ZMP
extl3
Ensembl ID:
ZFIN ID:
Description:
exostosin-like 3 [Source:RefSeq peptide;Acc:NP_001008402]
Human Orthologue:
EXTL3
Human Description:
exostoses (multiple)-like 3 [Source:HGNC Symbol;Acc:3518]
Mouse Orthologue:
Extl3
Mouse Description:
exostoses (multiple)-like 3 Gene [Source:MGI Symbol;Acc:MGI:1860765]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17419 | Nonsense | Available for shipment | Available now |
sa23818 | Essential Splice Site | Available for shipment | Available now |
sa43541 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17419
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039499 | Nonsense | 398 | 917 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 50272572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 50157515 |
GRCz11 | 20 | 49960719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGCTGTACAGGACAGTCACCTAGACCAGRTTCTTGTGGAGTTTACTTG[C/A]AAGAATCAAGCCAAGCCAAGTTTACCAACAGAGTGGGCATTGTGTGGCAA
Long Flanking Sequence:
ATAGCTCTTGTTGGGGAAATACAAGAATCACCCTCCTCTCCGCTTGCTTCACCTTCAGACCTTGAAAAACAGCTCAAGGCTTTGCCGTATTGGAGGTCGGATGGTCACAACCACCTGCTTGTACACCTTTCTATAAATTCTCTGACACAGAACTTCCTCTATAATGTGAGCACGGGACGAGCAGCAGTAGCACAGTCTACCTTTTTTGAACGACAGTATAGAGAAGGTTTTGACTTGGTGGTGTCTCCACTAGTCCATGCTCTGTCTGAGCCTAACTTCTTGGAGGTTCCTCCGCAAGTCCCAGTTAAGAGGAAGTACCTCTTTACCTTTCAGGGAGAAAAAGTTGAGTCTTTGAGAAGCAGTTTGCTTGAAGCCCCTCCACAATCCTTTGAGGAGGAAATGGAAGGGGATCCACCAGCAGACTATGATGATCGAATCATTGGCACACTTAAAGCTGTACAGGACAGTCACCTAGACCAGGTTCTTGTGGAGTTTACTTG[C/A]AAGAATCAAGCCAAGCCAAGTTTACCAACAGAGTGGGCATTGTGTGGCAAGCGTGAGGATCGTTTAGAGGTACTGAAAGTCTCTACATTTGCCTTGGTAATATCTCCAGGTGATGGACAGCTGGTGGCATCTGCTGGCTGTAGCATGAGACTTTTTGAGGCTTTGGAAGTTGGGGCAATACCTGTGGTACTTGGTGACCACTCAAAGTTACCCTACCATCATCTCATACGCTGGAGTGAAGCAGTCATAATGGTGCCAAAACCCCGCATTACGGAACTACACTTTCTGTTGCGTAGCATCTCAGACAATGATCTTCTTGCTATGCGGCGACAAGGACGGTTTCTTTGGGAAACATATTTCTCCACTTCAGAAAGCATCTTCAATACCATTTTGGCTAGTGTACGTACCAGCATCCAGATCCCAGCAGCACCCATACGTGAAGAACCTGCTCAGGAGATTCCCCACAAAGCTGGAAAGTTGGCCGGGACCGATGCTAACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23818
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039499 | Essential Splice Site | 805 | 917 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 50265042)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 50149985 |
GRCz11 | 20 | 49953189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTGCGAGCTCTCCATGGTGCTGACGGGTGCGGCCTTCTTCCACAAGG[T/C]GAAACTGTGACCGCTTTCACACTTCCAGAGCACGATTATGTCAAAAATAG
Long Flanking Sequence:
