ZMP
SHROOM2 (1 of 2)
Ensembl ID:
Description:
shroom family member 2 [Source:HGNC Symbol;Acc:630]
Human Orthologue:
SHROOM2
Human Description:
shroom family member 2 [Source:HGNC Symbol;Acc:630]
Mouse Orthologue:
Shroom2
Mouse Description:
shroom family member 2 Gene [Source:MGI Symbol;Acc:MGI:107194]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2290 | Essential Splice Site | F2 line generated | Not yet available |
sa31513 | Nonsense | Available for shipment | Available now |
sa38554 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa943 | Nonsense | F2 line generated | Not yet available |
sa11469 | Nonsense | Available for shipment | Available now |
sa40712 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2290
Status:
F2 line generated
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108943 | Essential Splice Site | 245 | 1324 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 30120613)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30445508 |
GRCz11 | 6 | 30432422 |
KASP Assay ID:
554-2570.1 (used for ordering genotyping assays)
KASP Sequence:
AGTGATAGCTTTGCAGCTACCAAGGTTCAYGAGAAGGGTCTGATCACAGG[T/C]ACTTCAGAGGGCCTTGGTGGTCATTCTCAAGTAAAGCCTCAAGCGAAACC
Long Flanking Sequence:
CTAGAACATAGTTCTCATCCCTATCCACCTGGCCGTCTTTCCCCAAACAAATCCAACAATAATAGCATTGAACATTTGGGTAGTGGTAAACGGGACTCGGCATACAGCTCTTTTTCTACAAGTTCGGGAACCCCAGATTACACACTGTCCAAAAGTAACACGGCATCCACTGAGAACATGCTGTACAAAATAAATCAGTGGGATTCAAGTGCCAGGCACAGCAATGGCAGGCACAGCCAAAACCTAAGCGAAGGGGTACGACAAGATGAGAGGCCTGGATACCTGCACCACCTCTCAAGTACAGGTAACCACGAGATCCCAAGAGCTGAAGAACTGCCTGGCAACCGTCATTCAAGCTCTGGAAGAGTTAATATTGGACCTGTCTGGCATGTTCCAGATATGAAGAAAAACATGATATCATCTACTCCACCTCCCACTCCACCCACACGCAGTGATAGCTTTGCAGCTACCAAGGTTCACGAGAAGGGTCTGATCACAGG[T/C]ACTTCAGAGGGCCTTGGTGGTCATTCTCAAGTAAAGCCTCAAGCGAAACCACAACAAAAGCCAGGAGAAACCCATGAAAGCACACAAAGGTCTAACCAAGTCATCGAGATTTGTCTTGAGGGTCGACGGGATTATAATCTACAATCCAAAAATGATTCCTCAAATAGCTGCATTTCATCTGATTCTCATCATCAGTATATCCAACGTACATCATCAGATAAGACATACTCCCTATCAACCACAGACATAAGAGATAGCCATCCATCCTATGGCCATGCTCCATACCATGCACAGCAGTACAGTGACGAAGGCACTTTCCATGCTCAAACTAGAACAGCAATGAAACCTCCATTCAGTGGCTATTTCAGTAGTATGCAGGAACTGCACACAAACAACCACATGCAACTCAACAGCCAGAATCAAACTGGAAGACCAGCTGCATCACTGTCAGTTAATTTAGGAGTCAATTCCCACCATATCTCTCAGGGATTAACACAGGC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa31513
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 |
---|---|---|---|---|---|
