ZMP
arfip2b
Ensembl ID:
ZFIN ID:
Description:
ADP-ribosylation factor interacting protein 2b [Source:RefSeq peptide;Acc:NP_001017649]
Human Orthologue:
ARFIP2
Human Description:
ADP-ribosylation factor interacting protein 2 [Source:HGNC Symbol;Acc:17160]
Mouse Orthologue:
Arfip2
Mouse Description:
ADP-ribosylation factor interacting protein 2 Gene [Source:MGI Symbol;Acc:MGI:1924182]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13726 | Essential Splice Site | Available for shipment | Available now |
sa17908 | Essential Splice Site | Available for shipment | Available now |
sa41668 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13726
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 |
---|---|---|---|---|---|
ENSDART00000079194 | Essential Splice Site | 33 | 355 | 2 | 9 |
ENSDART00000130920 | Essential Splice Site | 33 | 355 | 1 | 8 |
ENSDART00000132019 | Essential Splice Site | 33 | 140 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 26852685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26256542 |
GRCz11 | 10 | 26218255 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGTAATGGGGACTCTCGAAATCTGGCAGAAGATGACAGTTTGGAGCAG[G/A]TGAGCAATACATGGTGATTCAGTAAAACTGGAACAGTTTTTTTTTTTTAA
Long Flanking Sequence:
CTTGAACTTCTTTGCAGTTCCTTTCATAGTAATGACTGGGTTGGGCTCAGCCAGATCTGATAAGAGCTTTTGAAGAGAACATTCCTGAGGAAGCTCTTTTCCATCTACACTTTCCGGCAAACGTATGCATACAGAAGCCATATTATAATTAAATACAGGACATATCTACAGTGTCATGTCATCATTTATTCAACCACCTGTTTTCTTTTTTCCACAAAATCTTGTCTCAATCTTTCGAGTTAACCTGTAACAATCAAGCCATTGTTATCTGAACAACATTGTTAATTAGGAGCTATTTAAATGTATGTATCTGAAGGCTTTTGTAATACACTTAAGAGCTTTTTTTGTTTTATTTACTTTTCTTTATTTCTCATCTGGCTCTGTTTCAGTAACACTCAAGTATGGCGGACAGTATGATGAGTAAAGCCGCCACAATGGAGATTCCTATTAGCAGTAATGGGGACTCTCGAAATCTGGCAGAAGATGACAGTTTGGAGCAG[G/A]TGAGCAATACATGGTGATTCAGTAAAACTGGAACAGTTTTTTTTTTTTAAACAGTGATTTTTGTCAAAAGTAGCCCAGTTTTCCTGAACTTTCCAAAAAAGTTTGACTTTTAAATCTATTACATTTAGAGCTTGAACCATGTCAAAAGCATCAGAATGTGGATGTCTGTGCTTTGTTCCCATGCGTTTAGGTTTTCATAGCTTAAGAGGATAATATCTAGCTGTCCATCCAGTTTGTTTAGCTTGCTTGTCTAAGTTTCACAATATCAGTCTGAGAAAAAGTCTCAAGGTAGCAGGTGATGCAAACATTTAGTTTATAATTGTTCTGCTCTTTTGTTTTTTGAAAATTTTAATCCTTTAGCATTCCTGTAATTAATGTCTTGTTGTACTATGGACAGAAAACTGGAACACTAAGGGGTTAAGCAACCTTTAAAAAATAATGTTCTGATAGACTTGTTAATAAGTAATAGAATTTATTTATAAAAATGCCTTGTGTGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17908
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079194 | Essential Splice Site | 194 | 355 | 7 | 9 |
ENSDART00000130920 | Essential Splice Site | 194 | 355 | 6 | 8 |
ENSDART00000132019 | None | None | 140 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 26842467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26246324 |
