ZMP
necab2
Ensembl ID:
ZFIN ID:
Description:
N-terminal EF-hand calcium-binding protein 2 [Source:RefSeq peptide;Acc:NP_001025366]
Human Orthologue:
NECAB2
Human Description:
N-terminal EF-hand calcium binding protein 2 [Source:HGNC Symbol;Acc:23746]
Mouse Orthologue:
Necab2
Mouse Description:
N-terminal EF-hand calcium binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:2152211]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13964 | Nonsense | Available for shipment | Available now |
sa36646 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13964
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 |
---|---|---|---|---|---|
ENSDART00000100853 | Nonsense | 183 | 269 | 7 | 9 |
ENSDART00000140161 | Nonsense | 251 | 428 | 7 | 13 |
The following transcripts of ENSDARG00000056745 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21350599)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21580822 |
GRCz11 | 18 | 21569888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTATGACCTAGATCTTACCCCAGTAAGACCAGCCCACGCGTCCCAGAT[C/T]GACGCTATGAGGCACCGGTGCCAGATTATCCTCCCAACAACAGAGTCAGT
Long Flanking Sequence:
TAAGAGCATGTCTATTACCAGAAAAACTAAATTAAAATTATATTTTAATTGAACACATCACATCACATACAGTAAGCTACGCCTACAGAACAGTCTGTTTAGCATTGTGAAAAGGCAAAGCTGAATATCTGTGGTTAAAGTGCCACCCAGCGGTCAAATGCTGCTGGCGCATCAAGTACCGCCGTCGCCGCGGCATGAATGGCGGCACAAGGAACACATTGAAGTAGTAACATCTGTACATCTTGCACCTTATTGCATCGGGTGTATGATAGGGCTCATTGACTTCCATAGTATTTTTGCTTCTACATGTCAATGGTTGCTTTCCCCCAAAAATTTTTAATAAAATAAAAAAAAATCATAAATGTTTTATAACCACTTGAGTGTGAGTAAATGGTGAGGGAAAATTTGAAATATTCTTTAACCATCTGTATTCCTTGTCCTTGTTTTCCCTGTTATGACCTAGATCTTACCCCAGTAAGACCAGCCCACGCGTCCCAGAT[C/T]GACGCTATGAGGCACCGGTGCCAGATTATCCTCCCAACAACAGAGTCAGTGCAAAGGAGAGCATGAGGAACATCAACACAGGTGCAGGTGAGGGGATTACATGTCTCCAAACACCTCCTTTTGAAAACAAAACACACTATTAGTTGTTTACAAAAGGCATAATTTAGGTTTATTTTCTTACTTGGATTTTTAGTCTTGTTTCTAGTCTAAAAATTCAAAAATTCTTAAATTAAGAAACATTTTCTAGACAAGCAAAAGTTATTATCTTGTTTTAAGAAATATTATGTCAACATTAAGTGAGTTTTTTCCTAAAACACATAAAATAATCTGCCAGTGGAGCAAGCAAAATAAACTTATGTCAAAAGAAAAAACAAGATCATTTTGCTTGTTTTTAATTCTAGAAAATGCTTCTTGACTGAAAGGCATTTTTGCAGTGCAGTTCCAAAAATAATGCATACGGTGTGAGTTTTTAAGCATCACATAATACACACCAGACTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36646
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100853 | Nonsense | 266 | 269 | 9 | 9 |
ENSDART00000140161 | None | None | 428 | None | 13 |
The following transcripts of ENSDARG00000056745 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21371707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21601930 |
GRCz11 | 18 | 21590996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACACTGATGGCACAACTAGCGCAGTAAGTACTAAAGCACGTCTTATATA[C/G]CAAAGAGCATGACAAAAAAAATACACCAAATCGTAAAAGACAATGCATGC
Long Flanking Sequence:
AGAGTTATATTTTTAACATCAGAAGTTGTTATAGTGTAGCTTTAATCAAACTGAAAGCACACAGTAAATAAGCACCCGTGAATAAGAAGATAAGGGCTATTTCTGATCCCATACACACAGTTTATGTGAGTGATTTAAATACAAATATGATAAATAATTGACATTATTGTTACACATGCATTATTGATCCATGCTAAATGACGGTCATTTTACATACTTTTAAAAATAAAAACTAAGCTCGTATGAACTTGTTCAAATGATTTTTAATGACTACTTAATACAAACACATATATTATATTTGTAATCTCAGTCTTTCTTGTTAAAGTCAGGTACACATGTTTTGTGATTGATCATCAAGGGGCAGTTCAGGGGGGCAGTGAATTCACTAGTGGCTTTTCTGTTCTGGTTTTGTTGCAGACAGTTTGGTTTGACCTACATCAGCGACTAACAGACACTGATGGCACAACTAGCGCAGTAAGTACTAAAGCACGTCTTATATA[C/G]CAAAGAGCATGACAAAAAAAATACACCAAATCGTAAAAGACAATGCATGCCCAATTTCACCTGTTCCCTCCTTGTAAAAACACCAAATTGATAAATAAAGCCCAGTCAAGTGCAGCTTAACTCCTCACAGGTTTCCCCGTGCTGTTCCACACACCTGCAGCAGATCTGCCACCTGTTCCTCAGGATTTACTCACATTTCTTTTTTTCCATATATGAAAGCCCCTGCTCAGTGTGTTCAATAACAGCCTGCTCCGAGAGTCATTTGTGCGTCTGAAAGATAAGAGGCAGTATCACACTACACCTCGCCTAGCCACAAATCAGTCTCGCTCTGTGATACACACAGCAGTGCATGATGGGAACACAGAAAATCATAGCTGTTTTTGTTAAGTGGAAGTGTAGAAGTGCTGAGATTTAATCTCTCGTAGAACTGTGAGGTTTAAAAGTTTTCCATCTAATAAAGCAAGGATTGCTGGGTTTAAAAGAAATGGCTGGAATAGTGC
Associated Phenotype:
Not determined