ZMP
gltscr1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human glioma tumor suppressor candidate region gene 1 (GLTSCR1) [Source:Uni
Human Orthologue:
KIAA0240
Human Description:
KIAA0240 [Source:HGNC Symbol;Acc:21111]
Mouse Orthologue:
BC032203
Mouse Description:
cDNA sequence BC032203 Gene [Source:MGI Symbol;Acc:MGI:2673855]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43165 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36722 | Nonsense | Available for shipment | Available now |
sa29089 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16525 | Nonsense | Available for shipment | Available now |
sa23374 | Nonsense | Available for shipment | Available now |
sa13301 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43165
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098540 | Essential Splice Site | 30 | 1800 | 3 | 13 |
ENSDART00000144271 | None | 1 | 1771 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 43048443)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 44638334 |
GRCz11 | 18 | 44631788 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAAATGTGACTGGGTCTAGTTTTTAAAAAGTCTGTCTGTGTTTTCCA[G/T]GGCCATGTTCCTGAGGTTCCGGCACAGGTTCAGCTGTCGACAAGTGAGCC
Long Flanking Sequence:
CCTGTTTGCTTGGCTTTTTAACTTGGTTGTGCCTGCATTTTGTTCTGGTTGATTGGTGCACTGTCCTCACTTTTCTCTTCCCTTGCCTTTTCCTCTTTGTCTGCCTATTTGCCCCTTGTGCGTCTTCTCCCTGTCGCTTTCACACGCCTGTCTGTGTGCTGTGGTGATTTCTGCCTGTCCTATCCTGGGTATATCTGTCTGTAGCTGGACACTGATGACCTATTGGATGGCTCAGGTGACCCGTCCAGCTCGTTCTTCTCCAGCACTGGGGTGAGTAAAATCCCCCATTTGCGCCAACCTCCTGGCTCCATCCTTTTTTTCGTAGCATGTGCTCCTCAACCCCACCATCCAAATCAGATGCATTGTGCACCAGATCTGCAACTACAGCAGTCAGTCCCAAAGGAGTGCCACCATCCCAAATCCATCCTTAGCATGTTATTTCATATGATTCTGAAAATGTGACTGGGTCTAGTTTTTAAAAAGTCTGTCTGTGTTTTCCA[G/T]GGCCATGTTCCTGAGGTTCCGGCACAGGTTCAGCTGTCGACAAGTGAGCCGGGCCTTCCAAGAGTCAGCGTTGATTTGGACTTCTTGGAGGACGATGACATATTGGGGGGATCGCCAGGAGGAGACAATGGAAGTAATGGTGTTGGGACAAATCATGAGCCCTGTGACATTTTGCAGCAGAGCTTGGCGGAGGCTAACATCACAGAGCAGAGCCTTCAAGAGGCAGATGCTGAGCTTGACCTCAGTTCCTTTGGGCTAACTGGCCTTACGCAGGTGGTTCAACCCCTGCCTGATGCCGGCCTGTCTGGGGTGGGCATTGGAGGTGCAACTCAGATTTTTCCAAACCAAGGCACCCCTACCGCACCCTCAAATCCCACTCCAGACATGCTTGGTTCTGTCCTGGCACATCCAGGTCTGCAGCTTCAACAACAGGTCATGAACAAGGCTATCAGCGTCCAGCCTTTTGTACAACAAGTCGGACTTGGAAATGTAACACTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36722
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098540 | Nonsense | 217 | 1800 | 3 | 13 |
ENSDART00000144271 | Nonsense | 188 | 1771 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 43049005)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 44638896 |
