ZMP
itln3
Ensembl ID:
ZFIN ID:
Description:
intelectin 3 [Source:RefSeq peptide;Acc:NP_001153056]
Human Orthologues:
ITLN1, ITLN2
Human Descriptions:
intelectin 1 (galactofuranose binding) [Source:HGNC Symbol;Acc:18259]
intelectin 2 [Source:HGNC Symbol;Acc:20599]
intelectin 2 [Source:HGNC Symbol;Acc:20599]
Mouse Orthologues:
Gm9765, Itln1
Mouse Descriptions:
intelectin 1 (galactofuranose binding) Gene [Source:MGI Symbol;Acc:MGI:1333831]
predicted gene 9765 Gene [Source:MGI Symbol;Acc:MGI:3642721]
predicted gene 9765 Gene [Source:MGI Symbol;Acc:MGI:3642721]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35654 | Nonsense | Available for shipment | Available now |
sa7386 | Missense | Mutation detected in F1 DNA | Not yet available |
sa28277 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35654
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 |
---|---|---|---|---|---|
ENSDART00000003040 | Nonsense | 151 | 314 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 14 (position 14036648)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16043030 |
GRCz11 | 14 | 16348683 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAATCTGATGGTTTAATACTGTCACATCCTACAGAATCCTGGATATTA[T/A]GACATTTCTGCACAAGACGTCTCAGTGTGGCATGTTCCCAATAATGAGCA
Long Flanking Sequence:
GAGACTTTCAACCAGCACAACAAAAATAGCTTCTGAAGAACCATACTGCATCTTTAAATTATGTTGATTCTACAAATAATTTTTTGAGTGTACTTTACTTCTTTATTGAGTATCTTTTCTACAAAGTGAACTCTGGGGTTGTTGTTTGTCTTCAGATGGCATGTACATCCTGACAACAGAGAGCGGCACATATTACCAGACTTTCTGTGACATGACCACAGCCGGAGGTGGATGGACTCTTGTGGCCAGCGTCCACGAGAACAACATCAATGGGAAATGTTCTTTCGGCGATCGCTGGTCGAGCCAGCAGGGAAATGACCAAAGCCTGCCTGAAGGAGAAGCATCATGGGCAAACACTGCTACGTTTGGCAGTGCAGAAGGCTCTACCAGTGATGACTATAAGGTACATTAGAACATGGAACTTCAGCCATATACTAAGAGGATATTGATGTCAATCTGATGGTTTAATACTGTCACATCCTACAGAATCCTGGATATTA[T/A]GACATTTCTGCACAAGACGTCTCAGTGTGGCATGTTCCCAATAATGAGCAGTTGAAAAAGTGGACATCTTCTGCCATCCTGCGCTACCATACTGAAAGCCAGTTCCTGAAGGAGCATGGAGGAAATCTTTACCACTTATTTAAGGTCAATCACACTTCTGTGCCCCTTAATTTCATTTCAATTTTATTTCAATTTCATTTCAAGGATTAATTTTATTTTAAAGTAATTTAATGACAGTTACTTGTAATGTACTTCCCTTAAATGTTGTAAACAAATGTTTTAGTTTGGTAAAAATCTATTCAGTGAAGCAGATACAGTTGAAGTCAGAATTATTAGCCCCCATTTGATTTTTTTCTTTTTTAAATATTTCCTAAATGATTTTTAACAACAAGGAAATTTTCACAGTGTGTCTGATAATATTTGTTCTTCTTGAAAAAGTCTTATTTGTTTTATTTCGGGTAGAATAAAAGCAGTTTTTAGTTTTTTTAACTATTTTACGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7386
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 > T
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003040 | Missense | 163 | 314 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 14 (position 14036682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16043064 |
GRCz11 | 14 | 16348717 |
KASP Assay ID:
554-4228.1 (used for ordering genotyping assays)