GRCz11 | 10 | 26208037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATATATTGATRATGTATAATATTGAGGTTTGTGCTATTGTTCATGTAC[A/T]GGATGAGTTTGGATACAATGCAGAAACGCAAAAGTTGTTGTGCAAGAATG
Long Flanking Sequence:
GTGTCTCAGTGGATTCAGACACTTAAACAGGCCTATCCGATGGAAGAAAATGACTGCATGTCTACAAAGGAAGACTGATCTTTTTCTGAAGAGGTGGAAAAGTATTACAACATATTTAGATATGTACATTTAGAGGTTTCTTAACCTATAATCAATGTAATTTGAGGTAACTACAATGTAACACAATGTAACTTGATGTACAAATGTACCTTGAAATGTACCCTGAAAAGTAATTATAATGGCAGTACCTTTTATTCATTTATTTATTTATTGTTGTATTATTTTTATTTTATTTATTTATTTAGTTTATGTATTCCCTCATCTGTAAGGGTTTAAATTGTTGGGCAAGGGGTTGTTCTGGAAAAAATATATATTGAGAAAACATAAATCATTTTTTTTTTTTAATTAACAAAAATAAAATAAAAAAATATATATAATATAAATATAAATATATATATTGATAATGTATAATATTGAGGTTTGTGCTATTGTTCATGTAC[A/T]GGATGAGTTTGGATACAATGCAGAAACGCAAAAGTTGTTGTGCAAGAATGGAGAGACTCTGCTTGGTGCCATCAATTTTTTTGTGTCCAGCATCAACACACTTGTGAACAAAACGATGGAAGACACACTGATGACTATCAAGATGTATGAGAATGCCAGGTAAAAGCTGCTCCTGCTCTATCCTCTAGTATTGTAGCTTTCATTTGTTTTGAAATGCTCTATTGTGTTTTATTTATTTATGTATTTTTAACCTCTGATGCTACTGGATGTTATGGTTATTATGTGTTGCAGTTGTTTGGTTTATCATTGAATATTGGCATTGATACCTACCGATTGGAACTCTAACTCAGTCTTTAGATTAAAAATAAAAGGGCGGTAGGATATCCACTTTCACAGTTATCTATTTTGTATGGTTCAAGCTGAGACCTTTGGAAACATTTGATGCTGTTGTGCTGTTACTTGATGTACCTACTTCTGCTTAGCTGTCTACATTTAAGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41668
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079194 | Nonsense | 306 | 355 | 9 | 9 |
ENSDART00000130920 | Nonsense | 306 | 355 | 8 | 8 |
ENSDART00000132019 | None | None | 140 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 26840693)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26244550 |
GRCz11 | 10 | 26206263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGCTTTTTGTTTTCTGACACGGTGTGTTTGTCTCTCTTCTACAGGTC[A/T]AAGTGATGCACAAGCAACTTCTGCTGTTCCATAATGCCATCTCTGCCTAC
Long Flanking Sequence:
GCTAACTGTAAATGTAATTCATTACATGGCCAGTGCTTGAGCATAAGGCTCTGTCATTGGGGCTTTAGGCCATGGTAAAAGTAAATACATGTTGTTTATACATGTTTTACACTGTGTATATTCAATTTTGTTTGCTTAACAAACATTTTAGAGCATCAAAAGTTATCATGTGAAAGGTTTTGGTGGCTATATCTCAGGAAGAAAAGGCATTTGTTTTCTAACGTTGCTTTGTTCTGTAGGCTGGAGTTCGACGCGTACAGGGCAGATCTGGAGGAGTTGAACATGGGCCCACGGGACGCTGTTACTATGGCTCGTATCGAGGCTGCTCAGCAGCAGTACCAGATCCACAAGGACAAATATGAACGTCTCCGCAGTGATGTCACCATCAAAATTAAGTTCCTAGAAGAAAATAAGGTGCCAGACCACCTGCATAACTTCCTCTGCAAGTCCTGTTGCTTTTTGTTTTCTGACACGGTGTGTTTGTCTCTCTTCTACAGGTC[A/T]AAGTGATGCACAAGCAACTTCTGCTGTTCCATAATGCCATCTCTGCCTACTTTGCTGGAAACCAGCAGCAGCTGGAACAGACCCTCAAGCAGTTCAACATTAAACTCAAACCACCAGGGGCCGACAAACCCTCTTGGCTGGAGGAACAGTGAAAGTGCTCCATTACCCCTGGTTTCCTGTTGTATTTCTTTAGCCCCGCAGAGCAACACAGTAGGACCCTGAGAGACCAGCGATCTGAGATGCTAGAAGAGACAAGGCTCCAACAGAGAGCCCCTTTCACACTAACTCTCTTTACACTTCTCTTCCTTTATTCTTCTTCTCATCCTATTCCTGCTCTGAGACTGTTTTCAAGTGTCTGAATTGTGACCAGTCCTTAAAGCTCCAATCAAATGTCAAGGGTATCCAGTGCAAGCTTCATCCTTATAAATGTCATTAAACCGACTGAAAAAAAAACTTCTGATATATCAGTCAGAACAGCAGACAATTGTCAATATTCTCTC
Associated Phenotype:
Not determined