ZMP
si:dkey-74f15.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate Rho guanine nucleotide exchange factor (GEF) 4 (ARHGEF4) [Source
Human Orthologue:
ARHGEF4
Human Description:
Rho guanine nucleotide exchange factor (GEF) 4 [Source:HGNC Symbol;Acc:684]
Mouse Orthologue:
Arhgef4
Mouse Description:
Rho guanine nucleotide exchange factor (GEF) 4 Gene [Source:MGI Symbol;Acc:MGI:2442507]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32868 | Nonsense | Available for shipment | Available now |
sa13647 | Nonsense | Available for shipment | Available now |
sa19710 | Nonsense | Available for shipment | Available now |
sa17428 | Nonsense | Available for shipment | Available now |
sa12665 | Nonsense | Available for shipment | Available now |
sa19709 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32868
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 |
---|---|---|---|---|---|
ENSDART00000057216 | Nonsense | 1139 | 3063 | 3 | 16 |
ENSDART00000133708 | None | None | 665 | None | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 16091459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16602286 |
GRCz11 | 2 | 16270876 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCAACAGTACACAGCCAATCACAAACTTCAGTGGGACAAAGCCAATCC[C/T]AGGATTTGGTAGAACAAAGTCGATCACCAGCTGCAGCCGAAAACAGTCAA
Long Flanking Sequence:
AATCACATGATTTAATAGAACACTTCAAATCACTAGACAACACAGAGCACAAGCAATCAGACATGAGTTATATAAACTGCAGTCAATCACAGGCCTCAGTAGAAATCTTGCAATCACACGAGTCTGTTGAACACAGCCAATCAGAACAGTCAGTAAAACACAGCCAGTCACAAGACACTGACAATTTTAGCCAGACACAGGATTTAATTAAGCACAGCCAATCACAGACTTTCATAAAATGCAAACACAACCAATCACTGGATGGCGTACAATATGATCAGTCAAAGATCTTAATAGAACAAACCCAATCACAGGATTCCGTAAAGGACAATCCATCCCAAGATCTTGTCAAACATAGCCAATCACAGGACACAGTAGAACCGAGTCAATCACAGGTCTCAGTAGAACACATCCAATCACAGGATTCCCAAGACTGCAGCCATTCACAGAACTCAACAGTACACAGCCAATCACAAACTTCAGTGGGACAAAGCCAATCC[C/T]AGGATTTGGTAGAACAAAGTCGATCACCAGCTGCAGCCGAAAACAGTCAATCACAGACTTCAGTGGAACACAGCCAATCACTGGATTCAGTGGAACACATGAAATCTCAGACTTCGGTGGAACACAGGCAATCACAGGTTGAATTGATTAAGGCACATTCCATGAACACCCGGTGGATGGTGACTGAGTCAGACACAGTAGCGTTTTATGACAAGGTGCGATTAAAACAAGACTGCATGGATGTTTGCGCAGATTGTGAAGTCGTTGAATCCTTGGGAGTTTTATCAAAACATGCTGACAATTTGAACTTCGAAAATAACGAAAGACTAAATTTCAAAACACAGGACTTAAATGACACTTCACCTGTTGTTTCTGAATACGAGTGTTTCCCACATGTGCCTAATGCATCTTCTATTGGAGTGCCAGATTCACTGCATCAGTGCACGATTAGCAATTCACCCTCAGACCTGCAGGTTAAAACTCAGCAGAGTTGGCCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13647
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 |
---|---|---|---|---|---|
ENSDART00000057216 | Nonsense | 1240 | 3063 | 3 | 16 |
