ZMP
si:ch211-134m17.7
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to vertebrate multimerin family [Source:UniProtKB/TrEMBL;Acc:B8A4A4]
Human Orthologues:
MMRN1, MMRN2
Human Descriptions:
multimerin 1 [Source:HGNC Symbol;Acc:7178]
multimerin 2 [Source:HGNC Symbol;Acc:19888]
multimerin 2 [Source:HGNC Symbol;Acc:19888]
Mouse Orthologues:
Mmrn1, Mmrn2
Mouse Descriptions:
multimerin 1 Gene [Source:MGI Symbol;Acc:MGI:1918195]
multimerin 2 Gene [Source:MGI Symbol;Acc:MGI:2385618]
multimerin 2 Gene [Source:MGI Symbol;Acc:MGI:2385618]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22282 | Nonsense | Available for shipment | Available now |
sa22281 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22282
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114773 | Nonsense | 287 | 1093 | 5 | 8 |
ENSDART00000136808 | Nonsense | 281 | 544 | 5 | 7 |
The following transcripts of ENSDARG00000076135 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 22768157)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22497495 |
GRCz11 | 13 | 22627945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAGGTCTAATGTATGAAGCTCAGCAACCTGATGTGGAGAATCAAACT[G/T]GACCGTCCATAGAGGATTATGAGCATATCCCTCCTGCTGGTCAAGAAAAC
Long Flanking Sequence:
GCGAGCCCACACAGGGCGTGAACGCGTGTGACCGTGCTTCAGTCCGAGCATGGACAAAACAAAAATACACACATGCACTGGAGCACGCTAGAATAACAGCGTTTCAGACGAGGTCGTCAATTCCACAGCTCTAAAAATAATCCTTTGAGCTGGTTGTTGGGACACAAACAAAGGCTTTGGACGCAAACTTGGAAATTCCCATGCTGCTGATTCATCTGATACTAAGCACTCTTATTAATGACCTTCCTGAGATTCAAACCAACAGTTCAAAGTGCACAGGTCATAATCTGCCTGTGAAAAACACGAGAACAAGAATTGATGGAAAAGGACCAACTTTTATTAAATGCCAAAGAAAAGGTGTAACATTTGGTACAACTTGTTTCTCTTCTCTCTCCTAAGGATTTAACAATCTAACTCCGGAAAACAGAGAGCAGAATGATTACCAAACGTTTGGAGGTCTAATGTATGAAGCTCAGCAACCTGATGTGGAGAATCAAACT[G/T]GACCGTCCATAGAGGATTATGAGCATATCCCTCCTGCTGGTCAAGAAAACCATAACAAACATCACTTTGAGAGGAGAGGTATGTTATGACTACAAGTAAAATACCTTGTCAACTTCCATAAACCATGACGATTTTCTAAAATCATTTGATTCAATAGTTTTGAGAGTACTCCATAAAACCTAAGGTCTTTCACCTAACAATAAAATCTCCCAGAAACCACTTATGGAGGGCTTCGGCCAACTCTAAAGGGCTTTCCTTGCCACTAATGCTTTGATAACACACCTGTCTCTTTTCATTACAAATATGGCTGCTACTCTGCTTATTTTGCAATGCGGATGTACGCTCTTTTCTGCACTTTGTGATTAATTTAAATATGGGTAAACAACTAGGAATATAAAATGGAGGGAACCATAAACAACTAAATTAAAACTAAATTAAAACTTTAAACATTTAAATTAGGGTGACTTGGTTGTGCAGTAGGTAGCACGAACACCTCACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22281
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114773 | Nonsense | 609 | 1093 | 7 | 8 |
ENSDART00000136808 | None | None | 544 | None | 7 |
The following transcripts of ENSDARG00000076135 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 22762208)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22491546 |
GRCz11 | 13 | 22621996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTGCAGGATGTGGAGACTGATGTCGACAACATTTATATCGATTTTTAC[A/T]AAAATATAAGTTCAGCAAGTGGAGAATGTGACTGCATTGCTCTTGGAGCA
Long Flanking Sequence:
TTTTATGTGCACGGGAAACAACTAAACTAAAAGTGTGTTTCTGGCTCTAGGTCAATCTCCAATCGCTCAACACATCCATGTCTGAAGTGAGGCAGGAGCAAGAGAGGCTGGACGAGGAGCTTCAGAAGATTTGGCCTGAAAAGAGGACAGATCCCACTGAGAGCCAGAGTCATGTAAGCACTGCTGTCTGGGAGGCCATTACACGTCTAGACAACAAAGTTGTCAACAACACAGTGAGACTTAGTGCCTTGATTGAAGAACAAGAACAAGTGACCGAAAACATCAGGGGCCTTCATAATGGTTGGAAAGATCTGAATGATAAAATAGTCCAGACTGGCCGTAACAGTCAGGTTCAGTTTATGGAGACCGGTTTGGAGGTGGAGGCAGCCAAGGTCAGAGTCCTTGATCGTATTGATGAGCTGAGCAGCAATATTAGTGTTATCCAGAGTGCCCTGCAGGATGTGGAGACTGATGTCGACAACATTTATATCGATTTTTAC[A/T]AAAATATAAGTTCAGCAAGTGGAGAATGTGACTGCATTGCTCTTGGAGCAACTGTGACCCATTTGGAACAAACTGTAGCTGATGTGATGAAGACAGTAAATGAAAATATTTTAGCACAGGAAATGATGGCCAATCGACACAATAGGGCATGGGTACCATCTGTGGAAGATCTCAAATTAGGCCTACTGAATGTGCAAAATTCCCTTGCTTTTCAGCAGGAAAAGAGCAGAACGTTACAACACAATGTGACCCAGGCACTTGCCTCTCTCCTGGGCAGCCAGCAGGACATTGAAATGCTCCAGAAGCAGGACAGGGCCAAGGTTGAGAAGATCAAGCAGCTAGAGGGCACTTTCAACACCTTGCTTCAGGATGCCACTCGTCACTCAGATGTACTGGAAATTTTGCTTGGGGAAGAGGTGCTGGAGTTCACAAAGTGGTCTCAACAGGACAAGAGACGTTTCTCAATACCGCAGCTGGATGAAAGAATGAAAGACATGCAA
Associated Phenotype:
Not determined