GRCz11 | 18 | 44632350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTCAGGCCCTACCGAACGGCAGCCAGTCTGGACCGTTGGGCATTGGA[C/T]AAATTCAAGTGGTGGGTCAGCCCACTGTAATGACTATAAATCCATCTGGG
Long Flanking Sequence:
GAGTCAGCGTTGATTTGGACTTCTTGGAGGACGATGACATATTGGGGGGATCGCCAGGAGGAGACAATGGAAGTAATGGTGTTGGGACAAATCATGAGCCCTGTGACATTTTGCAGCAGAGCTTGGCGGAGGCTAACATCACAGAGCAGAGCCTTCAAGAGGCAGATGCTGAGCTTGACCTCAGTTCCTTTGGGCTAACTGGCCTTACGCAGGTGGTTCAACCCCTGCCTGATGCCGGCCTGTCTGGGGTGGGCATTGGAGGTGCAACTCAGATTTTTCCAAACCAAGGCACCCCTACCGCACCCTCAAATCCCACTCCAGACATGCTTGGTTCTGTCCTGGCACATCCAGGTCTGCAGCTTCAACAACAGGTCATGAACAAGGCTATCAGCGTCCAGCCTTTTGTACAACAAGTCGGACTTGGAAATGTAACACTTCAGCCAATTTCGAGCCTTCAGGCCCTACCGAACGGCAGCCAGTCTGGACCGTTGGGCATTGGA[C/T]AAATTCAAGTGGTGGGTCAGCCCACTGTAATGACTATAAATCCATCTGGGCAGCAAATCTTGACGAAAACCATGGGTGGCTACCAACTGCATCAACCTGGGCCGGAGGCAGCAAGCGCTGGAACGCAGGCTGGGCTTGGAAGCTCTGTTTTGAGTTCAGGAGGTGGACTTGTAATTCAAGGGGGCAAGGCCACTCTCGGGTCCCCTGCCTTAAATGGGCCAGCTGTCTGCTTAGGCAGCACAAATACCAACAACAGTGCAACTACAATGGCCACTGCTGGTGGTATAGTGGGTTTTAGTAATGCCTCTTTGGGTGCAGGAATTGGATCTCAGACCCAGCCTCAAGGCCAAATCATGCAGAATGTCATCATCCAGCGAACGCCAACGCCAATACAGCCCAAACCTCCTCAAGGGGGTACAATCCAACCCAAAATCTTCAAGCAACAACAACAACAGCTTCCTGCCCCACATGCCTTGCCAAATGATGCTAATAAAGCTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29089
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 |
---|---|---|---|---|---|
ENSDART00000098540 | Nonsense | 427 | 1800 | 3 | 13 |
ENSDART00000144271 | Nonsense | 398 | 1771 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 43049635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 44639526 |
GRCz11 | 18 | 44632980 |
KASP Assay ID:
2261-2568.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACACAGGCAGCGTCGCAGGGAACACAGTTTTCTCAAGCGCTCTTTAAA[C/T]AGCAGGGCCCTCAAACTTCAGGCAAACCCCTCAGTGTTCACTTGTTAAAC
Long Flanking Sequence:
CTGGGCTTGGAAGCTCTGTTTTGAGTTCAGGAGGTGGACTTGTAATTCAAGGGGGCAAGGCCACTCTCGGGTCCCCTGCCTTAAATGGGCCAGCTGTCTGCTTAGGCAGCACAAATACCAACAACAGTGCAACTACAATGGCCACTGCTGGTGGTATAGTGGGTTTTAGTAATGCCTCTTTGGGTGCAGGAATTGGATCTCAGACCCAGCCTCAAGGCCAAATCATGCAGAATGTCATCATCCAGCGAACGCCAACGCCAATACAGCCCAAACCTCCTCAAGGGGGTACAATCCAACCCAAAATCTTCAAGCAACAACAACAACAGCTTCCTGCCCCACATGCCTTGCCAAATGATGCTAATAAAGCTCTGGGGGTACAGCAAATCCCAGTGTCAGCTGGTCAGAATGTAACGTTCCTCACCGGGAAGCCTGGCTCTAACGTAGTTTTGAGCACACAGGCAGCGTCGCAGGGAACACAGTTTTCTCAAGCGCTCTTTAAA[C/T]AGCAGGGCCCTCAAACTTCAGGCAAACCCCTCAGTGTTCACTTGTTAAACCAACAGGGCAGCATTGTCATTCCCTCGCAAACTGTCCTGCAGGGCCAAAACCACCAGTTCCTCTTACCAGGGCTTCAAGCAGGAGGCCAGATCCTGGCTCAGCATCCTGGTGGACACATCATAACCAGTCAGGGGCCTGGAGGGCAGATAATCGCTAATCAGATCTTGACAGCCAATCAGAACATCAACTTGGGACAGGTGTTGGCTTCACAGGGCCACCCTGGTGCAGCCCACATTCTCTCTGGACACATCCAGCTCCAGCCTGGTCAGATGGGTCAGCCTGCACTGTTCCAAATGCCGGTGTCTTTGGCGCATACTCAGACACAATCTCATCCGGTAACCGGGCATGTACAAACGGTCATTCAGGGCATGCCTATACAGAATTCCCTGTCTGTGGAGAGCCTTAGCCCAGCAGTCAGTTTACAGACGTTGCAGCAGTCTGGCGGCGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16525
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098540 | Nonsense | 698 | 1800 | 3 | 13 |
ENSDART00000144271 | Nonsense | 669 | 1771 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 43050448)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 44640339 |
GRCz11 | 18 | 44633793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTGTTCACGTCACCTGGTTCCGGCATGATCCTGAGCCAGGAGCCTCTT[C/T]AAATGTTCCTGCACCAGGTCAGTGTGCTCTCTTTAAACTTTATCTGCTGT
Long Flanking Sequence:
CTGGTCAGATGGGTCAGCCTGCACTGTTCCAAATGCCGGTGTCTTTGGCGCATACTCAGACACAATCTCATCCGGTAACCGGGCATGTACAAACGGTCATTCAGGGCATGCCTATACAGAATTCCCTGTCTGTGGAGAGCCTTAGCCCAGCAGTCAGTTTACAGACGTTGCAGCAGTCTGGCGGCGTCCCTAATAATGGTAGCAGTGGATCGACGGCAATGGCGCCATGCCAGCCAGGAGAGGGTATCACTGTATTGGGCGGCTCTTCTGACTCTGCTGCTCAACCAGCACAGACGCAACCTCAGCCCTCAATTCTCACGGTTCAGACGACGCCTCCAGTTTCAGTAGCAGCTTCGGTTCCTTCCTCTTCATCTCCATCCCCAACGATGGCCACGTCTGCATCCACAATGGTGGGTCTGTGTTCACAGGCCCAGCACAGCCCTGGAAAAGTGTTGTTCACGTCACCTGGTTCCGGCATGATCCTGAGCCAGGAGCCTCTT[C/T]AAATGTTCCTGCACCAGGTCAGTGTGCTCTCTTTAAACTTTATCTGCTGTTTGCAAACTGTGTGCTAACATAACAACATTTAGAGCCCCAAGCTGACCTCTGGACCAGTTTGAATGATTGTTTTACCTCTCCCATTCCTGAACTGATAAATGTACCTATGTTAGGAGCAACAGCATCACGCAGGAAAAGACCCACCTGCCGCTGTGGGTGTACCTGCATCTGTTATCGTCAGCGGCAGCAGTTCTGGTCCCGTCCCTTCAGGCCATGACAACTTGTTAGCTGAGACTCGGCAGAGGCAGAGTCCCAGTCCCTCCCTTGGTCCTGCCCACATGGCAACAGTGGTTAACAAGGTAGATGAGCTCATGCTCTGTGCTAAGCCCCACCCACTTGTTGCTGCCACTGCTGCGTATTGGACCACTGTCTCCCAGCAGAATTCCCTCTTTTTCTGTCCTCTTGTCCTTCTACTGTCATTGCTCAGGCTACTGCTCTTTCACTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23374
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 |
---|---|---|---|---|---|
ENSDART00000098540 | Nonsense | 917 | 1800 | 5 | 13 |
ENSDART00000144271 | Nonsense | 888 | 1771 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 43054654)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 44644545 |
GRCz11 | 18 | 44637999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGCAGCCACTTCCCACACAGTTCCAGTTCCAGCCCCCAGTCTCCAGCT[C/A]GTCTCCAGCTGCAGCAGTGAAACAGCAGGTGACGGTGGTGCCTGGGCTGA
Long Flanking Sequence:
ACTGACAATTTCTCTCATCCCCCACCTCCTCTTTTTTACCATATAGGTTCCATCGTCAGCACATTCACAGTCTATAAAGATCCAAAACGCCTCCCAATCTCAGCCTGTGGTCACCCCTTCGCCAGCACCCACACTGTCCGACAGCCCTCAACCTGCTCAAGTTTCCCCTCTCACTCTCGGGCAGCAGATCCAGTCTCCCCATCAACAGTCTCGGCCTCCCTCGCAGCCCCAGCCTCCTTCACAGGCACAGACTCCTTCACGCTCATGCACCCCTTCCTCTCTACCGCCTCTCTTCATCATTCACAATCAGATGGGAGGTTCTCCACAGCCGGCTCCACCACCTCAGCAACAGCAGCCTCAGCAGTTACAAGTGCAGCTCCAGCCTCAAGTTCTTCCTCAGCCTGCTGCTCTGCAGCCAGACGTACCTCCTTCCTCGTGCTCCCCAAAGCCTCCGCAGCCACTTCCCACACAGTTCCAGTTCCAGCCCCCAGTCTCCAGCT[C/A]GTCTCCAGCTGCAGCAGTGAAACAGCAGGTGACGGTGGTGCCTGGGCTGACCGCAGAACAGCAGCATCACCTACAGCTGGTCAGTGCGCAGCTGCAGACCATGTCATCAATCACACAGCCCTCCCCTCAACAAAAGCAGCTCTTGGAAAAACTTCACCAGGTATTGTATCATCAGTTTATCCCAAATACCTCGCTCTAAGTGCTTGTGAAGTGTATAGACATGAGTGGATGAAAATTCTGGAGAGAAACAGAAGATTCTGACTGGATCTTTTAACAGATGTTCCCTCCATGAACATTTTTGTTTGGTCTTTATTCATGGACACAAATGTACTGGATTGATCAACTCATTCTAAATACCCTGCTCTAAGTGTTTGTGATGCGGGTTTGCGTGGAAACAATGTTAGTTTTCGCCAACTATATTTATTTTACTGACGAAAAGGAAATAAAAATAAGTTTTAATGACAAAATCTATGACAAAATGTACTGATGTTTTTGTCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13301
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 |
---|---|---|---|---|---|
ENSDART00000098540 | Nonsense | 1694 | 1800 | 13 | 13 |
ENSDART00000144271 | Nonsense | 1665 | 1771 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 43062262)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 44652153 |
GRCz11 | 18 | 44645607 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGTCTTCCTGCACAAGAGACTCGTCACTTCCTGCCAAACGCTGCAAGT[C/A]GGACTCTCCRGACATGGACAATGCAAGCTTCTCCAGCGGCAGCCCGCYGC
Long Flanking Sequence:
AACGTGCAGGCTCCCGCTCCGAAAGACATACCGTGAGAACATCAGTCCCCGTCACAGGCCTGGAGTACCAGGAGGTGGTGGAGATACACTACCCATTCTGCCTGCAGGACCTCCTGTTACCTCTTCGCCCCAACCGCAAAGCTCGTCCCCTCAACCCGAACGAACTGTGATAGCCAGTGTGAAACTGGAGCGGCAAGGTGGACACGGGCGATCTCACCCCCATGCGGAGTCACAAAGCCTGGCAGCCGTTGAAGACGTCCTTTATCGGGGAATAAAAAACGCGTACCAACATCATCGGGAGTTTGATAAAGACGATGAGGATGATATGGAGGAAGGTGGTGGTGGTGGTGGTGCTTTGGGGCGGTTAAAGGGCATAGGAAGCAAACACCGGGAAGGGGGACGGGGCGCCTTCAGGATGGATCAGCATGCCCCAGGGCCGCCCTCTCCCGGAGAGTCTTCCTGCACAAGAGACTCGTCACTTCCTGCCAAACGCTGCAAGT[C/A]GGACTCTCCGGACATGGACAATGCAAGCTTCTCCAGCGGCAGCCCGCCGCCTGACGACTCGCTAAATGAGCACCTGCAGTGTGCCATAGACAGTATACTAAACCTCCAACAGGGCCCTCCTGGACACGGAGGCTCAGGGAGAGGGGATTTAGGGAGGGTTCATGGGGCAAACCTGCCTAACCAGCACCAAACCCATCCCTCCTACAGACAGTCCATGCCTCCCCTCTCAACACAGCCCTCGTCCGCCCCCATGTCCCAGCATTCACAGGTAGGAGGGCGAGGGCAGAATGGAAATCTGGTTTCACAGACGCACAGTAGATAACAGCCCCTTCAGCCCACGTCGACTGAAAGACTGAAAAAGCAGGATGTCAGTGCATAGGGGGAAGAAAATGGAGACATTTTCCCATGTTCAGCTGTGTTTGCTTTGTTTGTCTGTGGTTCGTGCTGATCAAACGTGTTCTTTTGGTTTACATATGGCCCTTTAAGTGTACTTTCTAAGT
Associated Phenotype:
Not determined