ZMP
ARHGEF37
Ensembl ID:
Description:
Rho guanine nucleotide exchange factor (GEF) 37 [Source:HGNC Symbol;Acc:34430]
Human Orthologue:
ARHGEF37
Human Description:
Rho guanine nucleotide exchange factor (GEF) 37 [Source:HGNC Symbol;Acc:34430]
Mouse Orthologue:
Arhgef37
Mouse Description:
Rho guanine nucleotide exchange factor (GEF) 37 Gene [Source:MGI Symbol;Acc:MGI:3045339]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu3278 | Essential Splice Site | Available for shipment | Available now |
sa45516 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22474 | Essential Splice Site | Available for shipment | Available now |
sa18496 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
hu3278
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106039 | Essential Splice Site | 252 | 709 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 14 (position 25852718)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24555809 |
GRCz11 | 14 | 24853054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCAGATCAACTGCAGGATCAATGAATACAAACGCTTCCGTGAAGTGGG[T/A]GAGAGAACATGCTCGCAATTTATCACGCAAAGCTGGCTGAACACAAGTAC
Long Flanking Sequence:
TATTTTATTTCCCAGGTGACTCTTTCTTGAGTCTGTCTCAAGATATTGAAATGGCTTATAAGGAGTATCTTGCCAACTACAACAATATCACCGCTCTGGAAAACAGCTACAAACAGAAAGAGGCCCTGTGGATGGAGATGGTCAGAATCATCAAATCCTCTGCGTAAGTCTAACAACAACCAACAGAGGATGTATACATCTTCAACCCTGTTGAGAGAAGAATGACTTCTTAGAAAAACACACTAGTCTTTTACCCAGCATTCCTTTCATTTTTGACCCCTGATCTTGTCTGTCTTCAGTCCTGATGTGAACGCGTCTACTTTGAGCTTCTTCCTGGTAATGCCGGTCCAGAGAATCGCCCGTTACCCCCTACTTTTCCAGACCATTCAGAAACACACAGACCCCCAACACCCTGCCTACCCTGAACTGGAGCACACCGCTCACACGGCCATCCAGATCAACTGCAGGATCAATGAATACAAACGCTTCCGTGAAGTGGG[T/A]GAGAGAACATGCTCGCAATTTATCACGCAAAGCTGGCTGAACACAAGTACGTCAATTTATTCAGAACAGCATCACATAAACATGAGTAATTATTGTCATTCTCTTGACTACCACAGCTGACAAGTACAAGAAGACAGAAAACCTGACCATCAAGGACAAGCTTAATCGGTTGAGTGGCCACAGCATTGCTAAGAAGACAGCCCGGTTCAGCCAGTATATAAAGCATGAGACCGGAATAGTGCCAAAGGTAACTTCTGTACAATTATGCTATACATAGAAGAACAATACCTTGTGTACACACAGACATTTAAATGTTTAACTTGTTGAAAGAACCACATTGTTTTCCTAAAACCTAAGACGCCATTGCCTATTTTAAAAGTTAAAGGGATAGTTCACCCAAAATTTAATTATTTACTCATCCTTTACTAGTTCAAATTAGATTGAAAGTATTTCTTGGTTGTGTTGGACATAAAAGAAGAATTATTAAAAAATGTTGGAAA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa45516
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 |
---|---|---|---|---|---|
ENSDART00000106039 | Nonsense | 362 | 709 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 14 (position 25855167)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24558258 |
GRCz11 | 14 | 24855503 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGGGAGAAAACCGCCTTGTTCTCCAAAGAAATCACAGTGGCGCTCAGA[C/T]AGTGGATATACCCCTCATATGTAAGACTTTTAGATAATTATTACAGTTTG
Long Flanking Sequence:
AATCCCATTGTAGTTAAAGGATGAAGAATTCGATGCCCTAGCTGGCTTCTTCTTTGTCCTGGAAAGGGGCGTCTCAGAGCTTCATGATAACCTGCTGACTTATCTCCACCATTTACAGGTTTGGATTTACATTTCTTCCACATAATGACTGCAGCTAAACCTAGACAAAGAGTCTGTCTAATTTGTTTTGGTGTTCCCTTAGTATGAACCCAGTACGCCCATGAAAACTTCTGAAATGTTTTTCACTGTTATTCCAGCTGGTGAATAAAAGAAAAAAATCTACAGAAGGGTTGATCCCAGGGCTGATGGATGGGGTTATTGGAGATTGTAAAGTTCAGATGTTTGCTATGTGTGCTTGCAGTGTTTGTAAAGATTTATTTAACATCCTGAGCTGTTTCTGTGTACAGAGGTTCCTCAGCTGCAGACCAGAGGAAGCAGATCTTGATCTTGAAGGGGAGAAAACCGCCTTGTTCTCCAAAGAAATCACAGTGGCGCTCAGA[C/T]AGTGGATATACCCCTCATATGTAAGACTTTTAGATAATTATTACAGTTTGTGTCCCTGGGCCACAATACTTGTCATAAGTGTGCTATTTTTATTTCTGAAAAATTAAGCTTTCAATTAATGTTTGGCTTCTTAGAATAGGAAATCTAGAATTTGAAGTTTTAAAAAAAACATAATACTGAGAAAATCACCTTTAATGTGTCTAAATTAATTGGTTAGCTATGCATATTATTAATGAAAAAAAGAGTTTTGATATATTTACAGTATGATGTTTACAAAATATCTTCATGAAGCATGATCTTTACTTAATATTTGAATGATTTTTAGCCTATACAATGTATTTTTGGCCTATGCTACAATATACTCCTGCAACTTAATACTGAGGTTCTAAGACTGAAGTTAGGCTAGACTACAGTCACATTACTTCAACATTTCCATCATAACTTTTTAGTCTTTATTTAAATTCTGAAAGTTGGAAAATGTGTTAAAATAGTTTGCAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22474