KASP Sequence:
AGAATCCTGGATATTATGACATTTCTGCACAAGACGTCTCAGTGTGGCAT[G/T]TTCCCAATAATGAGCAGTTGAAAAAGTGGACATCTTCTGCCATCCTGCGC
Long Flanking Sequence:
GAAGAACCATACTGCATCTTTAAATTATGTTGATTCTACAAATAATTTTTTGAGTGTACTTTACTTCTTTATTGAGTATCTTTTCTACAAAGTGAACTCTGGGGTTGTTGTTTGTCTTCAGATGGCATGTACATCCTGACAACAGAGAGCGGCACATATTACCAGACTTTCTGTGACATGACCACAGCCGGAGGTGGATGGACTCTTGTGGCCAGCGTCCACGAGAACAACATCAATGGGAAATGTTCTTTCGGCGATCGCTGGTCGAGCCAGCAGGGAAATGACCAAAGCCTGCCTGAAGGAGAAGCATCATGGGCAAACACTGCTACGTTTGGCAGTGCAGAAGGCTCTACCAGTGATGACTATAAGGTACATTAGAACATGGAACTTCAGCCATATACTAAGAGGATATTGATGTCAATCTGATGGTTTAATACTGTCACATCCTACAGAATCCTGGATATTATGACATTTCTGCACAAGACGTCTCAGTGTGGCAT[G/T]TTCCCAATAATGAGCAGTTGAAAAAGTGGACATCTTCTGCCATCCTGCGCTACCATACTGAAAGCCAGTTCCTGAAGGAGCATGGAGGAAATCTTTACCACTTATTTAAGGTCAATCACACTTCTGTGCCCCTTAATTTCATTTCAATTTTATTTCAATTTCATTTCAAGGATTAATTTTATTTTAAAGTAATTTAATGACAGTTACTTGTAATGTACTTCCCTTAAATGTTGTAAACAAATGTTTTAGTTTGGTAAAAATCTATTCAGTGAAGCAGATACAGTTGAAGTCAGAATTATTAGCCCCCATTTGATTTTTTTCTTTTTTAAATATTTCCTAAATGATTTTTAACAACAAGGAAATTTTCACAGTGTGTCTGATAATATTTGTTCTTCTTGAAAAAGTCTTATTTGTTTTATTTCGGGTAGAATAAAAGCAGTTTTTAGTTTTTTTAACTATTTTACGGTCAAAATTATTAGCCTTTTTAAGCTATATTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28277
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003040 | Nonsense | 290 | 314 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 14 (position 14041025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16046331 |
GRCz11 | 14 | 16351984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGTATTGTATTGGCGGAGGAGGATTTTTTGTCCAGCCTGAGCAGTGT[G/T]GAGACTTCACAGCACTGGACCTGAAAGAAACATTTAAACAACCCACTCAG
Long Flanking Sequence:
TTTACTAAGTAGTTAAGTGGTGCAAAAATGACCCAGAAATGGTTTTATATGCTCATTTATACTCACAGGAGTAACCTCTATATGAGAAGCGTGGTTTTGACCATATTTGGAATGGTCATAAATAATAATGAGCTCTGCCTATTGTATCATTACAAACATATCAGTTAAATTTCACAGTATACATGTTAAACTAACAAAAGATCAAGTTAAACAGACTTTATGCCTGTTCAGGAGGGGGTACTTAATTAATTTTAATCTGTATATCCAGCATTTTGTGCTCTGACAAAGGTATGTGATGAGATAAGATACTCCATGATTTCATTGACTGAAAGCTCTAAAATGTTTTAAAAATCAAGAATAATACAAGTTTAGATCAGCTTTAAAAATAAGGGGAAACATTTAAATAAATCATAAATATTAGAATGAAATCAGACTAACATGATTGTGTTTTGCAGTATTGTATTGGCGGAGGAGGATTTTTTGTCCAGCCTGAGCAGTGT[G/T]GAGACTTCACAGCACTGGACCTGAAAGAAACATTTAAACAACCCACTCAGTCAGCTGTGCTTCTCTTCTACCGTTAAAGAGTCCTATTCGTTATATGTACATCATGGGAATCAGTGTTGTTACACATTAAGTCAAGTGCTGATCTGAACTGTATGTGCATAGTTGAGAAAACTGTGGTTCTGTTTTATCCATGAATGTTGATATCAATAAATATATTAAATGCAAGTTTCCCGGTGTGTTTAGTATAACTACACCAATTTCTAGCTATAGAAACATAAAAATTAATTTTCTGTTCAAGCAGTGTATATAAGAACAAATCATTCATCTGTCTTAAAACGTGTTATGGTGAGTTCATGTTTTACAAAGTTTTAATTGAATATATTTGCAGCCGCATTTTAAAAATGTTTAAATAATGAATTCCTCAAGCAATGTATCACAGGAGAAATGCTGAGTGTAAAACATTTCAGATATAATTTAAAAAGTAGCAAAGAGGGAGTGAA
Associated Phenotype:
Not determined