ENSDART00000133708 | None | None | 665 | None | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 16091155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16601982 |
GRCz11 | 2 | 16270572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGAAGTCRTTGAATCCTTGGGAGTTTTATCAAAACATGCTGACAATT[T/A]GAACTTCGAAAATAACGAAAGACTAAATTTCAAAACACAGGACTTAAATG
Long Flanking Sequence:
CCAATCACAGGATTCCGTAAAGGACAATCCATCCCAAGATCTTGTCAAACATAGCCAATCACAGGACACAGTAGAACCGAGTCAATCACAGGTCTCAGTAGAACACATCCAATCACAGGATTCCCAAGACTGCAGCCATTCACAGAACTCAACAGTACACAGCCAATCACAAACTTCAGTGGGACAAAGCCAATCCCAGGATTTGGTAGAACAAAGTCGATCACCAGCTGCAGCCGAAAACAGTCAATCACAGACTTCAGTGGAACACAGCCAATCACTGGATTCAGTGGAACACATGAAATCTCAGACTTCGGTGGAACACAGGCAATCACAGGTTGAATTGATTAAGGCACATTCCATGAACACCCGGTGGATGGTGACTGAGTCAGACACAGTAGCGTTTTATGACAAGGTGCGATTAAAACAAGACTGCATGGATGTTTGCGCAGATTGTGAAGTCGTTGAATCCTTGGGAGTTTTATCAAAACATGCTGACAATT[T/A]GAACTTCGAAAATAACGAAAGACTAAATTTCAAAACACAGGACTTAAATGACACTTCACCTGTTGTTTCTGAATACGAGTGTTTCCCACATGTGCCTAATGCATCTTCTATTGGAGTGCCAGATTCACTGCATCAGTGCACGATTAGCAATTCACCCTCAGACCTGCAGGTTAAAACTCAGCAGAGTTGGCCAGTATTACAAATACACACCGAAAAAGACGATTACTCAGTTAGTAGGTATCACATGGATGGTTACTGTTTGCAGGACAGTGAGCAAACAGAGTTTTACAAAACCTACCAGTGCCCTAACAGTACCATTAATTTTAATACACAGGGTGAGTTCACTGAAGCTCGGAAGGTTGTATCAACTGAAGGTGTATTTACTAGAGGTTGTATCAACACCAAACTTTTTGATGGCAAAAGTGTTGACATTGTAGGAGGACCGCAGAAGGACAGCAACAAGCATCACGTTATGAAAGGGAAAGAATGTACAATAGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19710
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 |
---|---|---|---|---|---|
ENSDART00000057216 | Nonsense | 1576 | 3063 | 3 | 16 |
ENSDART00000133708 | None | None | 665 | None | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 16090148)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16600975 |
GRCz11 | 2 | 16269565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATAATAACATTAAAGCCATTACTTTAGAAGAGTGTGCCTCGGGAGTA[C/T]AAATGTCATTGCCTAGTTCATTGCAGAAATACAGTAGGTTTACAAATAAT
Long Flanking Sequence:
TAGAGCAGTCAGTAATTTACTCTGACAGTTCAGGATGCATAGAATATAAAAGGCCCAAAACGTTGAGCATTGCTTGTCCTGACATGACGACTGCTGAATCTGAAGGGTGTCCTGTAGACAGTCCTGTTGAATCACTTTCTACACTGTTTGAGATTCCACATGACAGATCTACAGTCAGCCCCACAGACATTTGCTTTGAGTTTAGTGATGGCCCTCATATGAACTGTACACAAGTAGCACAGAGTGTTATAGAATATTCAGATGCCCCCAAACTATTTCACCAGTTTGACACCCTGTCTGACAAACAAAGAAGACCTAATGAGTCAGCTGAAGCAATTGCGTCGAATGTTGATATTTTGTCTGGTGCACGTTCCGATCCTTTCACAAATGCACAGACTCCTTTTGATTATTCCCAGGTGAACAGCAGGAACTATACACAGAGCTCAGACACAAATAATAACATTAAAGCCATTACTTTAGAAGAGTGTGCCTCGGGAGTA[C/T]AAATGTCATTGCCTAGTTCATTGCAGAAATACAGTAGGTTTACAAATAATGCTGAATGCTTAGTCTCAAAAAGGGGTGATTACAAAAACATTGATTCTTTTAGTGCTCGTAATACTCTGGCTACCCCCTTCAAAGCACCTGAAATGAAGACTGAAGTGAACAGCAGAGAAAATGTTGTGAAATCTAGCAGTCACATAGATGTTACACAGAGGAAGCTCTGTGATTGCTGCGGTGGAAAGGAGTGCCAGCTGCAGACAGCGGGTGTATTTCAGTTCAAGGGCACAGACGCCATCAGTCAGCGCAGAACTGCAGTGTTGCAAACCTTGAGTCCCCTCCACACAGATGACAGCACACATGAAGCGGTAAAAGTAGACTCTACAAGCTGTGAATTTTCACATATGGTCAGTTTGCTTACACACAAACATCCGAATCTTGTCCAAGAAGACTTCGTATTACCACTGACTGGAGCTCATAAGGCTGATGATACTCATGTATTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17428
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057216 | Nonsense | 2133 | 3063 | 3 | 16 |
ENSDART00000133708 | None | None | 665 | None | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 16088477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16599304 |
GRCz11 | 2 | 16267894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGAAGCAGAACTTTGCAAAAGAACTCNNNCTGTTCCTGGGACGGTCTGTGAC[A/T]AGTGCATAMATCAGAGCCAAATTGATTGTGYYTTCTGTGCTTATCAGAAC
Long Flanking Sequence:
AACAAGATGAGATGAAGAACAACAGGTCACCCACATGCAGCAAATCTCACTCTTCACTGTACAAGACCCCTATATCTCAAAGTGCAGATCACCTTACTGATATTACAAAGCATTCTGACCACTCAAATGATGATGTTTTTGAAAGGGCTTTTGCTTTAAATGTGCAAAATAGAGAGAAACACATGCAACCTCAACACCCGTTTGAGCAGCAGCAGCAGAAAGATGGAGATGCACTCAGTTTTAGAGCTGGCCAGACAACAGAGGGGTTGCAACAAAAAAGATGCAAGAGCATTGATAACTTAAACTTACGCATGAAGCTGGCATTGGCTCACAAGTCTATTTCTAGCCTGTTTGAGACCAGATATCCTGAGAGGGACCAAGAGCAAATCTTACAGTTAGAGAATGAGGATGGGAAAACCAAGCAATCATGGAGAAAGACCAAACGATGTAACGAAGCAGAACTTTGCAAAAGAACTCCTGTTCCTGGGACGGTCTGTGAC[A/T]AGTGCATACATCAGAGCCAAATTGATTGTGCCTTCTGTGCTTATCAGAACCGGTCCATATTAACCAACTTACCAAATGTCCAAGCAAGATTGAAGAACACGTGCCATTCTGACCCGCAGAGTTTGAAATCTGCACCTCAGGAAGGGTTTGAAGATGGTAAATATCTGGAGGAAGGTGAGCAGCCTTGTGGTGCTTTCTCAGATTCAGACCAAGCATCGGTAGATGGTTTTGAGTCCAGTGTAGAGGACAGGTCGCTGTCACCTGCACACCCCACTGTTCTTGCACTTTCAAACCAAATGTCACCTACCTGGACAAGGTCCCTAAGCTGCTTCGAGACAACTGATACACCGACAAGGCCCATGAGCCCCAAACCACACAGTCCTGGTCTGGGCTGGACACAGCGGAGGAGCTTCCGCTACCCCTCAAGATCTGTTGCATCTTCTCTCTGCTTGCTTGGTCAGGGAGTGAGCACTGACGGTCTCTTAGACCCACCTCAGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12665
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 |
---|---|---|---|---|---|
ENSDART00000057216 | Nonsense | 2502 | 3063 | 6 | 16 |
ENSDART00000133708 | None | None | 665 | None | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 16077693)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16588520 |
GRCz11 | 2 | 16257110 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTCTCCACAGAAACGAACCTCAGCGCMCCGGAAAAAGAGGCACATGGA[C/T]AGGTYGCACCTCTCGGTGAGTTTACTTTCTCAGCTAAATCTTGANNNNNAACACA
Long Flanking Sequence:
CAAAATATGTGAACAAAACTCATAAGGTATGCTTACACAACTACTTATTTAATCCTGTTAGAATAGCGTAAAATGGACTAAGCAGTGAACTCGTTGATCTCTAATATTGATTCTTTTCTGAAACTCTCATCTGAACTAAGACTTCTTGATCATTTGTGTTTTACTGTTCAGTTTATTTATGTAAAACATTCCTCCCACTATTGAAGCCATGACATGCTTTGTGTGTTTTGCAAGGCCTCTGAAAGCACTGCCTTATGAAATATGGATTCAAATGAGGAGAAAGACACAATGACCTCGTTTTGCTACTTGCTGACATCATGCCCCCTCTACAACCTTACTTTACACCACATGACAAGCCAAAGGGGCATTTCTTTTTCAGTTATGCTCATCTAGATCTTGAATCTTAACTTGTTTTTTTAGTACAGGAGAGAAACTAACTCTGATACATGCTGCTCTCCACAGAAACGAACCTCAGCGCACCGGAAAAAGAGGCACATGGA[C/T]AGGTCGCACCTCTCGGTGAGTTTACTTTCTCAGCTAAATCTTGAAACACAGTATGAGCTTGTACTTTTAAGAAATACAGTGCTGGTGTGTTGAAGATATACAGGAAGAGTGGAACAGTTGATCCTGGTGATTTGACTGATGGGTTTAACATATTTTCTTTACTCTTTTTATGAATATTGTTTATTATGGCTTAACTTGTGGATTCATTTTATGTATGATTTAAACCAGAGATAATATATAGTTCTCAGCATATATAAGTACACCCCTCACAATTCTACCTTTTAAATTTATATGTTTAATAGGAATCTATACAATATTACATTTGTGTATATACATTAGATTAGTCAGTACTGAAGCCAAATCTGGAGCTTACCTAACAAAATAACCTACGAGAACGGTCCAAAAACTAGTACAGCCAAATGTATATGTTATAGAAAAATATTAAATACTACCAAAAAAAGGAAAAATCAAAAGAAATAGAACAATTGAAAAATTTAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19709
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 |
---|---|---|---|---|---|
ENSDART00000057216 | Nonsense | 2984 | 3063 | 14 | 16 |
ENSDART00000133708 | Nonsense | 542 | 665 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 16027325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16538152 |
GRCz11 | 2 | 16206742 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGCTGAGAGCCTTCACAGATGAGCGGGAGCAGGTCCAGCATGACCTC[G/T]AGACAGGTGAACGGCGCTTCTGGAGCTGTATAAAAACACTGCTTTTGCTG
Long Flanking Sequence:
GTGGTCTCACGGTCTCTTTCTCATTTCATTAGGGTGAAGACGTCTTGAGCAGGAGCTCTGATCTGATCTTTTCTGGAGACCTGACCAAGATCTCCCAGCCACAGGCTAAAGGCCAGCAGAGAATGTTCTTCCTCTTTGACCACCAACTGGTTTTCTGTAAGAAGGTCAGTCACTTGATGTGCCAGTGAGAGCAGTCACTGTTAGTCACGGCAGATGGTGTTCATGCAGGTATTAAAGTTTTACCGTCTTTTTAAAAACCACAGGATCTGCTTCGGAGGGATATCTTGTACTACAAGGGTCGGTTAGACATGGATGAGATGGAGGTGGTGGATGTGGAGGATGGGAAGGATAAGGACTTTAATGTGAGTGTGAAGAATGCCTTGAAATTGTGTTCTCCTGGAGGAGAGGAGGTTCATCTCCTGTGTGCCAAGAAGCCCGAACAAAAGCAGCGCTGGCTGAGAGCCTTCACAGATGAGCGGGAGCAGGTCCAGCATGACCTC[G/T]AGACAGGTGAACGGCGCTTCTGGAGCTGTATAAAAACACTGCTTTTGCTGTTCATAGCTAGTCTTTAAATTGATTATTTAATTATTATTATTTCCTTTATTTTACACTCTTAGTTCATATCCAAAAACATTTAAACATATATAAATATCTTATTATCATTTAAAAAAACATACAAACATTATTTCAATGCTTCCAATACCAGGAGTAGTAATTAGTACCGCTTAGTGTGGGATAATTTGAAACCTTTATAAATGTATTTCTTGGGATATTCAATCGACACATACAATTATACATAGTTGGACTATCCATGATTATGTTTGCAGTTTATGATAAAACTTTATACAGAATCTTTGTTGTTAAATGACAAAAATAGTTAAGAATTCCATTATATACAGTAAATTCTTAGTTCTCCAAAAATATGTTCTACCATTCCAGGTTATAAACAATCTCGCTTTCTCTCATTGACACACACACACACACACACACACACACACACACAC
Associated Phenotype:
Not determined