ZMP
zgc:172112
Ensembl ID:
ZFIN IDs:
Description:
connector enhancer of kinase suppressor of ras 3 [Source:RefSeq peptide;Acc:NP_001107119]
Human Orthologues:
CNKSR3, IPCEF1
Human Descriptions:
CNKSR family member 3 [Source:HGNC Symbol;Acc:23034]
interaction protein for cytohesin exchange factors 1 [Source:HGNC Symbol;Acc:21204]
interaction protein for cytohesin exchange factors 1 [Source:HGNC Symbol;Acc:21204]
Mouse Orthologues:
Cnksr3, Ipcef1
Mouse Descriptions:
Cnksr family member 3 Gene [Source:MGI Symbol;Acc:MGI:2674130]
interaction protein for cytohesin exchange factors 1 Gene [Source:MGI Symbol;Acc:MGI:2444159]
interaction protein for cytohesin exchange factors 1 Gene [Source:MGI Symbol;Acc:MGI:2444159]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23627 | Essential Splice Site | Available for shipment | Available now |
sa23628 | Essential Splice Site | Available for shipment | Available now |
sa18621 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23627
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114830 | Essential Splice Site | 73 | 546 | 3 | 13 |
ENSDART00000125798 | Essential Splice Site | 73 | 546 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 4223350)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 4165029 |
GRCz11 | 20 | 3866870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGCCTGGCTGGTGGCCTTGCTTAATGCTTTGTTACTGTGTATTTTGC[A/G]GAACTGTGGCGTGGAGACTGATAACTTGAAGACTCTGGTTGGTCAGATGC
Long Flanking Sequence:
TCCACAAGTATCGCTTTAGCAGCCAAGAGGAGAGGAAAAGTTACCTCGAAAACACACCAGCAGGTCAAATGTCTAAAGAAAAAGAGGTAAAGATGGAGTTTTACAGCATTTCTTCATAGTAGTGAAATAGCGGCTTGTGTGCTGTGCCTTCTTCATTGTAGTAAGAGCGTTATTTAGTCGCCCTCGCCTCCTTCCTCATAGTATTCTACTGCGACATCGCGCATAGGAGATAAATGACGTCAGTACGTAATAACCGGTTATGATCTATTACTGAACCGATATCAATAATTTTGACAGCCCTAGTGACGAGTAACGATGCGGCACATAAAAAATCTGTCAGAGTAAAACTCATCGAATATACAGTATGTACTGAAGTAAAAGTGAAAGTAGGAGAAAAAAAACAATCCTCCAGTAGAGTACAGATACAGCCTTTTAGTACTTAAGTACAGTAGTGGCCTGGCTGGTGGCCTTGCTTAATGCTTTGTTACTGTGTATTTTGC[A/G]GAACTGTGGCGTGGAGACTGATAACTTGAAGACTCTGGTTGGTCAGATGCGAGCAGCATCCAATAACTTGCAGAACTGTGCATCGGAGCGTAGGAAAAACCCTTCGTACGATGGAGGAAGTCCAAACAAACCACCAAACGTGTTCCTCACTGCTGTGGTGGAGCTGATCGGGGCTGCCAAGAGCATGCTGGCCTGGCTGGACAGGTAGGAGAGATTTACACTCCAACTCTCTCTCTTTCCATCACAAGGAATGTTCAGAGCGCTTTGGCTAAGTCTGCGCACACATTTGGAAATCATGTTCCTAAAATAGCATTAGCAGAAAACTGTATATTACTGTGTGTTTAGAGTAGACTCGTGTCTTCTACAGTTTATTATTACTGATTGATGATGAAAAACCATCTACGTTCAGAGAGATTTTTAGCAGTGACATTTTATAAACGTTTTAAATGAAACAGATATGAACACAGTGAACTAAACTTAACATTGTAAAACAGAGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23628
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 |
---|---|---|---|---|---|
ENSDART00000114830 | Essential Splice Site | 183 | 546 | 5 | 13 |
ENSDART00000125798 | Essential Splice Site | 183 | 546 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 4227731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 4169066 |
