ZMP
si:ch211-222h17.4
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC566016 [Source:RefSeq peptide;Acc:NP_001038560]
Human Orthologue:
TULP4
Human Description:
tubby like protein 4 [Source:HGNC Symbol;Acc:15530]
Mouse Orthologue:
Tulp4
Mouse Description:
tubby like protein 4 Gene [Source:MGI Symbol;Acc:MGI:1916092]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20166 | Essential Splice Site, Missense | Available for shipment | Available now |
sa12777 | Splice Site, Nonsense | Available for shipment | Available now |
sa20167 | Nonsense | Available for shipment | Available now |
sa33350 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18049 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20166
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067486 | Missense | 251 | 1595 | 5 | 17 |
ENSDART00000132625 | Essential Splice Site | 242 | 1639 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 4 (position 55146)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 331423 |
GRCz11 | 4 | 344871 |
KASP Assay ID:
2259-4278.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAATGAGTTAAAGTAATCTGTGAGTGCTAATACTTGTGTTGTTGTTGCA[G/A]TGCACACCCTGAAGCCGCTGCTGACCGTCTGCTTCACGTCCGGAGACATC
Long Flanking Sequence:
TATCCAAAATTGTGGAGTTTGTGTTCTGAACTTCATTTAATGGTCAGATTTTTTCTACTAGTCAATAAAGAAAGAAAAGCTGAACAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTCCCCTCAGGTGTTGTTTGGCACTGCAGACGGGCAGGTGATCGTGATGGACTGCCACGGCCGCATGTTGGCTCATATTCTGCTCCATGAGGCCGAGGGCATCGCCAGCATGGCCTGGAACTATCCCAGCTTCCTGGTGGAGGACAGCAGCGAGAGCGACTCCGATTCAGACGACAGCACGCCTCCGCAGGGTAAACACTCCATTACTACACTCCATTACTACACTTCTGCATCCTGGGATCACCTTAAAACACAGTGCACTGCAAAATCTGCCCAAACACAGTCTTGTTTTCAGAAATAATGAGTTAAAGTAATCTGTGAGTGCTAATACTTGTGTTGTTGTTGCA[G/A]TGCACACCCTGAAGCCGCTGCTGACCGTCTGCTTCACGTCCGGAGACATCAGTTTGATGAGCAATTATGATGACCTTTCACCTCTGCTGATACGCACGGGCCTCAAAGGTTGGGTTTTATTCTTTAAATCTGTTTACAAGCTCATTTAAATCATTGCATTTTATTCTGCATTTGACAATTACATTGACCAGACCAGAGCAGGATATAGATAGTTTAGTGACCAAACTTTAATATCTCCTGCTGATCTCCAATTCAAGCGCTGACTAATTCTCTTTATTAGCCAAACACCTGGATAATTGTTGTGCATTAATAATATATATTGTTATTAATTGATTAGAGACACATCTAGGCAGTGCTTCTGCAGAATTCCCTTACAGAAAGATCATTCAGAAAGCAGAAATGTTTGGATGTTAGCATCATTGAGCCATAGCAATCTATGCTACCATAACTGTAAGTACATTCGTGTGCTTTTCATACACTTTCTATTCTGATTTGCAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12777
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067486 | Splice Site, Nonsense | 594 | 1595 | 10 | 17 |
ENSDART00000132625 | Splice Site, Nonsense | 589 | 1639 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 4 (position 60288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 336565 |
GRCz11 | 4 | 350013 |
KASP Assay ID:
2259-4279.1 (used for ordering genotyping assays)
KASP Sequence:
TTGGCTCTCCAAGTCTGACTCGCAGAGAGTTCCCACTTGATGACATCACA[C/T]AGGTGATTACCRGAGTTTTAMAGCTAAATTATAGATCGTGTTGGCTCTAG
Long Flanking Sequence:
ATTGGGTAGGAAAGAAATCACCAAAGATCTCCAGAGGGAGCAAGTCTCCCAAACTTCCCAGGTACAACATTTTTGAGAACATTAGGTGCTCGATCACCTCATTTCATATGGTTTATTATTGACCATTAAGGTCACCTTTGCAAGAGCATCTGCAAGCTTGAATAGTTTGAAATCGCATGTGTGTCTGTTAACAAGAAATGCGAGATGAAATGCTTTACTAAGATTGCTGGAATGTAGCTTGCCCACATTTATTACTTAGCTGCAATTTTACACTGCATGCTGCTGGAAACTCACCTTGAACTTTTCTCTTCGTGTGCTGCCTTCTCTGTAGAGACTTAGTGTGTCCCTTTACCAACAGGATAAATATAGATCCTCGCAAGTCCCCCAAGCTGTCCCGCACCACACAGGAAATATCCCGATCGCCACGGTTACCCATTCGCAAGCCCTCTATTGGCTCTCCAAGTCTGACTCGCAGAGAGTTCCCACTTGATGACATCACA[C/T]AGGTGATTACCGGAGTTTTACAGCTAAATTATAGATCGTGTTGGCTCTAGACTGCGTTTTCTAATCATAACAACTTCTGTCTTTTTGCGTTTTAGCACAATTACCTTGCGCAAGTTACATCTAACATATGGGGAACAAAGTTCAAAATTGTGGGACTTGCAGCATTTTTGCCAACAAATCTTGGTGCAGGTATTGCATTTTTACAATACTACATGGTTATACTACATATTTTTACGCATCCAACTTTGTCTACATTACAAATTCTTTCCCATCTCACTAGTTATCTACAAGACAAGTCTGCTTCACCTCCAGCCCAGACAGATGACCATCTACCTCCCTGAGGTGAGGAAGATCTCGGTGGAATACATTAACCTTCCTATGTTCAGTCCTAATGTCTTCAGTGAGGACGAGGACGACCTGCCTGTCACAGGAGCTTCAGGAATCACTGATGATAATCCACCTTGCACTGTTAACATACCCATTGCCCCCATACACAGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20167
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 |
---|---|---|---|---|---|
ENSDART00000067486 | Nonsense | 961 | 1595 | 15 | 17 |
ENSDART00000132625 | Nonsense | 980 | 1639 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 4 (position 61937)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 338214 |
GRCz11 | 4 | 351662 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGCTGTAGAGGGGAAGAAGGTGCAGCTGCCCTATGCCTCTGCTACGT[T/A]GAACCGTCTCACTGTGCCAAGGTACTCTATACCCAGTGGGGACCCTCCTC
Long Flanking Sequence:
GCATGAGCTCCTGCTTAAAATTAAAACCACTCGTTCTGCCCCACAACTAGCTGAAGGTGATGCAGTGGTTTTTACAGCACCTCTTGAGATTAGCAAAATGAACCCGCCCCCTCCTTACCCTGGCACAGTCGCCGCTGCAGTGGCAGCTGCTACTGCTGCAGTTTCGGCTGCTGCTTCTGCAAGTTCCACCTCTGGGGCAGTGGGAAGCAGCTCTAGCACGTCATCCTCAGGGGAAGTTTGTCTGAAGAAAGGGGATCTGACCTTGTATCCACCTAGTGCACAAGGGGCTCAGTACCCAACTCCATTGGGCTATGAACGCATCACCACATTTGACAGCAGTGGAAATGTGGAAGAGGTGTGCCGACCCCGCACACGACTTGTTTGCAACCAGAATGTTTACACGCTGCAGGGCCCAGGAAGCTCTGCCACCCTCAGGGTCTCATCATCTTCCTCTGCTGTAGAGGGGAAGAAGGTGCAGCTGCCCTATGCCTCTGCTACGT[T/A]GAACCGTCTCACTGTGCCAAGGTACTCTATACCCAGTGGGGACCCTCCTCCATACCCTGATACAGCTAACCAGGGCGGAGCAGGGCGCAACCCTGGCCAGAGACTGGACAGCAGCTTGATTCATGCTACCTTGAGGCGCAACAGTCGGGAAGCTGCATTGAAGGTTTCCCAAATGCTGGATCACCAGCGGACTTTACCCCCCAAGGCTAAAGCCAGTACTTTGTCTGCTTCCTATCAACCAAGAGGGCCGACAGCTCTTTATACATGCAGTCAGTGCAGTAGCAACAGTAGTGGAACCACAAGCAGTGGAAGTAACGGAATAGCTGGGGGCACAATCATTAGGCAAGATTTCCCACCAACTGGGGGTGCTGCACCTCATAGCACTGTTATAGTGCACTCCAACAGTGCCTCGCCTCTGCCTTCTCAATCCTCCTACAGTCTGCTCAGTCTGGATGGCACCGGTGGAGTGGCTACTGGAGCTGGAAACAGGGAAAGAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33350
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 |
---|---|---|---|---|---|
ENSDART00000067486 | Nonsense | 1230 | 1595 | 16 | 17 |
ENSDART00000132625 | Nonsense | 1274 | 1639 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 4 (position 62818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 339095 |