ENSDART00000108943 | Nonsense | 508 | 1324 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 30121652)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30446547 |
GRCz11 | 6 | 30433461 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATGAAGCCCTTGACAGTCTCAGTAGTAAACAGGTTAGACGGAATGAC[C/T]GATTTGCCACCACTTTGCGCAACGAGATCCAGATGAGAAGGGCGCATCTC
Long Flanking Sequence:
TCTCAGAAATGTCCCACAATGGACGGGACAGAATGTCCATAGGTTCTCAAGGAGGGAATAAAGAGCGGTATTTCCCTCCTCAATCGCAGCACCATGATAATAAAGAAAGAAGTGCCTCCTTTAAACAAAATGAAAACCAACATTATGTTTCTGCACCAAGTAATCCCTTGAATATGTCTGATTCAACAAAACATAATGAGCTTAGGGGATGCCAAAAGCAGCACCATGTGCATGGCTCAGATGAGCTTTCTGGTAGTTATCCACCCAGTAAGCAGCCCGAGCACAGGAGAAGTGCTGGCCATCTTCATCATAAGGAATACTCGCAACAACCCTTTCCAACTAAAAGCGAATCAAAGATATGTCCCCAGAAAACACCTATGTTGTATTCTCTGGCCCAAGGGCACAATGACACAGATGACTGTTCTAATCAGATCAAAAGTGGAAGCGCACAACATGAAGCCCTTGACAGTCTCAGTAGTAAACAGGTTAGACGGAATGAC[C/T]GATTTGCCACCACTTTGCGCAACGAGATCCAGATGAGAAGGGCGCATCTCCAAAAGAGTCAAAGTGCAGCCACTTTAGAAAGTCCAGTTGAAACTGTAGAAGAGTCTGCTTTGTGGAAGACCACAGGGACTGCTTCTCCCTCATCAGATGGCTGCTTTTCCATTTCTTATAAAGACCATCTTAAAGAAGCTCAGGCCAGAGTCCTCCAGGCTACATCATTCAGGAGAAAAGACCTAGAGCCAGTATTATTTGAGCATCCAGGTACTGAAGGTCCCACACGAAAAGATGTACCTCCTTCAAGTGTCTCAGAGGTCACACCTAGCAAACCCACCTCAGGGAGTAATCATGTGCTTCGCATTGGAGGCCGTAAGCGGATATCTGCTGAAAAGAAAGTGACGTCTTTTTCTGAGCCAGATAAAATTCATGAAGTAGGAGCTGATGAACGCTCCACTATGCCTGAAAATGTTGCACACTTAGAAAATCAACAAAGATTCTTTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38554
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108943 | Nonsense | 801 | 1324 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 30122532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30447427 |
GRCz11 | 6 | 30434341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGAGCGACGGAGTAACCCCACCTGTGTGCATGAAAGATCTAGATCCT[C/A]ACCTTCTGCTGACTTTTATGGGCAGGTTTGTGACCTTGTTTAAATGAATC
Long Flanking Sequence:
TGCTGAAAAGAAAGTGACGTCTTTTTCTGAGCCAGATAAAATTCATGAAGTAGGAGCTGATGAACGCTCCACTATGCCTGAAAATGTTGCACACTTAGAAAATCAACAAAGATTCTTTGAGACAACAGGGAAACCAGTTTTCCCTAAGCCTATGCCAAAGCAAAACCTGCAGATATCAGAAGACCCCAGACTGTCCAAGCCTGGAGGCATGCACTATTCTGCAAACAGTGATATGGCAGGGCGGAATAATGGTGAAAGCTCAACCCCCATTGAACACCACATTAATGAAGGTCTGGATGGCCCTAACTCAGTGAACCATCAAGCATTGCTAGAACAACAGCGACTAGGCACATTTGCAGAGTATGAGGCCAAATGGAACACCCAGAGGAAGACTACAGAACCAAGAGTATCTGGCCGATACCACTCTGCTGATAACATCCTCGATACAGGAAAAGAGCGACGGAGTAACCCCACCTGTGTGCATGAAAGATCTAGATCCT[C/A]ACCTTCTGCTGACTTTTATGGGCAGGTTTGTGACCTTGTTTAAATGAATCCCACAACTTTCAGTATTGCATTTGTTGAAGTTTTCTGATTTGCCATCTACACTACCATTTACAAAAACATGTATTGTCAGTTTTTTTTTTTTTTTCAAAACTATAATAAATCAAATGTGACCTGTCTCTCACATATAACTACAATGATGGCAATATAAAACTTAGTCAAATATTAAACTAAGTACAGAAAGTCACACCTACAAACAAGAGAAGTTGCAGGTGAGATCACAGTCATGTCAATAGACCAAGATAATTATGAGAATAGACAGTAGGCTAAAAAAACGAAAGTTCACACTAATTGAGGTATATCAATTTCTGGATAAAAAGATTCAAATTTGTGTATTCAAATCCTCACAGAAACTTCCACCACAAGAAAAGAAGTCAGCTGACTGTTTCAAATCTGAAAAGAGTCCTTGCCAACAGGACAAGAATAGTACAAGGTAGGTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa943
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000108943 | Nonsense | 831 | 1324 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 30123003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30447898 |
GRCz11 | 6 | 30434812 |
KASP Assay ID:
554-0848.1 (used for ordering genotyping assays)
KASP Sequence:
AAGAAAAGAAGTCAGCTGACTGTTTCAAATCTGAAAAGAGTCCTTGCCAA[C/T]AGGACAAGAATAGTACAAGGTAGGTGCTGTTTCATTTTCCCATTGCACTT
Long Flanking Sequence:
CACCTGTGTGCATGAAAGATCTAGATCCTCACCTTCTGCTGACTTTTATGGGCAGGTTTGTGACCTTGTTTAAATGAATCCCACAACTTTCAGTATTGCATTTGTTGAAGTTTTCTGATTTGCCATCTACACTACCATTTACAAAAACATGTATTGTCAGTTTTTTTTTTTTTTTCAAAACTATAATAAATCAAATGTGACCTGTCTCTCACATATAACTACAATGATGGCAATATAAAACTTAGTCAAATATTAAACTAAGTACAGAAAGTCACACCTACAAACAAGAGAAGTTGCAGGTGAGATCACAGTCATGTCAATAGACCAAGATAATTATGAGAATAGACAGTAGGCTAAAAAAACGAAAGTTCACACTAATTGAGGTATATCAATTTCTGGATAAAAAGATTCAAATTTGTGTATTCAAATCCTCACAGAAACTTCCACCACAAGAAAAGAAGTCAGCTGACTGTTTCAAATCTGAAAAGAGTCCTTGCCAA[C/T]AGGACAAGAATAGTACAAGGTAGGTGCTGTTTCATTTTCCCATTGCACTTTTAAGTGTAAAAAGATAGTGTTTAAATGTGATTATCAGAGTACTTTTTATAAGTCTTGATGTCTGTGATACTCCTGGGCATGTTTGAGAGACTAAACCGGACAACTTTTCCTTTGTAATGTAAATAATACAGATGCTAACTGTGCTGGCTAGGATTGTGTCAGTGTGTCAGTGAAACTATTCCAGCACTAATGGCTCTGATCTTGGCTTTGCTGCAAACAGAAATCCACAGTTGGGCCATCAGTCGGCCCTCGCTGGGTCAAAGGCAAACACTAGACTCTTTGTGGTCTTTGCAATGTTGGGATTTAGCCCAGCTGTGACAGCACTGCTATCCTCACTGACTGAGCTTTGTGTTACAAGGAGATGGCTTTGAGGTATAGGCATGCGGCTATGACATAGGAAGTGTCCAACCAGTCCATTCATAATCAGGCCAAAGAGTAAAATAGCAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11469
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 |
---|---|---|---|---|---|
ENSDART00000108943 | Nonsense | 1075 | 1324 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 30129942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30454837 |
GRCz11 | 6 | 30441751 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATGGAGGGGATTTTCCCTCAAGGAGATCAGCTACTGGAGGAGGCCYAA[C/T]AGCGYAGGAARGCTCAACCTAAACCACTCTCCCCTCGAAACTCTGTTGAG
Long Flanking Sequence:
ACACATCTGTGAAGAAAGTGCCCATTAAGATAGTCCATTCAGAGAGTGACACGGAAAAAGAAAGTCGGCAATATCTAGACCTGCCCAGCGAGACGCCTGTCAACTCGCAGGGACTTGTGGGAGCTCATCTTCAAAGTTTGGGGAACCCGGATCAGTCATACTCTTTGTTTTGTACATACACCAGACAAAAAGATCAGGTTCCTGGTCTTAGAGACCCAGACATGGGCCCTCTAAAAGACCAGGGGCCACAAAGCAATATAAACCCAGTGTCTTATGTGGAACCTGGCCTTCAGACAGGTCCACCATTGGATCAGAGTACCAATGGAGTGTCTTTGCATCCTTCACATTCAGAGGATGATAAAAGAAAGGAGCTGGCTAGAGACATAATGGACAAAGACAAGTCCCTCGCTGACATTTTAGACCAGAGTAAGATGAAGACCACTATGGATCTGATGGAGGGGATTTTCCCTCAAGGAGATCAGCTACTGGAGGAGGCCCAA[C/T]AGCGTAGGAAGGCTCAACCTAAACCACTCTCCCCTCGAAACTCTGTTGAGAAGTCAGTATTTCTTATTTGTAATCCTACTCTATTCACTTTTCCTACATCACTAAAAGAGCTCCTCTTTTTTCCCAAAGTAGGCAAATTTTACAACTCTCCTAGAGTTAAACAACTAAGTGTTACCATTTTTTATCTATTCAGTCAATCTCTGGTCTGGTGAGAGCACTTATAGCCTAGCTTAGCATAGATCATTGAATCAGACTAGACCATTAGCATCTCACTCAAAAATAACCACAATAGTTACACTGTGTACAAAAACTGAGCAAAAATGAAAAGTTGCCATTTTCTAGACCGATATCAGGGTGTCCGCGGGGTCTTAAAGTATTAGAAGTTGATAAATCAATTATGAGAAAATTAAGGCCCTTAAAAGGTATTTAAAAATCTTAATCGTGTTTTTACGAGGTCTTAAAATTAATTAAACCTTTGTCCAAAGTGTTTGATTTCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40712
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108943 | Essential Splice Site | 1146 | 1324 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 30139445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30463312 |
GRCz11 | 6 | 30450226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTTCCTACCTACCAGTTGACTGAATCTAATGGCATTCTCTGTCTTTGC[A/T]GCACGAGTTGATTGAAAGTCTCAGTAAGAAGTTGCAGGTCTTAAAAGAAG
Long Flanking Sequence:
TTTTTTCCTGTGGAGAAAGTGAGTATTGAGTTTTTATTTCTGGAACTGGAGTGTTTTTGGCTGTTGTTTATTGAAAAATATTTCATTATTATTAAACTCCCCTGAATGTCTCCGATCGGTCACACAATTAGTCCCATATCCTTAAAACAAAGCAAAACTGTGTAATCATTTTGCATTTAATATATATTTCCTTTGCTTTTTTGCTTGTTTTTCTTACAACAATCACTTATGGATTTTCAGGAAAGAGGAAGACAGCCTGGTGGCGGCCGCTGCTTTAGTGAGCAACTCTACCTACTACAGCACATCTGCACCCAAAGCAGAGCTGCTGATCAAGATGAAGGACATGCAGGACCAGGCGTTGAACACAACTCAGAAGAGGAGCTGGAGGAGGACAATGAAAGTGACCTCGCCTGCAAGAAGGTACAAACACTTTGCGTTGTACAGTCGGATGGTTTCCTACCTACCAGTTGACTGAATCTAATGGCATTCTCTGTCTTTGC[A/T]GCACGAGTTGATTGAAAGTCTCAGTAAGAAGTTGCAGGTCTTAAAAGAAGCTCAGGAGAGCCTGCAGGAGGACGTGCAGGACAACAACGCTCTTGGAGAAGAAGTGGAGGCCATCGTACAGGGCGTCTGCAAGCCTAATGAACTCGACAAATTCCGCATGTTCGTCGGGGATCTTGATAAAGTGGTCAACCTTCTGCTGTCTCTGTCAGGACGTTTGGCCAGGGTAGAGAATGCCCTGAACAGCCTGGAGGAAGATGCTTCGCTGGAGGAAAGGGTGAGGATGTGGGAAAGCTTTAGGAGGCATACTGAATTTTATGACGTTTTTCAAAACTACACTAATGTGTAGTAATTTAATAAATCTACCATGTTGTGTGAGAACAACCTCTTTTGGTAACAATTTTTTAACTAAATTTTAAATGGACTCTAGAATATTAAAGTGCATTTATTTTCACACAGCTTTTATCAGATAGAAAATGGGCTTCACAAATAATCGAAAAAGT
Associated Phenotype:
Not determined