGCTTTACAGTAGCCAAGTTGTTATCTTAAGCAAGTAGCGCAGTAACGTCCACAGAAGCTACATTTACCGATCACGGATCATTAAGTGACATTCACAGAGCTGCAATCAGGCAGTGTCTGGCCGATGAAAGTGAATACAAAATAGCAAGAATGACAAATTCTTTTTCTTTGTGTTTTACGGTGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38849
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 |
---|---|---|---|---|---|
ENSDART00000131165 | Nonsense | 1258 | 1342 | 27 | 27 |
Genomic Location (Zv9):
Chromosome 11 (position 30212397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29088383 |
GRCz11 | 11 | 29335557 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACCGTCTACGCTCAACCTCAGGGTTACCCGGACGGCCATTAACCGCA[C/T]GAGGAGACGAAGCCTCAGACTCATCTCTAGAGTCTCTGGAGCACAGCATG
Long Flanking Sequence:
TCAAAAGTTCTTCTTTTGTTCTCCACAGAATAGAAATATATATGCAAATGTTAATGGGAACTATGAAGGATGAACAAATTATGATCAATTTTTCAAGTTAATTTATTTCAAAGTAATTTCCGTATGCAATATGCACTTCAACATGTAATAATGCAAATCAGTTATCAAAGGTTCTTTCTGCTTTTTACTAATGAAAGCGATTTGTGATTTAATGTGGCCCAGGTAAGGGGATGATGTCCTTCAATGCTCACTGCGGGCCTGTGGATTTCTTAGTTGCCCTTTCCAGCACATTGTCCCCTGATCTTCTAAAACGGGACTCTGTGATAGAAGGTCACGATTCGGGCTGTGGAGTGGAGGACCGCAGCGACTCATCCTCTCAGGAATCCCTCCAGCAGCCCAGTGTTTCTACCCAGGTGGATGGAAAAGGGAAGGGACGGGGTGTTTTACTACAGTACCGTCTACGCTCAACCTCAGGGTTACCCGGACGGCCATTAACCGCA[C/T]GAGGAGACGAAGCCTCAGACTCATCTCTAGAGTCTCTGGAGCACAGCATGGAAGATGGCTCAATTTATGAACTCAGCGATGATCCAGACATGTGGGTCCGGGGTCGACCCTGCGAGAGGGAAGGGGTGAGGCGGGACAGGGTCACCTCGGTCGCAGTCATTTCGGGAGGTAAAGGTTTCCGTCGACTAAGGGAGGGATCGGTGACAGCCACTATGGAAAGCACACTTATGATCTGGCAGCTTCCTCTCACTGTTTGAGCTGAAATTTGTTGATTTACTCATCCTCATGTCATTCCAATACCCTCTTGACTTCCTCTTGAATTTATACACCGGTCACTCTTTTCAGTTCAGTTATGATAAATAGACCATAATTGGGTTTAAAGCTATGTTGAATTGAATGGAGATACGAGGCTGTGAGTGATAAACTAATCGAACACAGTTATGATGGTCTTAGAGAACAGAGTATCCATAACTTTTACTGTTGTTTTTTTTTTTTTTTTT
Associated Phenotype:
Not determined