GRCz11 | 4 | 352543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCCTATCCATCAAGTGCTGCATACAGTAGTCCCCCACTGCAGGCAGTG[C/T]AAGCATCTCCACGGCCGCCTTCTCCTAAAGAGGCGGTTGCTCCACTTTCC
Long Flanking Sequence:
GCACTGTTATAGTGCACTCCAACAGTGCCTCGCCTCTGCCTTCTCAATCCTCCTACAGTCTGCTCAGTCTGGATGGCACCGGTGGAGTGGCTACTGGAGCTGGAAACAGGGAAAGAGCTGACTATATCAACTCAGCTTTTACAGAGGACGAGGCATTGAATCAGTCTCTGAGGCAAATGGCCCTTAATACCGAGGTAGTGGGTTTGACAGTCAAACGGCCTCCACCGTATCAATGGGACCCATCTGTTACAGAAGAGATTTGGGTTCCTCAAGAGCGCACAGCGACTCTGCCCCCTTCTGGACCTCCTGCACCTCACAAACCTCCTCCGCTCATCCTCGGTCCTGCACAGCATCTGGACGTTTCTCGTCTTCCGTTTGTCCTCTCACCTAAATCTCCAACAAGTCCTAACAACACCACTTTTCCACTAGCAGGAGCTTATCAGATTGCATTGCCCTATCCATCAAGTGCTGCATACAGTAGTCCCCCACTGCAGGCAGTG[C/T]AAGCATCTCCACGGCCGCCTTCTCCTAAAGAGGCGGTTGCTCCACTTTCCTTTCCCCAGCAAGACCAGTCAGTGGTCTTGCCTCCTGGTTATCCACCAAATTTGCCCAACCTGGCTTGCTGTCCCCTCCCACCAATGTACCCTGGCACAGCTTCTTGTTCTAGCCTGCCTGTAACCGCCATTCCTCTTCATCCATGGGGTTCTTACAATCCCTGTCCCCCCATGCCAAGCCCCCCGGGTCCCGCCCCATCTCTCCCACCCAAGGCCTCCCACATGCTGGATAAACCTGTTCGTTCTCCACCTCCTCAACCGCCGCCTTTGCCTTCGCCTCCCCCAGACCTCCAGACTGCGGTCAGTCCCCCAGAAGCAATAGCTGAAGCCGGGGAAGGCTTTCAAGAGGTGCTCTCGCTTAACGAAAGCCCTGTTCCTCAACGAGCAGACAGGTTTGGCAAGAAGAATCGAAAGCGTTTGGACAACACTCGGGCAGATGAAGCTAATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18049
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067486 | Nonsense | 1569 | 1595 | 17 | 17 |
ENSDART00000132625 | Nonsense | 1613 | 1639 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 4 (position 63919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 340196 |
GRCz11 | 4 | 353644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTATTCTGCCTAGGTGATGCAGTTCGGAAGGATCGACGGGAAYGCATA[T/G]ATCCTGGACTTTCAGTACCCCTTCTCAGCTGTGCAAGCTTTTGCTGTAGC
Long Flanking Sequence:
AAAAGAAACCTAAAGGTCAAAAAGAGCAGCTGAAAGCCAAAAAGCTAAGCAAGGCCACCACAAATGAGTTCCAGGACAGCTCAGAGAGCGAGCCTGAGCTCTTTATCAGTGGAGATGAGCTGATGAACCAGAGCCAGAGTGGGAAGAAGAGTTGGAAAGCCAAAAGGAACCTGCGGGCAGGAGGTTGTGAGCTGGATGAGATCAAATGTCGAAAAGCGAATGAGAAAGAGGACCGAGGCCTCGGCAGCCAGGGCTTCGTCTACATCATGGCCAACAAACAGCCTCTCTGGAATGAAGCCACGCAGGTCTACCAGCTAGACTTTGGAGGGAGAGTCACACAGGAATCAGCAAAGAACTTCCAGATTGAGCTTGAGGGGAGACAGGTATGCAAATAAGCTTTAGATTCTGTTTGAGTTTATTGAATTTATGCAGTTGTTCGCTTCTAACCTGCTTTATTCTGCCTAGGTGATGCAGTTCGGAAGGATCGACGGGAACGCATA[T/G]ATCCTGGACTTTCAGTACCCCTTCTCAGCTGTGCAAGCTTTTGCTGTAGCACTTGCTAATGTCACCCAGCGCCTCAAGTGATCGACTGGGCAGGAACGTTTTAGCCAATTAAACCATTTCTTTCTTTGCTCTTTTGTTGATTTTTAGTAATTCTCCCAGTTAAAGATGCAGTACTAATACTTGAAAACTACATCTGGGAAGTTATTGCCACATTTTCCGAGTGTTAGAGGTACTACTGGGCACTGAAATCTATTGCTGTACAACATACTGTCATTACTAATTCCTTTTTCTTGTTTTGCTTAGGATACTAATGTTTGTCACACTTCCAGGAGGTCATATCTAAACTCCAGGGACTTTACCCTTGGAGATCAATTGCTAGCATCTAATTAGATGCTTCTTGGCTTGCAGTCATAACGTGTATTTTAATAAGACATAGTAAGACTGAATATGCAGTCTGTAGCTGATACGCTCTAGGTATTTCTGTAAGGATGGACTTGCTT
Associated Phenotype:
Not determined