ZMP
gro1
Ensembl ID:
ZFIN ID:
Description:
Protein groucho-1 [Source:UniProtKB/Swiss-Prot;Acc:O13168]
Human Orthologue:
TLE3
Human Description:
transducin-like enhancer of split 3 (E(sp1) homolog, Drosophila) [Source:HGNC Symbol;Acc:11839]
Mouse Orthologue:
Tle3
Mouse Description:
transducin-like enhancer of split 3, homolog of Drosophila E(spl) Gene [Source:MGI Symbol;Acc:MGI:10
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20989 | Nonsense | Available for shipment | Available now |
sa13620 | Essential Splice Site | Available for shipment | Available now |
sa17548 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20989
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 |
---|---|---|---|---|---|
ENSDART00000100020 | Nonsense | 325 | 771 | 12 | 20 |
ENSDART00000130553 | Nonsense | 325 | 771 | 13 | 21 |
The following transcripts of ENSDARG00000069006 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 34989403)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 33383743 |
GRCz11 | 7 | 33654893 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCTCCATTCCTTCATCTCGCAGAACGACAAGTCCTCCACCCCAGGTT[T/A]GAAGTCCAACACCCCTACCCCACGCAACGACGCTCCCACCCCAGGAACCA
Long Flanking Sequence:
ACGCCCCAAACAGCCCAGCTTCCGTGGCGTCCTCTGGGAGCACCCCATCCTCCAAAGCGAAGGACCACCCACATGTAAGCATTAAAATTGAGGATGGACATTTGTGGTGTCAAGTCTTCGCAAACCCTTTTCCTCTAAGCAGCTATATGTCTGCGGCATAGATGTCAGTTTGAAGCATAACATGAATACATCAGCTGCTGTCAGACAAACAGCGGCTTGGCTGCTAGCCTCGGCTAATATCTCAATGCGCTTAGCTAGCCTCTGAGGGAACAGGAGAAAAGAGAGTGTGATTAAAGATGAGTGAGAGGATGAGGTCTCGGGGAAGGGTTCGGTCTGAAGTTTAGCTTTATCCTTCTCAGCTATAATGAGCTGTCAGTGTTTGACTGGATTAGTGCGAGCGAGCTCTCTGGATTTGAGCATTTGTGGTATGTAGCTTTAGCTCCGTTAATTCCATCTCCATTCCTTCATCTCGCAGAACGACAAGTCCTCCACCCCAGGTT[T/A]GAAGTCCAACACCCCTACCCCACGCAACGACGCTCCCACCCCAGGAACCAGCAACACCCCCGGGCTCAGGCCCCATCCCGGAAAACCACCTGGCATGGAAGCACTGAGTAAGTAGTAAATACACGGAATATAAAGATATGCAGCTATGGAAAACTTTAAGAGAATTTTGTTTTTATTCTTTAAACTTCTGATATTTAAATGTCCAGTTTGTTGCATAAAATAACACACAAGGTGACCCAAATAACCCTGATTCTCAATCCCAACAAAGCATCATTCTTACCAATTGTTAATTTTTGAAGGAAAAGAAAGTTAGAAGAAATGTTATACCCTTTTAGAATAGGGGTGCTTTACACCTAGACTTTTGTTCCGGAACCTGGCGCAGTTCCCCAGTTAGCGCGGTTTGTTTGGATATGTAATTTGCATATATGGCTATATAAAGAGAGAATTATGAGTAGGGTGTGATTTCCAAAAACCAAATTCATTTATTTAAATCATTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13620
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 |
---|---|---|---|---|---|
ENSDART00000100020 | Essential Splice Site | 660 | 771 | 17 | 20 |
ENSDART00000130553 | Essential Splice Site | 660 | 771 | 18 | 21 |
The following transcripts of ENSDARG00000069006 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 34984409)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 33378749 |
GRCz11 | 7 | 33649899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGACCTGAGAGAGGGTCGCCAGCTTCAGCAGCATGACTTCACAYCACAG[G/A]TTATCTTAATGCACACTTATACACCTYAAAAATGCACTTGTAATKGAAAT
