ZMP
srrm2
Ensembl ID:
ZFIN ID:
Description:
Srrm2 protein [Source:UniProtKB/TrEMBL;Acc:Q6IQN3]
Human Orthologue:
SRRM2
Human Description:
serine/arginine repetitive matrix 2 [Source:HGNC Symbol;Acc:16639]
Mouse Orthologue:
Srrm2
Mouse Description:
serine/arginine repetitive matrix 2 Gene [Source:MGI Symbol;Acc:MGI:1923206]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12827 | Essential Splice Site | Available for shipment | Available now |
sa2088 | Nonsense | Available for shipment | Available now |
sa14000 | Nonsense | Available for shipment | Available now |
sa33218 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9943 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12827
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 |
---|---|---|---|---|---|
ENSDART00000055337 | Essential Splice Site | 177 | 643 | 4 | 10 |
ENSDART00000129339 | Essential Splice Site | 63 | 1168 | 1 | 11 |
ENSDART00000129377 | Essential Splice Site | 177 | 1282 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 32774586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32505896 |
GRCz11 | 3 | 32637610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGAGCAGGAGAGACTGGAACGMGAGAAGCAGCAGCAGCAACAGTAYCAG[T/C]GAGTAGACAGAGAAGAGATTAAAGGGGTGCTATCATGAAAAAKCACTTTT
Long Flanking Sequence:
TGAGACTCTGATTGGTTTATTCTCAAAACACACCTATTACTCATTAAGAGAATAAGCACAACCCTGTTAGACCATGCACCATGGCGCAGAGCAGATTTTACCATCCTTAAAATAGCAAAAGTGGATTCGGACACGCCCTTAAATCTTTTGCGCCCTGCGCTTCAGACTTTGCACGTAGATTGTTAAAATAGAGCCCTAAATGTTTACCATACTGTACCAAACAGCTTGGTGGAAATGGGCAGTTCGGATTTTGCCACAGGCTTTTCTGTGTCTTAAATAGTAGTTTTCATCCATTTTTCTTCATTTTCAACAGTGTGACAGAGACTCATGCTCTGGCAGCCGCTAACCAGCAAAAAAATGACCGCCTGAGACAAGCGTTCGGCATCAGCTCTGACTATGTTGACGGCTCATCCTTTAACCCTGACCGGAAGGAGCGAGAAAAGGAGAAGAGGGAGCAGGAGAGACTGGAACGAGAGAAGCAGCAGCAGCAACAGTATCAG[T/C]GAGTAGACAGAGAAGAGATTAAAGGGGTGCTATCATGAAAAATCACTTTTTCCTTTATCCTTTGAGATAAAAGGGCTCTGAAAACGCTACTGTAACTTTTAGAAGTCAAACCTTTCATGTGCTTACTGACTTTTCTGTCCGTTTCTCCTCATTTCTTTTCAGAATTATTGAGTCTGATGACTCTGATTCATCTACTGAGCCAAAAAAGAGCCGCAAGAAGAAGAAAAAGAAAAACAAAAGTAGAGAGAGGTAAATAGAGAAGAATATTGAAACACTTAAAAAAACAAGAAATAGGAATTAGTTGTATATTAATATTATTTTTTACTCTTGTCAAATAGCTCTGAAAGCCCCTCCCCATCCCCTCACAGAGAGAAGAAAAAGGACAAGAAGAAGAAAAAGAAAAGGTTTTTAAAGTTACTTACTTAAAAAAAAAAACACATTATGGTGTTGTCCTCATAGGTGAGGCTTCAAGTATGCAGTGTCCCACTTTAATTAGTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2088
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 |
---|---|---|---|---|---|
ENSDART00000055337 | Nonsense | 548 | 643 | 10 | 10 |
ENSDART00000129339 | Nonsense | 434 | 1168 | 7 | 11 |
ENSDART00000129377 | Nonsense | 548 | 1282 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 32779328)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32510638 |
GRCz11 | 3 | 32642352 |
KASP Assay ID:
554-2515.1 (used for ordering genotyping assays)
KASP Sequence:
CACCTTTCGCCAATGGAAGACAGAAAGAACGAGAACTGGAGAAGGAAAGA[C/T]AAGAACAGCGAGACAGGGAGAAAAGACGAGAGGAGGAGATGAGGGAAGAA
Long Flanking Sequence:
CTCAAACAAGAAGACATGACTCCTCTTCACCATCTCCACCACCAAACAAGCAGCGGCAAGACAGAAGACAAAGGAGTGAGGAGAGACTGAAAGCCCCTCTGCGGAAAAGGCCTGACTCTTCACCCCGATCTCCCTCTCCTAAGCAGCAGAGAGACCGAAGGGACGATGGGAAGAAGAACAAAGTTCAAAGTAGACATGACTCCTCCTCCTCATCATCAACATCATCGCCATCCCCATCTCCTTCCCCACGTAAAGACAGAATGAGAAGAGGACACAGTGGAGAGAAAGCGAGAGCTCCTTCACCAAGAGACAGAGAGAAAGAGAGGGCAAGAGGAGGGGAGAGGATTAGCGACAGGGATAAAAGCAGAAAAGAAGACAGAGGACGAGATGGTGATAAAGCAAAGGAGCAAGCTCGAAACCGATCTAGTGACTCTGTGTCTCCTAAGCGTTCACCTTTCGCCAATGGAAGACAGAAAGAACGAGAACTGGAGAAGGAAAGA[C/T]AAGAACAGCGAGACAGGGAGAAAAGACGAGAGGAGGAGATGAGGGAAGAAGCTCTGAGGAAAGCCAGAGAGAGCGACAGAGAAAAGGAGAGAAACCGTAGTAGAAGAGAAGAAGTGTCCCATTCAGACAGGACGTCCTCCTCTAGGTGTCAGCCTGAGAACAGACGAGGAATTAGAGGAAGTGAGGCAGAGCAAGAGGTGCTCAAGAAAGACAGGAGAATGGAAGAGGACAAGAGGCAGGAGAAAAGTCCCCCGCACCAAAAGATGGAGAAACTGGCTCAAAAAGAAAAGACTGGACAGAAAGACAAAGCTAAAGCTGTGAGCAGTAGCAGTAGTAGTAGCAGCAGCAGCAGCAGTAGCAACAGTGAGAGTGATAGTGACAGCTCCTCCTCCTCATCTTCCTCCTCCTCCTCCTCTTCCTCCTCTTCTTCATCCTCAGATGATGACAAGAAAAAAAAGCAGAGTTCAAAAGACAGCACCTCGGCCAGTAAGTCTGTTCCT
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:
sa14000
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 |
---|---|---|---|---|---|
ENSDART00000055337 | None | None | 643 | None | 10 |
ENSDART00000129339 | Nonsense | 747 | 1168 | 7 | 11 |
ENSDART00000129377 | Nonsense | 861 | 1282 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 32780267)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32511577 |
GRCz11 | 3 | 32643291 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTGGAACAAGAGTCGTYACKTCCTTCACCTAGCAGAGGAAGAGATCGA[C/T]AGAGTGACCAAAGGAAAGAGGCACCGCCTTTGTCTCCAAGAGAAAAAGGA
Long Flanking Sequence:
ATGATGACAAGAAAAAAAAGCAGAGTTCAAAAGACAGCACCTCGGCCAGTAAGTCTGTTCCTAATGCTGTCATCGCTCAGGCAATTGCACGCAGAGAGAAGGAGAACCGAGTAAGGAATGGGGAGAGTGATGAGGGCAGGAAGACTTACCCTCCCATACAAAGACAGAGCTCACCTCCTGAGCCCCAAAGTAAAAGAGATGATGTTGAAAAGAAGCAGCGAGACCCTGAGAGAGAGCGGAGACCTGGTCAGTCCTCATCTTCGTTCACAGTAATGAATGATCGGGAACGTGGTAAAGAGAGGTACACTCCCACTGAGACTTCCAGCCCCCCTCTTTCTCCCCCTCAGAGAGTCCTGGACAGAGCAGCTCAGGTTGGGGAAAGGTACATGCCTTCAGGAGAAAGCCAATCTCAGAGCAGAGGTCGAGGAGGTGAGCGATATTCACCATCAGAGCTGGAACAAGAGTCGTCACGTCCTTCACCTAGCAGAGGAAGAGATCGA[C/T]AGAGTGACCAAAGGAAAGAGGCACCGCCTTTGTCTCCAAGAGAAAAAGGAAGGATTGACGCCCCTCAGGTTAAACAAGCAGCTTCTCGGCCTTCCCCAAAACGCACTCCACCAAGACAATACCAGGACCCTCAACGTTCACTTTCCCCAAGTCCAAGACGGGGGGTCAGAAGACTGTCACCTCCACGCAACTATTCCCCTTCTAGACGGGACCGCAGCCGGGAACGCCTTCGAGAACGGGACCGATTTAGAGCAAGACCAGCAGACAGAGATCGAGAGCGTTCCAGGGAGAGGAGGACGAGGAACAGCAGATCAAGGAGTCCCCGAAGACCGAGTCCTCCGTACAGGTTAGTCAGATGACCAGGTTTTGGAAATGCAAGAGGCAATGGAGACTGTAGTAGTGCTGTGCGTTATTTGTTTAACTCTTTAAGGTAACGTGCTGACAGACTGACTGACTGACAGGTGCGTGAGGCCAGGAAACACAGCGTAGCTTTCAGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33218
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055337 | None | None | 643 | None | 10 |
ENSDART00000129339 | Essential Splice Site | 862 | 1168 | 7 | 11 |
ENSDART00000129377 | Essential Splice Site | 976 | 1282 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 32780615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32511925 |