GRCz11 | 20 | 3862841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGCAGGACTGCACTGTTTTTGAAATGGAGGAGAAGATATTAGAAGTG[G/A]TGAGTAGAACGTTTTGCCGTCAGCCATTTTGCACACATTCACATATTCAC
Long Flanking Sequence:
TAGTATCCATTTAGTTAATCCATAAAACAACTATGGAAGTCAATGGGTCCAGGTTTCCAGCATTCTTCAAAATATCTTCTTTTAATTTTTGGGTCAACTTTAACTTTTGAACAGTGCTGTTTTCAGGTATATCCCGATGAACTCTTTACACACAGATGTGTGCTGCAGCGCAGAGAAACATATGGTTTGAGTGAGTCTGAGCGCCTCGTAACCGTGATGGATGTCTTCACAAGCCTCAAACTCGACAGCAATTACCCTGTCAGGAGTTGTCCTTAAATCTGAATTAAACACAGCCAATAGGCCCTCCTCCATCAGCACATTCCACATCTCCAGTCCTCATATTACATTTCATAAATACCTTCTTTGGTATTTTGATTTCATGTTTACCATTGCGTGTTTTCCTGTGGGAACTCGACATAATGTGGCGTCTCATGCGAATCCTCCCTTTTTAATTGCAGGACTGCACTGTTTTTGAAATGGAGGAGAAGATATTAGAAGTG[G/A]TGAGTAGAACGTTTTGCCGTCAGCCATTTTGCACACATTCACATATTCACGCAAAAGGTCAGAGATTCGGCTGTTATCTGGGATGCTTTTGGGTTCATCGGGAGTCAAAAGAGGCTACTCTATTGTTCAGTCGAGATGTTTTTACCTCAATAACATCCTGCAGTAGATATCAGCATCTCGCAGTCTCTGCTAAAAGAATATTCTGGATGCGATACAATCATTTTGACAGTTTGTAGAAACCAGTGTGAGTTGCATTTATTTTTCAGCCAATCATAAACAAATGTTTTACCGTTATGATCACGGTAGCCAATCAGAGGAGTTTATGTTACATTATATAGTCATAAATACACTGACCAGCCACTTTATTAAGTACACCTTACTAGTACCGGGTTGGACCCCCTTTTTGCCTTCAGAAGTGCCTTAATTCTTTGAAGCATAGATTCAACAAGGTACTGTAAATCAGGGGTTCTCAACTAGTTTGGCCATGGGACCCACATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18621
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 |
---|---|---|---|---|---|
ENSDART00000114830 | Essential Splice Site | 223 | 546 | 6 | 13 |
ENSDART00000125798 | Essential Splice Site | 223 | 546 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 4231413)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 4172748 |
GRCz11 | 20 | 3859159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTTTRGAGGAGGTRCCCATCAGCAATATCAAAYCTGGCGAGGGACTGG[T/A]GCGTGTCAACAGCCTTTACACTTCTCCACCTGCTGCCTTTGTTTACTCGT
Long Flanking Sequence:
TTAATTTAAAACTGAATAGAAAATTAAACACATTTACACAAGTAAATAAACAGAGTCAATGATGGGCTAAAAATCTGCAGAATTCTGCGTGTGCAGATTCTGTGTGGGACTACTTATGAGTTAGTAACCACAGCAAAAATATATTTCTGTCTAAAGCAATACCTTTTAAAAACTAGGTTTTTATGAAAAATGGTACTTTCGTCCCTGGTCTGCTCTACGCTTACGAGGAACATCTGCGTCAGCAAATGCATTTTTGTCTATAATTGTAATTTTCACACTTTTAGCAGAAAATTTGCCATAGGCAAGCCTTGGTTGTCACTTATGAAGTCATTATTGCCACTATGTCATTAACTAACACTCAGTTTTCTGTTCATTTCAGTCACAGGTTTTGACAGGCATTTGTGATTCCACCATGAGAATGACTTCTGACCCCTTGAAGACCCAAGTGACCTGTTTGGAGGAGGTACCCATCAGCAATATCAAACCTGGCGAGGGACTGG[T/A]GCGTGTCAACAGCCTTTACACTTCTCCACCTGCTGCCTTTGTTTACTCGTAGCATAACAACTGCATATTGTTTGCTTATTTTTTTTTCAAAGGGAATGTATATCAAATCCACTTACGACGGGCTGCACGTCATCACCGGAACCACGGAAAATGTGAGTCAAGTGACTTGAGAATTACAGACAGATCACTGGGGCTTTTGTTTGCTGTTAAAGCATCAAAATGGAGCGTCATACAAGCCTGTGACCAATGGATTGCCGAGATCCATAAAACACAAGAAACAGTTTACAAGGCTGGGACAGCTACAACCATTTTTTGGATTTTTTTTGGATACTCTAGTAATCTTTTGATACAAAAAGATTGGTGGTTTAGGGTGTGTTGGGCCCCCGATGCTGTGTTCACACCAGATACGGAACGCACGGATATATCCCAATATTGGCACGTAAATAGACCCTTGAACATACTGAGTTTTCTTGCGTCATTCGCACATCAAATTCACCGAG
Associated Phenotype:
Not determined