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106039 | Essential Splice Site | 368 | 709 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 14 (position 25855189)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24558280 |
GRCz11 | 14 | 24855525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAAAGAAATCACAGTGGCGCTCAGACAGTGGATATACCCCTCATATG[T/A]AAGACTTTTAGATAATTATTACAGTTTGTGTCCCTGGGCCACAATACTTG
Long Flanking Sequence:
GAAGAATTCGATGCCCTAGCTGGCTTCTTCTTTGTCCTGGAAAGGGGCGTCTCAGAGCTTCATGATAACCTGCTGACTTATCTCCACCATTTACAGGTTTGGATTTACATTTCTTCCACATAATGACTGCAGCTAAACCTAGACAAAGAGTCTGTCTAATTTGTTTTGGTGTTCCCTTAGTATGAACCCAGTACGCCCATGAAAACTTCTGAAATGTTTTTCACTGTTATTCCAGCTGGTGAATAAAAGAAAAAAATCTACAGAAGGGTTGATCCCAGGGCTGATGGATGGGGTTATTGGAGATTGTAAAGTTCAGATGTTTGCTATGTGTGCTTGCAGTGTTTGTAAAGATTTATTTAACATCCTGAGCTGTTTCTGTGTACAGAGGTTCCTCAGCTGCAGACCAGAGGAAGCAGATCTTGATCTTGAAGGGGAGAAAACCGCCTTGTTCTCCAAAGAAATCACAGTGGCGCTCAGACAGTGGATATACCCCTCATATG[T/A]AAGACTTTTAGATAATTATTACAGTTTGTGTCCCTGGGCCACAATACTTGTCATAAGTGTGCTATTTTTATTTCTGAAAAATTAAGCTTTCAATTAATGTTTGGCTTCTTAGAATAGGAAATCTAGAATTTGAAGTTTTAAAAAAAACATAATACTGAGAAAATCACCTTTAATGTGTCTAAATTAATTGGTTAGCTATGCATATTATTAATGAAAAAAAGAGTTTTGATATATTTACAGTATGATGTTTACAAAATATCTTCATGAAGCATGATCTTTACTTAATATTTGAATGATTTTTAGCCTATACAATGTATTTTTGGCCTATGCTACAATATACTCCTGCAACTTAATACTGAGGTTCTAAGACTGAAGTTAGGCTAGACTACAGTCACATTACTTCAACATTTCCATCATAACTTTTTAGTCTTTATTTAAATTCTGAAAGTTGGAAAATGTGTTAAAATAGTTTGCAAGAACACAGTTGAGCATAATTTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18496
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106039 | Nonsense | 498 | 709 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 14 (position 25859532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24562623 |
GRCz11 | 14 | 24859868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGGTGACTTCTGGAAGTGGGCAGAGACCTCTGTGCTGGAGGGTTCGTG[G/A]AGGATGGAGAGCCTGTGTCGGAGTRTTCAAGATGAGCTCAATGCTCCCAT
Long Flanking Sequence:
CTTTTTTAATAAATCTGCAAATATTTCAACAAGTCAGTGTTTTTCTGTCAATATGGCGTGCTGTGTGTGCATAAATAAGGAAAAATGAACTTAAATGACTTTAGCAATTGACTGGGGGTCTGAACACCTTTCGTACCCACTGTATACAAGACATTGTGTAGTTTTTTTAGCATGGGAATATTACAGAAGAAGTGCACCTTTGTTTTATCTGTATCTGTGTCTGTGGAACTCTTCTTTCCAGGTCATCTAGTTTAGTTATCCTCATGACTTCAGTTACACATAAATACCCTTCAGTTTCTCAAACTGTTGCACATTTTGTGCAATAATCCACCATTGAACGACAGCAGCAAACATGTGGTTGGAAAAGTGATTGAATTTAGCTTTTTGTAGGCTGGCAGTGTTTATGAATTGCTCTCTGTCTGCTGACAGCTCCCACACAGTTATTTGGAGGCTGGTGACTTCTGGAAGTGGGCAGAGACCTCTGTGCTGGAGGGTTCGTG[G/A]AGGATGGAGAGCCTGTGTCGGAGTGTTCAAGATGAGCTCAATGCTCCCATTGTGCAGGTCAGTTCCTAAACAGAGATGCACTATTGTCTGTTGCCTGGTGGAGATGTCTTCATAAGAGATTGTTTGTCCCCTTATTGTGGTTTAATATTGGCTGTGGACGGTTCTGGAATGAAACCACAAGTTGATGTCATTCATTAATCTTGGTATGGATTAGCCCTCATATGTTATGCATCAGTTTATCCATTATGAACACTTAGCAAAAATATGCTGGGTCCTGTGGTTATAGTTTTTTTATTGTGTGGTTATTTGTTCTCTGAACATCTGCTTTTCATTTAGTTAAATGCAAATTACAGTTGATCAACAACCATGTTATGAATTAAATTTTAAATCCTTAATCAAAAAGAAGTTTAACCAAAACGTAACAAGATAACCGGGATCATAACATAATCCCTGGTGCCCCTGTGCTCTCTCCCCACCAAACATAAACCAAAACACAAACC
Associated Phenotype:
Not determined