Long Flanking Sequence:
ATAACTATATCCGTTCCTGTAAGCTGCTTCCGGATGGCCGTACTCTGATTGTTGGAGGGGAAGCCAGCACTCTGACCATATGGGATTTGGCCTCTCAGACTCCTCGTATCAAAGCAGAGCTCACCTCTTCTGCCCCGGCTTGTTATGCGCTGGCGATCAGCCCTGATGCCAAGGTCTGCTTCTCCTGCTGCAGTGATGGAAATATTGCCGTCTGGGACCTTCATAACCAAACCCTTGTGAGGTAGGAATCAAATGGGTGTTGCCATGTGCAAAAATTGTCTCTGCGATGTATGCAAACGTATGTGTGTTCTGCTAATGCAATAAAAGACTGCATGATTGTTTGTGTTTGTAGGCAGTTCCAGGGTCACACAGATGGGGCGAGTTGTATAGATATTTCCCATGATGGCACCAAACTGTGGACAGGTGGACTGGACAACACTGTACGGTCCTGGGACCTGAGAGAGGGTCGCCAGCTTCAGCAGCATGACTTCACATCACAG[G/A]TTATCTTAATGCACACTTATACACCTTAAAAATGCACTTGTAATTGAAATTGTAGCACAAGTATGTGGAAAAACTTTGATAATAAATGGGTGAAATAGTTTTAAATATTTATCCACGATTTAGGGTTTTCATCTTGAGTGAGTTTCTTTTAAAGTCTTGTTATTCCTTATTCCTTATTATCTTGTTAATCCTTATTCAATGTCATTAAATAAAAATAAATAAATAAGCTTTAAAATTAGTCATGGATGAAAATTGTGCAGTTTGTAAACTTTCACATCTTATCTGCACTTCACGATGAAAGATGAAGAGACTCATTCACAGCTTCAGTGCTTTATGACAGGTTTTGTGTGAAAATGCATGACTTGTCATGAACTGACATGTTAGCCGCAATATGACTTTTTTAATTTTGAATCATCAACAGCCACCAGCAAAACCCAATTTTTTGGTTATAATAAACACTCCACAAGCTTCATGCTTTAGATGGGCATGTGGCATTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17548
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 |
---|---|---|---|---|---|
ENSDART00000100020 | Nonsense | 701 | 771 | 18 | 20 |
ENSDART00000130553 | Nonsense | 701 | 771 | 19 | 21 |
The following transcripts of ENSDARG00000069006 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 34983762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 33378102 |
GRCz11 | 7 | 33649252 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCATCACACCAAGCCTGACAAGTACCAGCTGCACCTGCACGAGAGCTG[T/A]GTCCTCTCCCTCAAATTTGCYTACTGTGGTAAGACGCTGTTACTTTACCT
Long Flanking Sequence:
TTTTAAAGTCTTGTTATTCCTTATTCCTTATTATCTTGTTAATCCTTATTCAATGTCATTAAATAAAAATAAATAAATAAGCTTTAAAATTAGTCATGGATGAAAATTGTGCAGTTTGTAAACTTTCACATCTTATCTGCACTTCACGATGAAAGATGAAGAGACTCATTCACAGCTTCAGTGCTTTATGACAGGTTTTGTGTGAAAATGCATGACTTGTCATGAACTGACATGTTAGCCGCAATATGACTTTTTTAATTTTGAATCATCAACAGCCACCAGCAAAACCCAATTTTTTGGTTATAATAAACACTCCACAAGCTTCATGCTTTAGATGGGCATGTGGCATTTGTTCATTTATTTATTTTTTTGTCTTAGATCTTCTCTCTGGGCTACTGTCCGACGGGCGAGTGGCTGGCTGTGGGAATGGAGAGCAGTAATGTGGAGGTGCTTCATCACACCAAGCCTGACAAGTACCAGCTGCACCTGCACGAGAGCTG[T/A]GTCCTCTCCCTCAAATTTGCTTACTGTGGTAAGACGCTGTTACTTTACCTTACATAAAGTGCAACATCTTGCACCTGAGAATAAATGAGGGAAGAAACCTTATACTTAATGTAAAATAGGGCCAAAACATGACATACAAACTTCAGCTTTAGCTTTGTATTCAGTGGTGTTTTTCCATTTTAGTTTGGCAAGGTTGCACTTTGTACACCCCCCCCCCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTAATGGCTCACTTTACTTCCAAAAAAGTCGAGTTGTAGTGAATCAAGTCATTCAGATCAACCTTGACTCTGTACCCATTAGTGCATATGTGTTTGTTCCATTTCCTAAAGGTAAATGGTTTGTGAGCACTGGGAAGGACAATCTCTTGAATGCCTGGAGGACTCCCTATGGTGCCAGCATTTTCCAGGTATGTCAGTCAATACTGTATTCCCTCTC
Associated Phenotype:
Not determined