ZMP
zgc:136839
Ensembl ID:
ZFIN ID:
Description:
PDZ domain-containing protein GIPC3 [Source:RefSeq peptide;Acc:NP_001038783]
Human Orthologue:
GIPC3
Human Description:
GIPC PDZ domain containing family, member 3 [Source:HGNC Symbol;Acc:18183]
Mouse Orthologue:
Gipc3
Mouse Description:
GIPC PDZ domain containing family, member 3 Gene [Source:MGI Symbol;Acc:MGI:2387006]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa29702 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa3151 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa29702
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075049 | Essential Splice Site | 220 | 333 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 3303854)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 3301168 |
| GRCz11 | 22 | 3320436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGATGGTTTGTGTGTGTTTCTCTTTTCTCTGTGTGTTTGTGTGATTCA[G/A]ACATGATCGGTCAGAGGACTCGGGCCCCTAAGTCCAGCGAGGGGAAGCTG
Long Flanking Sequence:
CATTAACATGCCTGTGTTTTAATTTCTGTAATAAATATGGCTGTCAAACCAGGATCTTGATGGTTTATTGTGGGTATGTTGTTTACATGAAGAAATCTGTTACAAGTTAAGCAAAAATTCTATTAAACAATTATATTTTGAATTTTAATTCTAATAAACAATTATATTTTGAATTTAAATAGTTTTTGTCTTGCGTTTACTTTAATTTTACATTTGAATAGCCAAAATTACAAGTTTCAGTATTTAAATGTGATTAATCACGATAATTTTTTTTTAAAACGGTGCGATTAATTAGTTAAATTTTTTTAATCGATTGACAGCACTAATATATATATATATATATATATATATATATATAATGTTTCTTTTCAACTTTTCTTGATTTTTTTTTTTTGTTACTGAACATTCATTTCTTTTTTAACTAGGAGTAAACACTGAAGTGATGAAGATTTTGATGGTTTGTGTGTGTTTCTCTTTTCTCTGTGTGTTTGTGTGATTCA[G/A]ACATGATCGGTCAGAGGACTCGGGCCCCTAAGTCCAGCGAGGGGAAGCTGTCGAGCGGCAAAGAAACTCTCCGCCTGCGAACTCGAGGATCAGCTTCACTGGAGGAGATTGTGAGTTTACTTATTTACTCACCCTTCAGTGACTTGATTCCAAACCTTTACGAGTTTCCACTGATCACAAAACAAGATATTTTGAAGAATGCTGGATATTGTGCATCAGTAACATCATGTGATTTAGTTTGAGCAGGTCATGTGATGATATTTATGTGTGATGGAATGCGTCAATGGACATCTGAAATGTTGTTTTGCTCATTTCTAAAACCCGTCAGCCTTCAGTCCATCATCACAGTGTATCAGTGTTATTACTATTTCCATCCAGAACTGTCTTGAGCATCTGTCTGTGCTCCTGAAGGACATCTCAGACCTCCAAAAGCCACCGCATTGCGTTCATTGTTTCGTTTTCATCTTCTGAGGCGCAACTCATTTATTAGAGAAGCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3151
Status:
F2 line generated
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075049 | Essential Splice Site | None | 333 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 3308168)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 3305482 |
| GRCz11 | 22 | 3324750 |
KASP Assay ID:
554-2471.1 (used for ordering genotyping assays)
KASP Sequence:
TCGATGTTTGGGGCGCTTTGGGCGACGTCAAGAATGGACGCCTTTAAAGG[T/C]GAGATCATGAAGGTAGAATTATTGGTAACTAATTTTGTTAACTAAGTCTT
Long Flanking Sequence:
ACTCATTATCCCTCCTTTCTGCTTTAAAGACATGCTTAGTGAAAGTAACATCATCATCATCATATTATATAAACTTTAGTCGACTTTCAAAACTCGCTGCGTGCCGACACCGCTGCACAAAAGGCTGTTACTCCGGTTTCACGGCGCATGAGCGGCGCCTATTTTGTCGGCGTGCATGCAAACAACCAACCGGGATTCACACAAGAGTGCGTGAGGCCTTCATTGTAGAGTATTTTACAACAGCTTAGAATGTGGCTCGACCAATCAGAATCAAGTAGCAGGACTGTATCTGTTTACTAAGAATATAAGTGATGATGTTTTTAACGTCGTGTGTCGTTCCTTCAGCGACGACTATAGTGGAGGCCGGGAAGAACAAGAAAAACCCAGATGATTTCGCCGAGGCTCTCGACTCAGTTCTGGGAGATTTCGGCTTTCCGGATGTTTTTCTGTTCGATGTTTGGGGCGCTTTGGGCGACGTCAAGAATGGACGCCTTTAAAGG[T/C]GAGATCATGAAGGTAGAATTATTGGTAACTAATTTTGTTAACTAAGTCTTTTGAAGCATTTATTAATCATAGTTCAACATTTATTAATGCATTATTAAAATCCAAAGGCGTGCTTGTTAACATTAGTTAATGCAGCAGGAGCTACCATGATTTTAAATTTAAGTTAAATAACATTAACTAACATGAACTATCGTTATTTACGTTAGGGTGATGTATGCAAGTTTGTGACTCTCCTAAAGCGTAAAAATACCATAATATGTTTGCAGATATTTCAGAAACATGCTAAGTAAACATTCCTGTTTATCTGAGAAACAATGCTGAAGTCAGATATTCTGCTTTGAAAATGTGAGTTACGTGCTGGAACGCTGTCTTTGTTTTGTTTTTTTTAACCTGCCTAATGCCAGTTCAGCCAATTATATTTCAGCACCCGGGTGGCCTTGATGGAAAACAGCATATTTCATTCATTCAGTCAGGAAGGCTCTCAAAGTGTGTGTCCACTA
Associated Phenotype:
Not determined