ZMP
hmmr
Ensembl ID:
ZFIN ID:
Description:
hyaluronan mediated motility receptor [Source:RefSeq peptide;Acc:NP_955874]
Human Orthologue:
HMMR
Human Description:
hyaluronan-mediated motility receptor (RHAMM) [Source:HGNC Symbol;Acc:5012]
Mouse Orthologue:
Hmmr
Mouse Description:
hyaluronan mediated motility receptor (RHAMM) Gene [Source:MGI Symbol;Acc:MGI:104667]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12528 | Essential Splice Site | Available for shipment | Available now |
sa13903 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12528
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 |
---|---|---|---|---|---|
ENSDART00000031785 | Essential Splice Site | 99 | 902 | 4 | 23 |
ENSDART00000105902 | Essential Splice Site | 100 | 904 | 4 | 20 |
ENSDART00000121921 | Essential Splice Site | 99 | 349 | 4 | 12 |
ENSDART00000125362 | Essential Splice Site | 99 | 903 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 29567604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 28241524 |
GRCz11 | 14 | 28547482 |
KASP Assay ID:
2260-7623.1 (used for ordering genotyping assays)
KASP Sequence:
GAGTAGTTTCACTCTTGAAATGAAACATCAGAGACTACTRGAGAAAGAGG[T/C]ACATCTGTTTGYACAAAACATTTTAAATRTTTCTTGGATGACCATTTATT
Long Flanking Sequence:
TATATAAAGTTATAAACAAACATCCTCTGGGAGATGAAATATAAACAAATTTTAAAAAGTTAAAGTTAAAAAATAAAAGAATGTAACAAGTTTATAATAAAAGATTAAAGAAAAGAAAAGTTACTCTAAGTAGTCAATATTTCCTCTCACCAGTTATTTACTGTGTATTAGATACCAACTGAGGGTAAGCCTTTGATATAGTCTAAAACAGGATTTAAAGTCATGTATGGTGAACTATTATTGTTATTTGAATTCTTAGGAAAAACTATGAATAAACTGAATAAAAAGTTTAATTTTAGTCTTTTTATTTTCAGAATTCTAAATGTCGAAGAACAGATGTCATTTCTTTCACATTTTTTCTTTTTATATGTTGACCACACTGTTTTAAAAATGTGCTCATATTGTTTTTTCTCCATTTTAGGCTGATGCATTAAGCTCCAAAAAAGACAAGAGTAGTTTCACTCTTGAAATGAAACATCAGAGACTACTAGAGAAAGAGG[T/C]ACATCTGTTTGCACAAAACATTTTAAATATTTCTTGGATGACCATTTATTGCTTTGAGGCCTGATCAGTTTATTTGCCCCTTTTCTTTCCCTAATTTCAACCATCATTGCTAATGCTTGGAGTATAGATCCGTTCCTTGGTGCAGCAGAGAGGAGAGCAGGACCGCAGGCTGCTGGCCCTGGAGGAAGAACTGAAGAAACTGGAGTCTAAATTGCTTGTGGCAGTCAGAGAGAAGACTGGCCTCGCAGCGAATGTAATATCTCTCGAGAGGCAGCTAGCAGAGTTAAAGAAAGCTAATGAATTCCTGAAGACCAAGGTGACTAGTCTTTCTGTACCTGTGTGCTTTGGGATCTGTTTTGTTTTGTAGACCCCTTCAGGTAAAGAGGAATGTCTTGGATTTTCACAGGTCTCTGCAGATATCACCAAGAAAAAGATCAACGCTCTTTCCATGGAGCTCATTGAAGCTAAAAATAAACTGGATGCCAAAGACAAGGCGAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13903
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 |
---|---|---|---|---|---|
ENSDART00000031785 | Nonsense | 512 | 902 | 13 | 23 |
ENSDART00000105902 | Nonsense | 513 | 904 | 13 | 20 |
ENSDART00000121921 | None | None | 349 | None | 12 |
ENSDART00000125362 | Nonsense | 512 | 903 | 13 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 29575159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 28249079 |
GRCz11 | 14 | 28555037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGGCGAGGAGTTRGAGGAYGCGCTTGAGGAGCTGGTGGAGCTGGAGAAG[C/T]AGGAGCARTGCAGTGRAGAGGCCATCCAGCAGCTCACACTGAACAACCAG
Long Flanking Sequence:
ATACACAAGCCATTTGAGATTAGTTTTTATGTATTTGTTGTTGTTGTTTCTGACCTTTTCTGTGGCTGACTTTTAGAAACTGGAACCTATTTCATTAGCTTGACTAAGTGTCTGTGTCTTTGGACTCAAATGGGAAAACAGTTTTGCTAGAATGTCATTGTGATTTGTTGTGCTACTTTTAGAGGAAAAAATCAATAGTGAATATAAGTGTAATGTGATTTATACCAGTTTGAGTGGGACAATTAAGTGAAGAGTGCATCTTAATAGACTTTAAGCAGGTTGTACTGCATCGTGTCTGAATCAGGAAGTCAAAGTCTCCCTGATCGACTTTGTGGATTAGGCTAATGTCTCTTAAGCTCCTCTAATGTGTGTTGCTGTAGACTCACAGCGGCTCCCTGGCTAGCTTGCTTGAGCGCCTGAGAGATGACACCGAGGCGGAGAGGAGACAGCTTGGCGAGGAGTTAGAGGACGCGCTTGAGGAGCTGGTGGAGCTGGAGAAG[C/T]AGGAGCAGTGCAGTGAAGAGGCCATCCAGCAGCTCACACTGAACAACCAGACACTGGAACAAGAGCTGAAGAAATCCTGTGCGGAGTTGCAAAAGTGAGCACCAATGATGACTTGTAGTTAAGCTGAGATGGATCACATTTTGTTTGGTAAAATAGTAAGCAGTTTTTGTTATTTCTTATGGCAGGACTTGTGCTGAAATGCAAGCTTTAGAAGAAGCTCACGTGAGGGCGATCAAAAAGTTAGAAGAGGATCACACCAGTTGTCTCGCAAAGCTGGGAGATGTAACAACTGACTTTGAGAGGTATTACTTAAAACACCTATTTGTTTAAACAAAGCCCAAAGAATGCTTCCATACAAAGCATATGCAAACAGTTAAATGTACAACCTTTCAATGTATACTGTACGTCAGTTGTCTGGTATGTATCCACAAATGTTTCATTGCACATGCAGTATGACAACTCTCAATATATGCTGGCCTATAGGATTCCTCCTGTGCACC
Associated Phenotype:
Not determined