GRCz11 | 3 | 32643639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAGGAACAGCAGATCAAGGAGTCCCCGAAGACCGAGTCCTCCGTACAGG[T/C]TAGTCAGATGACCAGGTTTTGGAAATGCAAGAGGCAATGGAGACTGTAGT
Long Flanking Sequence:
GAGTCCTGGACAGAGCAGCTCAGGTTGGGGAAAGGTACATGCCTTCAGGAGAAAGCCAATCTCAGAGCAGAGGTCGAGGAGGTGAGCGATATTCACCATCAGAGCTGGAACAAGAGTCGTCACGTCCTTCACCTAGCAGAGGAAGAGATCGACAGAGTGACCAAAGGAAAGAGGCACCGCCTTTGTCTCCAAGAGAAAAAGGAAGGATTGACGCCCCTCAGGTTAAACAAGCAGCTTCTCGGCCTTCCCCAAAACGCACTCCACCAAGACAATACCAGGACCCTCAACGTTCACTTTCCCCAAGTCCAAGACGGGGGGTCAGAAGACTGTCACCTCCACGCAACTATTCCCCTTCTAGACGGGACCGCAGCCGGGAACGCCTTCGAGAACGGGACCGATTTAGAGCAAGACCAGCAGACAGAGATCGAGAGCGTTCCAGGGAGAGGAGGACGAGGAACAGCAGATCAAGGAGTCCCCGAAGACCGAGTCCTCCGTACAGG[T/C]TAGTCAGATGACCAGGTTTTGGAAATGCAAGAGGCAATGGAGACTGTAGTAGTGCTGTGCGTTATTTGTTTAACTCTTTAAGGTAACGTGCTGACAGACTGACTGACTGACAGGTGCGTGAGGCCAGGAAACACAGCGTAGCTTTCAGTTATGTTGAATACAGTTTCCATAATTATACTTCATAGATAAAGGTCTTGAGCTCTGCATATAATGACTTTATCCTGCTGGAGTTTATAGACGTTTCACTTTACTTCAGGACCCAATAATGCCGCTCTGTTGGTCTATTGAAGACATTCATATTCCTAGCAAATGTAATAAATGTTTGAGATATACTCGTTATATAAACGCACTAAATCGCACTTCGGCAGCGTTTATTTGGGGGAATGCAAAAAGTTTTGTGCATGAGCTGAGAAAATCGGCGCACAAGCACAGAGATTTGCATGCTCGTATTACATGAATGCAATCTCGACTTGTAATACTGCGCTCACGACATTTGTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9943
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 |
---|---|---|---|---|---|
ENSDART00000055337 | None | None | 643 | None | 10 |
ENSDART00000129339 | Nonsense | 1023 | 1168 | 8 | 11 |
ENSDART00000129377 | Nonsense | 1137 | 1282 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 32784233)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32515543 |
GRCz11 | 3 | 32647257 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCGGGAGGTCGGTTAAGAAGGCAATCCCCAACATCWGTTCATGARCCAT[C/A]AGCAAGAGGAAAGACTGCAGTAAACGGGAAATCAGAGAAAGAGAGCTCTG
Long Flanking Sequence:
CTCTCTTTCTATACCTAGATCTCGCCGTTCTCCCTCTCCGGCACGTCGGCGCAGAAGTAGTCGCTCCTTATCAAGGGAAAGGGAGAGAGAGCAGGAGAGGAGGAGGAATCGAGAGCGGGACAGGCAGCGTGAACAGGAGAGAGAGAAAGAGCGAGAACAAAGGACAAGGGTGCCACCTAAAGATCTTACTCCTCCACGCCGCTCGCCATCCTCTTCCTCTAGTTCCTCCTCTTCATCCTCACCTTCTCCTCAGAGACCCATGAGGGGTGTAAAACCAACTGATACAGATAAAGATAGATCAAGGGAAGCTAATGAACAGGCTAGGAATAAGCAACCAGAAAGGACCTCCAAACATCGATCTCCCTCCTCTCCTCGAGAGTCTCGCCTCTCTCTTCCTCTGTCTTATCGTGATGTACCTGCCCGATCAAAATCACCAACAAGCACTGATCCTCCGGGAGGTCGGTTAAGAAGGCAATCCCCAACATCTGTTCATGAGCCAT[C/A]AGCAAGAGGAAAGACTGCAGTAAACGGGAAATCAGAGAAAGAGAGCTCTGGCAAACAGCAGAAAAGAAGCAGCTCAAGTTCTTCATCCTCCTCCTCCTCCTCCTCTTCTTCATCCTCATCATCCTCCTCATCAGACAGTTCAGACTCTGAAGCAGAAAAAGAAAAGGCGTAAGTGCCCAATAATAAAGTTTTTTTTCACTCATTTAAAAGAGATCTTCATATTAATTGTTGTTTTTACAGGGGTGTTAAAGCAAGCACAAATAAAAATGCTGGAAAGACAGCAAAAGGAAGAGCTTCTTCATCGTCATCCTCATCTGAAAGTGAGAAAGAAAAGAAAACAAAAAGGTAAGATATTTGGCTATTTTCATGTCATTTAAGTCATCGGCTGTTTCTCAATATGCATTCTTGTCTATACTTGCAATCTTGTGTTCTCGTAAACATCATCAACTGTTGCTGAAATACTCCAATTCAAAGTTCACACCTTACCAAAAAAACAGCAT
Associated Phenotype:
Not determined