CTAATTCTCTAGATTATAAGTAAACTGTTCGGTTGGGGTTAGGGTTGATGTTAGGGTTAGTAAGTTGACATGTACTTGCTAAGTTTCTTATAGTGAGTTAAATGTCTGTTGAAGGAGCAGAATCAACAGATATGAAGCAGACAGTATACTAATACTCAAATTGACCATCAAAATAAAGTGTTGCCAAAAACTACATATGCTTTTTGGCCAACTGATAATCCTTTAAAATAATCATGATTACAATTATGACCACAATAATTTTGATTTAAATTTTTCTCATAATTGAGCAGCCCTAATGAGTATTATAATAACCACTGATCCTTCACTTAGGTCTTTTTCTTTCTCTGTGCTCAGAGTGTGGAGGGAGGCGAGAGACCGGATCGTGGGCTTTCCGGGAAGGTTTCACGCCTGGGATTTAAATCACCAATCTTGGCTCTACAACTCCAACTACTCCTGCGAGCTCTCCATGGTGCTGACGGGTGCGGCCTTCTTCCACAAGG[T/C]GAAACTGTGACCGCTTTCACACTTCCAGAGCACGATTATGTCAAAAATAGACCCTGAGCTTTTGTAGTTTTACCCAAGTAACCTCAGGTAATCGGGCCAGGAATTGGTTTAGTTGGTTAAAACTGGTAATGCTGTATTGCTGTCCAAGGCATAACTTTCCAGATAATAAGCTAACAGAACAATGTGTTTTATTTAGGGCTGCATGATATTGGACAAAAAAACGGATGTTGCAATGTTTAGCTTTTGCTGCGATTTATGTTGCGATATAAATTAGGTCATCTTGTAAAATTATATTCGTTTTTCAATATCATTCAGCCCTTGTCATGATTAATTTCAAGTGATTTTTTTAAATATAATTTTTAAATTAAAACTCACAATTTCTTCATCTCCTCAGTATTACGCGTATCTCTATTCCTACGTCATGCCTCGAGCCATCCGAGACATGGTGGATGAGTACATCAACTGTGAGGATATCGCCATGAACTTCCTGGTGTCGCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43541
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039499 | Nonsense | 857 | 917 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 50253265)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 50138208 |
GRCz11 | 20 | 49941412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCTGGCGTATCCCCTCTCAGGTGACGTCCCGTTGGACCTTCCGCTG[T/A]CCCGGCTGCCCACAGGCTCTATCGCATGACGATTCGCACTTCCACGAGCG
Long Flanking Sequence:
AGTGCAAACCAACAACATCAGTCACTCAGTTGCCTATTAATAATGTTAAAGAGGTTTAATATGTATTTACAGTTTTGTTTAGAGTGCAGTGTTTGTTATTTAAATGTTTCTGTCATGTGTATCGCTTTTGGTGCAGACAGAAAAATTGCTTGTTGCTGAAATCTTGTATTTTTAGGACAGTGTTTAAAAGTTAAAAGTGTTTCTGACTCACCCAGAGATTGACTGAATTAATTTAAAAGTGGTAAAACTCAACTGTTTAACCCTAGTGGACTTTAAAAATTTGCCTATTTGCAAAAAAAGTGTAGTGTTTCTTTAAAATCATAGTTGACTCAACTTATAATTGGTTTTAAAGGAAAAATGCATCCAGCTTATGCACTATATTCTGAGTTTTCTGAATGTGCATGACGTATTGTGTGCGAAACTGCCTGAATTTCCTTTATAAAGTGTCCTTTTCTCTGGCGTATCCCCTCTCAGGTGACGTCCCGTTGGACCTTCCGCTG[T/A]CCCGGCTGCCCACAGGCTCTATCGCATGACGATTCGCACTTCCACGAGCGTCACAAGTGCATCAACTTCTTCGTAAAAGTTTACGGATACATGCCGCTGTTATACACTCAGTTCAGAGTGGACTCTGTACTCTTCAAGACTCGACTGCCCCACGACAAAACCAAATGTTTTAAATTCATTTAGCGGGAGCGTGGGGACATCCGGCGGACGTGGGACGATCTCTCTCTCTGGGAGCGGGAAGGGAATTAAAGCTTTCTTGTAAATACTGGAGGATTTTACTTTGAACTCGTCTTCCTTGAAGCCAAGGGAGAACTATTATGAAACGAACGATTACCGTCAGGCGTTCTTGAACATGCGTTATTCATCAGCAACCACTGCAGGCTTGATTTGCACCACTTTTCATGGGTCGCCTGAGACAAGGACGCTTTAATGGACATCCAACCGATGTTATACTGACGGAACGTGCAAAATGATGAACTAACGGAGGCTGTTTTTAAAGG
Associated Phenotype:
Not determined